Translocation of SLC2A4 (GLUT4) to the plasma membrane (Homo sapiens)

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3, 5, 6, 10, 22...7, 15, 19, 249, 251, 12, 13, 18, 2816, 297, 15202112, 1723cytosolcytoplasmic vesicle lumenATPSTX4 MYO1C SNAP23 MYH4 EXOC4 LNPEP GTP MYH13 p-T309,S474-AKT2RAB13 EXOC7 STXBP3 p-T308,S473-AKT114-3-3 dimerSNAP23KIF3B RAB8A RAB11A YWHAQ RAB14 YWHAB EXOC6 STX4 EXOC1 AMP KIF3ADPMYO1C:CALM1GTP ADPADPRAB10 STX4:STXBP3(MUNC18C)RAB4A YWHAG YWHAH p-S237-TBC1D1:14-3-3RAB8A,10,13,14:GDPSFN RAB8A,10,13,14:GTPRAB4A MYH6 KIF3B CALM1 MYH13 GTP Ca2+ GDPMYH15 p-5S,T642-AS160:14-3-3:IRAPCALM1 MYH6 RALA:GTP:MYO1C:ExocystRALGAPB YWHAZ GTP RAB10 SFN YWHAB SFN MYH2 YWHAB ATPEXOC1 MYH2 ASPSCR1p-S1652-MYO5A:F-actinYWHAE MYH4-like proteinsf-actin (ADP) RALA:GTP:MYO1C:Calmodulin:F-actin14-3-3 dimerYWHAZ p-S197-C2CD5:2xCa2+RAB8A YWHAH EXOC5 YWHAZ RALA YWHAQ MYH1 MYO1C RALA KIFAP3 PRKAG1 GGC-PalmC-RAC1 EXOC5 EXOC6 GTP p-5S,T642-TBC1D4 RALA MYO5AMYH7B EXOC4 ADPRHOQ:GTPRHOQ RAB14 f-actin (ADP) RALGAPA2 MYH2-like proteinsGTPGLUT4:TUGf-actin (ADP)p-S237-TBC1D1MYO1C VAMP2:STX4:SNAP23VAMP2 EXOC3 YWHAG RAB4A:GTP:KIF3:microtubuleATPTBC1D1YWHAG TBC1D4 RAB4A:GTPCa2+ YWHAQ RALA RALGAPB ATPRAC1:GTPRALA:GDPAS160:IRAPExocyst ComplexCALM1 p-S237-TBC1D1 MYH8 KIFAP3 PiYWHAE GTP ASPSCR1 RGC1:p-486,696-T715-RGC2RALA:GTPYWHAE ATPp-T172-PRKAA2 p-S197-C2CD5 PRKAB2 GTP MYH8 LNPEP EXOC8 ADPLNPEP ADPAMPK-alpha2:AMPK-beta:AMPK-gamma:AMPTBC1D4SFN RAB13 YWHAH GDPMYH3 p-5S,T642-TBC1D4 p-5S,T642-AS160:IRAPGTP RGC1:RGC2YWHAG VAMP2C2CD5:2xCa2+SLC2A4YWHAE f-actin (ADP) MYH7 EXOC8 PRKAG2 EXOC7 Microtubule protofilament GTP C2CD5 ATPYWHAB MYH3 KIF3A EXOC2 MYH7 GDP GDP RAB11A:GTPMicrotubuleGTPYWHAQ PRKAG3 p-Y521-STXBP3p-S1652-MYO5A EXOC2 p-S486,S696,T715-RALGAPA2 Microtubule protofilament SLC2A4 YWHAH YWHAZ KIF3A EXOC3 PRKAB1 MYH1 2, 48, 14, 267, 19227187, 197, 2411


Description

In adipocytes and myocytes insulin signaling causes intracellular vesicles carrying the GLUT4 (SLC2A4) glucose transporter to translocate to the plasma membrane, allowing the cells to take up glucose from the bloodstream (reviewed in Zaid et al. 2008, Leney and Tavare 2009, Bogan and Kandror 2010, Foley et al. 2011, Hoffman and Elmendorf 2011, Kandror and Pilch 2011). In myocytes muscle contraction alone can also cause translocation of GLUT4.
Though the entire pathway leading to GLUT4 translocation has not been elucidated, several steps are known. Insulin activates the kinases AKT1 and AKT2. Muscle contraction activates the kinase AMPK-alpha2 and possibly also AKT. AKT2 and, to a lesser extent, AKT1 phosphorylate the RAB GTPase activators TBC1D1 and TBC1D4, causing them to bind 14-3-3 proteins and lose GTPase activation activity. As a result RAB proteins (probably RAB8A, RAB10, RAB14 and possibly RAB13) accumulate GTP. The connection between RAB:GTP and vesicle translocation is unknown but may involve recruitment and activation of myosins.
Myosins 1C, 2A, 2B, 5A, 5B have all been shown to play a role in translocating GLUT4 vesicles near the periphery of the cell. Following docking at the plasma membrane the vesicles fuse with the plasma membrane in a process that depends on interaction between VAMP2 on the vesicle and SNAP23 and SYNTAXIN-4 at the plasma membrane. View original pathway at:Reactome.

Comments

Reactome-Converter 
Pathway is converted from Reactome ID: 1445148
Reactome-version 
Reactome version: 62
Reactome Author 
Reactome Author: May, Bruce

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Bibliography

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  2. Ramm G, Larance M, Guilhaus M, James DE.; ''A role for 14-3-3 in insulin-stimulated GLUT4 translocation through its interaction with the RabGAP AS160.''; PubMed Europe PMC Scholia
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  6. Karlsson HK, Zierath JR, Kane S, Krook A, Lienhard GE, Wallberg-Henriksson H.; ''Insulin-stimulated phosphorylation of the Akt substrate AS160 is impaired in skeletal muscle of type 2 diabetic subjects.''; PubMed Europe PMC Scholia
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  15. Foley K, Boguslavsky S, Klip A.; ''Endocytosis, recycling, and regulated exocytosis of glucose transporter 4.''; PubMed Europe PMC Scholia
  16. Kandror KV, Pilch PF.; ''The sugar is sIRVed: sorting Glut4 and its fellow travelers.''; PubMed Europe PMC Scholia
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  20. Hoffman NJ, Elmendorf JS.; ''Signaling, cytoskeletal and membrane mechanisms regulating GLUT4 exocytosis.''; PubMed Europe PMC Scholia
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  27. Treebak JT, Frøsig C, Pehmøller C, Chen S, Maarbjerg SJ, Brandt N, MacKintosh C, Zierath JR, Hardie DG, Kiens B, Richter EA, Pilegaard H, Wojtaszewski JF.; ''Potential role of TBC1D4 in enhanced post-exercise insulin action in human skeletal muscle.''; PubMed Europe PMC Scholia
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History

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CompareRevisionActionTimeUserComment
115083view17:03, 25 January 2021ReactomeTeamReactome version 75
113525view12:00, 2 November 2020ReactomeTeamReactome version 74
112724view16:12, 9 October 2020ReactomeTeamReactome version 73
101640view11:50, 1 November 2018ReactomeTeamreactome version 66
101176view21:37, 31 October 2018ReactomeTeamreactome version 65
100702view20:10, 31 October 2018ReactomeTeamreactome version 64
100252view16:55, 31 October 2018ReactomeTeamreactome version 63
99804view15:19, 31 October 2018ReactomeTeamreactome version 62 (2nd attempt)
99352view12:48, 31 October 2018ReactomeTeamreactome version 62
94027view13:52, 16 August 2017ReactomeTeamreactome version 61
93648view11:29, 9 August 2017ReactomeTeamreactome version 61
88359view16:37, 1 August 2016FehrhartOntology Term : 'pathway pertinent to protein folding, sorting, modification, translocation and degradation' added !
86764view09:25, 11 July 2016ReactomeTeamreactome version 56
83070view09:51, 18 November 2015ReactomeTeamVersion54
81775view10:34, 26 August 2015ReactomeTeamVersion53
77058view08:35, 17 July 2014ReactomeTeamFixed remaining interactions
76763view12:12, 16 July 2014ReactomeTeamFixed remaining interactions
76087view10:15, 11 June 2014ReactomeTeamRe-fixing comment source
75798view11:33, 10 June 2014ReactomeTeamReactome 48 Update
75149view14:09, 8 May 2014AnweshaFixing comment source for displaying WikiPathways description
74796view08:53, 30 April 2014ReactomeTeamNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
14-3-3 dimerComplexR-HSA-1445138 (Reactome)
ADPMetaboliteCHEBI:16761 (ChEBI)
AMP MetaboliteCHEBI:16027 (ChEBI)
AMPK-alpha2:AMPK-beta:AMPK-gamma:AMPComplexR-HSA-1454683 (Reactome)
AS160:IRAPComplexR-HSA-1445125 (Reactome)
ASPSCR1 ProteinQ9BZE9 (Uniprot-TrEMBL)
ASPSCR1ProteinQ9BZE9 (Uniprot-TrEMBL)
ATPMetaboliteCHEBI:15422 (ChEBI)
C2CD5 ProteinQ86YS7 (Uniprot-TrEMBL)
C2CD5:2xCa2+ComplexR-HSA-5260209 (Reactome)
CALM1 ProteinP0DP23 (Uniprot-TrEMBL)
Ca2+ MetaboliteCHEBI:29108 (ChEBI)
EXOC1 ProteinQ9NV70 (Uniprot-TrEMBL)
EXOC2 ProteinQ96KP1 (Uniprot-TrEMBL)
EXOC3 ProteinO60645 (Uniprot-TrEMBL)
EXOC4 ProteinQ96A65 (Uniprot-TrEMBL)
EXOC5 ProteinO00471 (Uniprot-TrEMBL)
EXOC6 ProteinQ8TAG9 (Uniprot-TrEMBL)
EXOC7 ProteinQ9UPT5 (Uniprot-TrEMBL)
EXOC8 ProteinQ8IYI6 (Uniprot-TrEMBL)
Exocyst ComplexComplexR-HSA-264974 (Reactome)
GDP MetaboliteCHEBI:17552 (ChEBI)
GDPMetaboliteCHEBI:17552 (ChEBI)
GGC-PalmC-RAC1 ProteinP63000 (Uniprot-TrEMBL)
GLUT4:TUGComplexR-HSA-1449566 (Reactome)
GTP MetaboliteCHEBI:15996 (ChEBI)
GTPMetaboliteCHEBI:15996 (ChEBI)
KIF3A ProteinQ9Y496 (Uniprot-TrEMBL)
KIF3B ProteinO15066 (Uniprot-TrEMBL)
KIF3ComplexR-HSA-2316334 (Reactome)
KIFAP3 ProteinQ92845 (Uniprot-TrEMBL)
LNPEP ProteinQ9UIQ6 (Uniprot-TrEMBL)
MYH1 ProteinP12882 (Uniprot-TrEMBL)
MYH13 ProteinQ9UKX3 (Uniprot-TrEMBL)
MYH15 ProteinQ9Y2K3 (Uniprot-TrEMBL)
MYH2 ProteinQ9UKX2 (Uniprot-TrEMBL)
MYH2-like proteinsComplexR-HSA-4127437 (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.
MYH3 ProteinP11055 (Uniprot-TrEMBL)
MYH4 ProteinQ9Y623 (Uniprot-TrEMBL)
MYH4-like proteinsComplexR-HSA-4127445 (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.
MYH6 ProteinP13533 (Uniprot-TrEMBL)
MYH7 ProteinP12883 (Uniprot-TrEMBL)
MYH7B ProteinA7E2Y1 (Uniprot-TrEMBL)
MYH8 ProteinP13535 (Uniprot-TrEMBL)
MYO1C ProteinO00159 (Uniprot-TrEMBL)
MYO1C:CALM1ComplexR-HSA-2316345 (Reactome)
MYO5AProteinQ9Y4I1 (Uniprot-TrEMBL)
Microtubule protofilament R-HSA-8982424 (Reactome)
MicrotubuleComplexR-HSA-190599 (Reactome)
PRKAB1 ProteinQ9Y478 (Uniprot-TrEMBL)
PRKAB2 ProteinO43741 (Uniprot-TrEMBL)
PRKAG1 ProteinP54619 (Uniprot-TrEMBL)
PRKAG2 ProteinQ9UGJ0 (Uniprot-TrEMBL)
PRKAG3 ProteinQ9UGI9 (Uniprot-TrEMBL)
PiMetaboliteCHEBI:18367 (ChEBI)
RAB10 ProteinP61026 (Uniprot-TrEMBL)
RAB11A ProteinP62491 (Uniprot-TrEMBL)
RAB11A:GTPComplexR-HSA-1458542 (Reactome)
RAB13 ProteinP51153 (Uniprot-TrEMBL)
RAB14 ProteinP61106 (Uniprot-TrEMBL)
RAB4A ProteinP20338 (Uniprot-TrEMBL)
RAB4A:GTP:KIF3:microtubuleComplexR-HSA-1458522 (Reactome)
RAB4A:GTPComplexR-HSA-1458538 (Reactome)
RAB8A ProteinP61006 (Uniprot-TrEMBL)
RAB8A,10,13,14:GDPComplexR-HSA-1445130 (Reactome)
RAB8A,10,13,14:GTPComplexR-HSA-1445137 (Reactome)
RAC1:GTPComplexR-HSA-217289 (Reactome)
RALA ProteinP11233 (Uniprot-TrEMBL)
RALA:GDPComplexR-HSA-1458466 (Reactome)
RALA:GTP:MYO1C:Calmodulin:F-actinComplexR-HSA-2316344 (Reactome)
RALA:GTP:MYO1C:ExocystComplexR-HSA-2316343 (Reactome)
RALA:GTPComplexR-HSA-1458506 (Reactome)
RALGAPA2 ProteinQ2PPJ7 (Uniprot-TrEMBL)
RALGAPB ProteinQ86X10 (Uniprot-TrEMBL)
RGC1:RGC2ComplexR-HSA-1458509 (Reactome)
RGC1:p-486,696-T715-RGC2ComplexR-HSA-1458472 (Reactome)
RHOQ ProteinP17081 (Uniprot-TrEMBL)
RHOQ:GTPComplexR-HSA-2316453 (Reactome)
SFN ProteinP31947 (Uniprot-TrEMBL)
SLC2A4 ProteinP14672 (Uniprot-TrEMBL)
SLC2A4ProteinP14672 (Uniprot-TrEMBL)
SNAP23 ProteinO00161 (Uniprot-TrEMBL)
SNAP23ProteinO00161 (Uniprot-TrEMBL)
STX4 ProteinQ12846 (Uniprot-TrEMBL)
STX4:STXBP3 (MUNC18C)ComplexR-HSA-2263479 (Reactome)
STXBP3 ProteinO00186 (Uniprot-TrEMBL)
TBC1D1ProteinQ86TI0 (Uniprot-TrEMBL) As inferred from rat L6 muscle cells, TBC1D1 is located in the perinuclear cytosol (Chen et al. 2008). TBC1D1 is observed throughout the cytosol and, based on its homology to TBC1D4 and its interaction with membrane-bound RAB proteins, TBC1D1 is expected to be concentrated near vesicle membranes.
TBC1D4 ProteinO60343 (Uniprot-TrEMBL)
TBC1D4ProteinO60343 (Uniprot-TrEMBL)
VAMP2 ProteinP63027 (Uniprot-TrEMBL)
VAMP2:STX4:SNAP23ComplexR-HSA-1449628 (Reactome)
VAMP2ProteinP63027 (Uniprot-TrEMBL)
YWHAB ProteinP31946 (Uniprot-TrEMBL)
YWHAE ProteinP62258 (Uniprot-TrEMBL)
YWHAG ProteinP61981 (Uniprot-TrEMBL)
YWHAH ProteinQ04917 (Uniprot-TrEMBL)
YWHAQ ProteinP27348 (Uniprot-TrEMBL)
YWHAZ ProteinP63104 (Uniprot-TrEMBL)
f-actin (ADP) R-HSA-202998 (Reactome)
f-actin (ADP)R-HSA-202998 (Reactome)
p-5S,T642-AS160:14-3-3:IRAPComplexR-HSA-1445124 (Reactome)
p-5S,T642-AS160:IRAPComplexR-HSA-1445133 (Reactome) AS160 (TBC1D4) phosphorylated on serines 318, 341, 570, 588, and 751 and threonine 642 binds to all 14-3-3 proteins, although binding to 14-3-3 delta (YWHAZ) is comparatively low (Ramm et al. 2006, Howlett et al. 2007, Ngo et al. 2009, Treebak et al. 2009, Koumanov et al. 2011). As inferred from mouse, binding to 14-3-3 does not interfere with the interaction between AS160 and IRAP (LNPEP).
p-5S,T642-TBC1D4 ProteinO60343 (Uniprot-TrEMBL)
p-S1652-MYO5A ProteinQ9Y4I1 (Uniprot-TrEMBL)
p-S1652-MYO5A:F-actinComplexR-HSA-2316339 (Reactome)
p-S197-C2CD5 ProteinQ86YS7 (Uniprot-TrEMBL)
p-S197-C2CD5:2xCa2+ComplexR-HSA-5260210 (Reactome)
p-S237-TBC1D1 ProteinQ86TI0 (Uniprot-TrEMBL) As inferred from rat L6 muscle cells, TBC1D1 is located in the perinuclear cytosol (Chen et al. 2008). TBC1D1 is observed throughout the cytosol and, based on its homology to TBC1D4 and its interaction with membrane-bound RAB proteins, TBC1D1 is expected to be concentrated near vesicle membranes.
p-S237-TBC1D1:14-3-3ComplexR-HSA-1454696 (Reactome)
p-S237-TBC1D1ProteinQ86TI0 (Uniprot-TrEMBL) As inferred from rat L6 muscle cells, TBC1D1 is located in the perinuclear cytosol (Chen et al. 2008). TBC1D1 is observed throughout the cytosol and, based on its homology to TBC1D4 and its interaction with membrane-bound RAB proteins, TBC1D1 is expected to be concentrated near vesicle membranes.
p-S486,S696,T715-RALGAPA2 ProteinQ2PPJ7 (Uniprot-TrEMBL)
p-T172-PRKAA2 ProteinP54646 (Uniprot-TrEMBL)
p-T308,S473-AKT1ProteinP31749 (Uniprot-TrEMBL)
p-T309,S474-AKT2ProteinP31751 (Uniprot-TrEMBL)
p-Y521-STXBP3ProteinO00186 (Uniprot-TrEMBL)

Annotated Interactions

View all...
SourceTargetTypeDatabase referenceComment
14-3-3 dimerR-HSA-1445149 (Reactome)
14-3-3 dimerR-HSA-1454689 (Reactome)
ADPArrowR-HSA-1445144 (Reactome)
ADPArrowR-HSA-1449574 (Reactome)
ADPArrowR-HSA-1449597 (Reactome)
ADPArrowR-HSA-1454699 (Reactome)
ADPArrowR-HSA-1458463 (Reactome)
ADPArrowR-HSA-5260201 (Reactome)
AMPK-alpha2:AMPK-beta:AMPK-gamma:AMPmim-catalysisR-HSA-1454699 (Reactome)
AS160:IRAPR-HSA-1445144 (Reactome)
ASPSCR1ArrowR-HSA-1449574 (Reactome)
ATPR-HSA-1445144 (Reactome)
ATPR-HSA-1449574 (Reactome)
ATPR-HSA-1449597 (Reactome)
ATPR-HSA-1454699 (Reactome)
ATPR-HSA-1458463 (Reactome)
ATPR-HSA-5260201 (Reactome)
ArrowR-HSA-2316352 (Reactome)
C2CD5:2xCa2+R-HSA-5260201 (Reactome)
Exocyst ComplexR-HSA-2316352 (Reactome)
GDPArrowR-HSA-2255342 (Reactome)
GDPArrowR-HSA-2255343 (Reactome)
GLUT4:TUGR-HSA-1449574 (Reactome)
GTPR-HSA-2255342 (Reactome)
GTPR-HSA-2255343 (Reactome)
KIF3R-HSA-2316347 (Reactome)
MYH2-like proteinsmim-catalysisR-HSA-2316352 (Reactome)
MYH4-like proteinsmim-catalysisR-HSA-2316352 (Reactome)
MYO1C:CALM1R-HSA-2316349 (Reactome)
MYO5AR-HSA-1449597 (Reactome)
MicrotubuleR-HSA-2316347 (Reactome)
PiArrowR-HSA-1458485 (Reactome)
R-HSA-1445143 (Reactome) RAB proteins have intrinsic weak GTPase activity that is enhanced by RAB-GTPase activating proteins (RAB-GAPs, Sano et al. 2007). The GTPase activity of RAB13 is inferred from other RAB proteins. AS160 (TBC1D4) and TBC1D1 are GAPs that activate the GTPase activity of RAB8A/10/13. Insulin signaling activates AKT, which phosphorylates and inactivates AS160 and TBC1D1, allowing GTP-bound (active) RABs to accumulate.
R-HSA-1445144 (Reactome) As inferred from mouse, AKT2 and, to a lesser extent, AKT1 phosphorylate AS160 (TBC1D4) in response to insulin signaling (Howlett et al. 2007, Karlsson et al 2005). AS160, a RAB GTPase activating protein, interacts with IRAP (LNPEP) and is associated with cytoplasmic vesicles containing GLUT4 (SLC2A4).
R-HSA-1445149 (Reactome) AS160 (TBC1D4) phosphorylated on serines 318, 341, 570, 588, and 751 and threonine 642 binds to all 14-3-3 proteins, although binding to 14-3-3 delta (YWHAZ) is comparatively low (Ramm et al. 2006, Howlett et al. 2007, Ngo et al. 2009, Treebak et al. 2009, Koumanov et al. 2011). As inferred from mouse, binding to 14-3-3 does not interfere with the interaction between AS160 and IRAP (LNPEP).
R-HSA-1449574 (Reactome) After docking at the membrane VAMP2 on the vesicle interacts with SYNTAXIN-4 and SNAP23 on the plasma membrane to catalyze fusion of the vesicle with the plasma membrane. STXBP3 (MUNC18C) bound to STX4 prevents fusion until STXBP3 is phosphorylated.
R-HSA-1449597 (Reactome) As inferred from mouse, AKT2 phosphorylates Myosin 5A on serine-1652. The phosphorylation promotes association of Myosin 5A with actin and ATPase activity of Myosin 5A.
R-HSA-1454689 (Reactome) TBC1D1 phosphorylated on serine-237 binds 14-3-3 proteins in assays with yeast 14-3-3 proteins BMH1 and BMH2 (Chen et al. 2008, Frosig et al. 2010). Binding with human 14-3-3 proteins is inferred.
R-HSA-1454699 (Reactome) In response to muscle contraction and insulin signaling, AMPK-alpha2 phosphorylates TBC1D1 on serine 237 and probably other residues (Frosig et al. 2010, Vichaiwong et al. 2010). As inferred from rat L6 muscle cells TBC1D1 colocalizes with perinuclear vesicles bearing GLUT4 (SLC2A4) and may be involved in an early step that mobilizes them (Chen et al. 2008). Human TBC1D1 appears cytosolic and is believed to be concentrated near vesicle membranes (Park et al. 2011).
R-HSA-1458463 (Reactome) As inferred from mouse, AKT2 (PKB-beta) phosphorylates RBC2 (RALGAPA2) on serine-486, serine-696, and threonine-715 in response to insulin. The phosphorylation prevents RBC1:RBC2 from activating RALA GTPase and allows RALA:GTP to accumulate.
R-HSA-1458485 (Reactome) RALA is a guanine nucleotide binding protein that hydrolyzes bound GTP to yield GDP and phosphate. RGC1 and RGC2 are GAPs (GTPase-activating proteins) that activate the GTPase activity of RALA. Insulin activates AKT, which phosphorylates RGC2, inactivating the GAP activity of RGC1:RGC2 and allowing RALA:GTP to accumulate.
R-HSA-2255342 (Reactome) RALA releases GDP and binds GTP, producing the active form of RALA. The reaction is accelerated by guanine nucleotide exchange factors (GEFs) and opposed by GTPase-activating proteins (GAPs) which enhance the conversion of RALA:GTP back to RALA:GDP by activating the GTPase activity of RALA.
R-HSA-2255343 (Reactome) RAB8A/10/13/14 release GDP and bind GTP to yield the active complex. Guanine nucleotide exchange factors (GEFs) stimulate the reaction. GTPase-activating proteins (GAPs) oppose the reaction by stimulating the intrinsic GTPase activity of the RAB proteins.
R-HSA-2316347 (Reactome) As inferred from mouse adipocytes, insulin signals via PKC-lambda to cause Rab4 to load GTP and associate with Kif3, which then has higher affinity for microtubules. Motor activity of Kif3 along microtubules is believed to transport vesicles containing Glut4 (Slc2a4) across the cytosol to the cortical actin network.
R-HSA-2316349 (Reactome) As inferred from mouse, insulin causes phosphorylation and inactivation of the Ral GTPase activating complex RGC, causing RALA:GTP to accumulate and associate with the unconventional myosin MYO1C. MYO1C, with calmodulin as a light chain, motors across cortical actin and interacts with the exocyst complex to tether vesicles at the plasma membrane (Chen et al. 2007).
R-HSA-2316352 (Reactome) As inferred from mouse, GLUT4 (SLC2A4) initially translocates from endosomes to insulin-responsive vesicles (IRVs, GSVs). RAB11 appears to play a role in this process. IRVs bearing GLUT4 are then translocated across the cortical actin network to the plasma membrane. Myosins 2A, 2B, 5A, and 5B contribute to translocation and are presumed to be involved in this step. Myosin 1C appears to act close to the plasma membrane and may facilitate fusion of the vesicle with the plasma membrane. RAB:GTP complexes coupled to the vesicles may interact with myosins to regulate their activity.
R-HSA-5260201 (Reactome) The protein kinase B beta (AKT) pathway mediates insulin-stimulated glucose transport by increasing glucose transporter GLUT4 translocation from intracellular stores to the plasma membrane. C2 domain-containing protein 5 (C2CD5 aka C2 domain-containing phosphoprotein 138kDa) has been shown to be required for optimal insulin-stimulated GLUT4 translocation and fusion of GLUT4 vesicles with the plasma membrane in adipocytes. It is also able to bind Ca2+ and lipid membranes in its C2 domain. C2CD5 is a substrate for RAC-beta serine/threonine-protein kinase (AKT2), which phosphorylates C2CD5 at serine 197. Phosphorylated C2CD5 optimises GLUT4 translocation to the plasma membrane. The role of human C2CD5 is inferred from the role of the orthologous mouse protein (Xie et al. 2011).
RAB11A:GTPArrowR-HSA-2316352 (Reactome)
RAB4A:GTP:KIF3:microtubuleArrowR-HSA-2316347 (Reactome)
RAB4A:GTPR-HSA-2316347 (Reactome)
RAB8A,10,13,14:GDPArrowR-HSA-1445143 (Reactome)
RAB8A,10,13,14:GDPR-HSA-2255343 (Reactome)
RAB8A,10,13,14:GTPArrowR-HSA-2255343 (Reactome)
RAB8A,10,13,14:GTPArrowR-HSA-2316352 (Reactome)
RAB8A,10,13,14:GTPR-HSA-1445143 (Reactome)
RAB8A,10,13,14:GTPmim-catalysisR-HSA-1445143 (Reactome)
RALA:GDPArrowR-HSA-1458485 (Reactome)
RALA:GDPR-HSA-2255342 (Reactome)
RALA:GTP:MYO1C:Calmodulin:F-actinArrowR-HSA-2316349 (Reactome)
RALA:GTP:MYO1C:Calmodulin:F-actinR-HSA-2316352 (Reactome)
RALA:GTP:MYO1C:Calmodulin:F-actinmim-catalysisR-HSA-2316352 (Reactome)
RALA:GTP:MYO1C:ExocystArrowR-HSA-2316352 (Reactome)
RALA:GTPArrowR-HSA-2255342 (Reactome)
RALA:GTPR-HSA-1458485 (Reactome)
RALA:GTPR-HSA-2316349 (Reactome)
RALA:GTPmim-catalysisR-HSA-1458485 (Reactome)
RGC1:RGC2ArrowR-HSA-1458485 (Reactome)
RGC1:RGC2R-HSA-1458463 (Reactome)
RGC1:p-486,696-T715-RGC2ArrowR-HSA-1458463 (Reactome)
SLC2A4ArrowR-HSA-1449574 (Reactome)
SNAP23R-HSA-1449574 (Reactome)
STX4:STXBP3 (MUNC18C)R-HSA-1449574 (Reactome)
TBC1D1ArrowR-HSA-1445143 (Reactome)
TBC1D1R-HSA-1454699 (Reactome)
TBC1D4ArrowR-HSA-1445143 (Reactome)
VAMP2:STX4:SNAP23ArrowR-HSA-1449574 (Reactome)
VAMP2R-HSA-1449574 (Reactome)
f-actin (ADP)R-HSA-1449597 (Reactome)
f-actin (ADP)R-HSA-2316349 (Reactome)
mim-catalysisR-HSA-1445144 (Reactome)
p-5S,T642-AS160:14-3-3:IRAPArrowR-HSA-1445149 (Reactome)
p-5S,T642-AS160:IRAPArrowR-HSA-1445144 (Reactome)
p-5S,T642-AS160:IRAPR-HSA-1445149 (Reactome)
p-S1652-MYO5A:F-actinArrowR-HSA-1449597 (Reactome)
p-S1652-MYO5A:F-actinmim-catalysisR-HSA-2316352 (Reactome)
p-S197-C2CD5:2xCa2+ArrowR-HSA-2316352 (Reactome)
p-S197-C2CD5:2xCa2+ArrowR-HSA-5260201 (Reactome)
p-S237-TBC1D1:14-3-3ArrowR-HSA-1454689 (Reactome)
p-S237-TBC1D1ArrowR-HSA-1454699 (Reactome)
p-S237-TBC1D1R-HSA-1454689 (Reactome)
p-T308,S473-AKT1mim-catalysisR-HSA-1445144 (Reactome)
p-T309,S474-AKT2mim-catalysisR-HSA-1449597 (Reactome)
p-T309,S474-AKT2mim-catalysisR-HSA-1458463 (Reactome)
p-T309,S474-AKT2mim-catalysisR-HSA-5260201 (Reactome)
p-Y521-STXBP3ArrowR-HSA-1449574 (Reactome)
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