Signaling by the B Cell Receptor (BCR) (Homo sapiens)

From WikiPathways

Revision as of 09:22, 11 July 2016 by ReactomeTeam (Talk | contribs)
Jump to: navigation, search
3, 10, 11, 22, 34...32, 119, 131, 13527, 48, 89, 103, 112...23, 63, 971, 13, 3319, 24, 40, 94, 114...16, 39, 57, 67, 95...2, 4, 31, 45, 47...9, 26, 66, 145, 1517, 56, 140, 14420, 30, 76, 116, 12033, 46, 59, 126, 1461, 46, 5911, 77, 7937, 42, 70, 74, 81...11, 77, 798, 23, 63, 73, 9719, 24, 40, 94, 114...6, 36, 86, 98, 111...70, 124, 139, 1523, 22, 34, 42, 70...49, 65, 8551, 129, 130, 13725, 50, 88, 102, 1226, 98, 111, 11521, 60, 92, 116, 1214, 17, 18, 28, 29, 82...10, 12, 38, 108, 124...35, 45, 68, 80, 90...107105, 113, 1541plasma membranenucleoplasmendoplasmic reticulum lumencytosolIg kappa chain V-I region CAR CHUK PSMD12 Ig lambda chain V-IV region Hil IGLC2 Ig heavy chain V-III region HIL Ig heavy chain V-II region WAH Ig heavy chain V-I region EU Ig heavy chain V-II region SESS Ig lambda chain V-V region DEL CBL Ig lambda chain V-II region MGC CALM1 IGKC Ig kappa chain V-III region VH Ig kappa chain V-III region WOL Ig lambda chain V-IV region Bau PSMB2 Ig lambda chain V-II region BOH Ig heavy chain V-III region TRO Ig kappa chain V-I region Walker Ig lambda chain V-I region NIG-64 Ig heavy chain V-I region HG3 p-6Y-CD19 Ig lambda chain V-IV region MOL PSMB5 STIM1 p-4Y-PIK3AP1 Ig heavy chain V-III region NIE Ig lambda chain V-I region EPS Ig heavy chain V-II region WAH Ig kappa chain V-I region Wes Ig kappa chain V-I region DEE Ig kappa chain V-III region HIC Ig heavy chain V-III region TIL Ig heavy chain V-III region GAL Ig kappa chain V-I region Scw Ig heavy chain V-III region GA Ig kappa chain V-I region Gal PSMD7 BLK-like proteinsIg kappa chain V-IV region Len Ig heavy chain V-I region WOL NFKBIA Ig kappa chain V-II region RPMI 6410 Ig kappa chain V-I region WEA PRKCBUBA52(1-76) p-Y196,Y207-CD79B Ig kappa chain V-I region Ni Ig lambda chain V-II region TOG CARMA1:BCL10:MALT1:TAK1:IKKIg heavy chain V-III region LAY Ig lambda chain V-II region NEI Ig kappa chain V-I region BAN Ig heavy chain V-III region WAS Ig heavy chain V-III region WEA Ig heavy chain V-III region POM Ig lambda chain V-II region TOG Ig heavy chain V-III region JON ATPIg heavy chain V-III region ZAP Ig heavy chain V-III region GAL ATPIKBKG Ig kappa chain V-III region B6 Ig heavy chain V-II region NEWM Ig heavy chain V-III region BRO CD79A Ig lambda chain V-I region WAH Ig heavy chain V-III region POM CBLB Ig lambda chain V-II region MGC Ig kappa chain V-III region SIE Ig kappa chain V-II region FR Ig lambda chain V-IV region Bau RPS27A(1-76) Ig heavy chain V-III region TRO p-S559,S644,S652-CARD11 Ig heavy chain V-III region TIL Ig lambda chain V-IV region Kern Ig lambda chain V-VII region MOT Ig heavy chain V-III region KOL Ig lambda chain V-III region LOI Ig kappa chain V-II region Cum Ig kappa chain V-I region Ni Ig kappa chain V-III region CLL Ig lambda chain V-VII region MOT Ig heavy chain V-III region BUR NFKB1(1-433) IGKV4-1(21-?) Ig kappa chain V-I region Mev Ig kappa chain V-I region Rei Ig kappa chain V-IV region Len Ig lambda chain V-II region NIG-58 Ig heavy chain V-III region KOL Ig heavy chain V-I region ND Ig kappa chain V-III region SIE IGLV(23-?) IGLC6 IGHD p-BCL10 PIK3CD Ig heavy chain V-I region ND p-S157,S161-NFKBIE Ig lambda chain V-IV region MOL Ig kappa chain V-III region VH Ig lambda chain V-II region BO GRB2-1 Ig kappa chain V-I region Gal Ig heavy chain V-III region GAL Ig lambda chain V-II region MGC p-6Y-SYK Ig heavy chain V-III region BRO STIM1:TRPC1Ig lambda chain V-I region NEWM Ig kappa chain V-II region MIL Ig heavy chain V-II region ARH-77 Ig heavy chain V-I region WOL Ig heavy chain V-III region BUR Ig kappa chain V-III region Ti Ig kappa chain V-I region Kue Ig kappa chain V-III region CLL Ig heavy chain V-I region EU Ig kappa chain V-I region Bi Ig heavy chain V-III region GA Ig kappa chain V-III region POM HRAS Ig kappa chain V-III region B6 Ig kappa chain V-I region Ka Ig heavy chain V-I region EU p-BCL10 Ig kappa chain V-IV region STH Ig kappa chain V-I region Ka Ig lambda chain V-II region BOH Ig kappa chain V-I region Gal Ig lambda chain V-I region NEWM Ig kappa chain V-IV region B17 Ig kappa chain V-II region RPMI 6410 Ig heavy chain V-II region NEWM Ig kappa chain V-III region B6 Ig kappa chain V-I region Lay IGKC p-6Y-SYK Ig kappa chain V-IV region Len Ig kappa chain V-III region B6 Ig lambda chain V-II region MGC Ig lambda chain V-IV region Bau Ig heavy chain V-I region WOL Ig heavy chain V-III region TUR Ig lambda chain V-I region VOR Active IKK complexIg kappa chain V-II region TEW Ig kappa chain V-III region CLL p-Y188,Y199-CD79A Ig kappa chain V-I region Bi IGLC7 Ig kappa chain V-II region RPMI 6410 CD79B CUL1 Ig kappa chain V-II region RPMI 6410 Ig heavy chain V-III region BRO Ig kappa chain V-II region MIL p-Y188,Y199-CD79A Ig kappa chain V-I region WAT Ig lambda chain V-II region MGC Ig kappa chain V-I region WEA Ig heavy chain V-I region Mot IGLC6 Ig kappa chain V-I region Walker CARD11 p-Y762,807,822-CD22 Ig lambda chain V-II region NIG-84 Ig heavy chain V-II region ARH-77 p-Y196,Y207-CD79B Ig kappa chain V-IV region Len Ig kappa chain V-II region FR Ig kappa chain V-III region VH IGHV(1-?) Ig heavy chain V-II region ARH-77 Ig heavy chain V-III region NIE Ig lambda chain V-VI region AR Ig lambda chain V-I region EPS p-S157,S161-Ub-NFKBIE Ig lambda chain V-VI region AR Ig lambda chain V-IV region Kern Ig heavy chain V-III region TEI Ig lambda chain V-II region NIG-84 CD19:VAV1Ig lambda chain V-VI region NIG-48 Ig heavy chain V-III region TUR Ig kappa chain V-I region WAT IGKV1-5(23-?) Ig kappa chain V-III region GOL Ig heavy chain V-III region HIL p-6Y-SYK Ig lambda chain V-IV region Bau Ig lambda chain V-II region TRO Ig heavy chain V-I region SIE IGHV7-81(1-?) IGLC3 PSMD11 NRAS IGHV7-81(1-?) Ig lambda chain V-I region MEM Ig kappa chain V-I region WAT Ig lambda chain V-II region TRO Ig heavy chain V-II region DAW Ig lambda chain V-I region NIG-64 Ig kappa chain V-I region Roy IGLV(23-?) Ig lambda chain V-III region LOI Ig lambda chain V region 4A Ig lambda chain V-IV region MOL Ig lambda chain V-I region NEW Ig kappa chain V-IV region STH Ig kappa chain V-I region EU Ig kappa chain V-I region Walker p-T184-RASGRP1 CBL Ig kappa chain V-I region Wes Ig kappa chain V-I region Hau Antigen:p-BCR:p-SYK:p-BLNKIg lambda chain V-VI region AR Ig kappa chain V-II region GM607 Ig lambda chain V-VI region EB4 p-T187-MAP3K7 Ig kappa chain V-I region AG p-12S-NFATC1 Ig kappa chain V-I region BAN IGLC1 Ig kappa chain V-I region Scw Ig lambda chain V-II region BO IGLC1 Ig kappa chain V-II region MIL IGHD Ig lambda chain V-II region BOH Ig kappa chain V-IV region JI Ig kappa chain V-II region FR Ig kappa chain V region EV15 IGLC7 Ig kappa chain V-II region FR Ig kappa chain V-I region Kue DAG NAc-CD22homo-oligomerFKBP1A:TacrolimusIGHD Ig kappa chain V-II region FR Ig heavy chain V-I region ND IGHM Ig heavy chain V-I region SIE Ig lambda chain V-II region NIG-84 Ig kappa chain V-III region IARC/BL41 Ig heavy chain V-III region TEI Ig lambda chain V-VI region AR Ig kappa chain V-IV region STH Ig heavy chain V-III region KOL Ig kappa chain V-III region SIE IGKC p-Y239,Y240,Y317-SHC1-2 Ig kappa chain V-III region VH CD22:Antigen:p-BCRIg lambda chain V-II region TRO Ig lambda chain V region 4A Ig kappa chain V-I region Roy DephosphorylatedNFATC1,2,3Ig kappa chain V-II region RPMI 6410 IGKV1-5(23-?) IGKVA18(21-?) Ig lambda chain V-VII region MOT ATPIg heavy chain V-III region HIL Ig lambda chain V region 4A Ig heavy chain V-II region WAH PPP3CB Ig lambda chain V-III region LOI Ig kappa chain V-I region HK101 PPP3R1 Ig lambda chain V-I region NEWM Ig lambda chain V-VI region SUT Ig lambda chain V-I region HA Ig heavy chain V-III region JON Ig heavy chain V-I region WOL REL RELA Ig lambda chain V-VI region NIG-48 Ig lambda chain V-II region BOH Ig lambda chain V-I region WAH Ig heavy chain V-I region WOL Ig heavy chain V-III region WAS IgH heavy chain V-III region VH26 precursor Ig heavy chain V-III region BUT PIK3CD Ig heavy chain V-III region LAY RASGRP1 Ig heavy chain V-III region TUR IGKV1-5(23-?) Ig lambda chain V-II region BOH Ig heavy chain V-III region WEA PLCG1 Ig kappa chain V-III region VG Ig heavy chain V-III region ZAP Ig lambda chain V-II region TRO Ig kappa chain V region EV15 Zn2+ Ig heavy chain V-I region EU Ig lambda chain V-VI region NIG-48 ADPIg kappa chain V-III region HAH Ig kappa chain V-III region GOL Ig heavy chain V-III region LAY Ig kappa chain V-I region Rei Ig kappa chain V-III region NG9 Ig heavy chain V-II region SESS Ig kappa chain V-I region Scw p-Y771,Y783-PLCG1 PI(3,4,5)P3ITPR3 CBLB IGKV1-5(23-?) Ig lambda chain V-III region LOI Ig kappa chain V region EV15 Ig kappa chain V-III region IARC/BL41 Ig kappa chain V-I region Roy Ig kappa chain V-I region Mev Ig lambda chain V-I region BL2 Ig heavy chain V-III region DOB Ig heavy chain V-II region MCE p-Y188,Y199-CD79A p-S157,S161-NFKBIE Ig lambda chain V-IV region Kern Ig kappa chain V-III region HIC Ig heavy chain V-I region EU Ig lambda chain V-II region BUR Ig kappa chain V-I region Gal SHC1-2 IGLV(23-?) SYK NCK1 Ig kappa chain V-I region WAT CALM1IGKV1-5(23-?) PSME3 Ig kappa chain V-II region FR Ig kappa chain V-I region Bi Ig lambda chain V-VII region MOT Ig lambda chain V region 4A Ig kappa chain V-III region CLL UBC(381-456) Ig lambda chain V-II region NEI Ig lambda chain V-IV region MOL Ig kappa chain V-I region EU Ig lambda chain V-IV region X p21 RAS:GDPCARMA1 oligomerIg lambda chain V-II region BUR Ig kappa chain V-III region GOL Ig heavy chain V-II region HE Ig kappa chain V-I region AU Ig lambda chain V-II region BO ITPR1 SHC1 p46,p52BLNK:GRB2:SOS1:CIN85:CBLIg lambda chain V-II region TOG Ig kappa chain V-II region GM607 Ig kappa chain V-III region B6 Ig lambda chain V-I region VOR PLCG2 Ig lambda chain V-I region NIG-64 p-T133-RASGRP3 Ig lambda chain V-II region VIL Ig heavy chain V-III region TEI Antigen:p-BCR:p-SYKCD79A IGHD Ig heavy chain V-II region SESS IGKV1-5(23-?) Ig heavy chain V-III region LAY Ig lambda chain V-I region VOR Ig heavy chain V-II region MCE Ig kappa chain V-I region HK101 IGKV4-1(21-?) SH3KBP1 Ig kappa chain V-II region MIL Ig heavy chain V-I region SIE Ig heavy chain V-I region HG3 MALT1Ig lambda chain V-I region EPS Ig kappa chain V-I region Bi p-Y188,Y199-CD79A Ig lambda chain V-II region BOH NCK1STIM1 Ig kappa chain V-II region GM607 Ig lambda chain V-VI region SUT PIK3R1 UBC(533-608) Ig kappa chain V-I region Hau Ig kappa chain V-II region MIL Ig heavy chain V-III region KOL p-Y196,Y207-CD79B Ig kappa chain V-IV region Len IGKC IGHD Ig lambda chain V-III region SH ADPIg heavy chain V-III region BUT Ig kappa chain V-I region AU Ig lambda chain V-II region BUR Ig kappa chain V-I region CAR Ig kappa chain V-III region GOL Ig heavy chain V-II region OU BLK IGHV7-81(1-?) Ig kappa chain V-III region WOL Ig kappa chain V-I region Ka Ig kappa chain V-I region Bi Ig kappa chain V-III region VH Ig heavy chain V-II region HE Ig kappa chain V-I region Daudi CBLB Ig lambda chain V-VI region EB4 IGLC7 26S proteasomeIg kappa chain V-II region GM607 Ig heavy chain V-I region ND Ig heavy chain V-III region JON Ig lambda chain V-II region MGC CyclophilinA:Cyclosporin AIg kappa chain V-IV region B17 Antigen:p-BCR:SYKPhosphorylatedNFATC1,2,3Ig heavy chain V-III region CAM Ig kappa chain V-II region Cum Ig kappa chain V-I region Bi PSMB6 Ig lambda chain V-I region WAH Ig kappa chain V-I region Daudi IGLC1 RELA REL NAD+ Ig lambda chain V-I region NIG-64 Ig lambda chain V-VI region WLT UBC(457-532) Ig heavy chain V-I region Mot Ig kappa chain V-I region AU Ig lambda chain V-II region TRO PIK3R1 Antigen Ig heavy chain V-III region DOB IP3 receptorhomotetramerIg kappa chain V-I region DEE Ig lambda chain V-I region WAH IGKV4-1(21-?) BLNK (SLP-65)SignalosomeIg kappa chain V-I region Mev PIK3CD:PIK3R1Ig kappa chain V-III region HAH Ig heavy chain V-III region WAS Ig heavy chain V-III region BUR Zn2+ p-Y194,Y195,Y272-SHC1-1(156-583) Ig heavy chain V-III region TUR IGHV(1-?) Ig kappa chain V-I region OU IGHV(1-?) Ig heavy chain V-III region LAY Ig kappa chain V-I region DEE Ig kappa chain V-II region Cum Ig lambda chain V-VI region NIG-48 Ig lambda chain V-I region NEWM Ig lambda chain V-VII region MOT Ig heavy chain V-II region HE Ig lambda chain V-II region NEI Ig lambda chain V-I region HA IGKC Ig kappa chain V-I region Daudi Ig heavy chain V-I region EU Ig kappa chain V-I region Hau Ig lambda chain V-I region MEM PLC gamma1,2Ig heavy chain V-III region BUR Ig kappa chain V-I region Daudi ITPR2 Ig lambda chain V-VI region AR IGLC3 Ig lambda chain V-II region NIG-58 Ig heavy chain V-III region GA CRAC channelIg kappa chain V-III region WOL Ig kappa chain V-II region TEW PSMC5 Ig kappa chain V-I region Rei Ig lambda chain V-VI region SUT IGKV1-5(23-?) IGLC7 Ig kappa chain V-III region WOL MALT1 Ig lambda chain V-I region WAH Ig lambda chain V-I region VOR Ig lambda chain V-IV region X Ig lambda chain V-I region NIG-64 FYNIg lambda chain V-I region VOR Cyclosporin A IGLC2 Ig kappa chain V-I region Roy Ig kappa chain V-II region RPMI 6410 Ig kappa chain V-III region B6 Ig heavy chain V-I region HG3 Ig kappa chain V-IV region JI Ig heavy chain V-III region LAY Ig lambda chain V-III region LOI I(1,4,5)P3 Ig kappa chain V-I region AU Ig lambda chain V-V region DEL Ig kappa chain V-III region GOL RASGRP3 Ig kappa chain V-IV region Len Ig lambda chain V-I region VOR Ca2+Ig lambda chain V-IV region X Ig lambda chain V-V region DEL IGHD Ig heavy chain V-II region WAH Ig kappa chain V-I region Mev IgH heavy chain V-III region VH26 precursor Ig kappa chain V-I region OU Ig lambda chain V-II region MGC Ig lambda chain V-I region EPS Ig kappa chain V-I region Hau Ig kappa chain V-III region VH Ig heavy chain V-III region TIL Ig lambda chain V-II region TOG Ig heavy chain V-II region ARH-77 Ig heavy chain V-II region HE IgH heavy chain V-III region VH26 precursor NF-kappa-Bp50,p65,c-Rel:p-IKBIg lambda chain V-VI region AR Ig lambda chain V-IV region Bau Ig kappa chain V-IV region JI Ig heavy chain V-III region DOB Ig heavy chain V-II region MCE Ig heavy chain V-I region HG3 Ig heavy chain V-I region Mot Antigen Ig lambda chain V-VI region SUT Ig heavy chain V-III region WEA Ig heavy chain V-II region OU Ig lambda chain V-I region EPS Ig kappa chain V-I region WEA Ig heavy chain V-I region SIE Ig lambda chain V-VI region EB4 Ig lambda chain V-VI region EB4 Ig kappa chain V-I region Rei Ig kappa chain V-III region HAH Ig kappa chain V-III region CLL Ig lambda chain V-I region NIG-64 Ig heavy chain V-III region ZAP Ig kappa chain V-III region HIC p-S177,S181-IKBKB Ig kappa chain V-I region WEA Ig heavy chain V-II region MCE Ig heavy chain V-I region EU STIM1:CalciumIg lambda chain V-I region HA Ig kappa chain V-III region HIC Ig kappa chain V region EV15 Ig heavy chain V-III region GAL Ig kappa chain V region EV15 p-S19,S23-NFKBIB ADPIg kappa chain V-III region Ti Ig heavy chain V-II region DAW Ig heavy chain V-II region COR Ig kappa chain V-I region OU Ig lambda chain V-II region NEI Ig heavy chain V-III region POM Ig kappa chain V-I region WEA Ig heavy chain V-II region SESS Ig kappa chain V-I region Ka Calcineurin (CaN)Ig kappa chain V-I region Walker Ig lambda chain V-VI region AR Ig lambda chain V-VI region NIG-48 PSMA1 CALM1 Ig heavy chain V-II region COR p-Y196,Y207-CD79B PIK3AP1Ig kappa chain V-IV region JI Ig lambda chain V-II region BO Ig heavy chain V-III region NIE Ig kappa chain V-III region WOL Ig kappa chain V-IV region B17 Ig lambda chain V-II region NEI IGKVA18(21-?) p-S32,S36-NFKBIA Ig kappa chain V-III region SIE Ig kappa chain V-I region Ni Ig heavy chain V-I region SIE Ig lambda chain V-V region DEL Ig heavy chain V-I region WOL Ig lambda chain V-II region WIN Ig heavy chain V-II region ARH-77 Ig kappa chain V-I region Walker Ig heavy chain V-III region TIL Ig heavy chain V-III region BUT UBC(77-152) p-5Y-BLNK Ig kappa chain V-III region HAH Ig heavy chain V-III region KOL Ig kappa chain V-I region Kue PIK3R1 IGHM Ig lambda chain V-II region BUR DAPP1Ig kappa chain V-I region Kue p-S559,S644,S652-CARD11 Ig heavy chain V-III region CAM IGLC2 Ig kappa chain V-I region Hau TRPC1DAG Ig lambda chain V-VII region MOT Ig kappa chain V-I region BAN Ig heavy chain V-III region DOB Ig lambda chain V-II region BOH NFKBIE PSMC2 Ig heavy chain V-III region GAL Ig lambda chain V-I region NEW IGLC2 CD22 IGKVA18(21-?) IGLC1 Ig lambda chain V-I region WAH Ig lambda chain V-II region TOG Ig lambda chain V-VI region NIG-48 Antigen Ig kappa chain V-III region GOL MALT1 Ig kappa chain V-I region Walker Ig kappa chain V-I region WAT Ig heavy chain V-I region WOL PSMB11 IGHV(1-?) Ig kappa chain V-IV region STH Ig lambda chain V-II region NIG-84 Ig heavy chain V-III region BRO ATPIg lambda chain V-I region EPS Ig heavy chain V-III region CAM MAP3K7Ig heavy chain V-III region HIL Ig heavy chain V-I region SIE SOS1 Ig kappa chain V-I region BAN IGLV(23-?) Ig kappa chain V-I region CAR Ig kappa chain V-I region BAN IGKV4-1(21-?) Ig heavy chain V-III region TEI IGLC3 Ig kappa chain V-I region AU IGLC3 PSMA6 Ig heavy chain V-III region KOL Ig lambda chain V-III region LOI PI(3,4,5)P3 Ig lambda chain V-I region NEW Ig heavy chain V-III region JON Ig lambda chain V-I region NEW Ig kappa chain V-I region Mev Ig heavy chain V-II region SESS Ig heavy chain V-I region ND Ig heavy chain V-III region WEA Ig lambda chain V-II region BUR Ig kappa chain V-II region FR Ig kappa chain V-I region AG Ig kappa chain V-III region HAH Ig heavy chain V-III region GA Ig lambda chain V-II region TRO Ig kappa chain V-I region Daudi Ig heavy chain V-III region TIL UBB(153-228) Ig lambda chain V-II region MGC Ig kappa chain V-III region HIC PSMD3 Ig heavy chain V-I region HG3 Ig lambda chain V-I region NEW Ig kappa chain V-II region Cum Ig kappa chain V-II region GM607 Ig lambda chain V-VI region WLT Ig heavy chain V-III region POM KRAS DAGIg heavy chain V-III region BUT Ig lambda chain V region 4A PTPN6:p-Y762,807,822-CD22:Antigen:p-BCRIg kappa chain V-I region Ni Ig kappa chain V-I region AU Ig kappa chain V-I region AG Ig kappa chain V-I region Gal Ig kappa chain V-II region RPMI 6410 Ig kappa chain V-II region TEW Ig lambda chain V-VII region MOT Ig lambda chain V-II region BO Ig lambda chain V-III region SH Ig kappa chain V-II region GM607 Ig lambda chain V-I region NEW Ig heavy chain V-III region JON NF-kappaB:p-IkB:SCF-betaTrCPIg kappa chain V-II region FR PSMD6 Ig lambda chain V-III region SH Antigen Ig kappa chain V-I region Scw AHCYL1:NAD+:ITPR1:I(1,4,5)P3 tetramerSTIM1 IGLC3 PIK3CD:PIK3R1BTRC Ig lambda chain V-I region EPS Ig heavy chain V-II region COR p-14S-NFATC2 Ig kappa chain V-III region Ti Ig heavy chain V-III region ZAP IGLV(23-?) Ig kappa chain V-I region Wes Ig lambda chain V-IV region MOL Ig lambda chain V-I region VOR IGLC2 Ig kappa chain V-II region GM607 Ig heavy chain V-I region Mot Ig lambda chain V-II region BO AHCYL1 Ig lambda chain V-I region HA Ig heavy chain V-I region SIE Ig kappa chain V-IV region Len Ig heavy chain V-III region GA Ig kappa chain V-I region Rei Ig kappa chain V-IV region Len Ig kappa chain V-II region FR Ig lambda chain V-II region VIL Ig kappa chain V-II region MIL Ig kappa chain V-I region HK101 Ig heavy chain V-II region NEWM FBXW11 Ig kappa chain V-I region Roy Ig lambda chain V-I region MEM Antigen:p-BCRIg heavy chain V-III region TRO Ig kappa chain V-IV region Len Ig lambda chain V-I region NEWM Ig kappa chain V-I region Mev Ig kappa chain V-III region NG9 p-BCL10 PIK3CD Ig lambda chain V-IV region X Ig kappa chain V-III region CLL Ig lambda chain V-III region SH IGKC Ig kappa chain V-I region Bi Ig heavy chain V-I region HG3 IGLC1 Fe3+ ATPIg lambda chain V-VI region WLT IGHD PPP3CB Ig heavy chain V-II region OU Ig lambda chain V-I region HA RELA Ig kappa chain V-III region HIC Ig heavy chain V-III region DOB IGKC Ig heavy chain V-III region WEA Ig heavy chain V-II region HE ITPR1 Ig lambda chain V-II region TOG Ig lambda chain V-II region VIL p-5Y-BLNK Ig lambda chain V region 4A Antigen Ig heavy chain V-III region WAS Ig kappa chain V-III region SIE Ig lambda chain V-II region TRO Ig lambda chain V-IV region Bau CD19 IGHV7-81(1-?) CARMA1:MALT1:BCL10BLKIg lambda chain V-I region NEWM Ig kappa chain V-I region Wes Ig heavy chain V-II region OU Ig heavy chain V-III region HIL Ig lambda chain V-I region NEW Ig heavy chain V-III region POM Ig lambda chain V-VI region WLT Ig lambda chain V-VI region WLT Ig lambda chain V-VI region EB4 Ig heavy chain V-II region OU Ig heavy chain V-I region Mot Ig lambda chain V-IV region Kern IGKVA18(21-?) IGKV4-1(21-?) Ig lambda chain V-VI region WLT p-14S-NFATC2 Ig heavy chain V-III region JON Ig heavy chain V-III region TRO Ig kappa chain V-III region HIC IGLC3 Ig lambda chain V-IV region Hil Ig kappa chain V-I region Gal SHC1-3 Ig kappa chain V-I region Ni PSMA4 Ig lambda chain V-VI region SUT Ig lambda chain V-IV region Hil Ig lambda chain V-I region BL2 Ig heavy chain V-III region TUR p-S243-NFATC2 SKP1 Ig lambda chain V-II region WIN Ig kappa chain V-I region EU Ig lambda chain V-I region BL2 Ig kappa chain V-I region Mev Ig kappa chain V-II region RPMI 6410 Ig lambda chain V-I region MEM PSME2 Ig heavy chain V-III region DOB Ig heavy chain V-II region SESS Ig heavy chain V-III region CAM Ig kappa chain V-I region Bi GRB2-1 PSMC4 Ig kappa chain V-III region Ti Ig heavy chain V-III region ZAP Ig kappa chain V-I region Roy Ig heavy chain V-III region DOB Ig heavy chain V-III region WAS Ig heavy chain V-II region ARH-77 IGLC1 PSMB1 Ig kappa chain V-I region AU Ig kappa chain V-I region Walker NFKB1(1-433) Ig lambda chain V-VI region AR Ig heavy chain V-I region HG3 UBC(609-684) Ig heavy chain V-III region TUR Ig kappa chain V-I region Kue Ig heavy chain V-III region BUR Ig heavy chain V-II region SESS UBB(77-152) Ig heavy chain V-III region DOB CALM1:4xCa2+Ig kappa chain V-IV region Len Ig kappa chain V-I region EU Ig heavy chain V-II region MCE Ig heavy chain V-III region TIL Orai1 dimerIg lambda chain V-II region NEI Ig kappa chain V-II region TEW p-Y762,807,822-CD22:Antigen:p-BCRp21 RAS:GTPIg kappa chain V-III region SIE Ig lambda chain V-I region NIG-64 Antigen:BCRIg lambda chain V-II region MGC Ca2+ Ig kappa chain V-III region NG9 Ig lambda chain V-VII region MOT Ig lambda chain V-I region NEW Ig kappa chain V-III region IARC/BL41 Ig lambda chain V-III region SH Ig kappa chain V-I region WEA Ig heavy chain V-III region BRO SOS1 Ig lambda chain V-II region BOH Ig lambda chain V-VI region WLT CHUK Ig heavy chain V-II region WAH Ig heavy chain V-II region HE Ig kappa chain V-I region OU Ig heavy chain V-III region TEI Ig lambda chain V-II region WIN Ig heavy chain V-II region OU Ig kappa chain V-III region POM Ig kappa chain V-I region DEE Ig lambda chain V-I region BL2 Ig kappa chain V-I region Kue Ig heavy chain V-I region Mot Ig kappa chain V-I region Wes Ig kappa chain V-III region POM Ig heavy chain V-III region CAM Ig lambda chain V-II region NIG-84 NFKB1(1-433) Ig lambda chain V-IV region X Ig lambda chain V-II region MGC Ig heavy chain V-III region TRO Ig kappa chain V-I region CAR IKBKG Ig lambda chain V-V region DEL p-13S-NFATC3 IGLC7 Ig lambda chain V-II region TOG Ig heavy chain V-III region ZAP Phosphatidylserine Ig kappa chain V-I region Ni PSME4 IGLC7 Ig kappa chain V-III region IARC/BL41 Ig lambda chain V-I region BL2 Ig lambda chain V-II region VIL Ig kappa chain V-I region CAR IGHV7-81(1-?) Ig heavy chain V-II region WAH Ig lambda chain V-IV region Hil Ig kappa chain V-III region POM Ig heavy chain V-II region NEWM Ig heavy chain V-II region SESS Ig lambda chain V-II region NEI Ig kappa chain V-III region WOL Ig lambda chain V-IV region X Ig lambda chain V-III region SH REL Ig heavy chain V-III region DOB Ig heavy chain V-III region BUR Ig lambda chain V-VI region EB4 Ig kappa chain V-III region SIE Ig heavy chain V-III region POM NFKB1(1-433) IGLV(23-?) Ig heavy chain V-I region Mot Ig kappa chain V-I region Bi PSMD13 Ig lambda chain V-II region TOG Ig lambda chain V-II region NIG-84 Ig lambda chain V-IV region Bau Ig lambda chain V-II region BOH Ig heavy chain V-I region ND Ig lambda chain V-VI region SUT Ig kappa chain V-IV region B17 GRB2-1Ig lambda chain V-VI region NIG-48 Ig lambda chain V-I region MEM Ig heavy chain V-III region POM Ig kappa chain V-I region Ka Ig kappa chain V-I region Kue Ig lambda chain V-II region NIG-84 Ig heavy chain V-III region GAL Ig lambda chain V-II region NEI Ig kappa chain V-I region Ni Ig lambda chain V region 4A p-Y139-DAPP1 IGLC6 Ig kappa chain V-I region WEA Ig heavy chain V-I region SIE CHUK Ig lambda chain V region 4A Ig kappa chain V-I region DEE Ig kappa chain V-II region Cum IGLV(23-?) IGKVA18(21-?) Ig lambda chain V-I region BL2 Ig kappa chain V-I region CAR Ig heavy chain V-III region HIL PSMB7 PSMC3 Ig kappa chain V-III region Ti Ig lambda chain V-I region MEM Ig lambda chain V-I region NEW VAV1 IGKVA18(21-?) Ig lambda chain V-VI region EB4 Ig lambda chain V-IV region Hil Ig kappa chain V-I region Lay PSMC1 IGLV(23-?) Ig heavy chain V-III region TEI BCRIg heavy chain V-II region HE Ig lambda chain V-II region VIL Ig lambda chain V-I region HA IGKV1-5(23-?) IGHM IGHV(1-?) Ig kappa chain V region EV15 Ig kappa chain V-I region WEA Ig kappa chain V-III region SIE Ig heavy chain V-II region NEWM Ig kappa chain V-I region Walker Ig kappa chain V-I region Hau Ig kappa chain V-III region HAH Ig kappa chain V-III region Ti p-RASGRP1,3:DAGIg kappa chain V-III region HIC Ig lambda chain V-I region NEW Ig kappa chain V-I region Lay Ig heavy chain V-III region HIL Ig heavy chain V-III region POM Ig kappa chain V-III region CLL Ig lambda chain V-I region WAH IGHM Ig heavy chain V-III region NIE Ig heavy chain V-III region POM Ig kappa chain V-I region Roy Ig kappa chain V-I region BAN Ig heavy chain V-III region TIL IGHV7-81(1-?) Ig heavy chain V-III region TUR Ig lambda chain V-II region WIN PSMD14 Ig kappa chain V-I region EU Ig heavy chain V-III region WEA Ig heavy chain V-III region NIE Ig kappa chain V-I region Roy IgH heavy chain V-III region VH26 precursor Ig lambda chain V-II region BUR Ig kappa chain V region EV15 Ig kappa chain V-I region EU Ig heavy chain V-III region JON Ig heavy chain V-I region ND Ig heavy chain V-III region CAM IgH heavy chain V-III region VH26 precursor Tacrolimus IGHM IGLC1 Ig heavy chain V-III region WAS Ig lambda chain V-IV region X Ig heavy chain V-III region GAL Ig heavy chain V-III region DOB FKBP1A Ig heavy chain V-III region TEI Ig lambda chain V-II region WIN Ig lambda chain V-I region EPS Ig lambda chain V-II region BO Ig kappa chain V-I region Scw Ig kappa chain V-III region POM Ig kappa chain V-III region SIE ADPATPIg lambda chain V-IV region Hil Ig kappa chain V-I region Rei Ig kappa chain V-I region Daudi Ig heavy chain V-II region NEWM Ig lambda chain V-III region LOI Ig heavy chain V-II region NEWM Ig heavy chain V-I region WOL Ig heavy chain V-II region HE Ig lambda chain V-IV region X Ig lambda chain V-II region NEI Ig heavy chain V-III region CAM Ig lambda chain V-IV region MOL Ig kappa chain V-I region WEA Ig heavy chain V-II region HE Ig kappa chain V-I region Wes BLNK PI(4,5)P2Ig kappa chain V-I region Scw IGHM ITPR2 Ig kappa chain V-I region OU CD79B Ig kappa chain V-III region CLL Ig kappa chain V-III region HAH Ig kappa chain V-I region Mev Ig heavy chain V-III region GA CUL1 Ig lambda chain V-VI region SUT GDP Ig kappa chain V-I region Ka Ig kappa chain V-I region Rei PSMA3 IGLC7 p-Y196,Y207-CD79B Ig lambda chain V-II region NIG-84 Ig kappa chain V-IV region STH Ig kappa chain V-I region Gal PI(4,5)P2Ig kappa chain V-I region Lay Ig kappa chain V-II region Cum Ig lambda chain V-VII region MOT Ig heavy chain V-III region TUR Ig lambda chain V-I region NEWM Ig kappa chain V-I region Ni Ig kappa chain V-I region EU AntigenIg lambda chain V-I region WAH Ig kappa chain V-III region IARC/BL41 p-S257-NFATC1 Ig kappa chain V-I region EU Ig kappa chain V-II region GM607 Ig kappa chain V-IV region STH GRB2-1 Ig kappa chain V-I region Daudi PSMA8 IGKV1-5(23-?) Ig heavy chain V-III region GAL Ig heavy chain V-II region SESS p-Y196,Y207-CD79B SYKIg heavy chain V-II region NEWM Ig lambda chain V-V region DEL Ig kappa chain V-IV region JI Ig kappa chain V-III region POM Ig heavy chain V-II region NEWM Ig lambda chain V-VII region MOT IGLC1 Ig kappa chain V-I region DEE Ig heavy chain V-II region OU IGLC6 IGHD Ig kappa chain V-IV region STH PPP3R1 Ig lambda chain V-I region HA Ig kappa chain V-II region Cum Ig lambda chain V-II region NIG-58 Ca2+RELA Ig heavy chain V-II region COR IGKV4-1(21-?) Ig heavy chain V-II region SESS Ig heavy chain V-III region GAL Ig heavy chain V-I region ND Ig kappa chain V-I region OU UbUb-21,22-p-S32,S36-NFKBIA Ig kappa chain V-I region Wes Ig kappa chain V-I region OU Ig kappa chain V-IV region STH Ig lambda chain V-II region WIN Ig heavy chain V-III region HIL Ig kappa chain V-IV region JI Ig heavy chain V-III region BUT Ig lambda chain V-I region NIG-64 Ig heavy chain V-I region SIE IGLC3 Ig lambda chain V-I region MEM Ig heavy chain V-III region BUR Ig lambda chain V-I region VOR Ig kappa chain V-II region GM607 p-S265-NFATC3 Ig heavy chain V-III region HIL Ig lambda chain V-IV region Bau ITPR1 Ig lambda chain V-II region NIG-84 Calcineurin:Phosphorylated NFATC1,2,3Ig lambda chain V-II region TOG Ig kappa chain V-IV region JI Ig heavy chain V-III region KOL Ig kappa chain V-I region WEA Ig lambda chain V-IV region MOL Ig heavy chain V-III region TEI Ig heavy chain V-III region CAM Ig kappa chain V-III region GOL Ig kappa chain V-II region TEW IGHD Ig lambda chain V-II region VIL PSMB3 IGKVA18(21-?) SH3KBP1 Ig heavy chain V-II region HE Ig kappa chain V-I region AU Ig kappa chain V-I region Rei IGLC6 PSMD1 Ca2+ Ig kappa chain V-I region Lay Ig lambda chain V-VI region WLT Ig heavy chain V-III region BRO Ig heavy chain V-III region TRO Ig heavy chain V-I region HG3 Ig kappa chain V-I region CAR IGHV7-81(1-?) Ig kappa chain V-I region CAR Ig lambda chain V-VI region AR Ig kappa chain V-I region Scw Ig lambda chain V-I region BL2 Ig kappa chain V-I region AG Ig kappa chain V-I region Hau Ig heavy chain V-II region ARH-77 Ig heavy chain V-II region COR PSMB8 Ig kappa chain V-I region Walker Ig kappa chain V-III region IARC/BL41 NAc-CD22IGKV1-5(23-?) IGHV7-81(1-?) Ig kappa chain V-I region DEE Ig lambda chain V-II region BUR Ig lambda chain V-V region DEL Ig heavy chain V-III region LAY Ig heavy chain V-III region JON Ig heavy chain V-I region ND Ig heavy chain V-I region Mot Ig kappa chain V-I region Kue IGHD Ig kappa chain V-III region VG Ig kappa chain V-III region WOL Ig kappa chain V-I region OU PSMA5 Ig kappa chain V-I region CAR Ca2+IGKV4-1(21-?) PIK3R1 p-Y188,Y199-CD79A Ig kappa chain V-II region FR STIM1 DimerIg heavy chain V-III region WEA IGKV4-1(21-?) Ig kappa chain V-III region WOL Ig heavy chain V-III region TUR Ig kappa chain V-I region Ka Ig kappa chain V-III region NG9 Ig heavy chain V-III region WAS Ig kappa chain V-I region Kue Ig heavy chain V-III region BRO Ig kappa chain V-III region B6 IGLC6 Ig heavy chain V-I region EU PTPN6Ig heavy chain V-III region BUT Ig kappa chain V-I region Lay Ig kappa chain V-IV region STH Ig kappa chain V-III region NG9 Ig kappa chain V-I region AG Ig kappa chain V-III region Ti Ig heavy chain V-III region WAS Ig heavy chain V-II region WAH SRMS PSMD4 PRKCB UBC(1-76) SOS1 Ig kappa chain V-III region Ti Ig kappa chain V-I region Kue p-S559,S644,S652-CARD11 Ig lambda chain V-I region NEWM Ig heavy chain V-III region KOL PSMF1 Antigen RELA Ig kappa chain V-III region WOL Ig kappa chain V-I region Rei IGLC7 Ig kappa chain V-III region Ti IGHV(1-?) RASGRP1,3UBC(153-228) Ig kappa chain V-I region BAN Ig kappa chain V-I region HK101 Ig heavy chain V-II region WAH IGKC Ig heavy chain V-II region DAW Ig heavy chain V-III region TRO Ig lambda chain V-IV region MOL Ig kappa chain V-III region VG Ig kappa chain V-I region Gal Ig heavy chain V-III region BRO NF-kappaBp50,p65,c-Rel dimerIg heavy chain V-II region COR Ig heavy chain V-III region TRO IgH heavy chain V-III region VH26 precursor Ig kappa chain V-I region WAT p-Y196,Y207-CD79B SCF-beta-TrCp1,2p-Y188,Y199-CD79A Ig kappa chain V-I region BAN PPIA Ig lambda chain V-IV region MOL VAV1STIM1 Ig lambda chain V-III region LOI BTRC Ig kappa chain V-I region Hau Ig kappa chain V-I region Daudi FBXW11 Ig heavy chain V-II region MCE Ig heavy chain V-II region DAW Ig lambda chain V-I region VOR Ig heavy chain V-III region TRO Ig lambda chain V-I region EPS NFKB1(1-433) Ig kappa chain V-I region AG KRAS Ig kappa chain V-I region Mev Ig kappa chain V-III region GOL IGKVA18(21-?) IGHV7-81(1-?) Ig heavy chain V-II region MCE Ig heavy chain V-III region WEA Ig lambda chain V-IV region X ORAI1 Ig lambda chain V-II region BUR Ig heavy chain V-III region BUR Ig lambda chain V-IV region Bau PSMA2 Ig kappa chain V-I region WAT Ig heavy chain V-II region MCE Ig kappa chain V-I region Wes Ig lambda chain V-IV region Hil Ig heavy chain V-III region BRO IGLV(23-?) Ig kappa chain V-III region IARC/BL41 SH3KBP1 BTKIg kappa chain V-I region HK101 VAV1 Ig kappa chain V-I region HK101 Ig lambda chain V-III region LOI Ig heavy chain V-III region WEA Ig heavy chain V-II region DAW p-Y762,807,822-CD22 Ig lambda chain V-VI region SUT Ig heavy chain V-II region DAW Ig kappa chain V-IV region STH Ig lambda chain V-II region BOH Ig lambda chain V region 4A Ig heavy chain V-II region WAH Ig kappa chain V-III region HAH PhosphatidylserinePIP3 activates AKTsignalingIGKVA18(21-?) Ig kappa chain V-I region DEE Ig kappa chain V-IV region B17 PSMD9 Ig heavy chain V-III region ZAP Ig lambda chain V-I region WAH PSMD8 Ig kappa chain V-II region Cum Ig lambda chain V-I region NEWM ORAI1 Ig heavy chain V-III region TIL Ig kappa chain V-III region IARC/BL41 Ig lambda chain V-II region VIL I(1,4,5)P3 Ig heavy chain V-III region BRO Ig kappa chain V-II region TEW Ig heavy chain V-II region DAW Ig lambda chain V-II region NIG-58 Ig kappa chain V-I region OU IKBKB Ig lambda chain V-IV region X Ig lambda chain V-II region WIN Ig kappa chain V-III region VG Ig heavy chain V-III region GA Ig lambda chain V-IV region MOL Ig kappa chain V-III region VG REL Ig heavy chain V-III region GA IgH heavy chain V-III region VH26 precursor PPP3CA Ig heavy chain V-II region DAW Ig lambda chain V-II region TRO Ig kappa chain V-III region VH Ig lambda chain V-I region MEM Ig kappa chain V-III region POM Ig lambda chain V-II region NEI Ig heavy chain V-III region LAY Ig lambda chain V-II region BO Ig lambda chain V-I region MEM Ig kappa chain V-I region BAN Ig heavy chain V-III region NIE Ig kappa chain V-III region HAH Ig lambda chain V-IV region Kern Ig lambda chain V-II region WIN Ig kappa chain V-I region Mev Ig heavy chain V-III region WAS Ig heavy chain V-I region Mot Ig heavy chain V-II region NEWM REL Ig kappa chain V-I region Lay Ig kappa chain V-I region Ka Ig heavy chain V-II region ARH-77 Ig lambda chain V-I region HA Ig heavy chain V-III region TEI Ig heavy chain V-II region OU IGKC Ig kappa chain V-I region AU Ig lambda chain V-III region SH Ig kappa chain V-I region EU p-CARMA1 OligomerIg lambda chain V-II region WIN Ig heavy chain V-I region ND IGHV(1-?) Ig kappa chain V-III region HIC Ig kappa chain V-I region Hau Ig kappa chain V-I region DEE Ig lambda chain V-VI region NIG-48 Ig kappa chain V-III region CLL Ig kappa chain V-I region HK101 Ig lambda chain V-II region VIL Ig kappa chain V-III region POM Ig heavy chain V-III region TRO Ig heavy chain V-III region BUT Ig kappa chain V-III region VG Ig lambda chain V-II region NIG-58 Ig kappa chain V-III region SIE Ig lambda chain V-II region NIG-58 PSMC6 Ig lambda chain V-II region VIL IGKV4-1(21-?) TRPC1 ITPR3 Activated PKC betaRELA Ig kappa chain V-I region HK101 Ig lambda chain V-II region NIG-58 Ig kappa chain V-II region TEW p-Y223,Y551-BTK NFKBIB Ig heavy chain V-II region WAH Ig lambda chain V-II region TOG Ig kappa chain V-I region WAT Ig heavy chain V-III region BUT Ig kappa chain V-I region AU Ig lambda chain V-IV region Kern Ig kappa chain V-I region WAT Ig lambda chain V-VI region AR Ig lambda chain V-IV region Kern IGHV(1-?) BCAP SignalosomePSMA7 Ig kappa chain V-IV region B17 IGLC6 Ig kappa chain V-II region TEW Ig kappa chain V-I region Wes PSMB10 Ig heavy chain V-III region ZAP Ig heavy chain V-III region BUT Ig kappa chain V-III region Ti Ig heavy chain V-III region JON Ig heavy chain V-III region BUT Ig kappa chain V-III region NG9 Ig lambda chain V-I region BL2 ATPIg lambda chain V-IV region Kern Ig heavy chain V-II region OU Ig kappa chain V-III region POM IGHV(1-?) p-12S-NFATC1 Ig kappa chain V-I region Lay Ig heavy chain V-III region BUR Ig kappa chain V-I region Gal Ig kappa chain V-I region Lay Ca2+ Ig lambda chain V-VI region EB4 Ig kappa chain V-I region Gal IGLC2 GRB2-1 Ig kappa chain V-I region AG Ig lambda chain V-VI region WLT p-Y753,Y759,Y1217-PLCG2 IGKV4-1(21-?) Ig heavy chain V-III region GA Ig kappa chain V-III region POM Ig lambda chain V-IV region Hil CD22Ig lambda chain V-III region SH Ig heavy chain V-III region LAY Ig lambda chain V-VI region SUT Ig lambda chain V-I region NEWM IGHM Ig heavy chain V-III region ZAP Ig kappa chain V-III region VG Ig kappa chain V-II region MIL Ig lambda chain V-I region HA IgH heavy chain V-III region VH26 precursor Ig heavy chain V-III region KOL Ig lambda chain V-II region NIG-58 Ig heavy chain V-I region SIE NRAS ADPIg heavy chain V-I region WOL Ig kappa chain V-III region B6 p-Y188,Y199-CD79A Ig heavy chain V-II region COR Ig heavy chain V-III region NIE Ig lambda chain V-III region LOI Ig lambda chain V-VI region NIG-48 I(1,4,5)P3p-Y188,Y199-CD79A IGLC6 Ig heavy chain V-II region ARH-77 Ig heavy chain V-III region TUR Ig kappa chain V-III region NG9 Ig lambda chain V-I region EPS Ig kappa chain V-III region NG9 Ig heavy chain V-III region CAM Ig kappa chain V-I region HK101 Ig kappa chain V-I region CAR PSME1 Ig lambda chain V-II region BO Ig lambda chain V-II region NIG-84 UBC(229-304) VAV1 Ig lambda chain V-III region SH Ig heavy chain V-III region POM PSMB9 REL Ig lambda chain V-I region VOR Ig kappa chain V-III region IARC/BL41 IGLC3 Ig heavy chain V-III region JON Ig kappa chain V-I region Daudi HRAS ADPNF-kappa-Bp50,p65,c-Rel:IKBIg kappa chain V-II region MIL Ig kappa chain V-I region AG Ig kappa chain V-III region IARC/BL41 Ig heavy chain V-I region EU Ig lambda chain V-IV region Kern Ig kappa chain V-I region Scw Ig kappa chain V-I region EU PPP3CA ADPIg lambda chain V-VI region EB4 Ig heavy chain V-III region GAL IGHV(1-?) IGLC2 Ig heavy chain V-II region OU Ig lambda chain V-I region NIG-64 p-S19,S23-NFKBIB Ig lambda chain V-V region DEL Ig heavy chain V-III region NIE Ig heavy chain V-I region EU Fe3+ Ig kappa chain V-I region Roy Ig heavy chain V-II region COR NF-kappaBp50,p65,c-Rel dimerIGKC Ig kappa chain V-II region MIL Ig lambda chain V-II region BO p-T187-MAP3K7 Ig heavy chain V-III region LAY Ig heavy chain V-III region ZAP Ig kappa chain V-III region WOL p-BCL10PSMD5 IGKVA18(21-?) ITPR2 GTP Ig kappa chain V-III region HIC Ig kappa chain V-III region VH Ca2+ Ig kappa chain V-III region NG9 Ig kappa chain V-II region MIL Ig kappa chain V-II region Cum IGLC1 Ig lambda chain V-II region BUR Ig kappa chain V-I region BAN PIK3CD Ig lambda chain V-IV region Kern Ig heavy chain V-III region WAS IGLC2 Ig kappa chain V-I region Wes Ig lambda chain V-I region HA IGLC7 Ig kappa chain V-IV region B17 Ig heavy chain V-II region MCE Ig heavy chain V-III region TEI Ig heavy chain V-I region HG3 Ig heavy chain V-III region NIE Ig kappa chain V-IV region JI Ig kappa chain V-III region B6 Ig heavy chain V-III region TIL Ig heavy chain V-I region Mot LYNIGLC3 Ig kappa chain V region EV15 Ig lambda chain V-I region WAH Ig kappa chain V-III region HAH UBC(305-380) Ig kappa chain V-IV region JI Ig kappa chain V-III region VG Ig heavy chain V-II region DAW CD19 SignalosomeIg kappa chain V-III region VH Ig kappa chain V-I region DEE Ig lambda chain V-III region SH Ig heavy chain V-III region BUR Ig kappa chain V-I region OU Ig kappa chain V-III region GOL Ig heavy chain V-II region COR p-S559,S644,S652-CARD11 Ig kappa chain V-III region B6 Ig heavy chain V-III region KOL IGHV7-81(1-?) Ig kappa chain V-II region RPMI 6410 IKBKB PTPN6 NFKB1(1-433) Ig lambda chain V-VI region WLT ADPIg lambda chain V-V region DEL p-13S-NFATC3 IGLC3 Ig kappa chain V-I region Ka Ig heavy chain V-II region MCE Ig heavy chain V-III region CAM Ig kappa chain V-I region Lay IGHM Antigen Ig kappa chain V-I region Ni Ig kappa chain V-I region Daudi Ig lambda chain V-II region TRO IKBKG Ig heavy chain V-I region WOL Ig lambda chain V-II region WIN Ig kappa chain V-I region AG IGHM Ig kappa chain V-I region Scw Ig kappa chain V-III region NG9 Ig kappa chain V-I region Ka Ig lambda chain V-I region BL2 Ig kappa chain V-II region RPMI 6410 CBL Antigen Ig lambda chain V-VI region EB4 Ig kappa chain V-III region VG p-S32,S36-NFKBIA Ig kappa chain V-I region AG Ig kappa chain V-IV region B17 Ig kappa chain V-IV region JI Ig lambda chain V-I region NIG-64 Ig kappa chain V-I region Bi Ig heavy chain V-II region DAW IGLC6 Ig kappa chain V-I region Roy Ig lambda chain V-I region MEM IGLC2 Ig kappa chain V-I region Rei ATPIGLC1 Ig heavy chain V-III region HIL IGLV(23-?) ITPR:I(1,4,5)P3tetramerIg kappa chain V-I region Walker Ig lambda chain V-IV region Hil Ig kappa chain V-I region Ni Ig kappa chain V-II region TEW IGLC7 Ig kappa chain V-III region GOL IGLC6 PI(4,5)P2Ig lambda chain V-IV region Hil PSMB4 Ig lambda chain V-IV region Bau Ig heavy chain V-III region TIL Ig kappa chain V-I region Scw PSMD10 Ig lambda chain V-II region BUR Ig lambda chain V-II region NIG-58 Ig heavy chain V-III region GA Ig kappa chain V-III region CLL Ig kappa chain V region EV15 IGHM IKKA:IKBKB:IKBKGIg heavy chain V-I region HG3 Ig heavy chain V-III region WEA Ig lambda chain V-I region BL2 Ig lambda chain V-II region NIG-58 Antigen Ig kappa chain V-III region VH Ig kappa chain V-I region HK101 Ig kappa chain V-IV region B17 Ig kappa chain V-I region Hau Ig heavy chain V-III region NIE Ig lambda chain V-V region DEL Ig lambda chain V-II region VIL IgH heavy chain V-III region VH26 precursor Ig lambda chain V region 4A ITPR3 Ig lambda chain V-VI region SUT Ig lambda chain V-II region TRO Ig heavy chain V-II region COR p-Y196,Y207-CD79B Ig kappa chain V region EV15 Ig kappa chain V-II region GM607 Ig kappa chain V-I region WAT Ig lambda chain V-VI region NIG-48 p-S19,S23-Ub-NFKBIB SKP1 IGLC2 Ig kappa chain V-II region Cum CARMA1:BCL10:MALT1:TAK1NF-kappaBp50,p65,c-Rel:ub-p-IKBUBB(1-76) IgH heavy chain V-III region VH26 precursor Ig kappa chain V-IV region B17 PSMD2 Ig kappa chain V-III region VG Ig kappa chain V-II region TEW Ig heavy chain V-II region ARH-77 MALT1 931275315450, 8811615546, 86, 111, 12313469, 87, 110, 1611355144, 28, 82, 83, 915441, 1314828, 64, 82, 9153, 125, 1604316, 84


Description

Mature B cells express IgM and IgD immunoglobulins which are complexed at the plasma membrane with Ig-alpha (CD79A, MB-1) and Ig-beta (CD79B, B29) to form the B cell receptor (BCR) (Fu et al. 1974, Fu et al. 1975, Kunkel et al. 1975, Van Noesel et al. 1992, Sanchez et al. 1993, reviewed in Brezski and Monroe 2008). Binding of antigen to the immunoglobulin activates phosphorylation of immunoreceptor tyrosine-based activation motifs (ITAMs) in the cytoplasmic tails of Ig-alpha and Ig-beta by Src family tyrosine kinases, including LYN, FYN, and BLK (Nel et al. 1984, Yamanashi et al. 1991, Flaswinkel and Reth 1994, Saouaf et al. 1994, Hata et al. 1994, Saouaf et al. 1995, reviewed in Gauld and Cambier 2004, reviewed in Harwood and Batista 2010).
The protein kinase SYK binds the phosphorylated immunoreceptor tyrosine-activated motifs (ITAMs) on the cytoplasmic tails of Ig-alpha (CD79A, MB-1) and Ig-beta (CD79B, B29) (Wienands et al. 1995, Rowley et al. 1995, Tsang et al. 2008). The binding causes the activation and autophosphorylation of SYK (Law et al. 1994, Baldock et al. 2000, Irish et al. 2006, Tsang et al. 2008, reviewed in Bradshaw 2010).
Activated SYK and other kinases phosphorylate BLNK (SLP-65), BCAP, and CD19 which serve as scaffolds for the assembly of large complexes, the signalosomes, by recruiting phosphoinositol 3-kinase (PI3K), phospholipase C gamma (predominantly PLC-gamma2 in B cells, Coggeshall et al. 1992), NCK, BAM32, BTK, VAV1, and SHC. The effectors are phosphorylated by SYK and other kinases.
PLC-gamma associated with BLNK hydrolyzes phosphatidylinositol-4,5-bisphosphate to yield inositol-1,4,5-trisphosphate (IP3) and diacylglycerol (Carter et al. 1991, Kim et al. 2004). IP3 binds receptors on the endoplasmic reticulum and causes release of calcium ions from the ER into the cytosol. The depletion of calcium from the ER in turn activates STIM1 to interact with ORAI and TRPC1 channels in the plasma membrane, resulting in an influx of extracellular calcium ions (Muik et al. 2008, Luik et al. 2008, Park et al. 2009, Mori et al. 2002). PI3K associated with BCAP and CD19 phosphorylates phosphatidylinositol 4,5-bisphosphate to yield phosphatidyinositol 3,4,5-trisphosphate.
Second messengers (calcium, diacylglycerol, inositol 1,4,5-trisphosphate, and phosphatidylinositol 3,4,5-trisphosphate) trigger signaling pathways: NF-kappaB is activated via protein kinase C beta, RAS is activated via RasGRP proteins, NF-AT is activated via calcineurin, and AKT (PKB) is activated via PDK1 (reviewed in Shinohara and Kurosaki 2009, Stone 2006). View original pathway at:Reactome.

Comments

Reactome Converter 
Pathway is converted from Reactome id:

Try the New WikiPathways

View approved pathways at the new wikipathways.org.

Quality Tags

Ontology Terms

 

Bibliography

View all...
  1. Scherer DC, Brockman JA, Chen Z, Maniatis T, Ballard DW.; ''Signal-induced degradation of I kappa B alpha requires site-specific ubiquitination.''; PubMed Europe PMC Scholia
  2. Saijo K, Mecklenbräuker I, Santana A, Leitger M, Schmedt C, Tarakhovsky A.; ''Protein kinase C beta controls nuclear factor kappaB activation in B cells through selective regulation of the IkappaB kinase alpha.''; PubMed Europe PMC Scholia
  3. Chan VW, Lowell CA, DeFranco AL.; ''Defective negative regulation of antigen receptor signaling in Lyn-deficient B lymphocytes.''; PubMed Europe PMC Scholia
  4. Zeng W, Yuan JP, Kim MS, Choi YJ, Huang GN, Worley PF, Muallem S.; ''STIM1 gates TRPC channels, but not Orai1, by electrostatic interaction.''; PubMed Europe PMC Scholia
  5. Mori Y, Wakamori M, Miyakawa T, Hermosura M, Hara Y, Nishida M, Hirose K, Mizushima A, Kurosaki M, Mori E, Gotoh K, Okada T, Fleig A, Penner R, Iino M, Kurosaki T.; ''Transient receptor potential 1 regulates capacitative Ca(2+) entry and Ca(2+) release from endoplasmic reticulum in B lymphocytes.''; PubMed Europe PMC Scholia
  6. Fu SM, Winchester RJ, Kunkel HG.; ''Similar idiotypic specificity for the membrane IgD and IgM of human B lymphocytes.''; PubMed Europe PMC Scholia
  7. Rowley RB, Burkhardt AL, Chao HG, Matsueda GR, Bolen JB.; ''Syk protein-tyrosine kinase is regulated by tyrosine-phosphorylated Ig alpha/Ig beta immunoreceptor tyrosine activation motif binding and autophosphorylation.''; PubMed Europe PMC Scholia
  8. Watanabe S, Take H, Takeda K, Yu ZX, Iwata N, Kajigaya S.; ''Characterization of the CIN85 adaptor protein and identification of components involved in CIN85 complexes.''; PubMed Europe PMC Scholia
  9. Wahl MI, Fluckiger AC, Kato RM, Park H, Witte ON, Rawlings DJ.; ''Phosphorylation of two regulatory tyrosine residues in the activation of Bruton's tyrosine kinase via alternative receptors.''; PubMed Europe PMC Scholia
  10. Miyamoto S, Maki M, Schmitt MJ, Hatanaka M, Verma IM.; ''Tumor necrosis factor alpha-induced phosphorylation of I kappa B alpha is a signal for its degradation but not dissociation from NF-kappa B.''; PubMed Europe PMC Scholia
  11. Krappmann D, Hatada EN, Tegethoff S, Li J, Klippel A, Giese K, Baeuerle PA, Scheidereit C.; ''The I kappa B kinase (IKK) complex is tripartite and contains IKK gamma but not IKAP as a regular component.''; PubMed Europe PMC Scholia
  12. Doody GM, Justement LB, Delibrias CC, Matthews RJ, Lin J, Thomas ML, Fearon DT.; ''A role in B cell activation for CD22 and the protein tyrosine phosphatase SHP.''; PubMed Europe PMC Scholia
  13. Stone JC.; ''Regulation of Ras in lymphocytes: get a GRP.''; PubMed Europe PMC Scholia
  14. Zheng Y, Liu H, Coughlin J, Zheng J, Li L, Stone JC.; ''Phosphorylation of RasGRP3 on threonine 133 provides a mechanistic link between PKC and Ras signaling systems in B cells.''; PubMed Europe PMC Scholia
  15. Chantry D, Vojtek A, Kashishian A, Holtzman DA, Wood C, Gray PW, Cooper JA, Hoekstra MF.; ''p110delta, a novel phosphatidylinositol 3-kinase catalytic subunit that associates with p85 and is expressed predominantly in leukocytes.''; PubMed Europe PMC Scholia
  16. Winston JT, Strack P, Beer-Romero P, Chu CY, Elledge SJ, Harper JW.; ''The SCFbeta-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IkappaBalpha and beta-catenin and stimulates IkappaBalpha ubiquitination in vitro.''; PubMed Europe PMC Scholia
  17. Kissinger CR, Parge HE, Knighton DR, Lewis CT, Pelletier LA, Tempczyk A, Kalish VJ, Tucker KD, Showalter RE, Moomaw EW.; ''Crystal structures of human calcineurin and the human FKBP12-FK506-calcineurin complex.''; PubMed Europe PMC Scholia
  18. Park S, Uesugi M, Verdine GL.; ''A second calcineurin binding site on the NFAT regulatory domain.''; PubMed Europe PMC Scholia
  19. Wu K, Kovacev J, Pan ZQ.; ''Priming and extending: a UbcH5/Cdc34 E2 handoff mechanism for polyubiquitination on a SCF substrate.''; PubMed Europe PMC Scholia
  20. Kohout SC, Corbalán-García S, Torrecillas A, Goméz-Fernandéz JC, Falke JJ.; ''C2 domains of protein kinase C isoforms alpha, beta, and gamma: activation parameters and calcium stoichiometries of the membrane-bound state.''; PubMed Europe PMC Scholia
  21. Rothwarf DM, Zandi E, Natoli G, Karin M.; ''IKK-gamma is an essential regulatory subunit of the IkappaB kinase complex.''; PubMed Europe PMC Scholia
  22. Fu SM, Winchester RJ, Kunkel HG.; ''Occurrence of surface IgM, IgD, and free light chains of human lymphocytes.''; PubMed Europe PMC Scholia
  23. Law CL, Sidorenko SP, Chandran KA, Draves KE, Chan AC, Weiss A, Edelhoff S, Disteche CM, Clark EA.; ''Molecular cloning of human Syk. A B cell protein-tyrosine kinase associated with the surface immunoglobulin M-B cell receptor complex.''; PubMed Europe PMC Scholia
  24. Chalupny NJ, Kanner SB, Schieven GL, Wee SF, Gilliland LK, Aruffo A, Ledbetter JA.; ''Tyrosine phosphorylation of CD19 in pre-B and mature B cells.''; PubMed Europe PMC Scholia
  25. Gauld SB, Cambier JC.; ''Src-family kinases in B-cell development and signaling.''; PubMed Europe PMC Scholia
  26. Hashimoto S, Iwamatsu A, Ishiai M, Okawa K, Yamadori T, Matsushita M, Baba Y, Kishimoto T, Kurosaki T, Tsukada S.; ''Identification of the SH2 domain binding protein of Bruton's tyrosine kinase as BLNK--functional significance of Btk-SH2 domain in B-cell antigen receptor-coupled calcium signaling.''; PubMed Europe PMC Scholia
  27. DiDonato JA, Mercurio F, Karin M.; ''Phosphorylation of I kappa B alpha precedes but is not sufficient for its dissociation from NF-kappa B.''; PubMed Europe PMC Scholia
  28. Van Noesel CJ, Borst J, De Vries EF, Van Lier RA.; ''Identification of two distinct phosphoproteins as components of the human B cell antigen receptor complex.''; PubMed Europe PMC Scholia
  29. Wienands J, Freuler F, Baumann G.; ''Tyrosine-phosphorylated forms of Ig beta, CD22, TCR zeta and HOSS are major ligands for tandem SH2 domains of Syk.''; PubMed Europe PMC Scholia
  30. Yuan JP, Zeng W, Huang GN, Worley PF, Muallem S.; ''STIM1 heteromultimerizes TRPC channels to determine their function as store-operated channels.''; PubMed Europe PMC Scholia
  31. Zhang W, Zhang X, Wu XL, He LS, Zeng XF, Crammer AC, Lipsky PE.; ''Competition between TRAF2 and TRAF6 regulates NF-kappaB activation in human B lymphocytes.''; PubMed Europe PMC Scholia
  32. Shinohara H, Yasuda T, Aiba Y, Sanjo H, Hamadate M, Watarai H, Sakurai H, Kurosaki T.; ''PKC beta regulates BCR-mediated IKK activation by facilitating the interaction between TAK1 and CARMA1.''; PubMed Europe PMC Scholia
  33. Tan P, Fuchs SY, Chen A, Wu K, Gomez C, Ronai Z, Pan ZQ.; ''Recruitment of a ROC1-CUL1 ubiquitin ligase by Skp1 and HOS to catalyze the ubiquitination of I kappa B alpha.''; PubMed Europe PMC Scholia
  34. Alkalay I, Yaron A, Hatzubai A, Orian A, Ciechanover A, Ben-Neriah Y.; ''Stimulation-dependent I kappa B alpha phosphorylation marks the NF-kappa B inhibitor for degradation via the ubiquitin-proteasome pathway.''; PubMed Europe PMC Scholia
  35. Ong HL, Cheng KT, Liu X, Bandyopadhyay BC, Paria BC, Soboloff J, Pani B, Gwack Y, Srikanth S, Singh BB, Gill DL, Ambudkar IS.; ''Dynamic assembly of TRPC1-STIM1-Orai1 ternary complex is involved in store-operated calcium influx. Evidence for similarities in store-operated and calcium release-activated calcium channel components.''; PubMed Europe PMC Scholia
  36. Otero DC, Omori SA, Rickert RC.; ''Cd19-dependent activation of Akt kinase in B-lymphocytes.''; PubMed Europe PMC Scholia
  37. Bradshaw JM.; ''The Src, Syk, and Tec family kinases: distinct types of molecular switches.''; PubMed Europe PMC Scholia
  38. Shi P, Zhu S, Lin Y, Liu Y, Liu Y, Chen Z, Shi Y, Qian Y.; ''Persistent stimulation with interleukin-17 desensitizes cells through SCFβ-TrCP-mediated degradation of Act1.''; PubMed Europe PMC Scholia
  39. Jin L, McLean PA, Neel BG, Wortis HH.; ''Sialic acid binding domains of CD22 are required for negative regulation of B cell receptor signaling.''; PubMed Europe PMC Scholia
  40. Van Noesel CJ, Brouns GS, van Schijndel GM, Bende RJ, Mason DY, Borst J, van Lier RA.; ''Comparison of human B cell antigen receptor complexes: membrane-expressed forms of immunoglobulin (Ig)M, IgD, and IgG are associated with structurally related heterodimers.''; PubMed Europe PMC Scholia
  41. Heilker R, Freuler F, Pulfer R, Di Padova F, Eder J.; ''All three IkappaB isoforms and most Rel family members are stably associated with the IkappaB kinase 1/2 complex.''; PubMed Europe PMC Scholia
  42. Müller J, Obermeier I, Wöhner M, Brandl C, Mrotzek S, Angermüller S, Maity PC, Reth M, Nitschke L.; ''CD22 ligand-binding and signaling domains reciprocally regulate B-cell Ca2+ signaling.''; PubMed Europe PMC Scholia
  43. Jardin I, Salido GM, Rosado JA.; ''Role of lipid rafts in the interaction between hTRPC1, Orai1 and STIM1.''; PubMed Europe PMC Scholia
  44. Baldock D, Graham B, Akhlaq M, Graff P, Jones CE, Menear K.; ''Purification and characterization of human Syk produced using a baculovirus expression system.''; PubMed Europe PMC Scholia
  45. Hombach J, Tsubata T, Leclercq L, Stappert H, Reth M.; ''Molecular components of the B-cell antigen receptor complex of the IgM class.''; PubMed Europe PMC Scholia
  46. Niiro H, Jabbarzadeh-Tabrizi S, Kikushige Y, Shima T, Noda K, Ota S, Tsuzuki H, Inoue Y, Arinobu Y, Iwasaki H, Shimoda S, Baba E, Tsukamoto H, Horiuchi T, Taniyama T, Akashi K.; ''CIN85 is required for Cbl-mediated regulation of antigen receptor signaling in human B cells.''; PubMed Europe PMC Scholia
  47. DeHaven WI, Smyth JT, Boyles RR, Putney JW.; ''Calcium inhibition and calcium potentiation of Orai1, Orai2, and Orai3 calcium release-activated calcium channels.''; PubMed Europe PMC Scholia
  48. Dowler S, Currie RA, Downes CP, Alessi DR.; ''DAPP1: a dual adaptor for phosphotyrosine and 3-phosphoinositides.''; PubMed Europe PMC Scholia
  49. Saouaf SJ, Mahajan S, Rowley RB, Kut SA, Fargnoli J, Burkhardt AL, Tsukada S, Witte ON, Bolen JB.; ''Temporal differences in the activation of three classes of non-transmembrane protein tyrosine kinases following B-cell antigen receptor surface engagement.''; PubMed Europe PMC Scholia
  50. Lin YC, Brown K, Siebenlist U.; ''Activation of NF-kappa B requires proteolysis of the inhibitor I kappa B-alpha: signal-induced phosphorylation of I kappa B-alpha alone does not release active NF-kappa B.''; PubMed Europe PMC Scholia
  51. Sekiya F, Poulin B, Kim YJ, Rhee SG.; ''Mechanism of tyrosine phosphorylation and activation of phospholipase C-gamma 1. Tyrosine 783 phosphorylation is not sufficient for lipase activation.''; PubMed Europe PMC Scholia
  52. Aiba Y, Kameyama M, Yamazaki T, Tedder TF, Kurosaki T.; ''Regulation of B-cell development by BCAP and CD19 through their binding to phosphoinositide 3-kinase.''; PubMed Europe PMC Scholia
  53. Yaron A, Hatzubai A, Davis M, Lavon I, Amit S, Manning AM, Andersen JS, Mann M, Mercurio F, Ben-Neriah Y.; ''Identification of the receptor component of the IkappaBalpha-ubiquitin ligase.''; PubMed Europe PMC Scholia
  54. Fuchs SY, Chen A, Xiong Y, Pan ZQ, Ronai Z.; ''HOS, a human homolog of Slimb, forms an SCF complex with Skp1 and Cullin1 and targets the phosphorylation-dependent degradation of IkappaB and beta-catenin.''; PubMed Europe PMC Scholia
  55. Cui J, Zhu L, Xia X, Wang HY, Legras X, Hong J, Ji J, Shen P, Zheng S, Chen ZJ, Wang RF.; ''NLRC5 negatively regulates the NF-kappaB and type I interferon signaling pathways.''; PubMed Europe PMC Scholia
  56. Baba Y, Hashimoto S, Matsushita M, Watanabe D, Kishimoto T, Kurosaki T, Tsukada S.; ''BLNK mediates Syk-dependent Btk activation.''; PubMed Europe PMC Scholia
  57. Harwood NE, Batista FD.; ''Early events in B cell activation.''; PubMed Europe PMC Scholia
  58. Carter RH, Park DJ, Rhee SG, Fearon DT.; ''Tyrosine phosphorylation of phospholipase C induced by membrane immunoglobulin in B lymphocytes.''; PubMed Europe PMC Scholia
  59. Flaswinkel H, Reth M.; ''Dual role of the tyrosine activation motif of the Ig-alpha protein during signal transduction via the B cell antigen receptor.''; PubMed Europe PMC Scholia
  60. Ghosh CC, Vu HY, Mujo T, Vancurova I.; ''Analysis of nucleocytoplasmic shuttling of NF kappa B proteins in human leukocytes.''; PubMed Europe PMC Scholia
  61. Uckun FM, Burkhardt AL, Jarvis L, Jun X, Stealey B, Dibirdik I, Myers DE, Tuel-Ahlgren L, Bolen JB.; ''Signal transduction through the CD19 receptor during discrete developmental stages of human B-cell ontogeny.''; PubMed Europe PMC Scholia
  62. Shinohara H, Kurosaki T.; ''Comprehending the complex connection between PKCbeta, TAK1, and IKK in BCR signaling.''; PubMed Europe PMC Scholia
  63. Nishizumi H, Horikawa K, Mlinaric-Rascan I, Yamamoto T.; ''A double-edged kinase Lyn: a positive and negative regulator for antigen receptor-mediated signals.''; PubMed Europe PMC Scholia
  64. Whiteside ST, Epinat JC, Rice NR, Israël A.; ''I kappa B epsilon, a novel member of the I kappa B family, controls RelA and cRel NF-kappa B activity.''; PubMed Europe PMC Scholia
  65. Loh C, Shaw KT, Carew J, Viola JP, Luo C, Perrino BA, Rao A.; ''Calcineurin binds the transcription factor NFAT1 and reversibly regulates its activity.''; PubMed Europe PMC Scholia
  66. Marshall AJ, Niiro H, Lerner CG, Yun TJ, Thomas S, Disteche CM, Clark EA.; ''A novel B lymphocyte-associated adaptor protein, Bam32, regulates antigen receptor signaling downstream of phosphatidylinositol 3-kinase.''; PubMed Europe PMC Scholia
  67. Baeuerle PA, Baltimore D.; ''Activation of DNA-binding activity in an apparently cytoplasmic precursor of the NF-kappa B transcription factor.''; PubMed Europe PMC Scholia
  68. Batiuk TD, Kung L, Halloran PF.; ''Evidence that calcineurin is rate-limiting for primary human lymphocyte activation.''; PubMed Europe PMC Scholia
  69. Chen L, Monti S, Juszczynski P, Daley J, Chen W, Witzig TE, Habermann TM, Kutok JL, Shipp MA.; ''SYK-dependent tonic B-cell receptor signaling is a rational treatment target in diffuse large B-cell lymphoma.''; PubMed Europe PMC Scholia
  70. Fagerlund R, Melén K, Cao X, Julkunen I.; ''NF-kappaB p52, RelB and c-Rel are transported into the nucleus via a subset of importin alpha molecules.''; PubMed Europe PMC Scholia
  71. Ohba Y, Mochizuki N, Yamashita S, Chan AM, Schrader JW, Hattori S, Nagashima K, Matsuda M.; ''Regulatory proteins of R-Ras, TC21/R-Ras2, and M-Ras/R-Ras3.''; PubMed Europe PMC Scholia
  72. Dinh M, Grunberger D, Ho H, Tsing SY, Shaw D, Lee S, Barnett J, Hill RJ, Swinney DC, Bradshaw JM.; ''Activation mechanism and steady state kinetics of Bruton's tyrosine kinase.''; PubMed Europe PMC Scholia
  73. Alicia S, Angélica Z, Carlos S, Alfonso S, Vaca L.; ''STIM1 converts TRPC1 from a receptor-operated to a store-operated channel: moving TRPC1 in and out of lipid rafts.''; PubMed Europe PMC Scholia
  74. Hata D, Nakamura T, Kawakami T, Kawakami Y, Herren B, Mayumi M.; ''Tyrosine phosphorylation of MB-1, B29, and HS1 proteins in human B cells following receptor crosslinking.''; PubMed Europe PMC Scholia
  75. Wesselborg S, Fruman DA, Sagoo JK, Bierer BE, Burakoff SJ.; ''Identification of a physical interaction between calcineurin and nuclear factor of activated T cells (NFATp).''; PubMed Europe PMC Scholia
  76. Matsuda M, Paterson HF, Rodriguez R, Fensome AC, Ellis MV, Swann K, Katan M.; ''Real time fluorescence imaging of PLC gamma translocation and its interaction with the epidermal growth factor receptor.''; PubMed Europe PMC Scholia
  77. Beals CR, Clipstone NA, Ho SN, Crabtree GR.; ''Nuclear localization of NF-ATc by a calcineurin-dependent, cyclosporin-sensitive intramolecular interaction.''; PubMed Europe PMC Scholia
  78. Buhl AM, Pleiman CM, Rickert RC, Cambier JC.; ''Qualitative regulation of B cell antigen receptor signaling by CD19: selective requirement for PI3-kinase activation, inositol-1,4,5-trisphosphate production and Ca2+ mobilization.''; PubMed Europe PMC Scholia
  79. Park CY, Hoover PJ, Mullins FM, Bachhawat P, Covington ED, Raunser S, Walz T, Garcia KC, Dolmetsch RE, Lewis RS.; ''STIM1 clusters and activates CRAC channels via direct binding of a cytosolic domain to Orai1.''; PubMed Europe PMC Scholia
  80. Shibasaki F, Price ER, Milan D, McKeon F.; ''Role of kinases and the phosphatase calcineurin in the nuclear shuttling of transcription factor NF-AT4.''; PubMed Europe PMC Scholia
  81. Weng WK, Jarvis L, LeBien TW.; ''Signaling through CD19 activates Vav/mitogen-activated protein kinase pathway and induces formation of a CD19/Vav/phosphatidylinositol 3-kinase complex in human B cell precursors.''; PubMed Europe PMC Scholia
  82. Irish JM, Czerwinski DK, Nolan GP, Levy R.; ''Kinetics of B cell receptor signaling in human B cell subsets mapped by phosphospecific flow cytometry.''; PubMed Europe PMC Scholia
  83. Li CC, Dai RM, Longo DL.; ''Inactivation of NF-kappa B inhibitor I kappa B alpha: ubiquitin-dependent proteolysis and its degradation product.''; PubMed Europe PMC Scholia
  84. Garcia-Cozar FJ, Okamura H, Aramburu JF, Shaw KT, Pelletier L, Showalter R, Villafranca E, Rao A.; ''Two-site interaction of nuclear factor of activated T cells with activated calcineurin.''; PubMed Europe PMC Scholia
  85. Luo C, Shaw KT, Raghavan A, Aramburu J, Garcia-Cozar F, Perrino BA, Hogan PG, Rao A.; ''Interaction of calcineurin with a domain of the transcription factor NFAT1 that controls nuclear import.''; PubMed Europe PMC Scholia
  86. Papp E, Tse JK, Ho H, Wang S, Shaw D, Lee S, Barnett J, Swinney DC, Bradshaw JM.; ''Steady state kinetics of spleen tyrosine kinase investigated by a real time fluorescence assay.''; PubMed Europe PMC Scholia
  87. Valentine MA, Bursten SL, Harris WE, Draves KE, Pollok BA, Ostrowski J, Bomsztyk K, Clark EA.; ''Generation of phosphatidic acid and diacylglycerols following ligation of surface immunoglobulin in human B lymphocytes: potential role in PKC activation.''; PubMed Europe PMC Scholia
  88. Cheng KT, Liu X, Ong HL, Swaim W, Ambudkar IS.; ''Local Ca²+ entry via Orai1 regulates plasma membrane recruitment of TRPC1 and controls cytosolic Ca²+ signals required for specific cell functions.''; PubMed Europe PMC Scholia
  89. Kochs G, Hummel R, Fiebich B, Sarre TF, Marmé D, Hug H.; ''Activation of purified human protein kinase C alpha and beta I isoenzymes in vitro by Ca2+, phosphatidylinositol and phosphatidylinositol 4,5-bisphosphate.''; PubMed Europe PMC Scholia
  90. Park J, Yaseen NR, Hogan PG, Rao A, Sharma S.; ''Phosphorylation of the transcription factor NFATp inhibits its DNA binding activity in cyclosporin A-treated human B and T cells.''; PubMed Europe PMC Scholia
  91. Voges D, Zwickl P, Baumeister W.; ''The 26S proteasome: a molecular machine designed for controlled proteolysis.''; PubMed Europe PMC Scholia
  92. Law CL, Aruffo A, Chandran KA, Doty RT, Clark EA.; ''Ig domains 1 and 2 of murine CD22 constitute the ligand-binding domain and bind multiple sialylated ligands expressed on B and T cells.''; PubMed Europe PMC Scholia
  93. Kim YJ, Sekiya F, Poulin B, Bae YS, Rhee SG.; ''Mechanism of B-cell receptor-induced phosphorylation and activation of phospholipase C-gamma2.''; PubMed Europe PMC Scholia
  94. Coughlin JJ, Stang SL, Dower NA, Stone JC.; ''RasGRP1 and RasGRP3 regulate B cell proliferation by facilitating B cell receptor-Ras signaling.''; PubMed Europe PMC Scholia
  95. Roifman CM, Wang G.; ''Phospholipase C-gamma 1 and phospholipase C-gamma 2 are substrates of the B cell antigen receptor associated protein tyrosine kinase.''; PubMed Europe PMC Scholia
  96. Huang GN, Zeng W, Kim JY, Yuan JP, Han L, Muallem S, Worley PF.; ''STIM1 carboxyl-terminus activates native SOC, I(crac) and TRPC1 channels.''; PubMed Europe PMC Scholia
  97. Fu C, Turck CW, Kurosaki T, Chan AC.; ''BLNK: a central linker protein in B cell activation.''; PubMed Europe PMC Scholia
  98. Chen Z, Hagler J, Palombella VJ, Melandri F, Scherer D, Ballard D, Maniatis T.; ''Signal-induced site-specific phosphorylation targets I kappa B alpha to the ubiquitin-proteasome pathway.''; PubMed Europe PMC Scholia
  99. Su YW, Zhang Y, Schweikert J, Koretzky GA, Reth M, Wienands J.; ''Interaction of SLP adaptors with the SH2 domain of Tec family kinases.''; PubMed Europe PMC Scholia
  100. Park H, Wahl MI, Afar DE, Turck CW, Rawlings DJ, Tam C, Scharenberg AM, Kinet JP, Witte ON.; ''Regulation of Btk function by a major autophosphorylation site within the SH3 domain.''; PubMed Europe PMC Scholia
  101. Chen TY, Illing M, Molday LL, Hsu YT, Yau KW, Molday RS.; ''Subunit 2 (or beta) of retinal rod cGMP-gated cation channel is a component of the 240-kDa channel-associated protein and mediates Ca(2+)-calmodulin modulation.''; PubMed Europe PMC Scholia
  102. Tanner MJ, Hanel W, Gaffen SL, Lin X.; ''CARMA1 coiled-coil domain is involved in the oligomerization and subcellular localization of CARMA1 and is required for T cell receptor-induced NF-kappaB activation.''; PubMed Europe PMC Scholia
  103. Suzuki H, Chiba T, Kobayashi M, Takeuchi M, Suzuki T, Ichiyama A, Ikenoue T, Omata M, Furuichi K, Tanaka K.; ''IkappaBalpha ubiquitination is catalyzed by an SCF-like complex containing Skp1, cullin-1, and two F-box/WD40-repeat proteins, betaTrCP1 and betaTrCP2.''; PubMed Europe PMC Scholia
  104. Meller N, Elitzur Y, Isakov N.; ''Protein kinase C-theta (PKCtheta) distribution analysis in hematopoietic cells: proliferating T cells exhibit high proportions of PKCtheta in the particulate fraction.''; PubMed Europe PMC Scholia
  105. Oellerich T, Bremes V, Neumann K, Bohnenberger H, Dittmann K, Hsiao HH, Engelke M, Schnyder T, Batista FD, Urlaub H, Wienands J.; ''The B-cell antigen receptor signals through a preformed transducer module of SLP65 and CIN85.''; PubMed Europe PMC Scholia
  106. Oellerich T, Grønborg M, Neumann K, Hsiao HH, Urlaub H, Wienands J.; ''SLP-65 phosphorylation dynamics reveals a functional basis for signal integration by receptor-proximal adaptor proteins.''; PubMed Europe PMC Scholia
  107. Brooks SR, Kirkham PM, Freeberg L, Carter RH.; ''Binding of cytoplasmic proteins to the CD19 intracellular domain is high affinity, competitive, and multimeric.''; PubMed Europe PMC Scholia
  108. Roifman CM, Ke S.; ''CD19 is a substrate of the antigen receptor-associated protein tyrosine kinase in human B cells.''; PubMed Europe PMC Scholia
  109. Clark MR, Friedrich RJ, Campbell KS, Cambier JC.; ''Human pre-B and B cell membrane mu-chains are noncovalently associated with a disulfide-linked complex containing a product of the B29 gene.''; PubMed Europe PMC Scholia
  110. Yamanashi Y, Kakiuchi T, Mizuguchi J, Yamamoto T, Toyoshima K.; ''Association of B cell antigen receptor with protein tyrosine kinase Lyn.''; PubMed Europe PMC Scholia
  111. Sundivakkam PC, Freichel M, Singh V, Yuan JP, Vogel SM, Flockerzi V, Malik AB, Tiruppathi C.; ''The Ca(2+) sensor stromal interaction molecule 1 (STIM1) is necessary and sufficient for the store-operated Ca(2+) entry function of transient receptor potential canonical (TRPC) 1 and 4 channels in endothelial cells.''; PubMed Europe PMC Scholia
  112. Zandi E, Chen Y, Karin M.; ''Direct phosphorylation of IkappaB by IKKalpha and IKKbeta: discrimination between free and NF-kappaB-bound substrate.''; PubMed Europe PMC Scholia
  113. Coggeshall KM, McHugh JC, Altman A.; ''Predominant expression and activation-induced tyrosine phosphorylation of phospholipase C-gamma 2 in B lymphocytes.''; PubMed Europe PMC Scholia
  114. Teixeira C, Stang SL, Zheng Y, Beswick NS, Stone JC.; ''Integration of DAG signaling systems mediated by PKC-dependent phosphorylation of RasGRP3.''; PubMed Europe PMC Scholia
  115. Dowler S, Montalvo L, Cantrell D, Morrice N, Alessi DR.; ''Phosphoinositide 3-kinase-dependent phosphorylation of the dual adaptor for phosphotyrosine and 3-phosphoinositides by the Src family of tyrosine kinase.''; PubMed Europe PMC Scholia
  116. Blasioli J, Paust S, Thomas ML.; ''Definition of the sites of interaction between the protein tyrosine phosphatase SHP-1 and CD22.''; PubMed Europe PMC Scholia
  117. Lorenzo PS, Kung JW, Bottorff DA, Garfield SH, Stone JC, Blumberg PM.; ''Phorbol esters modulate the Ras exchange factor RasGRP3.''; PubMed Europe PMC Scholia
  118. Huai Q, Kim HY, Liu Y, Zhao Y, Mondragon A, Liu JO, Ke H.; ''Crystal structure of calcineurin-cyclophilin-cyclosporin shows common but distinct recognition of immunophilin-drug complexes.''; PubMed Europe PMC Scholia
  119. Yamashita S, Mochizuki N, Ohba Y, Tobiume M, Okada Y, Sawa H, Nagashima K, Matsuda M.; ''CalDAG-GEFIII activation of Ras, R-ras, and Rap1.''; PubMed Europe PMC Scholia
  120. Leprince C, Draves KE, Geahlen RL, Ledbetter JA, Clark EA.; ''CD22 associates with the human surface IgM-B-cell antigen receptor complex.''; PubMed Europe PMC Scholia
  121. Ferguson KM, Kavran JM, Sankaran VG, Fournier E, Isakoff SJ, Skolnik EY, Lemmon MA.; ''Structural basis for discrimination of 3-phosphoinositides by pleckstrin homology domains.''; PubMed Europe PMC Scholia
  122. Saouaf SJ, Kut SA, Fargnoli J, Rowley RB, Bolen JB, Mahajan S.; ''Reconstitution of the B cell antigen receptor signaling components in COS cells.''; PubMed Europe PMC Scholia
  123. Sommer K, Guo B, Pomerantz JL, Bandaranayake AD, Moreno-García ME, Ovechkina YL, Rawlings DJ.; ''Phosphorylation of the CARMA1 linker controls NF-kappaB activation.''; PubMed Europe PMC Scholia
  124. Engels N, Wollscheid B, Wienands J.; ''Association of SLP-65/BLNK with the B cell antigen receptor through a non-ITAM tyrosine of Ig-alpha.''; PubMed Europe PMC Scholia
  125. Zhou H, Wertz I, O'Rourke K, Ultsch M, Seshagiri S, Eby M, Xiao W, Dixit VM.; ''Bcl10 activates the NF-kappaB pathway through ubiquitination of NEMO.''; PubMed Europe PMC Scholia
  126. Kim LJ, Ferguson HA, Seto AG, Goodrich JA.; ''Characterization of DNA binding, transcriptional activation, and regulated nuclear association of recombinant human NFATp.''; PubMed Europe PMC Scholia
  127. Tsang E, Giannetti AM, Shaw D, Dinh M, Tse JK, Gandhi S, Ho H, Wang S, Papp E, Bradshaw JM.; ''Molecular mechanism of the Syk activation switch.''; PubMed Europe PMC Scholia
  128. Rebhun JF, Castro AF, Quilliam LA.; ''Identification of guanine nucleotide exchange factors (GEFs) for the Rap1 GTPase. Regulation of MR-GEF by M-Ras-GTP interaction.''; PubMed Europe PMC Scholia
  129. Ozdener F, Dangelmaier C, Ashby B, Kunapuli SP, Daniel JL.; ''Activation of phospholipase Cgamma2 by tyrosine phosphorylation.''; PubMed Europe PMC Scholia
  130. Cheng KT, Liu X, Ong HL, Ambudkar IS.; ''Functional requirement for Orai1 in store-operated TRPC1-STIM1 channels.''; PubMed Europe PMC Scholia
  131. Traenckner EB, Wilk S, Baeuerle PA.; ''A proteasome inhibitor prevents activation of NF-kappa B and stabilizes a newly phosphorylated form of I kappa B-alpha that is still bound to NF-kappa B.''; PubMed Europe PMC Scholia
  132. Nore BF, Mattsson PT, Antonsson P, Bäckesjö CM, Westlund A, Lennartsson J, Hansson H, Löw P, Rönnstrand L, Smith CI.; ''Identification of phosphorylation sites within the SH3 domains of Tec family tyrosine kinases.''; PubMed Europe PMC Scholia
  133. Roifman CM, Mills GB, Stewart D, Cheung RK, Grinstein S, Gelfand EW.; ''Response of human B cells to different anti-immunoglobulin isotypes: absence of a correlation between early activation events and cell proliferation.''; PubMed Europe PMC Scholia
  134. Kabak S, Skaggs BJ, Gold MR, Affolter M, West KL, Foster MS, Siemasko K, Chan AC, Aebersold R, Clark MR.; ''The direct recruitment of BLNK to immunoglobulin alpha couples the B-cell antigen receptor to distal signaling pathways.''; PubMed Europe PMC Scholia
  135. Gold MR, Chan VW, Turck CW, DeFranco AL.; ''Membrane Ig cross-linking regulates phosphatidylinositol 3-kinase in B lymphocytes.''; PubMed Europe PMC Scholia
  136. Muik M, Frischauf I, Derler I, Fahrner M, Bergsmann J, Eder P, Schindl R, Hesch C, Polzinger B, Fritsch R, Kahr H, Madl J, Gruber H, Groschner K, Romanin C.; ''Dynamic coupling of the putative coiled-coil domain of ORAI1 with STIM1 mediates ORAI1 channel activation.''; PubMed Europe PMC Scholia
  137. Wang C, Deng L, Hong M, Akkaraju GR, Inoue J, Chen ZJ.; ''TAK1 is a ubiquitin-dependent kinase of MKK and IKK.''; PubMed Europe PMC Scholia
  138. Rolli V, Gallwitz M, Wossning T, Flemming A, Schamel WW, Zürn C, Reth M.; ''Amplification of B cell antigen receptor signaling by a Syk/ITAM positive feedback loop.''; PubMed Europe PMC Scholia
  139. Hanasaki K, Powell LD, Varki A.; ''Binding of human plasma sialoglycoproteins by the B cell-specific lectin CD22. Selective recognition of immunoglobulin M and haptoglobin.''; PubMed Europe PMC Scholia
  140. Nisitani S, Kato RM, Rawlings DJ, Witte ON, Wahl MI.; ''In situ detection of activated Bruton's tyrosine kinase in the Ig signaling complex by phosphopeptide-specific monoclonal antibodies.''; PubMed Europe PMC Scholia
  141. Kunkel HG.; ''Surface markers of human lymphocytes.''; PubMed Europe PMC Scholia
  142. Bohnenberger H, Oellerich T, Engelke M, Hsiao HH, Urlaub H, Wienands J.; ''Complex phosphorylation dynamics control the composition of the Syk interactome in B cells.''; PubMed Europe PMC Scholia
  143. Li Z, Nabel GJ.; ''A new member of the I kappaB protein family, I kappaB epsilon, inhibits RelA (p65)-mediated NF-kappaB transcription.''; PubMed Europe PMC Scholia
  144. Rodriguez R, Matsuda M, Perisic O, Bravo J, Paul A, Jones NP, Light Y, Swann K, Williams RL, Katan M.; ''Tyrosine residues in phospholipase Cgamma 2 essential for the enzyme function in B-cell signaling.''; PubMed Europe PMC Scholia
  145. Chiu CW, Dalton M, Ishiai M, Kurosaki T, Chan AC.; ''BLNK: molecular scaffolding through 'cis'-mediated organization of signaling proteins.''; PubMed Europe PMC Scholia
  146. Alland L, Peseckis SM, Atherton RE, Berthiaume L, Resh MD.; ''Dual myristylation and palmitylation of Src family member p59fyn affects subcellular localization.''; PubMed Europe PMC Scholia
  147. Smith KG, Tarlinton DM, Doody GM, Hibbs ML, Fearon DT.; ''Inhibition of the B cell by CD22: a requirement for Lyn.''; PubMed Europe PMC Scholia
  148. Sanchez M, Misulovin Z, Burkhardt AL, Mahajan S, Costa T, Franke R, Bolen JB, Nussenzweig M.; ''Signal transduction by immunoglobulin is mediated through Ig alpha and Ig beta.''; PubMed Europe PMC Scholia
  149. Wu C, Ghosh S.; ''beta-TrCP mediates the signal-induced ubiquitination of IkappaBbeta.''; PubMed Europe PMC Scholia
  150. Okamura H, Aramburu J, García-Rodríguez C, Viola JP, Raghavan A, Tahiliani M, Zhang X, Qin J, Hogan PG, Rao A.; ''Concerted dephosphorylation of the transcription factor NFAT1 induces a conformational switch that regulates transcriptional activity.''; PubMed Europe PMC Scholia
  151. Lin L, Czerwinski R, Kelleher K, Siegel MM, Wu P, Kriz R, Aulabaugh A, Stahl M.; ''Activation loop phosphorylation modulates Bruton's tyrosine kinase (Btk) kinase domain activity.''; PubMed Europe PMC Scholia
  152. Nel AE, Landreth GE, Goldschmidt-Clermont PJ, Tung HE, Galbraith RM.; ''Enhanced tyrosine phosphorylation in B lymphocytes upon complexing of membrane immunoglobulin.''; PubMed Europe PMC Scholia
  153. Padeh S, Levitzki A, Gazit A, Mills GB, Roifman CM.; ''Activation of phospholipase C in human B cells is dependent on tyrosine phosphorylation.''; PubMed Europe PMC Scholia
  154. Roose JP, Mollenauer M, Ho M, Kurosaki T, Weiss A.; ''Unusual interplay of two types of Ras activators, RasGRP and SOS, establishes sensitive and robust Ras activation in lymphocytes.''; PubMed Europe PMC Scholia
  155. Han S, Collins BE, Bengtson P, Paulson JC.; ''Homomultimeric complexes of CD22 in B cells revealed by protein-glycan cross-linking.''; PubMed Europe PMC Scholia
  156. Salim K, Bottomley MJ, Querfurth E, Zvelebil MJ, Gout I, Scaife R, Margolis RL, Gigg R, Smith CI, Driscoll PC, Waterfield MD, Panayotou G.; ''Distinct specificity in the recognition of phosphoinositides by the pleckstrin homology domains of dynamin and Bruton's tyrosine kinase.''; PubMed Europe PMC Scholia
  157. Wienands J, Schweikert J, Wollscheid B, Jumaa H, Nielsen PJ, Reth M.; ''SLP-65: a new signaling component in B lymphocytes which requires expression of the antigen receptor for phosphorylation.''; PubMed Europe PMC Scholia
  158. Brezski RJ, Monroe JG.; ''B-cell receptor.''; PubMed Europe PMC Scholia
  159. Luik RM, Wang B, Prakriya M, Wu MM, Lewis RS.; ''Oligomerization of STIM1 couples ER calcium depletion to CRAC channel activation.''; PubMed Europe PMC Scholia
  160. Leitges M, Schmedt C, Guinamard R, Davoust J, Schaal S, Stabel S, Tarakhovsky A.; ''Immunodeficiency in protein kinase cbeta-deficient mice.''; PubMed Europe PMC Scholia
  161. Burke JR, Wood MK, Ryseck RP, Walther S, Meyers CA.; ''Peptides corresponding to the N and C termini of IkappaB-alpha, -beta, and -epsilon as probes of the two catalytic subunits of IkappaB kinase, IKK-1 and IKK-2.''; PubMed Europe PMC Scholia
  162. Vasile S, Coligan JE, Yoshida M, Seon BK.; ''Isolation and chemical characterization of the human B29 and mb-1 proteins of the B cell antigen receptor complex.''; PubMed Europe PMC Scholia
  163. Wienands J, Hombach J, Radbruch A, Riesterer C, Reth M.; ''Molecular components of the B cell antigen receptor complex of class IgD differ partly from those of IgM.''; PubMed Europe PMC Scholia
  164. Fu C, Chan AC.; ''Identification of two tyrosine phosphoproteins, pp70 and pp68, which interact with phospholipase Cgamma, Grb2, and Vav after B cell antigen receptor activation.''; PubMed Europe PMC Scholia
  165. Roose JP, Mollenauer M, Gupta VA, Stone J, Weiss A.; ''A diacylglycerol-protein kinase C-RasGRP1 pathway directs Ras activation upon antigen receptor stimulation of T cells.''; PubMed Europe PMC Scholia
  166. Blank V, Kourilsky P, Israël A.; ''Cytoplasmic retention, DNA binding and processing of the NF-kappa B p50 precursor are controlled by a small region in its C-terminus.''; PubMed Europe PMC Scholia
  167. McConnell FM, Shears SB, Lane PJ, Scheibel MS, Clark EA.; ''Relationships between the degree of cross-linking of surface immunoglobulin and the associated inositol 1,4,5-trisphosphate and Ca2+ signals in human B cells.''; PubMed Europe PMC Scholia
  168. Wei SJ, Williams JG, Dang H, Darden TA, Betz BL, Humble MM, Chang FM, Trempus CS, Johnson K, Cannon RE, Tennant RW.; ''Identification of a specific motif of the DSS1 protein required for proteasome interaction and p53 protein degradation.''; PubMed Europe PMC Scholia
  169. Brooks SR, Li X, Volanakis EJ, Carter RH.; ''Systematic analysis of the role of CD19 cytoplasmic tyrosines in enhancement of activation in Daudi human B cells: clustering of phospholipase C and Vav and of Grb2 and Sos with different CD19 tyrosines.''; PubMed Europe PMC Scholia
  170. Su TT, Guo B, Kawakami Y, Sommer K, Chae K, Humphries LA, Kato RM, Kang S, Patrone L, Wall R, Teitell M, Leitges M, Kawakami T, Rawlings DJ.; ''PKC-beta controls I kappa B kinase lipid raft recruitment and activation in response to BCR signaling.''; PubMed Europe PMC Scholia

History

View all...
CompareRevisionActionTimeUserComment
112687view16:08, 9 October 2020ReactomeTeamReactome version 73
101604view11:47, 1 November 2018ReactomeTeamreactome version 66
101140view21:32, 31 October 2018ReactomeTeamreactome version 65
100668view20:06, 31 October 2018ReactomeTeamreactome version 64
100218view16:51, 31 October 2018ReactomeTeamreactome version 63
99769view15:17, 31 October 2018ReactomeTeamreactome version 62 (2nd attempt)
93934view13:46, 16 August 2017ReactomeTeamreactome version 61
93521view11:25, 9 August 2017ReactomeTeamreactome version 61
87188view08:07, 19 July 2016EgonwOntology Term : 'signaling pathway' added !
86619view09:22, 11 July 2016ReactomeTeamreactome version 56
83158view10:13, 18 November 2015ReactomeTeamVersion54
81511view13:03, 21 August 2015ReactomeTeamVersion53
76984view08:27, 17 July 2014ReactomeTeamFixed remaining interactions
76689view12:05, 16 July 2014ReactomeTeamFixed remaining interactions
76015view10:07, 11 June 2014ReactomeTeamRe-fixing comment source
75724view11:19, 10 June 2014ReactomeTeamReactome 48 Update
75074view14:02, 8 May 2014AnweshaFixing comment source for displaying WikiPathways description
74860view17:46, 2 May 2014EgonwMarked two metabolites as a DataNode type="Metabolite"...
74721view08:48, 30 April 2014ReactomeTeamNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
26S proteasomeComplexR-HSA-68819 (Reactome)
ADPMetaboliteCHEBI:16761 (ChEBI)
AHCYL1 ProteinO43865 (Uniprot-TrEMBL)
AHCYL1:NAD+:ITPR1:I(1,4,5)P3 tetramerComplexR-HSA-5226920 (Reactome)
ATPMetaboliteCHEBI:15422 (ChEBI)
Activated PKC betaComplexR-HSA-139829 (Reactome)
Active IKK complexComplexR-HSA-727820 (Reactome)
Antigen R-NUL-173548 (Reactome)
Antigen:BCRComplexR-HSA-983689 (Reactome)
Antigen:p-BCR:SYKComplexR-HSA-983693 (Reactome)
Antigen:p-BCR:p-SYK:p-BLNKComplexR-HSA-983687 (Reactome)
Antigen:p-BCR:p-SYKComplexR-HSA-983690 (Reactome)
Antigen:p-BCRComplexR-HSA-983691 (Reactome)
AntigenR-NUL-983667 (Reactome)
BCAP SignalosomeComplexR-HSA-2045909 (Reactome)
BCRComplexR-HSA-983677 (Reactome)
BLK ProteinP51451 (Uniprot-TrEMBL)
BLK-like proteinsComplexR-HSA-3902518 (Reactome) This CandidateSet contains sequences identified by William Pearson's analysis of Reactome catalyst entities. Catalyst entity sequences were used to identify analagous sequences that shared overall homology and active site homology. Sequences in this Candidate set were identified in an April 24, 2012 analysis.
BLKProteinP51451 (Uniprot-TrEMBL)
BLNK (SLP-65) SignalosomeComplexR-HSA-984818 (Reactome)
BLNK ProteinQ8WV28 (Uniprot-TrEMBL)
BLNK:GRB2:SOS1:CIN85:CBLComplexR-HSA-983692 (Reactome)
BTKProteinQ06187 (Uniprot-TrEMBL)
BTRC ProteinQ9Y297 (Uniprot-TrEMBL)
CALM1 ProteinP62158 (Uniprot-TrEMBL)
CALM1:4xCa2+ComplexR-HSA-74294 (Reactome)
CALM1ProteinP62158 (Uniprot-TrEMBL)
CARD11 ProteinQ9BXL7 (Uniprot-TrEMBL)
CARMA1 oligomerComplexR-HSA-1169088 (Reactome)
CARMA1:BCL10:MALT1:TAK1:IKKComplexR-HSA-1168620 (Reactome) TAK1 and the IKK complex are observed to migrate to lipid rafts containing phosphorylated CARMA1, BCL10, and MALT1. By analogy with NF-kappaB signaling pathways in other cells, the CARMA1:BCL10MALT1:TAK1:IKK complex in B cells may also contain TAB1, TAB2 and/or TAB3, TRAF6.
CARMA1:BCL10:MALT1:TAK1ComplexR-HSA-1168619 (Reactome) TAK1 and the IKK complex are observed to migrate to lipid rafts containing phosphorylated CARMA1, BCL10, and MALT1. By analogy with NF-kappaB signaling pathways in other cells, the CARMA1:BCL10MALT1:TAK1:IKK complex in B cells may also contain TAB1, TAB2 and/or TAB3, TRAF6.
CARMA1:MALT1:BCL10ComplexR-HSA-1168622 (Reactome)
CBL ProteinP22681 (Uniprot-TrEMBL)
CBLB ProteinQ13191 (Uniprot-TrEMBL)
CD19 ProteinP15391 (Uniprot-TrEMBL)
CD19 SignalosomeComplexR-HSA-2076233 (Reactome)
CD19:VAV1ComplexR-HSA-2076225 (Reactome)
CD22 ProteinP20273 (Uniprot-TrEMBL)
CD22:Antigen:p-BCRComplexR-HSA-5690660 (Reactome)
CD22ProteinP20273 (Uniprot-TrEMBL)
CD79A ProteinP11912 (Uniprot-TrEMBL)
CD79B ProteinP40259 (Uniprot-TrEMBL)
CHUK ProteinO15111 (Uniprot-TrEMBL)
CRAC channelComplexR-HSA-434679 (Reactome)
CUL1 ProteinQ13616 (Uniprot-TrEMBL)
Ca2+ MetaboliteCHEBI:29108 (ChEBI)
Ca2+MetaboliteCHEBI:29108 (ChEBI)
Calcineurin (CaN)ComplexR-HSA-2025977 (Reactome)
Calcineurin:Phosphorylated NFATC1,2,3ComplexR-HSA-2025899 (Reactome)
Cyclophilin A:Cyclosporin AComplexR-HSA-2026008 (Reactome)
Cyclosporin A MetaboliteCHEBI:4031 (ChEBI)
DAG MetaboliteCHEBI:17815 (ChEBI)
DAGMetaboliteCHEBI:17815 (ChEBI)
DAPP1ProteinQ9UN19 (Uniprot-TrEMBL)
Dephosphorylated NFATC1,2,3ComplexR-HSA-2025852 (Reactome)
FBXW11 ProteinQ9UKB1 (Uniprot-TrEMBL)
FKBP1A ProteinP62942 (Uniprot-TrEMBL)
FKBP1A:TacrolimusComplexR-HSA-2026019 (Reactome)
FYNProteinP06241 (Uniprot-TrEMBL)
Fe3+ MetaboliteCHEBI:29034 (ChEBI)
GDP MetaboliteCHEBI:17552 (ChEBI)
GRB2-1 ProteinP62993-1 (Uniprot-TrEMBL)
GRB2-1ProteinP62993-1 (Uniprot-TrEMBL)
GTP MetaboliteCHEBI:15996 (ChEBI)
HRAS ProteinP01112 (Uniprot-TrEMBL)
I(1,4,5)P3 MetaboliteCHEBI:16595 (ChEBI)
I(1,4,5)P3MetaboliteCHEBI:16595 (ChEBI)
IGHD ProteinP01880 (Uniprot-TrEMBL)
IGHM ProteinP01871 (Uniprot-TrEMBL)
IGHV(1-?) ProteinA2KUC3 (Uniprot-TrEMBL)
IGHV7-81(1-?) ProteinQ6PIL0 (Uniprot-TrEMBL)
IGKC ProteinP01834 (Uniprot-TrEMBL)
IGKV1-5(23-?) ProteinP01602 (Uniprot-TrEMBL)
IGKV4-1(21-?) ProteinP06312 (Uniprot-TrEMBL)
IGKVA18(21-?) ProteinA2NJV5 (Uniprot-TrEMBL)
IGLC1 ProteinP0CG04 (Uniprot-TrEMBL)
IGLC2 ProteinP0CG05 (Uniprot-TrEMBL)
IGLC3 ProteinP0CG06 (Uniprot-TrEMBL)
IGLC6 ProteinP0CF74 (Uniprot-TrEMBL)
IGLC7 ProteinA0M8Q6 (Uniprot-TrEMBL)
IGLV(23-?) ProteinA2NXD2 (Uniprot-TrEMBL)
IKBKB ProteinO14920 (Uniprot-TrEMBL)
IKBKG ProteinQ9Y6K9 (Uniprot-TrEMBL)
IKKA:IKBKB:IKBKGComplexR-HSA-168113 (Reactome)
IP3 receptor homotetramerComplexR-HSA-169686 (Reactome)
ITPR1 ProteinQ14643 (Uniprot-TrEMBL)
ITPR2 ProteinQ14571 (Uniprot-TrEMBL)
ITPR3 ProteinQ14573 (Uniprot-TrEMBL)
ITPR:I(1,4,5)P3 tetramerComplexR-HSA-169696 (Reactome)
Ig heavy chain V-I region EU ProteinP01742 (Uniprot-TrEMBL)
Ig heavy chain V-I region HG3 ProteinP01743 (Uniprot-TrEMBL)
Ig heavy chain V-I region Mot ProteinP06326 (Uniprot-TrEMBL)
Ig heavy chain V-I region ND ProteinP01744 (Uniprot-TrEMBL)
Ig heavy chain V-I region SIE ProteinP01761 (Uniprot-TrEMBL)
Ig heavy chain V-I region WOL ProteinP01760 (Uniprot-TrEMBL)
Ig heavy chain V-II region ARH-77 ProteinP06331 (Uniprot-TrEMBL)
Ig heavy chain V-II region COR ProteinP01815 (Uniprot-TrEMBL)
Ig heavy chain V-II region DAW ProteinP01816 (Uniprot-TrEMBL)
Ig heavy chain V-II region HE ProteinP01818 (Uniprot-TrEMBL)
Ig heavy chain V-II region MCE ProteinP01817 (Uniprot-TrEMBL)
Ig heavy chain V-II region NEWM ProteinP01825 (Uniprot-TrEMBL)
Ig heavy chain V-II region OU ProteinP01814 (Uniprot-TrEMBL)
Ig heavy chain V-II region SESS ProteinP04438 (Uniprot-TrEMBL)
Ig heavy chain V-II region WAH ProteinP01824 (Uniprot-TrEMBL)
Ig heavy chain V-III region BRO ProteinP01766 (Uniprot-TrEMBL)
Ig heavy chain V-III region BUR ProteinP01773 (Uniprot-TrEMBL)
Ig heavy chain V-III region BUT ProteinP01767 (Uniprot-TrEMBL)
Ig heavy chain V-III region CAM ProteinP01768 (Uniprot-TrEMBL)
Ig heavy chain V-III region DOB ProteinP01782 (Uniprot-TrEMBL)
Ig heavy chain V-III region GA ProteinP01769 (Uniprot-TrEMBL)
Ig heavy chain V-III region GAL ProteinP01781 (Uniprot-TrEMBL)
Ig heavy chain V-III region HIL ProteinP01771 (Uniprot-TrEMBL)
Ig heavy chain V-III region JON ProteinP01780 (Uniprot-TrEMBL)
Ig heavy chain V-III region KOL ProteinP01772 (Uniprot-TrEMBL)
Ig heavy chain V-III region LAY ProteinP01775 (Uniprot-TrEMBL)
Ig heavy chain V-III region NIE ProteinP01770 (Uniprot-TrEMBL)
Ig heavy chain V-III region POM ProteinP01774 (Uniprot-TrEMBL)
Ig heavy chain V-III region TEI ProteinP01777 (Uniprot-TrEMBL)
Ig heavy chain V-III region TIL ProteinP01765 (Uniprot-TrEMBL)
Ig heavy chain V-III region TRO ProteinP01762 (Uniprot-TrEMBL)
Ig heavy chain V-III region TUR ProteinP01779 (Uniprot-TrEMBL)
Ig heavy chain V-III region WAS ProteinP01776 (Uniprot-TrEMBL)
Ig heavy chain V-III region WEA ProteinP01763 (Uniprot-TrEMBL)
Ig heavy chain V-III region ZAP ProteinP01778 (Uniprot-TrEMBL)
Ig kappa chain V region EV15 ProteinP06315 (Uniprot-TrEMBL)
Ig kappa chain V-I region AG ProteinP01593 (Uniprot-TrEMBL)
Ig kappa chain V-I region AU ProteinP01594 (Uniprot-TrEMBL)
Ig kappa chain V-I region BAN ProteinP04430 (Uniprot-TrEMBL)
Ig kappa chain V-I region Bi ProteinP01595 (Uniprot-TrEMBL)
Ig kappa chain V-I region CAR ProteinP01596 (Uniprot-TrEMBL)
Ig kappa chain V-I region DEE ProteinP01597 (Uniprot-TrEMBL)
Ig kappa chain V-I region Daudi ProteinP04432 (Uniprot-TrEMBL)
Ig kappa chain V-I region EU ProteinP01598 (Uniprot-TrEMBL)
Ig kappa chain V-I region Gal ProteinP01599 (Uniprot-TrEMBL)
Ig kappa chain V-I region HK101 ProteinP01601 (Uniprot-TrEMBL)
Ig kappa chain V-I region Hau ProteinP01600 (Uniprot-TrEMBL)
Ig kappa chain V-I region Ka ProteinP01603 (Uniprot-TrEMBL)
Ig kappa chain V-I region Kue ProteinP01604 (Uniprot-TrEMBL)
Ig kappa chain V-I region Lay ProteinP01605 (Uniprot-TrEMBL)
Ig kappa chain V-I region Mev ProteinP01612 (Uniprot-TrEMBL)
Ig kappa chain V-I region Ni ProteinP01613 (Uniprot-TrEMBL)
Ig kappa chain V-I region OU ProteinP01606 (Uniprot-TrEMBL)
Ig kappa chain V-I region Rei ProteinP01607 (Uniprot-TrEMBL)
Ig kappa chain V-I region Roy ProteinP01608 (Uniprot-TrEMBL)
Ig kappa chain V-I region Scw ProteinP01609 (Uniprot-TrEMBL)
Ig kappa chain V-I region WAT ProteinP80362 (Uniprot-TrEMBL)
Ig kappa chain V-I region WEA ProteinP01610 (Uniprot-TrEMBL)
Ig kappa chain V-I region Walker ProteinP04431 (Uniprot-TrEMBL)
Ig kappa chain V-I region Wes ProteinP01611 (Uniprot-TrEMBL)
Ig kappa chain V-II region Cum ProteinP01614 (Uniprot-TrEMBL)
Ig kappa chain V-II region FR ProteinP01615 (Uniprot-TrEMBL)
Ig kappa chain V-II region GM607 ProteinP06309 (Uniprot-TrEMBL)
Ig kappa chain V-II region MIL ProteinP01616 (Uniprot-TrEMBL)
Ig kappa chain V-II region RPMI 6410 ProteinP06310 (Uniprot-TrEMBL)
Ig kappa chain V-II region TEW ProteinP01617 (Uniprot-TrEMBL)
Ig kappa chain V-III region B6 ProteinP01619 (Uniprot-TrEMBL)
Ig kappa chain V-III region CLL ProteinP04207 (Uniprot-TrEMBL)
Ig kappa chain V-III region GOL ProteinP04206 (Uniprot-TrEMBL)
Ig kappa chain V-III region HAH ProteinP18135 (Uniprot-TrEMBL)
Ig kappa chain V-III region HIC ProteinP18136 (Uniprot-TrEMBL)
Ig kappa chain V-III region IARC/BL41 ProteinP06311 (Uniprot-TrEMBL)
Ig kappa chain V-III region NG9 ProteinP01621 (Uniprot-TrEMBL)
Ig kappa chain V-III region POM ProteinP01624 (Uniprot-TrEMBL)
Ig kappa chain V-III region SIE ProteinP01620 (Uniprot-TrEMBL)
Ig kappa chain V-III region Ti ProteinP01622 (Uniprot-TrEMBL)
Ig kappa chain V-III region VG ProteinP04433 (Uniprot-TrEMBL)
Ig kappa chain V-III region VH ProteinP04434 (Uniprot-TrEMBL)
Ig kappa chain V-III region WOL ProteinP01623 (Uniprot-TrEMBL)
Ig kappa chain V-IV region B17 ProteinP06314 (Uniprot-TrEMBL)
Ig kappa chain V-IV region JI ProteinP06313 (Uniprot-TrEMBL)
Ig kappa chain V-IV region Len ProteinP01625 (Uniprot-TrEMBL)
Ig kappa chain V-IV region STH ProteinP83593 (Uniprot-TrEMBL)
Ig lambda chain V region 4A ProteinP04211 (Uniprot-TrEMBL)
Ig lambda chain V-I region BL2 ProteinP06316 (Uniprot-TrEMBL)
Ig lambda chain V-I region EPS ProteinP06888 (Uniprot-TrEMBL)
Ig lambda chain V-I region HA ProteinP01700 (Uniprot-TrEMBL)
Ig lambda chain V-I region MEM ProteinP06887 (Uniprot-TrEMBL)
Ig lambda chain V-I region NEW ProteinP01701 (Uniprot-TrEMBL)
Ig lambda chain V-I region NEWM ProteinP01703 (Uniprot-TrEMBL)
Ig lambda chain V-I region NIG-64 ProteinP01702 (Uniprot-TrEMBL)
Ig lambda chain V-I region VOR ProteinP01699 (Uniprot-TrEMBL)
Ig lambda chain V-I region WAH ProteinP04208 (Uniprot-TrEMBL)
Ig lambda chain V-II region BO ProteinP01710 (Uniprot-TrEMBL)
Ig lambda chain V-II region BOH ProteinP01706 (Uniprot-TrEMBL)
Ig lambda chain V-II region BUR ProteinP01708 (Uniprot-TrEMBL)
Ig lambda chain V-II region MGC ProteinP01709 (Uniprot-TrEMBL)
Ig lambda chain V-II region NEI ProteinP01705 (Uniprot-TrEMBL)
Ig lambda chain V-II region NIG-58 ProteinP01713 (Uniprot-TrEMBL)
Ig lambda chain V-II region NIG-84 ProteinP04209 (Uniprot-TrEMBL)
Ig lambda chain V-II region TOG ProteinP01704 (Uniprot-TrEMBL)
Ig lambda chain V-II region TRO ProteinP01707 (Uniprot-TrEMBL)
Ig lambda chain V-II region VIL ProteinP01711 (Uniprot-TrEMBL)
Ig lambda chain V-II region WIN ProteinP01712 (Uniprot-TrEMBL)
Ig lambda chain V-III region LOI ProteinP80748 (Uniprot-TrEMBL)
Ig lambda chain V-III region SH ProteinP01714 (Uniprot-TrEMBL)
Ig lambda chain V-IV region Bau ProteinP01715 (Uniprot-TrEMBL)
Ig lambda chain V-IV region Hil ProteinP01717 (Uniprot-TrEMBL)
Ig lambda chain V-IV region Kern ProteinP01718 (Uniprot-TrEMBL)
Ig lambda chain V-IV region MOL ProteinP06889 (Uniprot-TrEMBL)
Ig lambda chain V-IV region X ProteinP01716 (Uniprot-TrEMBL)
Ig lambda chain V-V region DEL ProteinP01719 (Uniprot-TrEMBL)
Ig lambda chain V-VI region AR ProteinP01721 (Uniprot-TrEMBL)
Ig lambda chain V-VI region EB4 ProteinP06319 (Uniprot-TrEMBL)
Ig lambda chain V-VI region NIG-48 ProteinP01722 (Uniprot-TrEMBL)
Ig lambda chain V-VI region SUT ProteinP06317 (Uniprot-TrEMBL)
Ig lambda chain V-VI region WLT ProteinP06318 (Uniprot-TrEMBL)
Ig lambda chain V-VII region MOT ProteinP01720 (Uniprot-TrEMBL)
IgH heavy chain V-III region VH26 precursor ProteinP01764 (Uniprot-TrEMBL)
KRAS ProteinP01116 (Uniprot-TrEMBL)
LYNProteinP07948 (Uniprot-TrEMBL)
MALT1 ProteinQ9UDY8 (Uniprot-TrEMBL)
MALT1ProteinQ9UDY8 (Uniprot-TrEMBL)
MAP3K7ProteinO43318 (Uniprot-TrEMBL)
NAD+ MetaboliteCHEBI:15846 (ChEBI)
NAc-CD22 homo-oligomerR-HSA-5690698 (Reactome)
NAc-CD22ProteinP20273 (Uniprot-TrEMBL)
NCK1 ProteinP16333 (Uniprot-TrEMBL)
NCK1ProteinP16333 (Uniprot-TrEMBL)
NF-kappa-B p50,p65,c-Rel:IKBComplexR-HSA-1168593 (Reactome)
NF-kappa-B p50,p65,c-Rel:p-IKBComplexR-HSA-1168588 (Reactome)
NF-kappaB p50,p65,c-Rel dimerComplexR-HSA-1168598 (Reactome)
NF-kappaB p50,p65,c-Rel dimerComplexR-HSA-1168608 (Reactome)
NF-kappaB p50,p65,c-Rel:ub-p-IKBComplexR-HSA-1168613 (Reactome)
NF-kappaB:p-IkB:SCF-betaTrCPComplexR-HSA-1168617 (Reactome)
NFKB1(1-433) ProteinP19838 (Uniprot-TrEMBL)
NFKBIA ProteinP25963 (Uniprot-TrEMBL)
NFKBIB ProteinQ15653 (Uniprot-TrEMBL)
NFKBIE ProteinO00221 (Uniprot-TrEMBL)
NRAS ProteinP01111 (Uniprot-TrEMBL)
ORAI1 ProteinQ96D31 (Uniprot-TrEMBL)
Orai1 dimerComplexR-HSA-434696 (Reactome)
PI(3,4,5)P3 MetaboliteCHEBI:16618 (ChEBI)
PI(3,4,5)P3MetaboliteCHEBI:16618 (ChEBI)
PI(4,5)P2MetaboliteCHEBI:18348 (ChEBI)
PIK3AP1ProteinQ6ZUJ8 (Uniprot-TrEMBL)
PIK3CD ProteinO00329 (Uniprot-TrEMBL)
PIK3CD:PIK3R1ComplexR-HSA-1045152 (Reactome)
PIK3CD:PIK3R1ComplexR-HSA-1806213 (Reactome)
PIK3R1 ProteinP27986 (Uniprot-TrEMBL)
PIP3 activates AKT signalingPathwayR-HSA-1257604 (Reactome) Signaling by AKT is one of the key outcomes of receptor tyrosine kinase (RTK) activation. AKT is activated by the cellular second messenger PIP3, a phospholipid that is generated by PI3K. In ustimulated cells, PI3K class IA enzymes reside in the cytosol as inactive heterodimers composed of p85 regulatory subunit and p110 catalytic subunit. In this complex, p85 stabilizes p110 while inhibiting its catalytic activity. Upon binding of extracellular ligands to RTKs, receptors dimerize and undergo autophosphorylation. The regulatory subunit of PI3K, p85, is recruited to phosphorylated cytosolic RTK domains either directly or indirectly, through adaptor proteins, leading to a conformational change in the PI3K IA heterodimer that relieves inhibition of the p110 catalytic subunit. Activated PI3K IA phosphorylates PIP2, converting it to PIP3; this reaction is negatively regulated by PTEN phosphatase. PIP3 recruits AKT to the plasma membrane, allowing TORC2 to phosphorylate a conserved serine residue of AKT. Phosphorylation of this serine induces a conformation change in AKT, exposing a conserved threonine residue that is then phosphorylated by PDPK1 (PDK1). Phosphorylation of both the threonine and the serine residue is required to fully activate AKT. The active AKT then dissociates from PIP3 and phosphorylates a number of cytosolic and nuclear proteins that play important roles in cell survival and metabolism. For a recent review of AKT signaling, please refer to Manning and Cantley, 2007.
PLC gamma1,2ComplexR-HSA-1169089 (Reactome)
PLCG1 ProteinP19174 (Uniprot-TrEMBL)
PLCG2 ProteinP16885 (Uniprot-TrEMBL)
PPIA ProteinP62937 (Uniprot-TrEMBL)
PPP3CA ProteinQ08209 (Uniprot-TrEMBL)
PPP3CB ProteinP16298 (Uniprot-TrEMBL)
PPP3R1 ProteinP63098 (Uniprot-TrEMBL)
PRKCB ProteinP05771 (Uniprot-TrEMBL)
PRKCBProteinP05771 (Uniprot-TrEMBL)
PSMA1 ProteinP25786 (Uniprot-TrEMBL)
PSMA2 ProteinP25787 (Uniprot-TrEMBL)
PSMA3 ProteinP25788 (Uniprot-TrEMBL)
PSMA4 ProteinP25789 (Uniprot-TrEMBL)
PSMA5 ProteinP28066 (Uniprot-TrEMBL)
PSMA6 ProteinP60900 (Uniprot-TrEMBL)
PSMA7 ProteinO14818 (Uniprot-TrEMBL)
PSMA8 ProteinQ8TAA3 (Uniprot-TrEMBL)
PSMB1 ProteinP20618 (Uniprot-TrEMBL)
PSMB10 ProteinP40306 (Uniprot-TrEMBL)
PSMB11 ProteinA5LHX3 (Uniprot-TrEMBL)
PSMB2 ProteinP49721 (Uniprot-TrEMBL)
PSMB3 ProteinP49720 (Uniprot-TrEMBL)
PSMB4 ProteinP28070 (Uniprot-TrEMBL)
PSMB5 ProteinP28074 (Uniprot-TrEMBL)
PSMB6 ProteinP28072 (Uniprot-TrEMBL)
PSMB7 ProteinQ99436 (Uniprot-TrEMBL)
PSMB8 ProteinP28062 (Uniprot-TrEMBL)
PSMB9 ProteinP28065 (Uniprot-TrEMBL)
PSMC1 ProteinP62191 (Uniprot-TrEMBL)
PSMC2 ProteinP35998 (Uniprot-TrEMBL)
PSMC3 ProteinP17980 (Uniprot-TrEMBL)
PSMC4 ProteinP43686 (Uniprot-TrEMBL)
PSMC5 ProteinP62195 (Uniprot-TrEMBL)
PSMC6 ProteinP62333 (Uniprot-TrEMBL)
PSMD1 ProteinQ99460 (Uniprot-TrEMBL)
PSMD10 ProteinO75832 (Uniprot-TrEMBL)
PSMD11 ProteinO00231 (Uniprot-TrEMBL)
PSMD12 ProteinO00232 (Uniprot-TrEMBL)
PSMD13 ProteinQ9UNM6 (Uniprot-TrEMBL)
PSMD14 ProteinO00487 (Uniprot-TrEMBL)
PSMD2 ProteinQ13200 (Uniprot-TrEMBL)
PSMD3 ProteinO43242 (Uniprot-TrEMBL)
PSMD4 ProteinP55036 (Uniprot-TrEMBL)
PSMD5 ProteinQ16401 (Uniprot-TrEMBL)
PSMD6 ProteinQ15008 (Uniprot-TrEMBL)
PSMD7 ProteinP51665 (Uniprot-TrEMBL)
PSMD8 ProteinP48556 (Uniprot-TrEMBL)
PSMD9 ProteinO00233 (Uniprot-TrEMBL)
PSME1 ProteinQ06323 (Uniprot-TrEMBL)
PSME2 ProteinQ9UL46 (Uniprot-TrEMBL)
PSME3 ProteinP61289 (Uniprot-TrEMBL)
PSME4 ProteinQ14997 (Uniprot-TrEMBL)
PSMF1 ProteinQ92530 (Uniprot-TrEMBL)
PTPN6 ProteinP29350 (Uniprot-TrEMBL)
PTPN6:p-Y762,807,822-CD22:Antigen:p-BCRComplexR-HSA-5690677 (Reactome)
PTPN6ProteinP29350 (Uniprot-TrEMBL)
Phosphatidylserine MetaboliteCHEBI:18303 (ChEBI)
PhosphatidylserineMetaboliteCHEBI:18303 (ChEBI)
Phosphorylated NFATC1,2,3ComplexR-HSA-2025924 (Reactome)
RASGRP1 ProteinO95267 (Uniprot-TrEMBL)
RASGRP1,3ComplexR-HSA-1169462 (Reactome)
RASGRP3 ProteinQ8IV61 (Uniprot-TrEMBL)
REL ProteinQ04864 (Uniprot-TrEMBL)
RELA ProteinQ04206 (Uniprot-TrEMBL)
RPS27A(1-76) ProteinP62979 (Uniprot-TrEMBL)
SCF-beta-TrCp1,2ComplexR-HSA-1168601 (Reactome)
SH3KBP1 ProteinQ96B97 (Uniprot-TrEMBL)
SHC1 p46,p52ComplexR-HSA-1169480 (Reactome) SHC1 isoforms p46 and p52 are found in B cells (Smit et al. 1994).
SHC1-2 ProteinP29353-2 (Uniprot-TrEMBL)
SHC1-3 ProteinP29353-3 (Uniprot-TrEMBL)
SKP1 ProteinP63208 (Uniprot-TrEMBL)
SOS1 ProteinQ07889 (Uniprot-TrEMBL)
SRMS ProteinQ9H3Y6 (Uniprot-TrEMBL)
STIM1 DimerComplexR-HSA-1168370 (Reactome)
STIM1 ProteinQ13586 (Uniprot-TrEMBL)
STIM1:CalciumComplexR-HSA-1168371 (Reactome)
STIM1:TRPC1ComplexR-HSA-2089954 (Reactome)
SYK ProteinP43405 (Uniprot-TrEMBL)
SYKProteinP43405 (Uniprot-TrEMBL)
TRPC1 ProteinP48995 (Uniprot-TrEMBL)
TRPC1ProteinP48995 (Uniprot-TrEMBL)
Tacrolimus MetaboliteCHEBI:61049 (ChEBI)
UBA52(1-76) ProteinP62987 (Uniprot-TrEMBL)
UBB(1-76) ProteinP0CG47 (Uniprot-TrEMBL)
UBB(153-228) ProteinP0CG47 (Uniprot-TrEMBL)
UBB(77-152) ProteinP0CG47 (Uniprot-TrEMBL)
UBC(1-76) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(153-228) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(229-304) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(305-380) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(381-456) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(457-532) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(533-608) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(609-684) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(77-152) ProteinP0CG48 (Uniprot-TrEMBL)
Ub-21,22-p-S32,S36-NFKBIA ProteinP25963 (Uniprot-TrEMBL)
UbComplexR-HSA-113595 (Reactome)
VAV1 ProteinP15498 (Uniprot-TrEMBL)
VAV1ProteinP15498 (Uniprot-TrEMBL)
Zn2+ MetaboliteCHEBI:29105 (ChEBI)
p-12S-NFATC1 ProteinO95644 (Uniprot-TrEMBL)
p-13S-NFATC3 ProteinQ12968 (Uniprot-TrEMBL)
p-14S-NFATC2 ProteinQ13469 (Uniprot-TrEMBL)
p-4Y-PIK3AP1 ProteinQ6ZUJ8 (Uniprot-TrEMBL)
p-5Y-BLNK ProteinQ8WV28 (Uniprot-TrEMBL)
p-6Y-CD19 ProteinP15391 (Uniprot-TrEMBL)
p-6Y-SYK ProteinP43405 (Uniprot-TrEMBL)
p-BCL10 ProteinO95999 (Uniprot-TrEMBL)
p-BCL10ProteinO95999 (Uniprot-TrEMBL)
p-CARMA1 OligomerComplexR-HSA-1168616 (Reactome) The coiled coil (CC) domain of CARMA1 interacts with the CC domain on other CARMA1 molecules to form oligomers of unknown stoichiometry.
p-RASGRP1,3:DAGComplexR-HSA-1168369 (Reactome) RasGRP3 binds diacylglycerol via its C1 domain.
p-S157,S161-NFKBIE ProteinO00221 (Uniprot-TrEMBL)
p-S157,S161-Ub-NFKBIE ProteinO00221 (Uniprot-TrEMBL)
p-S177,S181-IKBKB ProteinO14920 (Uniprot-TrEMBL)
p-S19,S23-NFKBIB ProteinQ15653 (Uniprot-TrEMBL)
p-S19,S23-Ub-NFKBIB ProteinQ15653 (Uniprot-TrEMBL)
p-S243-NFATC2 ProteinQ13469 (Uniprot-TrEMBL)
p-S257-NFATC1 ProteinO95644 (Uniprot-TrEMBL)
p-S265-NFATC3 ProteinQ12968 (Uniprot-TrEMBL)
p-S32,S36-NFKBIA ProteinP25963 (Uniprot-TrEMBL)
p-S559,S644,S652-CARD11 ProteinQ9BXL7 (Uniprot-TrEMBL)
p-T133-RASGRP3 ProteinQ8IV61 (Uniprot-TrEMBL)
p-T184-RASGRP1 ProteinO95267 (Uniprot-TrEMBL)
p-T187-MAP3K7 ProteinO43318 (Uniprot-TrEMBL)
p-Y139-DAPP1 ProteinQ9UN19 (Uniprot-TrEMBL)
p-Y188,Y199-CD79A ProteinP11912 (Uniprot-TrEMBL)
p-Y194,Y195,Y272-SHC1-1(156-583) ProteinP29353-3 (Uniprot-TrEMBL)
p-Y196,Y207-CD79B ProteinP40259 (Uniprot-TrEMBL) By homology with CD79A (Ig-alpha), CD79B (Ig-beta) is presumed to be phosphorylated on tyrosines 196 and 207.
p-Y223,Y551-BTK ProteinQ06187 (Uniprot-TrEMBL)
p-Y239,Y240,Y317-SHC1-2 ProteinP29353-2 (Uniprot-TrEMBL)
p-Y753,Y759,Y1217-PLCG2 ProteinP16885 (Uniprot-TrEMBL)
p-Y762,807,822-CD22 ProteinP20273 (Uniprot-TrEMBL)
p-Y762,807,822-CD22:Antigen:p-BCRComplexR-HSA-5690689 (Reactome)
p-Y771,Y783-PLCG1 ProteinP19174 (Uniprot-TrEMBL)
p21 RAS:GDPComplexR-HSA-109796 (Reactome)
p21 RAS:GTPComplexR-HSA-109783 (Reactome)

Annotated Interactions

View all...
SourceTargetTypeDatabase referenceComment
26S proteasomemim-catalysisR-HSA-1168640 (Reactome)
ADPArrowR-HSA-1168374 (Reactome)
ADPArrowR-HSA-1168635 (Reactome)
ADPArrowR-HSA-1168638 (Reactome)
ADPArrowR-HSA-1168641 (Reactome)
ADPArrowR-HSA-5690702 (Reactome)
ADPArrowR-HSA-983703 (Reactome)
ADPArrowR-HSA-983707 (Reactome)
ADPArrowR-HSA-983709 (Reactome)
AHCYL1:NAD+:ITPR1:I(1,4,5)P3 tetramerTBarR-HSA-169683 (Reactome)
ATPR-HSA-1168374 (Reactome)
ATPR-HSA-1168635 (Reactome)
ATPR-HSA-1168638 (Reactome)
ATPR-HSA-1168641 (Reactome)
ATPR-HSA-5690702 (Reactome)
ATPR-HSA-983703 (Reactome)
ATPR-HSA-983707 (Reactome)
ATPR-HSA-983709 (Reactome)
Activated PKC betaArrowR-HSA-1168373 (Reactome)
Activated PKC betamim-catalysisR-HSA-1168635 (Reactome)
Active IKK complexArrowR-HSA-1168641 (Reactome)
Active IKK complexmim-catalysisR-HSA-1168638 (Reactome)
Antigen:BCRArrowR-HSA-983696 (Reactome)
Antigen:BCRR-HSA-983709 (Reactome)
Antigen:p-BCR:SYKArrowR-HSA-983700 (Reactome)
Antigen:p-BCR:SYKR-HSA-983707 (Reactome)
Antigen:p-BCR:p-SYK:p-BLNKArrowR-HSA-983703 (Reactome)
Antigen:p-BCR:p-SYK:p-BLNKR-HSA-983704 (Reactome)
Antigen:p-BCR:p-SYK:p-BLNKmim-catalysisR-HSA-983704 (Reactome)
Antigen:p-BCR:p-SYKArrowR-HSA-983707 (Reactome)
Antigen:p-BCR:p-SYKR-HSA-983703 (Reactome)
Antigen:p-BCR:p-SYKmim-catalysisR-HSA-983703 (Reactome)
Antigen:p-BCR:p-SYKmim-catalysisR-HSA-983707 (Reactome)
Antigen:p-BCRArrowR-HSA-983709 (Reactome)
Antigen:p-BCRR-HSA-5690740 (Reactome)
Antigen:p-BCRR-HSA-983700 (Reactome)
AntigenR-HSA-983696 (Reactome)
BCAP SignalosomeArrowR-HSA-983704 (Reactome)
BCAP Signalosomemim-catalysisR-HSA-2045911 (Reactome)
BCRR-HSA-983696 (Reactome)
BLK-like proteinsmim-catalysisR-HSA-983709 (Reactome)
BLNK (SLP-65) SignalosomeArrowR-HSA-983704 (Reactome)
BLNK (SLP-65) Signalosomemim-catalysisR-HSA-1112666 (Reactome)
BLNK:GRB2:SOS1:CIN85:CBLR-HSA-983703 (Reactome)
BTKR-HSA-983704 (Reactome)
BTKmim-catalysisR-HSA-983704 (Reactome)
CALM1:4xCa2+ArrowR-HSA-74448 (Reactome)
CALM1:4xCa2+R-HSA-2025890 (Reactome)
CALM1R-HSA-74448 (Reactome)
CARMA1 oligomerR-HSA-1168635 (Reactome)
CARMA1:BCL10:MALT1:TAK1:IKKArrowR-HSA-1168637 (Reactome)
CARMA1:BCL10:MALT1:TAK1:IKKR-HSA-1168641 (Reactome)
CARMA1:BCL10:MALT1:TAK1:IKKmim-catalysisR-HSA-1168641 (Reactome)
CARMA1:BCL10:MALT1:TAK1ArrowR-HSA-1168641 (Reactome)
CARMA1:MALT1:BCL10ArrowR-HSA-1168644 (Reactome)
CARMA1:MALT1:BCL10R-HSA-1168637 (Reactome)
CD19 SignalosomeArrowR-HSA-983704 (Reactome)
CD19 Signalosomemim-catalysisR-HSA-2076220 (Reactome)
CD19:VAV1R-HSA-983704 (Reactome)
CD22:Antigen:p-BCRArrowR-HSA-5690740 (Reactome)
CD22:Antigen:p-BCRR-HSA-5690702 (Reactome)
CD22R-HSA-5690740 (Reactome)
CRAC channelArrowR-HSA-434700 (Reactome)
CRAC channelmim-catalysisR-HSA-434798 (Reactome)
Ca2+ArrowR-HSA-1168376 (Reactome)
Ca2+ArrowR-HSA-169683 (Reactome)
Ca2+ArrowR-HSA-2089943 (Reactome)
Ca2+ArrowR-HSA-434798 (Reactome)
Ca2+R-HSA-1168373 (Reactome)
Ca2+R-HSA-169683 (Reactome)
Ca2+R-HSA-2025890 (Reactome)
Ca2+R-HSA-2089943 (Reactome)
Ca2+R-HSA-434798 (Reactome)
Ca2+R-HSA-74448 (Reactome)
Calcineurin (CaN)R-HSA-2025890 (Reactome)
Calcineurin:Phosphorylated NFATC1,2,3ArrowR-HSA-2025890 (Reactome)
Calcineurin:Phosphorylated NFATC1,2,3R-HSA-2025882 (Reactome)
Calcineurin:Phosphorylated NFATC1,2,3mim-catalysisR-HSA-2025882 (Reactome)
Cyclophilin A:Cyclosporin ATBarR-HSA-2025882 (Reactome)
DAGArrowR-HSA-1112666 (Reactome)
DAGR-HSA-1168373 (Reactome)
DAGR-HSA-1168374 (Reactome)
DAPP1R-HSA-983704 (Reactome)
Dephosphorylated NFATC1,2,3ArrowR-HSA-2025882 (Reactome)
FKBP1A:TacrolimusTBarR-HSA-2025882 (Reactome)
FYNmim-catalysisR-HSA-983709 (Reactome)
GRB2-1R-HSA-983704 (Reactome)
I(1,4,5)P3ArrowR-HSA-1112666 (Reactome)
I(1,4,5)P3ArrowR-HSA-169683 (Reactome)
I(1,4,5)P3R-HSA-169680 (Reactome)
IKKA:IKBKB:IKBKGR-HSA-1168637 (Reactome)
IP3 receptor homotetramerR-HSA-169680 (Reactome)
ITPR:I(1,4,5)P3 tetramerArrowR-HSA-169680 (Reactome)
ITPR:I(1,4,5)P3 tetramermim-catalysisR-HSA-1168376 (Reactome)
ITPR:I(1,4,5)P3 tetramermim-catalysisR-HSA-169683 (Reactome)
LYNmim-catalysisR-HSA-5690702 (Reactome)
LYNmim-catalysisR-HSA-983709 (Reactome)
MALT1R-HSA-1168644 (Reactome)
MAP3K7R-HSA-1168637 (Reactome)
NAc-CD22 homo-oligomerArrowR-HSA-5690669 (Reactome)
NAc-CD22R-HSA-5690669 (Reactome)
NCK1R-HSA-983704 (Reactome)
NF-kappa-B p50,p65,c-Rel:IKBR-HSA-1168638 (Reactome)
NF-kappa-B p50,p65,c-Rel:p-IKBArrowR-HSA-1168638 (Reactome)
NF-kappa-B p50,p65,c-Rel:p-IKBR-HSA-1168642 (Reactome)
NF-kappaB p50,p65,c-Rel dimerArrowR-HSA-1168633 (Reactome)
NF-kappaB p50,p65,c-Rel dimerArrowR-HSA-1168640 (Reactome)
NF-kappaB p50,p65,c-Rel dimerR-HSA-1168633 (Reactome)
NF-kappaB p50,p65,c-Rel:ub-p-IKBArrowR-HSA-1168643 (Reactome)
NF-kappaB p50,p65,c-Rel:ub-p-IKBR-HSA-1168640 (Reactome)
NF-kappaB:p-IkB:SCF-betaTrCPArrowR-HSA-1168642 (Reactome)
NF-kappaB:p-IkB:SCF-betaTrCPR-HSA-1168643 (Reactome)
Orai1 dimerR-HSA-434700 (Reactome)
PI(3,4,5)P3ArrowR-HSA-2045911 (Reactome)
PI(3,4,5)P3ArrowR-HSA-2076220 (Reactome)
PI(4,5)P2R-HSA-1112666 (Reactome)
PI(4,5)P2R-HSA-2045911 (Reactome)
PI(4,5)P2R-HSA-2076220 (Reactome)
PI(4,5)P2R-HSA-983704 (Reactome)
PIK3AP1R-HSA-983704 (Reactome)
PIK3CD:PIK3R1R-HSA-983704 (Reactome)
PIK3CD:PIK3R1mim-catalysisR-HSA-983704 (Reactome)
PLC gamma1,2R-HSA-983704 (Reactome)
PRKCBR-HSA-1168373 (Reactome)
PTPN6:p-Y762,807,822-CD22:Antigen:p-BCRArrowR-HSA-5690701 (Reactome)
PTPN6:p-Y762,807,822-CD22:Antigen:p-BCRTBarR-HSA-983707 (Reactome)
PTPN6:p-Y762,807,822-CD22:Antigen:p-BCRTBarR-HSA-983709 (Reactome)
PTPN6R-HSA-5690701 (Reactome)
PhosphatidylserineR-HSA-1168373 (Reactome)
Phosphorylated NFATC1,2,3R-HSA-2025890 (Reactome)
R-HSA-1112666 (Reactome) Phospholipase C gamma (PLC-gamma) is activated by phosphorylation in response to antigen-binding by the B cell receptor (Carter et al. 1991, Roitman and Wang 1992, Rodriguez et al. 2001, Kim et al. 2004, Sekiya et al. 2004). Phospholipase C gamma hydrolyzes phosphatidylinositol-4,5-bisphosphate to yield inositol-1,4,5-trisphosphate and diacylglycerol (Carter et al. 1991, Kim et al. 2004). Human B cells contain both PLC-gamma1 and PLC-gamma2, with PLC-gamma2 predominating (Coggeshall et al. 1992).
R-HSA-1168373 (Reactome) Human Protein kinase C beta (PKC-beta) is activated by calcium ions, diacylglycerol, and binds phosphatidylserine (Kochs et al. 1991). Experiments in mice have shown that knocking out PKC-beta causes severe defects in B cells, leading to the conclusion that PKC-beta is the predominant signaling PKC in these cells (Leitges et al. 1996, Su et al. 2002, Saijo et al. 2002).
R-HSA-1168374 (Reactome) RasGRP1 and RasGRP3 translocate to the plasma membrane where they bind diacylglycerol (Lorenzo et al. 2001) and are phosphorylated (Teixeira et al. 2003, Zheng et al. 2005). Though RasGRP3 is phosphorylated in vitro and in some cell lines (e.g. Ramos cells) by protein kinase C theta (PKC-theta, Zheng et al. 2005), normal B cells do not contain PKC-theta (Meller et al. 1999). Both Rasgrp1 and Rasgrp3 participate in activating Ras in response to BCR signaling in mouse B cells (Coughlin et al. 2005).
R-HSA-1168376 (Reactome) In the resting state the luminal domain of STIM1 binds Ca2+ ions within the endoplasmic reticulum and this binding prevents dimerization of STIM1 (Luik et al. 2008). Upon depletion of Ca2+ ions from the endoplasmic reticulum, STIM1 is no longer bound to Ca2+ and forms homodimers (Muik et al. 2008, Luik et al. 2008, Park et al. 2009).
R-HSA-1168633 (Reactome) Nf-kappaB subunits contain nuclear localization sequences and, in the absence of IkB, are translocated to the nucleus (Bauerle and Baltimore 1988, Blank et al. 1991, Ghosh et al. 2008, Fagerlund et al. 2008). c-Rel binds to importins alpha5, alpha6, and alpha7; RelB binds to importins alpha5 and alpha6; p52 binds importin alpha3, alpha4, alpha5, and alpha6 (Fagerlund et al. 2008)
R-HSA-1168635 (Reactome) CARMA1 is phosphorylated at serines 559, 644, and 652 by Protein Kinase C beta (PKC-beta) (Sommer et al. 2005). CARMA1 is constitutively oligomerized (Tanner et al. 2007) and most CARMA1 in unstimulated cells is cytosolic (Sommer et al. 2005, Tanner et al. 2007), though a portion is constitutively associated with the plasma membrane (Gaide et al. 2002, Sommer et al. 2005). After phosphorylation, CARMA1 is associated with lipid rafts in the plasma membrane (Sommer et al. 2005). Note that some publications refer to CARMA1 with a different N-terminal methionine that is 7 amino acids shorter. In this case the phosphorylated serines are 552, 537, and 645.
R-HSA-1168636 (Reactome) RasGRP1 (Roose et al. 2007) and RasGRP3 (Ohba et al. 2000, Yamashita et al. 2000, Rebhun et al. 2000, Lorenzo et al. 2001) catalyze the exchange of GDP for GTP bound by RAS.
R-HSA-1168637 (Reactome) TAK1 and the IKK complex are observed to migrate from the cytosol to lipid rafts containing the CARMA1:BCL10:MALT1 (CBM) complex (Sommer et al. 2005, Shinohara et al. 2005 using chicken cells). By analogy with activation of NF-KappaB signaling in T cells, TAK1 in B cells may also be bound to TAB1 and TAB2 or TAB3, which bind K63-conjugated polyubiquitin on a TRAF protein bound to the CBM complex (reviewed in Shinohara et al. 2009).
R-HSA-1168638 (Reactome) Activated IKK complex phosphorylates the I-kappaB component of the cytoplasmic NF-kappaB complex (Zandi et al. 1998, Burke et al. 1999, Heilker et al. 1999). B cells contain I-kappaB-alpha, I-kappaB-beta, and I-kappaB-epsilon (Whiteside et al. 1997, Li and Nabel 1997).
R-HSA-1168640 (Reactome) Phosphorylated, ubiquitinated IkB is degraded by the proteasome (Miyamoto et al. 1994, Traenckner et al. 1994, Alkalay et al. 1995, DiDonato et al. 1995, Li et al. 1995, Lin et al. 1995, Scherer et al. 1995, Chen et al. 1995). IkB does not dissociate from NF-kB before it is proteolyzed (Miyamoto et al. 1994, Traenckner et al. 1994, DiDonato et al. 1995, Lin et al. 1995).
R-HSA-1168641 (Reactome) TAK1 phosphorylates IKK-beta (Wang et al. 2001). As inferred from chicken B cells, the reaction in human B cells may occur when TAK1 and the IKK complex are associated with the CARMA1:BCL10:MALT1 (CBM) complex. During T cell activation TAK1 forms a complex with TAB1 and TAB2, which binds K-63 conjugated polyubiquitin attached to TRAF6 associated with the CBM complex (Sun et al. 2004, reviewed in Shinohara et al. 2009). TRAF6 also polyubiquitinates IKK-gamma in T cells (Zhou et al. 2004). B cells contain functional TRAF6 and TRAF2 (Zhang et al. 2010) so the same mechanism may occur during activation of B cells.
R-HSA-1168642 (Reactome) SKP:Cul:F-box (SCF) complexes containing F-box factors Beta-TrCP1 (BTRCP, E3RSIkappaB) or beta-TrCP2 (BTRCP2, FBXW11, HOS) bind IkappaB (Yaron et al. 1998, Fuchs et al. 1999, Suzuki et al. 1999, Tan et al. 1999, Winston et al. 1999, Wu and Ghosh 1999).
R-HSA-1168643 (Reactome) SKP:Cul:F-box (SCF) complexes containing F-box factors Beta-TrCP1 (BTRCP, E3RSIkappaB) or beta-TrCP2 (BTRCP2, FBXW11, HOS) catalyze the polyubiquitination of IkappaB (Yaron et al. 1998, Fuchs et al. 1999, Suzuki et al. 1999, Tan et al. 1999, Winston et al. 1999, Wu and Ghosh 1999).
R-HSA-1168644 (Reactome) CARMA1 is phosphorylated and recruits BCL10 and MALT1 to the plasma membrane to form the CBM complex (Sommer et al. 2005, Tanner et al. 2007). Evidence from T cells (Jurkat cells) indicates that MALT1 and BCL10 oligomerize to activate the IKK complex (Zhou 2004).
R-HSA-169680 (Reactome) The IP3 receptor (IP3R) is an IP3-gated calcium channel. It is a large, homotetrameric protein, similar to other calcium channel proteins such as ryanodine. The four subunits form a 'four-leafed clover' structure arranged around the central calcium channel. Binding of ligands such as IP3 results in conformational changes in the receptor's structure that leads to channel opening.
R-HSA-169683 (Reactome) IP3 promotes the release of intracellular calcium.
R-HSA-2025882 (Reactome) As inferred from mouse (Okamura et al. 2000), calcineurin dephosphorylates NFATC2 at 13 serine residues (Batiuk et al. 1997, Kim et al. 2000). B lymphocytes also contain NFATC2 and NFATC3 which are inferred to undergo dephosphorylation at homologous serines. Dephosphorylation of NFATs exposes a nuclear localization signal which cause NFATs to be imported into the nucleus (Kim et al. 2000). In mouse, Calcineurin is observed to also transit into the nucleus in a complex with NFATs and may remain associated (Shibasaki et al. 1996).
R-HSA-2025890 (Reactome) Calcium activates calcineurin in two ways: binding the regulatory subunit of calcineurin directly and binding calmodulin which then interacts with the catalytic subunit of calcineurin. As inferred from mouse, B lymphocytes contain the R1 regulatory subunit (PPP3R1) and the beta catalytic subunit (PPP3CB).
In the presence of calcium and calcium:calmodulin calcineurin binds phosphorylated and unphosphorylated NFATs at 2 regions in the N-terminus (Luo et al. 1996, Garcia-Cozar et al. 1998, Park et al. 2000, evidence from mouse in Loh et al. 1996 and Wesselborg et al. 1996). Calcineurin also weakly interacts with NFATs in the absence of calcium (Garcia-Cozar et al. 1998).
R-HSA-2045911 (Reactome) PI3K generates phosphoinositol-3,4,5-trisphosphate (PIP3) from PIP2 after activation of the BCR (Gold et al. 1992, Chantry et al. 1997). Experiments in mice indicate that PI3K associated with BCAP is partly responsible for the activity (Aiba et al. 2008). (PI3K associated with CD19 is also partly responsible (Aiba et al. 2008).)
R-HSA-2076220 (Reactome) PI3K generates phosphoinositol-3,4,5-trisphosphate (PIP3) from PIP2 after activation of the BCR (Gold et al. 1992). Experiments in mice indicate that PI3K associated with CD19 is partly responsible for the activity (Buhl et al. 1997, Otero et al. 2001, Aiba et al. 2008). (PI3K associated with BCAP is also partly responsible (Aiba et al. 2008).)
R-HSA-2089927 (Reactome) The polybasic region of STIM1 interacts with 2 aspartate residues in the C-terminal region of TRPC1 (Zeng et al. 2008, Huang et al. 2006). The STIM1:TRPC1 complex can form a tenary complex with ORAI1 (Ong et al. 2007, Jardin et al. 2008) and ORAI participates in function of STIM1:TRPC1 channels (Cheng et al. 2008, Cheng et al. 2011). As inferred from chicken DT40 cells, TRPC1 (and possibly other TRP channels) participates in store-operated calcium influx during signaling by the B cell receptor (Mori et al. 2002).
R-HSA-2089943 (Reactome) TRPC1 forms a channel that transports Ca2+ across the plasma membrane. TRPC1 is gated by STIM1 (Ong et al. 2007).
R-HSA-434700 (Reactome) Sustained calcium signalling in lymphocytes and platelets requires the uptake of extracellular calcium when intracellular stores are depleted. The process whereby intracellular calcium depletion stimulates calcium uptake is often referred to as Store-operated calcium entry (SOCE). Store depletion is sensed by stromal interaction molecule 1 (STIM1), which then translocates to the plasma membrane and associates with 2 dimers of Orai1 to form a calcium-release activated calcium (CRAC) channel.
R-HSA-434798 (Reactome) Activation of Calcium-release-activated (CRAC) channels allows influx of calcium. The Orai component of CRAC is responsible for the selectivity of the channel, while the Stim component is responsible for activation.
R-HSA-5690669 (Reactome) In resting B cells, CD22 is a prominent cis ligand for itself, forming CD22 homo-oligomers. Cross-linking experiments showed that CD22 primarily recognizes alpha2,6-linked sialic acid (2,6Sia or N-acetylneuraminic acid (NAc)) on neighboring CD22 molecules present on the same B-cell (Han et al. 2005). NH2-terminal immuno globulin (Ig) domains, Ig1 and Ig2, mediate 2,6Sia binding (Law et al. 1998, Jin et al. 2002). Thus, CD22 recognizes self structures and triggers inhibitory signals, which may be relevant for suppression of autoimmune B-cell responses.
R-HSA-5690701 (Reactome) The phosphorylated ITIMs of CD22 facilitates recruitment of the tyrosine phosphatase SHP1 (Src homology region 2 domain-containing phosphatase-1 also referred as PTPN6/Tyrosine-protein phosphatase non-receptor type 6), which down modulates BCR signalling (Doody et al. 1995). Activation of SHP1 regulates the strength of the BCR-induced Ca+2 signal. Regulation of Ca+2 signalling occurs both by dephosphorylation of intracellular SHP1 substrates which are important for triggering of Ca+2 signals (Adachi et al. 2001, Stebbins et al. 2003), as well as by a SHP1 dependent activation of the Ca+2 plasma membrane pump PMCA4 which controls termination of the signal (Muller et al. 2013, Ghosh et al. 2006).
R-HSA-5690702 (Reactome) After ligation of membrane-bound IgM, CD22 is quickly tyrosine phosphorylated on its cytoplasmic ITIM sequence (immunoreceptor tyrosine-based inhibition motif). The tyrosine kinase involved in CD22 phosphorylation is LYN, a member of the Src kinase family (Smith et al. 1998). The CD22 cytoplasmic tail contains six tyrosines, three of which belong to the ITIM sequence (Nitschke & Tsubata 2004).
R-HSA-5690740 (Reactome) Physical association of CD22 with the BCR seems to have direct involvement in the regulation of BCR signalling, as antibody-mediated clustering of CD22 with the BCR leads to dampened signaling (Smith et al. 1998), and evidence of their association has been obtained by confocal microscopy, coimmunoprecipitation and chemical crossing (Zhang et al. 2004, Phee et al. 2001, Peaker et al. 1993, Law et al. 1994, Leprince et al. 1993, Collins et al. 2006). Forced ligation of CD22 to the BCR dramatically increases CD22 phosphorylation and suppression of BCR signalling (Macauley, 2013). This is relevant to suppression of BCR signalling to membrane antigens on B cells that contain self sialic acids (Lanoue, 2002; Macauley 2013). CD22 ligand binding modulates its activity as a negative regulator of B cell signalling.
R-HSA-74448 (Reactome) Upon increase in calcium concentration, calmodulin (CaM) is activated by binding to four calcium ions.
R-HSA-983696 (Reactome) Mature, unstimulated B cells express IgM and IgD immunoglobulins on their surfaces (Fu et al. 1974, Fu et al. 1975, reviewed in Kunkel 1975). The immunoglobulins form B cell receptor (BCR) complexes with disulfide-linked heterodimers of Ig-alpha (CD79A) and Ig-beta (CD79B), which have cytoplasmic tails containing immunoreceptor tyrosine-based activation motifs (ITAMs) (van Noesel et al. 1992, Saouaf et al. 1995, inferred from mouse Hombach et al. 1990, Wienands et al. 1990). Upon binding of antigen to the immunoglobulin a chain of phosphorylation events is triggered (Nel et al. 1984, Saouaf et al. 1994, Hata et al. 1994, Saouaf et al. 1995, reviewed in Harwood and Batista 2010).
R-HSA-983700 (Reactome) The SYK protein tyrosine kinase binds specifically to phosphorylated immunoreceptor tyrosine-activated motifs (ITAMs) on Ig-alpha (CD79A, MB-1) and Ig-beta (CD79B, B29) (Law et al. 1994, Saouaf et al. 1995, Rowley et al. 1995, Tsang et al. 2008). The binding activates the kinase activity of SYK (Rowley et al. 1995, Tsang et al. 2008).
R-HSA-983703 (Reactome) BLNK (SLP-65, BASH) forms a stable complex with GRB2, SOS1, and CIN85 in the cytosol. The complex is recruited to the plasma membrane where activated (phosphorylated) SYK phosphorylates BLNK at tyrosines 72, 84, 96, 178, and 189 (Fu et al. 1998, Chiu et al. 2002, inferred from mouse in Wienands et al. 1998, from chicken in Oellerich et al. 2009). Phosphorylated BLNK serves as a scaffold that binds effector molecules such as Phospholipase C. As inferred from mouse, BLNK interacts with phosphorylated tyrosines on CD79A (Ig-alpha) (Engels et al. 2001, Kabak et al. 2002).
R-HSA-983704 (Reactome) Phosphorylated SYK phosphorylates BLNK (SLP-65, Fu et al. 1998, Chiu et al. 2002) and BCAP (inferred from mouse, Okada et al. 2000). Effector molecules are then recruited: phosphoinositol 3-kinase (PI3K), Phospholipase C gamma (predominantly PLC-gamma2 in B cells, Coggeshall et al. 1992), NCK, BAM32, BTK, VAV1, and SHC. The effectors are phosphorylated by SYK and other kinases.
As inferred from chicken DT40 cells and mouse B cells (Okada et al. 2000), phosphorylated BCAP recruits PI3K, which is phosphorylated by a SYK-dependent mechanism (Kuwahara et al. 1996) and produces phosphatidylinositol-3,4,5-trisphosphate (PIP3). PIP3 recruits BAM32 (Marshall et al. 2000) and BTK (de Weers et al. 1994, Baba et al. 2001) via their PH domains. PIP3 also recruits and activates PLC-gamma1 and PLC-gamma2 (Bae et al. 1998). BTK binds phosphorylated BLNK via its SH2 domain (Baba et al. 2001). BTK phosphorylates Phospholipase C gamma-2 (Rodriguez et al. 2001), which activates phospholipase activity (Carter et al. 1991, Roifman and Wang 1992, Kim et al. 2004, Sekiya et al. 2004).
Phosphorylated BLNK recruits PLC gamma, VAV, GRB2, and NCK (Fu and Chan 1997, Fu et al. 1998, Chiu et al. 2002).
SYK phosphorylates SHC which then binds GRB2 (Saxton et al. 1994, Harmer and DeFranco 1997).
CD19 in a stable complex with VAV1 is phosphorylated by Src kinases (inferred from mouse, Xu et al. 2002) and possibly by LYN (inferred from mouse, Fujimoto et al. 2000) in response to BCR activation. Phosphorylated CD19 then binds PI3K (Roifman and Ke 1993, Chalupny et al. 1993, Uckun et al. 1993, Weng et al. 1994, Brooks et al. 2000, Brooks et al. 2004) and can bind PLC-gamma2, which competes with VAV1 for the same binding site on CD19 (Brooks et al. 2000, Brooks et al. 2004).
R-HSA-983707 (Reactome) The SYK protein tyrosine kinase autophosphorylates at tyrosines 131, 323, 348, 352, 525, and 526 (Law et al. 1994, Rowley et al. 1995, Baldock et al. 2000, Irish et al. 2006, Papp et al. 2007, Chen et al. 2008, Tsang et al. 2008). The autophosphorylation increases the kinase activity of SYK. SYK is also phosporylated on additional residues in response to BCR activation (Bohnenberger et al. 2011).
R-HSA-983709 (Reactome) The B cell receptor (BCR) comprises an immunoglobulin complexed with a heterodimer of Ig-alpha (CD79A, MB-1) and Ig-beta (CD79B, B29). After immunoglobulin IgM or IgD binds antigen the associated Ig-alpha and Ig-beta are each observed to be phosphorylated at two tyrosine residues in the cytoplasmic immunoreceptor tyrosine-activated motif (ITAM) (Sanchez et al. 1993, Hata et al. 1994, Saouaf et al. 1994, Saouaf et al. 1995). Saouaf et al. (1995) showed that the kinase Blk could phosphorylate both tyrosines of each ITAM and that the kinase SYK specifically bound phosphorylated but not unphosphorylated ITAMs. In mouse the kinase Lyn and other kinases phosphorylate one tyrosine and Syk is believed to phosphorylate the other (Yamanashi et al. 1991, Flaswinkel and Reth 1994, Rolli et al. 2002).
RASGRP1,3R-HSA-1168374 (Reactome)
SCF-beta-TrCp1,2ArrowR-HSA-1168643 (Reactome)
SCF-beta-TrCp1,2R-HSA-1168642 (Reactome)
SHC1 p46,p52R-HSA-983704 (Reactome)
STIM1 DimerArrowR-HSA-1168376 (Reactome)
STIM1 DimerR-HSA-2089927 (Reactome)
STIM1 DimerR-HSA-434700 (Reactome)
STIM1:CalciumR-HSA-1168376 (Reactome)
STIM1:TRPC1ArrowR-HSA-2089927 (Reactome)
STIM1:TRPC1mim-catalysisR-HSA-2089943 (Reactome)
SYKR-HSA-983700 (Reactome)
TRPC1R-HSA-2089927 (Reactome)
UbR-HSA-1168643 (Reactome)
VAV1R-HSA-983704 (Reactome)
p-BCL10R-HSA-1168644 (Reactome)
p-CARMA1 OligomerArrowR-HSA-1168635 (Reactome)
p-CARMA1 OligomerR-HSA-1168644 (Reactome)
p-RASGRP1,3:DAGArrowR-HSA-1168374 (Reactome)
p-RASGRP1,3:DAGmim-catalysisR-HSA-1168636 (Reactome)
p-Y762,807,822-CD22:Antigen:p-BCRArrowR-HSA-5690702 (Reactome)
p-Y762,807,822-CD22:Antigen:p-BCRR-HSA-5690701 (Reactome)
p21 RAS:GDPR-HSA-1168636 (Reactome)
p21 RAS:GTPArrowR-HSA-1168636 (Reactome)
Personal tools