Assembly of the primary cilium (Homo sapiens)

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16, 20, 38, 45, 60...2, 86, 125, 143, 1534, 37, 40, 58, 81...5, 47, 70, 12952, 92, 11528, 65, 67, 75, 89...16, 28, 65, 67, 73...523, 34, 48, 53, 55...15, 28, 97, 104, 138...22, 33, 66, 68, 85...19, 28, 32, 79, 89...52, 92, 11512, 16, 49, 61, 80...5, 45, 51, 72, 83...2, 70, 143, 1534, 37, 40, 58, 81...96, 106, 13140, 127, 13965, 75, 89, 93, 100...13, 30, 36, 57, 100...24, 4015, 28, 38, 42, 97...15, 28, 10473, 100, 12314840, 9016, 17, 60, 12882, 109, 116, 11954, 37, 40, 58, 81...12, 16, 61, 80, 1541, 9, 23, 82, 91...18, 33, 66, 68, 76...15, 28, 39, 41, 55...40, 12710, 15, 26, 28, 87...1, 9, 11, 23, 105...6, 31, 80, 94, 95, 106...5, 21, 27, 54, 62...16, 60, 70, 106, 120...5, 8, 14, 43, 45...38, 47, 70, 129, 132...3, 16, 25, 29, 35...61, 692, 7, 25, 29, 44...5212, 59-61, 80...20, 68, 73, 75, 1234028, 81, 108Golgi lumencytosolprimary ciliumGolgi-associated vesicleGolgi-associated vesicleGolgi-associated vesicleendoplasmic reticulum lumenWDR35 EXOC8 ASAP1 KIF3B TUBB4B CEP72 CEP135 DYNLL1 CCP110 YWHAG TUBA4A TUBA4A CEP290 TCTE3 RAB3IP RP2:ARL3:GTP:UNC119BASAP1 CNGB1 CEP57 SDCCAG8 TUBG1 KIF3A IFT74 DYNLL1 CC2D2A ASAP1 dimerRHO Golgi-derived vesicle PAFAH1B1 HAUS5 HAUS7 HAUS3 KIF24 B9D1 TCTN1 BBS4TUBA4A ARL6 TUBG1 PKD2 HAUS3 ARF4 RAB11FIP3 HSP90AA1 CEP41 NEK2 AHI1 TCTEX1D1 CEP78 PCM1 TUBB IFT88 RAB11A DCTN1-2 PRKAR2B OFD1 myristoylatedciliary cargoCLASP1 IFT20 SMO CEP78 BBS9 ARL3:GTP:UNC119B:myristoylated ciliary cargoTUBA4A TTC30A PPP2R1A IQCB1 RAB8A:GTPCEP76 GTP BBS2 SDCCAG8 TUBG1 acetylatedmicrotubulePKD2 DCTN2 ARF4 CEP83 BBS2KIF17 dimer:TNPO1NINL DCTN3 RAB8A RAB3IP BBS/CCT complexTCTE3 KIFAP3 DYNC2H1 HAUS5 IFT ACEP76 IFT20 SFI1 CDK1 AZI1 CEP83 PPP2R1A CSNK1E EXOC1 IQCB1 CNGA4 PRKAR2B GTP BBS5 CEP89 CEP83 TUBA4A IFT74 TUBB AKAP9 TUBB DCTN1-2 DCTN2 CSNK1D ODF2 BBIP1 IFT52 OFD1 IFT46 CEP78 MyrG2-NPHP3 HSPB11 TTC30A HSPB11 SSNA1 CETN2 EXOC5 PKD1 IFT46 C2CD3 NEDD1 CEP57 RAB11FIP3 TUBB YWHAG CNGB1 HAUS2 GTP TCTE3 BBS9DYNLRB1 CLASP1 TTC26 DYNLL1 YWHAE WDR34 NPHP complexHAUS6 TUBG1 CETN2 PRKACA WDR19 CSNK1D TTC21BRPGRIP1L KIF17 dimerCEP41 NINL CLASP1 KIFAP3 CEP250 mother centrioleCEP97HAUS4 EXOC5 YWHAG IFT88 CETN2 TMEM216 IFT172RP2 IFT57 RAB11A IFT27 TCTEX1D2 CEP70 PDE6D:INPP5EWDR19 CEP290 BBS9 IFT BTCTN3 CLUAP microtubuleDCTN3 NINL IQCB1 INPP5EDYNC1I2 FGFR1OP TTC21B IFT172 CEP57 CDK5RAP2 MAPRE1 UNC119B IFT27 WDR60 IQCB1 CCT8 FGFR1OP CNGA4 dynein-2TTC30B IFT81 YWHAG RABL5 Tectonic-likecomplexCSNK1D PKD1 TTC30A BBS4 HAUS4 UNC119B NINL RAB11A TUBA1A SCLT1 IFT80 WDR19 PKD1 MyrG2-NPHP3 ARF4 DYNLL2 RP2 TUBB4B CEP97 EXOC6 CEP78 WDR35 HSPB11 PKD1 TMEM67 DYNLRB2 YWHAE NPHP4 TTC8ARF4 TCTE3 PAFAH1B1 TUBB4B AZI1 PAFAH1B1 DYNC2LI1 BBIP1CEP164 TTC30B IFT80CEP72 DCTN3 IFT BPKD2 TCTEX1D1 NEK2 LZTFL1 oligomerTMEM67 IFT27 DYNC2LI1 BBS2 VxPx-containingciliary membraneproteinsIFT52 EXOC8 OFD1 CEP290 BBS1 HSPB11 LZTFL1oligomer:BBSomeCEP152 CENPJ CNTRL PDE6DCEP41 KIF24 CNGA4 CNGB1 CKAP5 ODF2 TUBG1 DYNLRB1 CEP152 CEP152 KIF24 HAUS7 CEP250 CEP192 ODF2 CEP72 TUBA1A CEP63 KIF3A RPGRIP1L CSNK1E TCTEX1D2 PAFAH1B1 RAB3IP:BBSomeTTBK2IFT46 CEP89 DCTN1-2 WDR60 HAUS6 RAB3IP:RAB11A:GTP:Golgi-derived vesicleGDP CDK1 DYNC2H1 ACTR1A IFT88 ARL13B:INPP5E:PDE6DPLK1 DCTN3 CEP290 HAUS8 IFT140 CEP97 MKS1 FBF1 CEP72 KIF3C UNC119BEXOC4 CEP162 HSPB11DCTN2 PCM1 IFT81 RAB11A CEP70 RAB3IP IFT74 PLK1 CEP250 PPP2R1A CENPJ HAUS2 CLUAP BBS7 HDAC6HAUS7 DYNC2LI1 KIF3B MAPRE1 NINL CEP63 KIF17 PLK4 RAB11A CEP250 RAB3IPWDR60 TCP1 FBF1 exocystcomplex:RAB8A:GTP:RAB3IP:RAB11:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsPPP2R1A NEK2 Ac-CoASDCCAG8 TCTN2 Centrosome:C2CD3:distal appendage proteins:TTBK2B9D1 AKAP9 CDK1 CNGA2 GTP PRKACA CKAP5 DYNC1H1 CNGA2 CDK5RAP2 HAUS4 CENPJ B9D2 TTC30A HAUS8 AZI1 EXOC7 KIF17 dimer:TNPO1IQCB1 PDE6D TTC26 IFT27 IFT88 CSNK1E RP2:ARL3:GDP:UNC119BBBS1 OFD1 RHO IFT80 WDR19 TTC8 KIF3A BBS10 DYNC1H1 NEK2 PPP2R1A PKD2 WDR60 RAB3IPALMS1 KIF17 TCTE3 ARL3:GDPPAFAH1B1 TUBA4A TTC21B IFT52 HAUS8 PCNT DYNC1I2 CEP41 RABL5 SDCCAG8 H2OAKAP9 CEP135 ASAP1 RAB3IP:RAB8A:GDPCEP57 KIF17 UNC119B DYNLL1 SDCCAG8 SSNA1 BBS9 CEP192 CEP152 GTP ALMS1 ACTR1A HAUS3 CETN2 HAUS8 CEP89GTPDYNLRB2 RAB11FIP3 ARL13B:INPP5EHSPB11 RAB11FIP3 PKD1 CNGA4 DYNLRB1 CDK1 MAPRE1 NPHP4 CEP76 SFI1 TTC30A SMO INPP5E TUBB4B PLK4 NEDD1 CENPJ NINL ACTR1A YWHAE TTBK2 CNTRL DCTN2 MARK4 PRKACA SEPT2TTC30B CSNK1D BBS7 CDK5RAP2 TTC30B HAUS6 TRAF3IP1 RHO PLK4 IFT172 ARF4:GTP:VxPx-containing ciliary membrane proteinsKIF3B CEP162 anterograde IFTtrainsCNGA2 CNTRL CCP110 CCP110 PRKAR2B HAUS3 CKAP5 CEP70 WDR35CEP76 CKAP5 ARL6 CEP250 CSNK1E NEK2 CEP290 CLUAP CCP110 KIF3B ALMS1 GTP CEP164 TUBA1A TRAF3IP1 WDR60 ASAP1 MAPRE1 acetylatedmicrotubuleNDE1 HAUS5 IFT27 PRKAR2B CEP72 KIF24 INPP5E IFT20 CEP83 CNGB1 ALMS1 RAB11A GTP OFD1 SFI1 ALMS1 DYNC1I2 DYNC1I2 CEP192 DYNC2LI1 SSTR3 CNGA2 ACTR1A RAB8A CEP162 IFT172 GTP ALMS1 NPHP4 CEP162 IFT122 CNGB1 FBF1 IFT80 CNTRL PKD1 TUBB4A SFI1 SFI1 ASAP1 KIF3B RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsCLUAP BBIP1 IFT140SSNA1 KIF3B KIF24 BBS5UNC119B ALMS1 TUBG1 TUBB4A IFT122GDP TCTEX1D1 RHO RAB11A:GTP:RAB11FIP3dimer:ASAP1dimer:ARF4:GTP:VxPx-containing ciliary membrane proteinsEXOC2 C2CD3 CEP164 CEP78 PKD1 CLASP1 PKD2 CEP72 acetylated microtubule GDP RAB3IP PLK4 NPHP1 CC2D2A CLUAPDYNC2H1 CNGA4 MCHR1 AKAP9 CEP57 CNGA2 DYNLL1 PKD2 AKAP9 TUBA1A MCHR1 KIF17 CEP63 MKS1 EXOC3 HAUS3 ODF2 IFT43 CEP57 CEP76 CNTRL HAUS8 CDK5RAP2 PKD1 HAUS2 PRKACA GDP DCTN3 CLUAP PCNT HAUS2 IFT122 ARL3 RAB11FIP3 WDR19 TUBB4A IFT46 RAB8A:GDP:RAB3IP:RAB11A:GTP:FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsTTC21B PLK1 HAUS6 AKAP9 CNGA2 DYNLL1 TCTEX1D1 ARL3 TCTEX1D1 IFT88CDK5RAP2 PCNT OFD1 SSTR3 TUBB AZI1 IFT74 HAUS2 CEP152 CNGB1 RAB8A exocyst complexCEP70 DYNC1H1 GTP WDR35 GTP PDE6D GTPCNGA2 IFT20 TTC30B TUBB4B MARK4 SCLT1 CNGA2 IFT43 CNGA4 ARL6 TTC26 ARF4 KIF17 CDK1 WDR19YWHAG YWHAE RAB8A:GDPNDE1 IFT57 TRIP11 GBF1BBIP1 TRAF3IP1 DCTN2 TRIP11TTC8 NEK2 CNTRL MyrG2-NPHP3 SCLT1CEP70 IFT80 BBS1 CEP152 DYNLL1 PLK4 CENPJ DYNC1H1 CENPJ HSP90AA1 TNPO1 GDP NPHP1 CNGB1 IFT81ACTR1A MCHR1 TUBA1A DCTN2 UNC119B:myristoylated ciliary cargoTUBB EXOC4 YWHAE ARL6:GTP:BBSome:ciliary cargoPLK1 CEP72 CEP135 MAPRE1 NDE1 YWHAG IFT122 TMEM216 PDE6D IFT81 CEP83 OFD1 Kinesin-2 motorsCEP250 IFT57 C2CD3 Kinesin-2 motorsDYNC2H1 EXOC3 IFT20 CKAP5 DYNLL2 TTC8 DYNC1I2 GTPFGFR1OP KIF24 retrograde IFTtrainsTTC30B CEP41 CEP97 DCTN1-2 KIF24 TUBG1 HSP90AA1 YWHAG HAUS2 DYNLL1 BBSome ciliary cargoHAUS5 CEP72 Golgi-derived vesicle CEP63 HSPB11 acetylated microtubule ALMS1 PRKACA CNGB1 HAUS3 KIF17 HAUS5 TRAF3IP1 DYNLL1 MAPRE1 SCLT1 NEK2 PCNT BBS7 TCTE3 NEDD1 ARL13B BBS5 CEP290 DCTN2 IFT52 HAUS4 SSNA1 MyrG2-CYS1 BBIP1 active kinesin-2motorsCKAP5 HAUS3 DCTN1-2 TTC8 CEP78 CLUAP HAUS1 TRAF3IP1RAB11A:GTPCEP89 IQCB1 KIF3A HAUS1 MyrG2-CYS1 acetylated microtubule NPHP1 RP2:ARL3:GTP:UNC119B(active)KIF3B CSNK1D CEP152 SCLT1 PLK1 GDPCEP162 CEP135 TTBK2 UNC119B:myristoylated ciliary cargoSDCCAG8 PPP2R1A IFT43DCTN3 TTBK2 CSNK1E HAUS7 RABL5 TTC30B CEP97 RAB11A KIF17 CEP164 DYNLRB2 DYNC2LI1 DYNLRB2 CEP250 NEDD1 SDCCAG8 MyrG2-CYS1 RAB11A Piacetylated microtubule GTP TRAF3IP1 DYNC1H1 IFT B*CEP152 HAUS1 CCP110 CEP162 MKS1 basalbody:transitionzone proteinscentrosome:C2CD2:distal appendage proteins:TTBK2:MARK4PCNT WDR60 CEP290 CETN2 NDE1 CCP110CETN2 MAPRE1 WDR35 FBF1 TTC30A DCTN3 HAUS7 CEP78 IFT81 TUBG1 AHI1 AZI1 CCT2 HAUS2 IFT122 BBS1 NDE1 TUBB4B TRAF3IP1 CLASP1 KIFAP3 IFT80 SFI1 anterograde IFTtrainsNEK2 BBS9 Golgi-derived vesicle CCT4 TTC30WDR34 IFT74 CC2D2A PAFAH1B1 YWHAE CNGB1 PLK1 RAB11A CCT5 PKD2 PAFAH1B1 TTBK2 AZI1 GDPMyrG2-CYS1 IFT74 TUBA1A EXOC1 CETN2 OFD1 IFT74YWHAE GTP RAB11FIP3 dimerIFT46 B9D2 FGFR1OP TCTE3 HAUS1 TUBB4A KIF24 TTC8 HAUS5 GTP PRKACA basalbody:transitionzoneproteins:RAB3IP:RAB11A:GTP:Golgi-derived vesiclePCNT CEP250 RAB11FIP3 ASAP1dimer:ARF4:GTP:VxPx-containing ciliary membrane proteinsCEP97 RAB3IP GTP AHI1 ARL6:GTPFGFR1OP HAUS3 IFT20 retrograde IFTtrainsB9D1 CENPJ HAUS1 NDE1 HSP90AA1 RP2 CEP76 DYNLL1 TUBA1A RABL5HAUS1 SSTR3 IFT43 CNGA2 TUBB PCM1 IFT52 CEP89 TCTEX1D2 TCTEX1D2 IFT74 PAFAH1B1 EXOC2 MyrG2-NPHP3 B9D2 SCLT1 ARL3 MyrG2-NPHP3 CEP70 TUBB4A CEP41 DCTN1-2 ARL13B IFT172 NINL RHO BBS5 CNGA4 KIFAP3 TTC30A SFI1 ASAP1 BBS4 CDK1 TUBA1A WDR35 MKKS HAUS6 BBS4 DYNLL2 ARL3 ODF2 IFT80 ARL6:GTP:BBSome:ciliary cargoWDR60 TCTN1 TCTEX1D2 HAUS6 ODF2 HAUS4 IQCB1 CNTRL DYNC1H1 RHO DYNC1H1 IFT20:TRIP11HAUS6 KIF3A TUBA4A CKAP5 WDR34 TUBA4A IFT20 GTP BBS2 IFT43 RAB3IP RPGRIP1L CEP76 CEP70 AZI1 CENPJ GTP BBS5 DYNC2H1 AKAP9 IFT81 BBS4 IFT172 ARF4:GTPHAUS8 CEP192 NEDD1 CDK1 PRKAR2B KIF3C TMEM216 TTC30B DYNC1H1 CEP164 CEP162 CLUAP CEP83TUBB4B WDR35 CEP63 BBIP1 INPP5E dynein-2IFT140 TTC30A KIFAP3 DYNLL2 TTC26 DCTN1-2 YWHAG CEP57 ACTR1A SSNA1 IFT140 WDR34 CEP192 PDE6D:INPP5ERAB8A GTP DYNLRB1 MARK4 mothercentriole:C2CD3PPP2R1A DYNLL1 ARL3 PCM1 DYNLRB2 RHO TNPO1TMEM67 FBF1 GTP HAUS2 IFT80 ASAP1 TTBK2 TTC26IFT172 RAB11A:GTP:RAB11FIP3dimer:ASAP1dimer:VxPx-containing ciliary membrane proteinsCSNK1D CEP162 HAUS7 CCT3 IFT88 GTP CEP63 PPP2R1A RAB8A RABL5 CNGA4 DYNLRB1 ARL3 IFT46 IFT57 DYNLL1 CEP83 KIF3C RABL5 FBF1NDE1 DCTN3 CEP135 PLK4 ARL3 UNC119BDYNC1I2 CEP164 HAUS4 IFT88 GTP TCTN3 IFT46HSP90AA1 CEP63 HAUS4 SDCCAG8 CEP41 KIFAP3 CLASP1 IFT20DYNC1I2 MAPRE1 CEP70 CEP192 PKD2 PCM1 FBF1 NDE1 MARK4WDR34 FGFR1OP CSNK1E ARL3:GTPC2CD3 DYNC2LI1 ARL3:GTP:UNC119BRAB11FIP3 C2CD3CEP78 PKD2 DYNC1I2 RP2DCTN1-2 WDR19 myristoylatedciliary proteinsDYNC2LI1 HSP90AA1 CKAP5 PCM1 BBS7 VxPx-containingciliary membraneproteinsIFT88 IFT122 C2CD3 IFT27 KIF3C CEP135 CoA-SHSCLT1 KIF17 DYNC2H1 MARK4 CEP57 KIF3A C2CD3 C2CD3 MyrG2-CYS1 TNPO1 IFT52PRKAR2B PLK4 IFT140 CEP76 HSP90AA1 SSNA1 NEDD1 IFT81 HSP90AA1 PCNT RAB11A:GTP:Golgiderived vesicleBBS12 CETN2 ARL13BIFT ABBS7TTC26 HAUS7 NEDD1 CEP135 DYNLRB1 PCNT CLASP1 IQCB1 ODF2 DYNC2H1 CDK5RAP2 TTC26 CEP63 PCM1 PRKACA TUBB4B ATATDYNLL1 IFT57 IFT57 DYNLRB2 GDP CSNK1D CEP41 ASAP1 active dynein-2motorsCLASP1 ARF4:GDPTCTEX1D1 AKAP9 KIF3C DCTN2 IFT57BBS5 YWHAE TRAF3IP1 ACTR1A PKD1 DYNLL2 acetylated microtubule CEP89 KIF17 CDK5RAP2 TCTN3 PLK1 HAUS5 PLK4 HAUS4 TTC21B DYNLL2 UNC119B NINL UNC119B CEP192 HAUS1 SSNA1 CDK5RAP2 SMO FGFR1OP HAUS8 CNGA2 HAUS8 BBS7 GTP BBS2 RAB3IP HAUS1 DYNLRB2 CEP135 WDR34 WDR34 PRKAR2B PLK1 RABL5 TTC21B TCTN2 TCTN1 INPP5E SSNA1 GDPKIFAP3 DYNLL2 KIF3C CSNK1D TTC21B PKD1 IFT43 RAB8A HAUS7 PRKAR2B TCTEX1D1 CNGA4 FGFR1OP IFT122 ACTR1A RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsCEP89 basal bodyEXOC6 BBS4 acetylated microtubule RAB3IP RABL5 CDK1 TUBB4A TCTN2 LZTFL1 PCM1 PRKACA DYNLRB1 RHO RHO CNGB1 PKD2 IFT57 SFI1 PDE6DEXOC7 KIF17 NEDD1 RHO TUBB HAUS6 BBS1 ODF2 HSPB11 IFT43 TCTEX1D2 IFT140 CEP164LZTFL1 UNC119B IFT52 BBSomeIFT27Centrosome:C2CD3:distal appendage proteinsBBS1IFT46 CEP192 IFT140 CSNK1E KIF3A IFT52 TCTEX1D2 CSNK1E TUBB4A RAB8A GTP HAUS5 KIF3C DYNLL1 AZI1 RAB11A BBS9 IFT27 CNGA4 BBS2 CNTRL DYNLL1 TUBB4A IFT172 TTC26 CEP290 IFT81 11821404325, 45, 51, 72125, 45, 51, 72119151804380161119106, 1231


Description

The primary cilium is one of two main types of cilia present on the surface of many eukaryotic cells (reviewed in Flieghauf et al, 2007). Unlike the motile cilia, which are generally present in large numbers on epithelial cells and are responsible for sensory function as well as wave-like beating motions, the primary cilium is a non-motile sensory organelle with roles in signaling and development and is present in a single copy at the apical surface of most quiescent cells (reviewed in Hsiao et al, 2012). Cilium biogenesis involves the anchoring of the basal body, a centriole-derived organelle, near the plasma membrane and the subsequent polymerization of the microtubule-based axoneme and extension of the plasma membrane (reviewed in Ishikawa and Marshall, 2011; Reiter et al, 2012). Although the ciliary membrane is continuous with the plasma membrane, the protein and lipid content of the cilium and the ciliary membrane are distinct from those of the bulk cytoplasm and plasma membrane (reviewed in Emmer et al, 2010; Rohatgi and Snell, 2010). This specialized compartment is established and maintained during cilium biogenesis by the formation of a ciliary transition zone, a proteinaceous structure that, with the transition fibres, anchors the basal body to the plasma membrane and acts as a ciliary pore to limit free diffusion from the cytosol to the cilium (reviewed in Nachury et al, 2010; Reiter et al, 2012). Ciliary components are targeted from the secretory system to the ciliary base and subsequently transported to the ciliary tip, where extension of the axoneme occurs, by a motor-driven process called intraflagellar transport (IFT). Anterograde transport of cargo from the ciliary base to the tip of the cilium requires kinesin-2 type motors, while the dynein-2 motor is required for retrograde transport back to the ciliary base. In addition, both anterograde and retrograde transport depend on the IFT complex, a multiprotein assembly consisting of two subcomplexes, IFT A and IFT B. The primary cilium is a dynamic structure that undergoes continuous steady-state turnover of tubulin at the tip; as a consequence, the IFT machinery is required for cilium maintenance as well as biogenesis (reviewed in Bhogaraju et al, 2013; Hsiao et al, 2012; Li et al, 2012; Taschner et al, 2012; Sung and Leroux, 2013). The importance of the primary cilium in signaling and cell biology is highlighted by the wide range of defects and disorders, collectively known as ciliopathies, that arise as the result of mutations in genes encoding components of the ciliary machinery (reviewed in Goetz and Anderson, 2010; Madhivanan and Aguilar, 2014). View original pathway at:Reactome.

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  33. Tanos BE, Yang HJ, Soni R, Wang WJ, Macaluso FP, Asara JM, Tsou MF.; ''Centriole distal appendages promote membrane docking, leading to cilia initiation.''; PubMed Europe PMC Scholia
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  35. Kozminski KG, Johnson KA, Forscher P, Rosenbaum JL.; ''A motility in the eukaryotic flagellum unrelated to flagellar beating.''; PubMed Europe PMC Scholia
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  42. Brown MT, Andrade J, Radhakrishna H, Donaldson JG, Cooper JA, Randazzo PA.; ''ASAP1, a phospholipid-dependent arf GTPase-activating protein that associates with and is phosphorylated by Src.''; PubMed Europe PMC Scholia
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  48. Insinna C, Humby M, Sedmak T, Wolfrum U, Besharse JC.; ''Different roles for KIF17 and kinesin II in photoreceptor development and maintenance.''; PubMed Europe PMC Scholia
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  56. Kozminski KG, Beech PL, Rosenbaum JL.; ''The Chlamydomonas kinesin-like protein FLA10 is involved in motility associated with the flagellar membrane.''; PubMed Europe PMC Scholia
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  60. Hsiao YC, Tuz K, Ferland RJ.; ''Trafficking in and to the primary cilium.''; PubMed Europe PMC Scholia
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  64. Halbritter J, Bizet AA, Schmidts M, Porath JD, Braun DA, Gee HY, McInerney-Leo AM, Krug P, Filhol E, Davis EE, Airik R, Czarnecki PG, Lehman AM, Trnka P, Nitschké P, Bole-Feysot C, Schueler M, Knebelmann B, Burtey S, Szabó AJ, Tory K, Leo PJ, Gardiner B, McKenzie FA, Zankl A, Brown MA, Hartley JL, Maher ER, Li C, Leroux MR, Scambler PJ, Zhan SH, Jones SJ, Kayserili H, Tuysuz B, Moorani KN, Constantinescu A, Krantz ID, Kaplan BS, Shah JV, UK10K Consortium, Hurd TW, Doherty D, Katsanis N, Duncan EL, Otto EA, Beales PL, Mitchison HM, Saunier S, Hildebrandt F.; ''Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.''; PubMed Europe PMC Scholia
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  154. Nachury MV, Seeley ES, Jin H.; ''Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier?''; PubMed Europe PMC Scholia
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History

CompareRevisionActionTimeUserComment
86366view09:16, 11 July 2016ReactomeTeamreactome version 56
83327view10:47, 18 November 2015ReactomeTeamVersion54
82435view13:12, 29 September 2015ReactomeTeamNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
ACTR1A ProteinP61163 (Uniprot-TrEMBL)
AHI1 ProteinQ8N157 (Uniprot-TrEMBL)
AKAP9 ProteinQ99996 (Uniprot-TrEMBL)
ALMS1 ProteinQ8TCU4 (Uniprot-TrEMBL)
ARF4 ProteinP18085 (Uniprot-TrEMBL)
ARF4:GDPComplexR-HSA-5623424 (Reactome)
ARF4:GTP:VxPx-containing ciliary membrane proteinsComplexR-HSA-5620917 (Reactome)
ARF4:GTPComplexR-HSA-5623423 (Reactome)
ARL13B ProteinQ3SXY8 (Uniprot-TrEMBL)
ARL13B:INPP5E:PDE6DComplexR-HSA-5637977 (Reactome)
ARL13B:INPP5EComplexR-HSA-5624905 (Reactome)
ARL13BProteinQ3SXY8 (Uniprot-TrEMBL)
ARL3 ProteinP36405 (Uniprot-TrEMBL)
ARL3:GDPComplexR-HSA-5624072 (Reactome)
ARL3:GTP:UNC119B:myristoylated ciliary cargoComplexR-HSA-5624104 (Reactome)
ARL3:GTP:UNC119BComplexR-HSA-5624076 (Reactome)
ARL3:GTPComplexR-HSA-5624073 (Reactome)
ARL6 ProteinQ9H0F7 (Uniprot-TrEMBL)
ARL6:GTP:BBSome:ciliary cargoComplexR-HSA-5624112 (Reactome)
ARL6:GTP:BBSome:ciliary cargoComplexR-HSA-5624114 (Reactome)
ARL6:GTPComplexR-HSA-5624106 (Reactome)
ASAP1

dimer:

ARF4:GTP:VxPx-containing ciliary membrane proteins
ComplexR-HSA-5623429 (Reactome)
ASAP1 ProteinQ9ULH1 (Uniprot-TrEMBL)
ASAP1 dimerComplexR-HSA-5623427 (Reactome)
ATATProteinQ5SQI0 (Uniprot-TrEMBL)
AZI1 ProteinQ9UPN4 (Uniprot-TrEMBL)
Ac-CoAMetaboliteCHEBI:15351 (ChEBI)
B9D1 ProteinQ9UPM9 (Uniprot-TrEMBL)
B9D2 ProteinQ9BPU9 (Uniprot-TrEMBL)
BBIP1 ProteinA8MTZ0 (Uniprot-TrEMBL)
BBIP1ProteinA8MTZ0 (Uniprot-TrEMBL)
BBS/CCT complexComplexR-HSA-5624117 (Reactome)
BBS1 ProteinQ8NFJ9 (Uniprot-TrEMBL)
BBS10 ProteinQ8TAM1 (Uniprot-TrEMBL)
BBS12 ProteinQ6ZW61 (Uniprot-TrEMBL)
BBS1ProteinQ8NFJ9 (Uniprot-TrEMBL)
BBS2 ProteinQ9BXC9 (Uniprot-TrEMBL)
BBS2ProteinQ9BXC9 (Uniprot-TrEMBL)
BBS4 ProteinQ96RK4 (Uniprot-TrEMBL)
BBS4ProteinQ96RK4 (Uniprot-TrEMBL)
BBS5 ProteinQ8N3I7 (Uniprot-TrEMBL)
BBS5ProteinQ8N3I7 (Uniprot-TrEMBL)
BBS7 ProteinQ8IWZ6 (Uniprot-TrEMBL)
BBS7ProteinQ8IWZ6 (Uniprot-TrEMBL)
BBS9 ProteinQ3SYG4 (Uniprot-TrEMBL)
BBS9ProteinQ3SYG4 (Uniprot-TrEMBL)
BBSome ciliary cargoComplexR-HSA-5624113 (Reactome)
BBSomeComplexR-HSA-5617794 (Reactome)
C2CD3 ProteinQ4AC94 (Uniprot-TrEMBL)
C2CD3ProteinQ4AC94 (Uniprot-TrEMBL)
CC2D2A ProteinQ9P2K1 (Uniprot-TrEMBL)
CCP110 ProteinO43303 (Uniprot-TrEMBL)
CCP110ProteinO43303 (Uniprot-TrEMBL)
CCT2 ProteinP78371 (Uniprot-TrEMBL)
CCT3 ProteinP49368 (Uniprot-TrEMBL)
CCT4 ProteinP50991 (Uniprot-TrEMBL)
CCT5 ProteinP48643 (Uniprot-TrEMBL)
CCT8 ProteinP50990 (Uniprot-TrEMBL)
CDK1 ProteinP06493 (Uniprot-TrEMBL)
CDK5RAP2 ProteinQ96SN8 (Uniprot-TrEMBL)
CENPJ ProteinQ9HC77 (Uniprot-TrEMBL)
CEP135 ProteinQ66GS9 (Uniprot-TrEMBL)
CEP152 ProteinO94986 (Uniprot-TrEMBL)
CEP162 ProteinQ5TB80 (Uniprot-TrEMBL)
CEP164 ProteinQ9UPV0 (Uniprot-TrEMBL)
CEP164ProteinQ9UPV0 (Uniprot-TrEMBL)
CEP192 ProteinQ8TEP8 (Uniprot-TrEMBL)
CEP250 ProteinQ9BV73 (Uniprot-TrEMBL)
CEP290 ProteinO15078 (Uniprot-TrEMBL)
CEP41 ProteinQ9BYV8 (Uniprot-TrEMBL)
CEP57 ProteinQ86XR8 (Uniprot-TrEMBL)
CEP63 ProteinQ96MT8 (Uniprot-TrEMBL)
CEP70 ProteinQ8NHQ1 (Uniprot-TrEMBL)
CEP72 ProteinQ9P209 (Uniprot-TrEMBL)
CEP76 ProteinQ8TAP6 (Uniprot-TrEMBL)
CEP78 ProteinQ5JTW2 (Uniprot-TrEMBL)
CEP83 ProteinQ9Y592 (Uniprot-TrEMBL)
CEP83ProteinQ9Y592 (Uniprot-TrEMBL)
CEP89 ProteinQ96ST8 (Uniprot-TrEMBL)
CEP89ProteinQ96ST8 (Uniprot-TrEMBL)
CEP97 ProteinQ8IW35 (Uniprot-TrEMBL)
CEP97ProteinQ8IW35 (Uniprot-TrEMBL)
CETN2 ProteinP41208 (Uniprot-TrEMBL)
CKAP5 ProteinQ14008 (Uniprot-TrEMBL)
CLASP1 ProteinQ7Z460 (Uniprot-TrEMBL)
CLUAP ProteinQ96AJ1 (Uniprot-TrEMBL)
CLUAPProteinQ96AJ1 (Uniprot-TrEMBL)
CNGA2 ProteinQ16280 (Uniprot-TrEMBL)
CNGA4 ProteinQ8IV77 (Uniprot-TrEMBL)
CNGB1 ProteinQ14028 (Uniprot-TrEMBL)
CNTRL ProteinQ7Z7A1 (Uniprot-TrEMBL)
CSNK1D ProteinP48730 (Uniprot-TrEMBL)
CSNK1E ProteinP49674 (Uniprot-TrEMBL)
Centrosome:C2CD3:distal appendage proteins:TTBK2ComplexR-HSA-5626178 (Reactome)
Centrosome:C2CD3:distal appendage proteinsComplexR-HSA-5626176 (Reactome)
CoA-SHMetaboliteCHEBI:15346 (ChEBI)
DCTN1-2 ProteinQ14203-2 (Uniprot-TrEMBL)
DCTN2 ProteinQ13561 (Uniprot-TrEMBL)
DCTN3 ProteinO75935 (Uniprot-TrEMBL)
DYNC1H1 ProteinQ14204 (Uniprot-TrEMBL)
DYNC1I2 ProteinQ13409 (Uniprot-TrEMBL)
DYNC2H1 ProteinQ8NCM8 (Uniprot-TrEMBL)
DYNC2LI1 ProteinQ8TCX1 (Uniprot-TrEMBL)
DYNLL1 ProteinP63167 (Uniprot-TrEMBL)
DYNLL2 ProteinQ96FJ2 (Uniprot-TrEMBL)
DYNLRB1 ProteinQ9NP97 (Uniprot-TrEMBL)
DYNLRB2 ProteinQ8TF09 (Uniprot-TrEMBL)
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)
FBF1 ProteinQ8TES7 (Uniprot-TrEMBL)
FBF1ProteinQ8TES7 (Uniprot-TrEMBL)
FGFR1OP ProteinO95684 (Uniprot-TrEMBL)
GBF1ProteinQ92538 (Uniprot-TrEMBL)
GDP MetaboliteCHEBI:17552 (ChEBI)
GDPMetaboliteCHEBI:17552 (ChEBI)
GTP MetaboliteCHEBI:15996 (ChEBI)
GTPMetaboliteCHEBI:15996 (ChEBI)
Golgi-derived vesicle R-NUL-5637956 (Reactome)
H2OMetaboliteCHEBI:15377 (ChEBI)
HAUS1 ProteinQ96CS2 (Uniprot-TrEMBL)
HAUS2 ProteinQ9NVX0 (Uniprot-TrEMBL)
HAUS3 ProteinQ68CZ6 (Uniprot-TrEMBL)
HAUS4 ProteinQ9H6D7 (Uniprot-TrEMBL)
HAUS5 ProteinO94927 (Uniprot-TrEMBL)
HAUS6 ProteinQ7Z4H7 (Uniprot-TrEMBL)
HAUS7 ProteinQ99871 (Uniprot-TrEMBL)
HAUS8 ProteinQ9BT25 (Uniprot-TrEMBL)
HDAC6ProteinQ9UBN7 (Uniprot-TrEMBL)
HSP90AA1 ProteinP07900 (Uniprot-TrEMBL)
HSPB11 ProteinQ9Y547 (Uniprot-TrEMBL)
HSPB11ProteinQ9Y547 (Uniprot-TrEMBL)
IFT AComplexR-HSA-5617795 (Reactome)
IFT AComplexR-HSA-5625350 (Reactome)
IFT B*ComplexR-HSA-5617798 (Reactome)
IFT BComplexR-HSA-5617799 (Reactome)
IFT BComplexR-HSA-5625418 (Reactome)
IFT122 ProteinQ9HBG6 (Uniprot-TrEMBL)
IFT122ProteinQ9HBG6 (Uniprot-TrEMBL)
IFT140 ProteinQ96RY7 (Uniprot-TrEMBL)
IFT140ProteinQ96RY7 (Uniprot-TrEMBL)
IFT172 ProteinQ9UG01 (Uniprot-TrEMBL)
IFT172ProteinQ9UG01 (Uniprot-TrEMBL)
IFT20 ProteinQ8IY31 (Uniprot-TrEMBL)
IFT20:TRIP11ComplexR-HSA-5617801 (Reactome)
IFT20ProteinQ8IY31 (Uniprot-TrEMBL)
IFT27 ProteinQ9BW83 (Uniprot-TrEMBL)
IFT27ProteinQ9BW83 (Uniprot-TrEMBL)
IFT43 ProteinQ96FT9 (Uniprot-TrEMBL)
IFT43ProteinQ96FT9 (Uniprot-TrEMBL)
IFT46 ProteinQ9NQC8 (Uniprot-TrEMBL)
IFT46ProteinQ9NQC8 (Uniprot-TrEMBL)
IFT52 ProteinQ9Y366 (Uniprot-TrEMBL)
IFT52ProteinQ9Y366 (Uniprot-TrEMBL)
IFT57 ProteinQ9NWB7 (Uniprot-TrEMBL)
IFT57ProteinQ9NWB7 (Uniprot-TrEMBL)
IFT74 ProteinQ96LB3 (Uniprot-TrEMBL)
IFT74ProteinQ96LB3 (Uniprot-TrEMBL)
IFT80 ProteinQ9P2H3 (Uniprot-TrEMBL)
IFT80ProteinQ9P2H3 (Uniprot-TrEMBL)
IFT81 ProteinQ8WYA0 (Uniprot-TrEMBL)
IFT81ProteinQ8WYA0 (Uniprot-TrEMBL)
IFT88 ProteinQ13099 (Uniprot-TrEMBL)
IFT88ProteinQ13099 (Uniprot-TrEMBL)
INPP5E ProteinQ9NRR6 (Uniprot-TrEMBL)
INPP5EProteinQ9NRR6 (Uniprot-TrEMBL)
IQCB1 ProteinQ15051 (Uniprot-TrEMBL)
KIF17 ProteinQ9P2E2 (Uniprot-TrEMBL)
KIF17 dimer:TNPO1ComplexR-HSA-5624928 (Reactome)
KIF17 dimer:TNPO1ComplexR-HSA-5624930 (Reactome)
KIF17 dimerComplexR-HSA-5624926 (Reactome)
KIF24 ProteinQ5T7B8 (Uniprot-TrEMBL)
KIF3A ProteinQ9Y496 (Uniprot-TrEMBL)
KIF3B ProteinO15066 (Uniprot-TrEMBL)
KIF3C ProteinO14782 (Uniprot-TrEMBL)
KIFAP3 ProteinQ92845 (Uniprot-TrEMBL)
Kinesin-2 motorsComplexR-HSA-5624910 (Reactome)
Kinesin-2 motorsComplexR-HSA-5625387 (Reactome)
LZTFL1 oligomer:BBSomeComplexR-HSA-5624121 (Reactome)
LZTFL1 ProteinQ9NQ48 (Uniprot-TrEMBL)
LZTFL1 oligomerComplexR-HSA-5624119 (Reactome)
MAPRE1 ProteinQ15691 (Uniprot-TrEMBL)
MARK4 ProteinQ96L34 (Uniprot-TrEMBL)
MARK4ProteinQ96L34 (Uniprot-TrEMBL)
MCHR1 ProteinQ99705 (Uniprot-TrEMBL)
MKKS ProteinQ9NPJ1 (Uniprot-TrEMBL)
MKS1 ProteinQ9NXB0 (Uniprot-TrEMBL)
MyrG2-CYS1 ProteinQ717R9 (Uniprot-TrEMBL)
MyrG2-NPHP3 ProteinQ7Z494 (Uniprot-TrEMBL)
NDE1 ProteinQ9NXR1 (Uniprot-TrEMBL)
NEDD1 ProteinQ8NHV4 (Uniprot-TrEMBL)
NEK2 ProteinP51955 (Uniprot-TrEMBL)
NINL ProteinQ9Y2I6 (Uniprot-TrEMBL)
NPHP complexComplexR-HSA-5626668 (Reactome)
NPHP1 ProteinO15259 (Uniprot-TrEMBL)
NPHP4 ProteinO75161 (Uniprot-TrEMBL)
ODF2 ProteinQ5BJF6 (Uniprot-TrEMBL)
OFD1 ProteinO75665 (Uniprot-TrEMBL)
PAFAH1B1 ProteinP43034 (Uniprot-TrEMBL)
PCM1 ProteinQ15154 (Uniprot-TrEMBL)
PCNT ProteinO95613 (Uniprot-TrEMBL)
PDE6D ProteinO43924 (Uniprot-TrEMBL)
PDE6D:INPP5EComplexR-HSA-5624934 (Reactome)
PDE6D:INPP5EComplexR-HSA-5624936 (Reactome)
PDE6DProteinO43924 (Uniprot-TrEMBL)
PKD1 ProteinP98161 (Uniprot-TrEMBL)
PKD2 ProteinQ13563 (Uniprot-TrEMBL)
PLK1 ProteinP53350 (Uniprot-TrEMBL)
PLK4 ProteinO00444 (Uniprot-TrEMBL)
PPP2R1A ProteinP30153 (Uniprot-TrEMBL)
PRKACA ProteinP17612 (Uniprot-TrEMBL)
PRKAR2B ProteinP31323 (Uniprot-TrEMBL)
PiMetaboliteCHEBI:18367 (ChEBI)
RAB11A ProteinP62491 (Uniprot-TrEMBL)
RAB11A:GTP:Golgi derived vesicleComplexR-HSA-5637979 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:ARF4:GTP:VxPx-containing ciliary membrane proteins
ComplexR-HSA-5623434 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:VxPx-containing ciliary membrane proteins
ComplexR-HSA-5623437 (Reactome)
RAB11A:GTPComplexR-HSA-5623431 (Reactome)
RAB11FIP3 ProteinO75154 (Uniprot-TrEMBL)
RAB11FIP3 dimerComplexR-HSA-5623435 (Reactome)
RAB3IP ProteinQ96QF0 (Uniprot-TrEMBL)
RAB3IP:BBSomeComplexR-HSA-5617806 (Reactome)
RAB3IP:RAB11A:GTP:Golgi-derived vesicleComplexR-HSA-5637982 (Reactome)
RAB3IP:RAB8A:GDPComplexR-HSA-5623440 (Reactome)
RAB3IPProteinQ96QF0 (Uniprot-TrEMBL)
RAB8A ProteinP61006 (Uniprot-TrEMBL)
RAB8A:GDP:RAB3IP:RAB11A:GTP:FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsComplexR-HSA-5623444 (Reactome)
RAB8A:GDPComplexR-HSA-5623441 (Reactome)
RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsComplexR-HSA-5623447 (Reactome)
RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsComplexR-HSA-5623450 (Reactome)
RAB8A:GTPComplexR-HSA-5623445 (Reactome)
RABL5 ProteinQ9H7X7 (Uniprot-TrEMBL)
RABL5ProteinQ9H7X7 (Uniprot-TrEMBL)
RHO ProteinP08100 (Uniprot-TrEMBL)
RP2 ProteinO75695 (Uniprot-TrEMBL)
RP2:ARL3:GDP:UNC119BComplexR-HSA-5637984 (Reactome)
RP2:ARL3:GTP:UNC119B(active)ComplexR-HSA-5637988 (Reactome)
RP2:ARL3:GTP:UNC119BComplexR-HSA-5637985 (Reactome)
RP2ProteinO75695 (Uniprot-TrEMBL)
RPGRIP1L ProteinQ68CZ1 (Uniprot-TrEMBL)
SCLT1 ProteinQ96NL6 (Uniprot-TrEMBL)
SCLT1ProteinQ96NL6 (Uniprot-TrEMBL)
SDCCAG8 ProteinQ86SQ7 (Uniprot-TrEMBL)
SEPT2ProteinQ15019 (Uniprot-TrEMBL)
SFI1 ProteinA8K8P3 (Uniprot-TrEMBL)
SMO ProteinQ99835 (Uniprot-TrEMBL)
SSNA1 ProteinO43805 (Uniprot-TrEMBL)
SSTR3 ProteinP32745 (Uniprot-TrEMBL)
TCP1 ProteinP17987 (Uniprot-TrEMBL)
TCTE3 ProteinQ8IZS6 (Uniprot-TrEMBL)
TCTEX1D1 ProteinQ8N7M0 (Uniprot-TrEMBL)
TCTEX1D2 ProteinQ8WW35 (Uniprot-TrEMBL)
TCTN1 ProteinQ2MV58 (Uniprot-TrEMBL)
TCTN2 ProteinQ96GX1 (Uniprot-TrEMBL)
TCTN3 ProteinQ6NUS6 (Uniprot-TrEMBL)
TMEM216 ProteinQ9P0N5 (Uniprot-TrEMBL)
TMEM67 ProteinQ5HYA8 (Uniprot-TrEMBL)
TNPO1 ProteinQ92973 (Uniprot-TrEMBL)
TNPO1ProteinQ92973 (Uniprot-TrEMBL)
TRAF3IP1 ProteinQ8TDR0 (Uniprot-TrEMBL)
TRAF3IP1ProteinQ8TDR0 (Uniprot-TrEMBL)
TRIP11 ProteinQ15643 (Uniprot-TrEMBL)
TRIP11ProteinQ15643 (Uniprot-TrEMBL)
TTBK2 ProteinQ6IQ55 (Uniprot-TrEMBL)
TTBK2ProteinQ6IQ55 (Uniprot-TrEMBL)
TTC21B ProteinQ7Z4L5 (Uniprot-TrEMBL)
TTC21BProteinQ7Z4L5 (Uniprot-TrEMBL)
TTC26 ProteinA0AVF1 (Uniprot-TrEMBL)
TTC26ProteinA0AVF1 (Uniprot-TrEMBL)
TTC30A ProteinQ86WT1 (Uniprot-TrEMBL)
TTC30B ProteinQ8N4P2 (Uniprot-TrEMBL)
TTC30ComplexR-HSA-5637976 (Reactome)
TTC8 ProteinQ8TAM2 (Uniprot-TrEMBL)
TTC8ProteinQ8TAM2 (Uniprot-TrEMBL)
TUBA1A ProteinQ71U36 (Uniprot-TrEMBL)
TUBA4A ProteinP68366 (Uniprot-TrEMBL)
TUBB ProteinP07437 (Uniprot-TrEMBL)
TUBB4A ProteinP04350 (Uniprot-TrEMBL)
TUBB4B ProteinP68371 (Uniprot-TrEMBL)
TUBG1 ProteinP23258 (Uniprot-TrEMBL)
Tectonic-like complexComplexR-HSA-5626670 (Reactome)
UNC119B ProteinA6NIH7 (Uniprot-TrEMBL)
UNC119B:myristoylated ciliary cargoComplexR-HSA-5624105 (Reactome)
UNC119B:myristoylated ciliary cargoComplexR-HSA-5624122 (Reactome)
UNC119BProteinA6NIH7 (Uniprot-TrEMBL)
VxPx-containing

ciliary membrane

proteins
ComplexR-HSA-5620919 (Reactome)
VxPx-containing

ciliary membrane

proteins
ComplexR-HSA-5623420 (Reactome)
WDR19 ProteinQ8NEZ3 (Uniprot-TrEMBL)
WDR19ProteinQ8NEZ3 (Uniprot-TrEMBL)
WDR34 ProteinQ96EX3 (Uniprot-TrEMBL)
WDR35 ProteinQ9P2L0 (Uniprot-TrEMBL)
WDR35ProteinQ9P2L0 (Uniprot-TrEMBL)
WDR60 ProteinQ8WVS4 (Uniprot-TrEMBL)
YWHAE ProteinP62258 (Uniprot-TrEMBL)
YWHAG ProteinP61981 (Uniprot-TrEMBL)
acetylated microtubuleR-HSA-5618327 (Reactome)
acetylated microtubuleR-HSA-5624939 (Reactome)
acetylated microtubule R-HSA-5624939 (Reactome)
active dynein-2 motorsComplexR-HSA-5625410 (Reactome)
active kinesin-2 motorsComplexR-HSA-5624943 (Reactome)
anterograde IFT trainsComplexR-HSA-5624945 (Reactome)
anterograde IFT trainsComplexR-HSA-5625417 (Reactome)
basal

body:transition zone

proteins:RAB3IP:RAB11A:GTP:Golgi-derived vesicle
ComplexR-HSA-5637989 (Reactome)
basal

body:transition

zone proteins
ComplexR-HSA-5626673 (Reactome)
basal bodyComplexR-HSA-5626181 (Reactome)
centrosome:C2CD2:distal appendage proteins:TTBK2:MARK4ComplexR-HSA-5626678 (Reactome)
dynein-2ComplexR-HSA-5624940 (Reactome)
dynein-2ComplexR-HSA-5625411 (Reactome)
exocyst complex:RAB8A:GTP:RAB3IP:RAB11:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsComplexR-HSA-5623455 (Reactome)
exocyst complexComplexR-HSA-5623453 (Reactome)
microtubuleR-HSA-190599 (Reactome)
mother centriole:C2CD3ComplexR-HSA-5626175 (Reactome)
mother centrioleComplexR-HSA-5626171 (Reactome)
myristoylated ciliary cargoComplexR-HSA-5624099 (Reactome)
myristoylated ciliary proteinsComplexR-HSA-5624102 (Reactome)
retrograde IFT trainsComplexR-HSA-5624947 (Reactome)
retrograde IFT trainsComplexR-HSA-5625425 (Reactome)

Annotated Interactions

View all...
SourceTargetTypeDatabase referenceComment
ARF4:GDPArrowR-HSA-5623513 (Reactome)
ARF4:GDPR-HSA-5623508 (Reactome)
ARF4:GTP:VxPx-containing ciliary membrane proteinsArrowR-HSA-5620914 (Reactome)
ARF4:GTP:VxPx-containing ciliary membrane proteinsR-HSA-5620918 (Reactome)
ARF4:GTPArrowR-HSA-5623508 (Reactome)
ARF4:GTPR-HSA-5620914 (Reactome)
ARL13B:INPP5E:PDE6DArrowR-HSA-5624953 (Reactome)
ARL13B:INPP5E:PDE6DR-HSA-5638012 (Reactome)
ARL13B:INPP5EArrowR-HSA-5638012 (Reactome)
ARL13BR-HSA-5624953 (Reactome)
ARL3:GDPArrowR-HSA-5638016 (Reactome)
ARL3:GTP:UNC119B:myristoylated ciliary cargoArrowR-HSA-5624133 (Reactome)
ARL3:GTP:UNC119B:myristoylated ciliary cargoR-HSA-5624130 (Reactome)
ARL3:GTP:UNC119BArrowR-HSA-5624130 (Reactome)
ARL3:GTP:UNC119BR-HSA-5638004 (Reactome)
ARL3:GTPR-HSA-5624133 (Reactome)
ARL6:GTP:BBSome:ciliary cargoArrowR-HSA-5624126 (Reactome)
ARL6:GTP:BBSome:ciliary cargoArrowR-HSA-5624127 (Reactome)
ARL6:GTP:BBSome:ciliary cargoR-HSA-5624127 (Reactome)
ARL6:GTPR-HSA-5624126 (Reactome)
ASAP1

dimer:

ARF4:GTP:VxPx-containing ciliary membrane proteins
ArrowR-HSA-5620918 (Reactome)
ASAP1

dimer:

ARF4:GTP:VxPx-containing ciliary membrane proteins
R-HSA-5620921 (Reactome)
ASAP1 dimerR-HSA-5620918 (Reactome)
ATATmim-catalysisR-HSA-5618328 (Reactome)
Ac-CoAArrowR-HSA-5618331 (Reactome)
Ac-CoAR-HSA-5618328 (Reactome)
BBIP1R-HSA-5624125 (Reactome)
BBS/CCT complexArrowR-HSA-5624125 (Reactome)
BBS1R-HSA-5624125 (Reactome)
BBS2R-HSA-5624125 (Reactome)
BBS4R-HSA-5624125 (Reactome)
BBS5R-HSA-5624125 (Reactome)
BBS7R-HSA-5624125 (Reactome)
BBS9R-HSA-5624125 (Reactome)
BBSome ciliary cargoR-HSA-5624126 (Reactome)
BBSomeArrowR-HSA-5624125 (Reactome)
BBSomeR-HSA-5617815 (Reactome)
BBSomeR-HSA-5624126 (Reactome)
BBSomeR-HSA-5624129 (Reactome)
C2CD3R-HSA-5626220 (Reactome)
CCP110ArrowR-HSA-5626227 (Reactome)
CEP164R-HSA-5626223 (Reactome)
CEP83R-HSA-5626223 (Reactome)
CEP89R-HSA-5626223 (Reactome)
CEP97ArrowR-HSA-5626227 (Reactome)
CLUAPR-HSA-5617820 (Reactome)
Centrosome:C2CD3:distal appendage proteins:TTBK2ArrowR-HSA-5626228 (Reactome)
Centrosome:C2CD3:distal appendage proteins:TTBK2R-HSA-5626699 (Reactome)
Centrosome:C2CD3:distal appendage proteinsArrowR-HSA-5626223 (Reactome)
Centrosome:C2CD3:distal appendage proteinsR-HSA-5626228 (Reactome)
CoA-SHArrowR-HSA-5618328 (Reactome)
CoA-SHR-HSA-5618331 (Reactome)
FBF1R-HSA-5626223 (Reactome)
GBF1mim-catalysisR-HSA-5623508 (Reactome)
GDPArrowR-HSA-5617816 (Reactome)
GDPArrowR-HSA-5623508 (Reactome)
GDPArrowR-HSA-5623521 (Reactome)
GTPR-HSA-5617816 (Reactome)
GTPR-HSA-5623508 (Reactome)
GTPR-HSA-5623521 (Reactome)
H2OR-HSA-5623513 (Reactome)
HDAC6mim-catalysisR-HSA-5618331 (Reactome)
HSPB11R-HSA-5617820 (Reactome)
IFT AArrowR-HSA-5617829 (Reactome)
IFT AArrowR-HSA-5625421 (Reactome)
IFT AArrowR-HSA-5625424 (Reactome)
IFT AR-HSA-5624949 (Reactome)
IFT AR-HSA-5624952 (Reactome)
IFT B*ArrowR-HSA-5617820 (Reactome)
IFT B*R-HSA-5617825 (Reactome)
IFT BArrowR-HSA-5617825 (Reactome)
IFT BArrowR-HSA-5625421 (Reactome)
IFT BArrowR-HSA-5625424 (Reactome)
IFT BR-HSA-5624949 (Reactome)
IFT BR-HSA-5624952 (Reactome)
IFT122R-HSA-5617829 (Reactome)
IFT140R-HSA-5617829 (Reactome)
IFT172R-HSA-5617820 (Reactome)
IFT20:TRIP11R-HSA-5617828 (Reactome)
IFT20ArrowR-HSA-5617828 (Reactome)
IFT20R-HSA-5617825 (Reactome)
IFT27R-HSA-5617820 (Reactome)
IFT43R-HSA-5617829 (Reactome)
IFT46R-HSA-5617820 (Reactome)
IFT52R-HSA-5617820 (Reactome)
IFT57R-HSA-5617820 (Reactome)
IFT74R-HSA-5617820 (Reactome)
IFT80R-HSA-5617820 (Reactome)
IFT81R-HSA-5617820 (Reactome)
IFT88R-HSA-5617820 (Reactome)
INPP5ER-HSA-5624956 (Reactome)
KIF17 dimer:TNPO1ArrowR-HSA-5624948 (Reactome)
KIF17 dimer:TNPO1ArrowR-HSA-5624951 (Reactome)
KIF17 dimer:TNPO1R-HSA-5624948 (Reactome)
KIF17 dimerR-HSA-5624951 (Reactome)
Kinesin-2 motorsArrowR-HSA-5625421 (Reactome)
Kinesin-2 motorsArrowR-HSA-5625424 (Reactome)
Kinesin-2 motorsR-HSA-5624952 (Reactome)
LZTFL1 oligomer:BBSomeArrowR-HSA-5624129 (Reactome)
LZTFL1 oligomer:BBSomeTBarR-HSA-5624127 (Reactome)
LZTFL1 oligomerR-HSA-5624129 (Reactome)
MARK4R-HSA-5626699 (Reactome)
NPHP complexR-HSA-5626681 (Reactome)
PDE6D:INPP5EArrowR-HSA-5624954 (Reactome)
PDE6D:INPP5EArrowR-HSA-5624956 (Reactome)
PDE6D:INPP5ER-HSA-5624953 (Reactome)
PDE6D:INPP5ER-HSA-5624954 (Reactome)
PDE6DArrowR-HSA-5638012 (Reactome)
PDE6DR-HSA-5624956 (Reactome)
PiArrowR-HSA-5623513 (Reactome)
R-HSA-5617815 (Reactome) The BBS1 component of the BBSome complex binds RAB3IP, a GEF for the small GTPase RAB8A. RAB3IP is required for RAB8A to localize to the cilium, and depletion of RAB3IP compromises cilia formation (Nachury et al, 2007; Loktev et al, 2008). GTP-bound RAB8A may promote ciliogenesis by promoting the traffic of post-Golgi vesicles to the base of the primary cilium (Nachury et al, 2007; reviewed in Zerial and McBride, 2001; Ishikawa et al, 2011; Hsiao et al, 2012; Sung and Leroux, 2013).
R-HSA-5617816 (Reactome) RAB3IP is a GEF for RAB8A, the only RAB GTPase localized in the cilium. GTP-bound RAB8A may play a role in recruiting vesicles from the Golgi to the ciliary base and is required for cilia formation (Nachury et al, 2007; Yoshimura et al, 2007; reviewed in Reiter et al, 2012).
R-HSA-5617820 (Reactome) Based on studies done in C. reinhardtii, C. elegans and mouse, the human IFT B complex likely consists of, minimally, IFT20, RABL5/IFT22, HSPB11/IFT25, IFT27, IFT46, IFT52, TRAF3IP1/IFT54, IFT74, IFT80, IFT81, IFT88, CLUAP/QILIN, IFT70/TTC30, and TTC26/IFT56, with IFT172 being an additional candidate (Follit et al, 2009; Piperno and Mead, 1997; Cole et al, 1998; Cole, 2003; Ou, 2007; Hallbritter et al, 2013; reviewed in Taschner et al, 2012). Work in C. reinhardtii and mouse suggests that IFT B consists of a salt stable core complex of IFT88, IFT81, IFT74, IFT70, IFT52, IFT46 IFT 27, IFT25 and IFT22 with peripheral, weakly associated subunits IFT 172, IFT80, IFT57, CLUAP, TTC26 and IFT20 (Lucker et al, 2005; Lucker et al, 2010; Follit et al, 2009; Bhogaraju et al, 2011). In Chlamydomonas, core components IFT81 and IFT74 have been shown to interact directly and a stable sub-complex of IFT81/74/27/25 has been demonstrated (Lucker et al, 2005; Taschner et al, 2011). Human IFT81 and IFT74 have likewise been shown to directly interact and to form a tubulin-binding complex (Bhogaraju et al, 2013). A recent study has elucidated more detail of the protein-protein interactions that direct the assembly of the IFTB complex (Taschner et al, 2014).
This reaction shows putative human IFT B proteins assembling in a single step; details of how and when this assembly occurs are not shown, nor are the specific protein-protein interactions within the complex or details of how IFT B is regulated. Moreover, this reaction shows the formation of a presumptive IFT B* complex, lacking IFT20, to allow the recruitment of IFT20 from the Golgi compartment to be depicted.
R-HSA-5617825 (Reactome) IFT20 is unique among IFT B components in that, in addition to being localized at the cilium and the centrosome, a pool of IFT20 exists at the Golgi in complex with the golgin protein TRIP11 (Follit et al, 2006; Follit et al, 2008; Follit et al, 2009). Independent of its interaction with TRIP11, IFT20 has been shown to interact with the IFT B complex member TRAF3IP1 at the cilium, and overexpression of TRAF3IP1 displaces IFT20 from the Golgi (Follit et al, 2009). Partial depletion of IFT20 disrupts the traffic of membrane proteins to the cilium (Follit et al, 2006; Follit et al, 2009). Taken together, these data suggest a model where TRAF3IP1 mediates recruitment of IFT20-carrying vesicles from the Golgi to the site of cilium assembly, thus completing assembly of the IFT B complex and delivering both lipid and protein cargo for cilium biogenesis (Follit et al, 2008; Follit et al, 2009; reviewed in Ishikawa et al, 2011).
R-HSA-5617828 (Reactome) IFT20 is a member of the IFT B anterograde complex that is required for cilia formation and that, uniquely among IFT proteins, is found at the Golgi in addition to the centrosome and the cilium. Fluorescently-labelled IFT20 shuttles between the Golgi complex and the cilium and the ciliary microtubules (Follit et al, 2006; Follit et al, 2009). Golgi-association of IFT20 depends on interaction with the peripheral membrane protein TRIP11 and this interaction occurs independently of the IFT B complex (Follit et al, 2008). Golgi-localization of IFT20 is abolished in cells lacking TRIP11, and cilia in these cells are short and have a depleted complement of polycystin-2, a ciliary-localized membrane protein (Follit et al, 2008). RNAi-depletion of IFT20 in mammalian cells similarly compromises the traffic of polycystin-2 to the cilium (Follit et al, 2006). These data suggest that IFT20 may have a role at the Golgi complex in sorting and transporting membrane proteins that are destined for the cilium (Follit et al, 2006; Follit et al, 2008; Follit et al, 2009). IFT54, another IFT B component that is localized at the cilia, interacts with IFT20 but not with TRIP11, and overexpression of IFT54 displaces IFT20 from the Golgi. This supports a model where, after dissociation of the TRIP11:IFT20 complex, IFT54 docks IFT20 at the primary cilium, possibly on the surface of Golgi-derived vesicles, thus completing assembly of the IFT B complex and delivering ciliary membrane and membrane proteins to the site of cilium assembly (Follit et al, 2009; Omori et al, 2008; Li et al, 2008).
R-HSA-5617829 (Reactome) The IFT A complex is believed to be composed of six components: WDR19/IFT144, IFT140, IFT122, TTC21B/IFT139, WDR35/IFT121 and IFT43 (Piperno et al, 1998; Cole and Snell, 2009; reviewed in Taschner et al, 2012). Each of these proteins was identified as a TULP3-interacting protein in human cells, supporting the notion established in other organisms that they are all components of the IFT A complex (Mukhopadhyay et al, 2010; reviewed in Taschner et al, 2012). The IFT A proteins are large and generally have similar domain organization, consisting of N-terminal WD motifs and C-terminal TPR repeats. These protein interaction domains may help the IFT A complex scaffold recruitment of the IFT B complex, as well as recruit ciliary cargo and motor proteins. Intriguingly, the domain structure of IFT A proteins is similar to that of nucleoporins and coat proteins and it has been suggested that they evolved from a coat protein precursor, consistent with a role in vesicle trafficking (Devos et al, 2004; Jekely and Arendt, 2006).
Details of protein-protein interactions within the IFT A complex are not known, nor are the details of how and where the complex assembles in a human cell.
R-HSA-5618328 (Reactome) Cilia are enriched in acetylated tubulin, a marker that is associated with stability, and the kinesin motor preferentially travels on acetylated microtubules (Johnson et al, 1998; Reed et al, 2006; Cai et al, 2009). Alpha tubulin acetyltransferase (ATAT), also known as MEC17, has been shown to catalyze the acetylation of alpha tubulin at K40 (Akella et al, 2010; Shida et al, 2010; Montagnac et al, 2013). ATAT preferentially acetylates polymerized alpha tubulin and may access the luminal K40 residue through 'breathing' of the microtubules protofilaments (Shida et al, 2010). ATAT was identified as an interacting protein with components of the BBSome, and siRNA knockdown of ATAT delays assembly of the primary cilium (Jin et al, 2010; Shida et al, 2010). BBIP1 is another component of the BBSome that has been shown to affect tubulin acetylation and stability, potentially through its interaction with HDAC6. BBIP1 exerts its effect on microtubule acetylation independently of its role as a component of the BBSome; it may exert its indirect effect by promoting ATAT-mediated acceleration, by counteracting HDAC6-mediated deacetylation, or by another mechanism (Loktev et al, 2008)
R-HSA-5618331 (Reactome) HDAC6 is a microtubule-associated deacetylase that targets the K40 acetyl groups of alpha tubulin (Hubbert et al, 2002; Loktev et al, 2008; Zhang et al, 2008). HDAC6 also interacts with BBIP1, a component of the BBSome that is required for BBSome assembly, and additionally (and independently of its role in the BBSome) plays a role in microtubule polymerization and acetylation (Loktev et al, 2008). Depletion of BBIP1 causes a marked reduction in cytoplasmic microtubule acetylation, and this defect is partially overcome by inhibition of HDAC6. These data suggest that BBIP1 may exert its effect on microtubule acetylation by negatively regulating HDAC6, although other mechanisms are also possible (Loktev et al, 2008).
R-HSA-5620914 (Reactome) ARF4 is a small GTPase that faciliates the targeting of some membrane proteins destined for the cilium. ARF4-mediated targeting of these cargo may depend in part on a VxPx-like motif in the C-terminal tails (Deretic et al, 2005; Geng et al, 2006; Jenkins et al, 2006; Mazelova et al, 2009; Ward et al, 2011; Wang et al, 2012; reviewed in Li et al, 2012). ARF4 is the only ARF protein with a role in ciliogenesis, and its localization at the TGN positions it to act as primary sorting mechanism for membrane proteins destined for the cilium (reviewed in Deretic, 2013; Li et al, 2012). ARF4 is myristoylated at the N-terminus and is membrane-associated in its GTP-bound form (reviewed in Li et al, 2012).
R-HSA-5620918 (Reactome) ASAP1 is a dimeric ARF GTPase activating protein (GAP) and scaffolding protein that is recruited to the trans-Golgi network (TGN) through interactions with activated ARF4, PI(4,5)P2 and acidic phospholipids (Brown et al, 1998; Che et al, 2005; Nie et al, 2006). Once at the TGN, ASAP1 forms a tripartite complex with ARF4 and ciliary cargo, possibly by interacting with a putative C-terminal FR targeting motif present in a number of membrane proteins destined for the cilium, although this remains to be conclusively demonstrated (Corbit et al, 2005; Wang et al, 2012; reviewed in Bhogaraju et al, 2013). In addition to its role as an ARF GAP, ASAP1 also scaffolds the recruitment of a number of other proteins required for ciliary targeting, including RAB11 and the RAB11 effector FIP3 (Mazelova et al, 2009; Inoue et al, 2008; reviewed in Deretic 2013).
R-HSA-5620921 (Reactome) Recruitment of ASAP1 to the TGN facilitates the subsequent recruitment of both RAB11A and the RAB11 effector protein FIP3 to the ciliary targeting complex. RAB11FIP3 functions as a homodimer and can bind simultaneously to RAB11 and ARF4 through its C-terminal region (Inoue et al, 2008; Mazelova et al, 2009; Wang et al, 2012; Shiba et al, 2006; Eathiraj et al, 2006; Schonteich et al, 2007). RAB11FIP3 also interacts with the BAR domain of ASAP1 and in this way may play a role in stimulating the ARF GAP activity of ASAP1, promoting the inactivation ARF4 and its subsequent dissociation from the TGN (Inoue et al, 2008; reviewed in Deretic, 2013).
R-HSA-5623508 (Reactome) GBF1 promotes guanine nucleotide exchange on ARF4 at the Golgi membrane, activating the small GTPase and promoting its association with the Golgi membrane (Szul et al, 2007; reviewed in Deretic, 2013). Activated ARF4 at the trans-Golgi network may represent the initial sorting point for membrane proteins destined for the primary cilium (reviewed in Li et al, 2012).
R-HSA-5623513 (Reactome) Recruitment of RAB11FIP3 to the trans-Golgi network (TGN) simulates ASAP1 to activate the ARF4 GTPase activity, causing the hydrolysis of GTP and the release of ARF4:GDP from the Golgi membrane (Mazelova et al, 2009; Inoue et al, 2008; reviewed in Deretic, 2013).
R-HSA-5623519 (Reactome) RAB8A is another small GTPase that is required for ciliogenesis. RAB8A is recruited to the ciliary targeting complex at the trans-Golgi network (TGN) through interactions of the RAB8A guanine nucleotide exchange factor (GEF) RAB3IP (also known as RABIN8) with ASAP1 and RAB11 (Wang et al, 2012; Westlake et al, 2011; Feng et al, 2012; reviewed in Deretic, 2013). RAB8A is recruited in the inactive GDP bound form, and is activated at the TGN by RAB3IP in a RAB11A-dependent fashion (Hatulla et al, 2002; Knodler et al, 2010; Westlake et al, 2012; Wang et al, 2012; Feng et al, 2012).
R-HSA-5623521 (Reactome) Once recruited to the ciliary targeting complex, RAB3IP/RABIN8 stimulates nucleotide exchange on RAB8A. Activated RAB8A is required for ciliogenesis and plays a role in mediating vesicle docking at the basal body, providing both lipid and protein content to the emerging cilium (Hattula et al, 2002; Knodler et al, 2010; Nachury et al, 2007; Wang et al, 2012; Westlake et al, 2011; Yoshimura et al, 2007; reviewed in Deretic, 2013; Sung and Leroux, 2013).


R-HSA-5623524 (Reactome) RAB3IP interacts directly with the EXOC6/SEC15 component of the exocyst, recruiting this membrane-targeting complex to the Golgi-derived vesicles (Feng et al, 2012; reviewed in Deretic, 2013). The exocyst is an octameric complex with roles in tethering and fusion of secretory vesicles with target membranes. A number of the exocyst components have been shown to be localized to the ciliary base and/or to be required for ciliogenesis. Consistent with this, IQCB1/NPHP5, a component of the basal body, has been shown to interact with members of the exocyst complex (Wu et al, 2005; Rogers et al, 2004; Zuo et al, 2009; Feng et al, 2012; Sang et al, 2011; reviewed in Das and Guo, 2011; Heider and Munson, 2012).
R-HSA-5623525 (Reactome) Membrane budding at the trans-Golgi network is promoted at least in part by the BAR domain of ASAP1, which is involved in sensing and inducing membrane curvature as well as providing the recognition site for small GTPases (Nie et al, 2006; Jian et al, 2009; Inoue et al, 2008; reviewed in Masuda et al, 2010). Oligomerization between ASAP1 and RAB11FIP3 may contribute to coat formation on vesicles budding from the TGN and destined for the plasma or ciliary membrane (Inoue et al, 2008; Mazelova et al, 2009; reviewed in Deretic, 2013).
R-HSA-5623527 (Reactome) Exocyst-mediated fusion of the Golgi-derived vesicle delivers the VxPx-containing membrane proteins to the ciliary membrane, although the precise mechanisms remain to be worked out (Mazelova et al, 2009; Wang et al, 2012; reviewed in Sung and Leroux, 2013). Vesicles carrying membrane proteins destined for the cilum may fuse at the periciliary membrane at the base of the cilium and deliver cargo to the IFT system. Ciliary membrane proteins may also diffuse laterally into the periciliary membrane after fusion of vesicles with the plasma membrane (reviewed in Hsiao et al, 2012; Sung and Leroux, 2013). Although not depicted in this reaction, there is evidence that some of the protein-protein interactions of the ciliary-targeting complex may persist into the periciliary or ciliary membrane region (Wang et al, 2012).
R-HSA-5624125 (Reactome) The BBSome is a complex of 8 conserved proteins with roles in ciliary trafficking (Nachury et al, 2007; Loktev et al, 2008; reviewed in Nachury et al, 2010; Hsiao et al, 2012). Mutations in the BBS genes leads to Bardet-Biedl syndrome, a heterogeneous ciliopathy characterized by obesity, blindness, cystic kidney disease, retinitis pigmentosa, polydactyly, mental retardation, and renal failure in some cases (reviewed in Tobin and Beales, 2009). The BBSome is the primary effector of ARL6/BBS3, a small GTPase that recruits the BBSome and associated membrane proteins destined for the primary cilium to membranes (Jin et al, 2010; Nachury et al, 2007; Zhang et al, 2011; Seo et al 2011). The BBSome also interacts with the RAB8A guanine nucleotide exchange factor RAB3IP, and in this way promotes the recruitment of RAB8A to the cilium (Nachury et al, 2007). Components of the BBSome are enriched in beta propeller and TPR domains and have been shown to form linear arrays on liposomes (Jin et al, 2010). Where these arrays form, and how they contribute to ciliary targeting remains to be elucidated (Jin et al, 2010; reviewed in Nachury et al, 2010).

In mammalian cells, formation of the BBSome depends on a BBS/CCT complex that consists of MKKS/BBS6, BBS10, BBS12 and 6 members of the CCT/TRiC family of chaperonins. The BBS/CCT complex interacts with a subset of the BBSome protein and plays a role in the BBS7 stability, promoting the formation of an intermediate "BBSome core complex" (Seo et al, 2010; Jin et al, 2010; Zhang el al, 2012).
R-HSA-5624126 (Reactome) ARL6 is a small GTPase that was also identified as BBS3, a gene that when mutated gives rise to the ciliopathy Bardet-Biedel syndrome (Chiang et al, 2004; Fan et al, 2004). In its GTP-form, membrane-associated ARL6 recruits the BBSome along with BBSome-associated cargo such as SSTR3, MHCR1 or SMO to the cilium (Jin et al, 2010; Zhang et al, 2011; Seo et al, 2011). Binding of IFT27 to the nucleotide-free form of ARL6 may also play a role in promoting the exit of the BBSome from the cilium (Liew et al, 2014). The BBSome, a complex consisting of BBS1, BBS2, BBS4, BBS5, BBS7, BBC9, TTC8/BBS8 and BBIP10 is thought to contribute to ciliary targeting, either by promoting budding of vesicles from the secretory pathway or through lateral diffusion of BBSome-enriched 'rafts' from the plasma membrane as indicated in this reaction (Jin et al, 2010; reviewed in Li et al, 2012; Sung and Leroux, 2013; Nachury et al, 2010). The interaction between the BBSome and ARL6 is mediated by the N-terminal B-propeller domain of BBSome component BBS1 (Jin et al, 2010). BBSome function is negatively regulated by LZTFL1, which forms a complex with the BBSome in the cytosol and inhibits its traffic to the cilium (Seo et al, 2011).
R-HSA-5624127 (Reactome) ARL6:GTP and the BBSome complex are required for the ciliary accumulation of proteins such as SSTR3, MHRC1 and SMO (Zhang et al, 2011; Jin et al, 2010; Seo et al, 2011; reviewed in Nachury et al, 2010; Sung and Leroux, 2013). BBSome localization to the primary cilium is negatively regulated by LZTFL1, and ciliary accumulation of some BBSome cargo is increased by LZTFL1 depletion (Seo et al, 2011).
R-HSA-5624129 (Reactome) LZTFL1 was identified as a tumor suppressor and as a protein that interacts with components of the BBSome (Wei et al, 2010; Seo et al, 2011). LZTFL1 forms cytosolic complexes with the BBSome and negatively regulates its entry into the cilium without affecting the assembly or stability of the BBSome complex. Both the BBSome and LZTFL1 have been shown to regulate the localization of the Hh signaling protein SMO (Seo et al, 2011). A recent study suggests that LZTFL1 may additionally play a role in coordinating the interaction between the BBSome and the IFT B component IFT27 and in this way contribute to the traffic of Hh pathway proteins into and out of the cilium (Eguether et al, 2014).
R-HSA-5624130 (Reactome) Binding of ARL3 to UNC119B induces a conformational change that obstructs UNC119B cargo-binding and promotes the release of the myrisoylated cargo into the ciliary membrane (Wright et al, 2011; Ismail et al, 2012).
R-HSA-5624131 (Reactome) UNC119B is an ARL3 effector that binds directly to the myristoyl moieties at glycine 2 of NPHP3 and CYS1 (Wright et al, 2011). Myristoylation is required for the ciliary localization of these proteins (Wright et al, 2011; Tao et al, 2006), and both mutation of the glycine 2 myristoylation target in NPHP3 and siRNA knockdown of UNC119B dramatically reduce the ciliary localization of NPHP3 and CYS1 (Tao et al, 2006; Wright et al, 2011; reviewed in Schwarz et al, 2012).
R-HSA-5624132 (Reactome) UNC119B promotes the translocation of myristoylated NPHP3 from the ER membrane to the primary cilium by an unknown mechanism. Ciliary localization depends both on myristoylation and UNC119B, as mutation of the glycine 2 acceptor site or siRNA knockdown of UNC119B drastically reduces the amount of NPHP3 or CYS1 in the cilium (Wright et al, 2011).
R-HSA-5624133 (Reactome) ARL3 is an ARF-like small GTPase that is localized to the primary cilium in both the GDP- and the GTP-bound form (Zhou et al, 2006; Wright et al, 2011). ARL3 binds UNC119B in a GTP-dependent fashion and is required for the ciliary localization of NPHP3 and CYS1. Upon GTPase activation, ARL3 promotes the transfer of the myristoylated cargo into the ciliary membrane (Wright et al, 2011).
R-HSA-5624948 (Reactome) Ciliary localization of the alternative kinesin-2 motor KIF17 depends on TNPO1 and the RAN:GDP/RAN:GTP gradient. Once in the cilium, the TNPO1:KIF17 complex is likely dissociated by RAN:GTP binding and subsequent GTP hydrolysis, freeing KIF17 to play its role in anterograde IFT transport (Dishinger et al, 2010).
R-HSA-5624949 (Reactome) IFT particles were first characterized in Chlamydomonas reinhardtii, where they were observed by differential interference contrast microscopy as electron-dense granules that move along doublet microtubules of the ciliary axoneme (Kozminski et al, 1993; Kozminski et al, 1995; reviewed in Pedersen et al, 2008). More recent ultrastructural analysis of Chlamydomonas flagella confirms the presence of two distinct types of IFT trains, a longer, less electron-opaque anterograde train and shorter, more opaque retrograde trains. Both the anterograde and retrograde trains are associated with the outer microtubule doublets and with the inner surface of the flagellar membrane (Pigino et al, 2009). Isolation and characterization of IFT particles revealed that they consist of 2 biochemically distinct subcomplexes, IFT A and IFT B that are widely conserved in ciliated organisms (Piperno et al, 1997; Cole et al, 1998; reviewed in Sung and Leroux, 2013). Anterograde traffic is driven by kinesin-2 type motors in an ATP-dependent manner. Evidence from C. elegans suggests distinct and sequential roles for the canonical heterotrimeric kinesin-2 motor and the alternate homodimeric kinesin-2, OSM-3 (homologue of human KIF17) in mediating anterograde transport, but this has not been demonstrated in human cells where the canonical kinesin-2 motor predominates (Evans et al, 2006; Snow et al, 2004; Ou et al, 2005). Human KIF17 appears to be required in some cell types for cilia formation, and plays a role in the import of some ciliary cargo (Jenkins et al, 2006; Insinna et al, 2008; Insinna et al, 2009; Dishinger et al, 2010; reviewed in Verhey et al, 2011). Assembly of the anterograde IFT trains at the base of the primary cilium may be facilitated by the BBSome complex, which has also been shown to display IFT-like movement along the axoneme; however, the BBSome is highly sub-stoichiometric with respect to the IFT complex, so this notion requires more substantiation (Ou et al, 2005; Wei et al, 2012; Blacque et al, 2004; Nachury et al, 2007; Lechtreck et al, 2009; reviewed in Sung and Leroux, 2013). Studies in C. elegans also suggest a role for ARL13B and ARL3 in regulating the stability of the anterograde IFT train (Li et al, 2010).
R-HSA-5624951 (Reactome) KIF17 is an alternate kinesin-2 motor that is required in some cell types for anterograde IFT and for the ciliary localization of CNG (Ou et al, 2005; Jenkins et al, 2006; Insinna et al, 2008; Insinna et al, 2009; Li et al, 2010; reviewed in Scholey, 2008; Verhey et al, 2011). KIF17 contains a C-terminal ciliary localization signal that mediates its interaction with nuclear import factor TNPO1 (importin beta-2). This interaction is required for the ciliary targeting of KIF17 and is regulated by RAN GTP levels such that the interaction is promoted in the cytosol where RAN:GTP levels are low, and is destabilized in the cilium where RAN:GTP levels are high (Dishinger et al, 2010). The roles of TNPO1 and the RAN:GTP gradient in promoting ciliary localization of KIF17 are analogous to their roles in nuclear import and provide evidence for the first time of conserved mechanisms governing nuclear and ciliary localization (Dishinger et al, 2010; Devos et al, 2004; Gruss, 2010).
R-HSA-5624952 (Reactome) Remodelling of IFT trains is thought to occur at the ciliary tip (Iomini et al, 2001; Buisson et al, 2013; reviewed in Snell and Cole, 2009). Retrograde transport is driven by the multi-subunit dynein-2 motor in an ATP-dependent fashion (Hou et al, 2004; Pazour et al, 1999; Porter et al, 1999; reviewed in Cole and Snell, 2009; Ishikawa et al, 2011). Mutations in genes encoding members of the IFT A complex or the dynein-2 motor generally result in short, swollen cilia that abnormally acccumulate IFT components (Iomini et al, 2009; Piperno et al, 1998; Pazour et al, 1999). The subunit composition of the human dynein-2 complex has recently been analyzed and preliminary characterization of the IFT A complex has begun, but detailed understanding of the molecular architecture of the retrograde IFT trains is still lacking (Assante et al, 2014; Piperno et al, 1998; Mukhopadhyay et al, 2010; reviewed in Taschner et al, 2012).
R-HSA-5624953 (Reactome) The small GTPase ARL13B is required for the ciliary localization of INPP5E. ARL13B binds directly to INPP5E and is thought to displace PDE6D from the complex (Humbert et al, 2012).
R-HSA-5624954 (Reactome) INPP5E is a ciliary peripheral membrane protein that is associated with the ciliopathy Joubert's Syndrome (Bielas et al, 2009; Jacoby et al, 2009). Ciliary localization of the full-length protein depends on a targeting sequence and interactions with PDE6D and ARL13B, although the detailed mechanism remains unresolved (Humbert et al, 2012).
R-HSA-5624956 (Reactome) The inositol polyphosphate phosphatase INPP5E is a ciliary localized peripheral membrane protein with a CaaX prenylation motif in its C-terminus (Jacoby et al, 2009; Bielas et al, 2009; Humbert et al, 2012). This motif is downstream of the ciliary targeting sequence and prenylation is not required for the ciliary localization of INPP5E. The CaaX motif is required for the interaction between INPP5E and the phosphodiesterase PDE6D, and PDE6D is required for the ciliary localization of full length INPP5E but not a truncated solubilized form. These data suggest that PDE6D may play a role in extracting prenylated INPP5E from a donor membrane prior to ciliary targeting (Humbert et al, 2012).
R-HSA-5625416 (Reactome) Anterograde trains travel along the axoneme of the primary cilium at an estimated rate of 2 micrometers per second in an ATP- and kinesin-2-dependent fashion (reviewed in Cole and Snell, 2009). Although the particulars of IFT train-cargo interactions have not been fully elaborated, recent studies in C. reinhardtii and human cells have shown that the IFT B components IFT74 and IFT81 have tubulin-binding sites, while IFT46 is required for the ciliary transport of the outer dynein arm, and more recently, TTC26 has been shown to be required for the transport of motility-related proteins into the flagella (Bhogaraju et al, 2013; Ahmed et al, 2008; Hou et al, 2007; Ishikawa et al, 2014; reviewed in Bhogarju et al, 2014).
R-HSA-5625421 (Reactome) Based on work done in C. reinhardtii and Trypanosoma brucei, anterograde IFT trains are believed to disassemble at the ciliary tip, releasing cargo and the IFT motors. Smaller retrograde trains are subsequently reassembled for transport back to the ciliary base (Iomini et al, 2001; Buisson et al, 2013; Pigino et al, 2009; reviewed in Ishikawa et al, 2011; Bhogaraju et al, 2013). A direct interaction between IFT27 and the nucleotide-free form of ARL6 may contribute to ARL6 activation and in this way contribute to ciliary exit of some cargo (Liew et al, 2014).
R-HSA-5625424 (Reactome) At the base of the cilium, retrograde trains are believed to disassemble and recycle for a subsequent round of IFT transport (Iomini et al, 2001; Buisson et al, 2013; reviewed in Ishikawa et al, 2011; Cole and Snell, 2009).
R-HSA-5625426 (Reactome) Retrograde trains are shorter than anterograde particles and travel along the axoneme of the primary cilium at an estimated rate of 3 micrometers per second (reviewed in Cole and Snell, 2009).
R-HSA-5626220 (Reactome) C2 domain-containing protein 3 (C2CD3) is basal body-localized protein that is required for ciliogenesis and Hh signaling (Hoover et al, 2008; Balestra et al, 2013). C2CD3 is recruited to the centrosome in a pericentriolar material 1 protein (PCM1)- and microtubule-dependent manner and is required for the subsequent recruitment of the distal appendage proteins to the mother centriole (Tanos et al, 2013; Sillibourne et al, 2013; Ye et al, 2014; reviewed in Winey and O'Toole, 2014). The distal appendage proteins are thought to be a component of the transition fibres that anchor the basal body to the membrane at the base of the cilium and are themselves required for the recruitment of Tau-tubulin kinase 2 (TTBK2) and for docking ciliary vesicles to the mother centriole (Tanos et al, 2013; Wei et al, 2013; Joo et al, 2013; Schmidt et al, 2012; Sillibourne et al, 2013; Burke et al, 2014).
R-HSA-5626223 (Reactome) C2CD3 and the centrosome component OFD1 are required for the recruitment of distal appendage proteins CEP164, CEP83/CCDC41, CEP89, FBF1 and SCLT1 to the mother centriole (Ye et al, 2014; Tang et al, 2013; Singla et al, 2010). Distal appendage proteins are believed to form part of the transition fibres that anchor the basal bodies to the actin rich cortex at the base of the emerging primary cilium, and are also required for the recruitment and binding of ciliary vesicles and intraflagellar transport (IFT) complexes (Tanos et al, 2013; Wei et al, 2013; Joo et al, 2010; Schmidt et al, 2012; Sillibourne et al, 2013; Ye et al, 2014; reviewed in Winey and O'Toole, 2014).
R-HSA-5626227 (Reactome) CCP110 is a negative regulator of ciliogenesis that caps the mother centriole. CCP110 may inhibit ciliogenesis in part by preventing the CEP290-dependent recruitment of RAB8A to the centrosome and cilia (Spektor et al, 2007; Tsang et al, 2008; reviewed in Tsang and Dynlacht, 2013). CCP110 and CEP97 also form a complex with the KIF24, a kinesin with centriolar microtubule depolymerizing activity that is required for the initial recruitment and/or stability of CCP110 at the centriole (Kobayashi et al, 2011). Recruitment of TTBK2 promotes the displacement of CCP110 and its binding partner CEP97. This results in the formation of a basal body and promotes recruitment of IFT complex members and allows axonemal extension to occur (Goetz et al, 2012; Ye et al, 2014; reviewed in Tsang and Dynlacht, 2013). Although the kinase activity of TTBK2 is required for cilium formation and TTBK2 has been shown to phosphorylate CEP164, the relevant physiological target during ciliogenesis has not been unambiguously identified (Cajanek et al, 2014). Similarly, the kinase activity of MARK4 is also required for ciliogenesis, and the interaction between MARK4 and ODF2, a putative substrate, is needed to promote the dissociation of the CCP110 and CEP97 proteins from the centriole (Kuhns et al, 2013; reviewed in Kim and Dynlacht, 2013).
R-HSA-5626228 (Reactome) C2CD3 and the distal appendage protein CEP164 are required for the recruitment of the kinase Tau tubulin kinase 2 (TTBK2) to the centriole (Ye et al, 2014; Cajanek et al, 2014). TTBK2 recruitment promotes the release of CCP110, a negative regulator of ciliogenesis that caps the mother centriole (Goetz et al, 2012; Ye et al, 2014; Tsang et al, 2008; Spektor et al, 2007). CCP110 is initially recruited and/or stabilized at the mother centriole in a KIF24-dependent manner; KIF24, a kinesin-like protein, also restricts ciliogenesis through its microtubule depolymerizing activity (Kobayashi et al, 2011). In addition to promoting the release of CCP110, TTBK2 also plays a role in the recruitment of intraflagellar transport (IFT) proteins and in this way contributes to extension of the ciliary axoneme (Goetz et al, 2012; Ye et al, 2014). Mutations in TTBK2 disrupt ciliogenesis and are associated with the development of spinocerebellar ataxia (Houlden et al, 2007; Bouskila et al, 2011; reviewed in Jackson, 2012).
R-HSA-5626681 (Reactome) The transition zone is a protein-rich zone at the base of the primary cilium that forms after maturation of the mother centriole and prior to or concurrent with the initiation of intraflagellar transport (IFT) (reviewed in Benzing and Schermer, 2011; Reiter et al, 2012). The transition zone consists of a growing number of proteins and protein complexes, many of whose genes are associated with ciliopathies such as nephronophthisis, Meckel-Gruber syndrome and Joubert's syndrome (Reiter et al, 2006; Hu et al, 2010; Sang et al, 2011; Williams et al, 2011; Garcia-Gonzalo et al, 2011; Chih et al, 2012; reviewed in Reiter et al, 2012). In conjunction with SEPT2, which was recently shown to form a septin ring diffusion barrier at the base of the cilium, the transition zone and its resident proteins contribute to protein sorting and ciliary membrane composition and act as a ciliary gate (Hu et al, 2010; Williams et al, 2011; Garcia-Gonzalo et al, 2011; Chih et al, 2012; reviewed in Reiter et al, 2012).
R-HSA-5626699 (Reactome) MARK4 (microtubule associated protein/microtubule affinity regulating kinase 4) was identified in a screen as a positive regulator of ciliogenesis (Kuhns et al, 2013). MARK4 interacts at the centriole with the subdistal appendage component ODF2 and this interaction is required to promote axonemal extension (Kuhns et al, 2013; reviewed in Kim and Dynlacht, 2013). Like Tau tubulin kinase 2 (TTBK2), MARK4 appears to have a role in promoting the dissociation of CCP110 and CEP97, uncapping the centriole and allowing axonemal extension to take place (Kuhns et al, 2013; Ye et al, 2014;; Goetz et al, 2012). Although this reaction shows that MARK4 is recruited to the centriole subsequent to TTBK2, the timing of the ODF2:MARK4 interaction is not known.
R-HSA-5638004 (Reactome) RP2 is an ARL3 GAP that is localized to the primary cilium and plays a role in trafficking proteins from the Golgi to the ciliary membrane (Veltel et al, 2008a; Hurd et al, 2011; Evans et al, 2010; Wright et al, 2011). RP2 forms a ternary complex with UNC119B and ARL3, activating the ARL3 GTPase activity and promoting the release of UNC119B (Veltel et al, 2008b; Wright et al, 2011; Kuhnel et al, 2006; reviewed in Schwarz et al, 2012; Li et al, 2012)
R-HSA-5638006 (Reactome) RP2 is an ARL3 GAP that is localized to the primary cilium and plays a role in trafficking proteins from the Golgi to the ciliary membrane (Veltel et al, 2008a; Hurd et al, 2011; Evans et al, 2010; Wright et al, 2011). RP2 forms a ternary complex with UNC119B and ARL3, activating the ARL3 GTPase activity and promoting the release of UNC119B (Veltel et al, 2008b; Wright et al, 2011; Kuhnel et al, 2006; reviewed in Schwarz et al, 2012; Li et al, 2012)
R-HSA-5638007 (Reactome) RP2 is an ARL3 GAP that is localized to the primary cilium and plays a role in trafficking proteins from the Golgi to the ciliary membrane (Veltel et al, 2008a; Hurd et al, 2011; Evans et al, 2010; Wright et al, 2011). RP2 forms a ternary complex with UNC119B and ARL3, activating the ARL3 GTPase activity and promoting the release of UNC119B (Veltel et al, 2008b; Wright et al, 2011; Kuhnel et al, 2006; reviewed in Schwarz et al, 2012; Li et al, 2012)
R-HSA-5638009 (Reactome) The distal appendage protein CEP164 interacts with RAB3IP, and in this way recruits Golgi-derived vesicles to the basal body to initiate ciliary membrane biogenesis (Schmidt et al, 2012; Westlake et al, 2011; Rohatgi and Snell, 2010). RAB3IP recruitment to the distal appendages of centrioles promotes the appropriate localization and activation of RAB8A (Nachury et al, 2007; Yoshimura et al, 2007; Westlake et al, 2011; Schmidt et al, 2012).
R-HSA-5638012 (Reactome) ARL13B promotes the ciliary localization of INPP5E by interacting with it directly and displacing PDE6D from the complex (Humbert et al, 2012).
R-HSA-5638014 (Reactome) The RAB8 guanine nucleotide exchange factor RAB3IP/RABIN8 is recruited to vesicles through interaction with membrane-tethered RAB11:GTP (Westlake et al, 2011; Knodler et al, 2010). Recruitment of RAB3IP may also depend on the TRAPPCII complex, a multiprotein complex with roles in vesicular trafficking (Westlake et al, 2011; reviewed in Sacher et al, 2008). RAB3IP is required for RAB8A to localize to the cilium, and depletion of RAB3IP compromises cilia formation (Nachury et al, 2007; Loktev et al, 2008). GTP-bound RAB8A may promote ciliogenesis by promoting the traffic of post-Golgi vesicles to the base of the primary cilium (Nachury et al, 2007; Westlake et al, 2011; Feng et al, 2012; reviewed in Reiter et al, 2012)
R-HSA-5638016 (Reactome) ARL3 hydrolysis of GTP promotes the release of UNC119B, dissociating the complex (Wright et al, 2011; reveiwed in Schwarz et al, 2012).
RAB11A:GTP:Golgi derived vesicleR-HSA-5638014 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:ARF4:GTP:VxPx-containing ciliary membrane proteins
ArrowR-HSA-5620921 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:ARF4:GTP:VxPx-containing ciliary membrane proteins
R-HSA-5623513 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:ARF4:GTP:VxPx-containing ciliary membrane proteins
mim-catalysisR-HSA-5623513 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:VxPx-containing ciliary membrane proteins
ArrowR-HSA-5623513 (Reactome)
RAB11A:GTP:RAB11FIP3

dimer:ASAP1

dimer:VxPx-containing ciliary membrane proteins
R-HSA-5623519 (Reactome)
RAB11A:GTPR-HSA-5620921 (Reactome)
RAB11FIP3 dimerR-HSA-5620921 (Reactome)
RAB3IP:BBSomeArrowR-HSA-5617815 (Reactome)
RAB3IP:RAB11A:GTP:Golgi-derived vesicleArrowR-HSA-5638014 (Reactome)
RAB3IP:RAB11A:GTP:Golgi-derived vesicleR-HSA-5638009 (Reactome)
RAB3IP:RAB8A:GDPR-HSA-5623519 (Reactome)
RAB3IPR-HSA-5617815 (Reactome)
RAB3IPR-HSA-5638014 (Reactome)
RAB8A:GDP:RAB3IP:RAB11A:GTP:FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsArrowR-HSA-5623519 (Reactome)
RAB8A:GDP:RAB3IP:RAB11A:GTP:FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsR-HSA-5623521 (Reactome)
RAB8A:GDP:RAB3IP:RAB11A:GTP:FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsmim-catalysisR-HSA-5623521 (Reactome)
RAB8A:GDPR-HSA-5617816 (Reactome)
RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsArrowR-HSA-5623521 (Reactome)
RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsArrowR-HSA-5623525 (Reactome)
RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsR-HSA-5623524 (Reactome)
RAB8A:GTP:RAB3IP:RAB11A:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsR-HSA-5623525 (Reactome)
RAB8A:GTPArrowR-HSA-5617816 (Reactome)
RABL5R-HSA-5617820 (Reactome)
RP2:ARL3:GDP:UNC119BArrowR-HSA-5638006 (Reactome)
RP2:ARL3:GDP:UNC119BR-HSA-5638016 (Reactome)
RP2:ARL3:GTP:UNC119B(active)ArrowR-HSA-5638007 (Reactome)
RP2:ARL3:GTP:UNC119B(active)R-HSA-5638006 (Reactome)
RP2:ARL3:GTP:UNC119B(active)mim-catalysisR-HSA-5638006 (Reactome)
RP2:ARL3:GTP:UNC119BArrowR-HSA-5638004 (Reactome)
RP2:ARL3:GTP:UNC119BR-HSA-5638007 (Reactome)
RP2ArrowR-HSA-5638016 (Reactome)
RP2R-HSA-5638004 (Reactome)
RP2mim-catalysisR-HSA-5638007 (Reactome)
SCLT1R-HSA-5626223 (Reactome)
SEPT2ArrowR-HSA-5626681 (Reactome)
TNPO1R-HSA-5624951 (Reactome)
TRAF3IP1R-HSA-5617820 (Reactome)
TRIP11ArrowR-HSA-5617828 (Reactome)
TTBK2R-HSA-5626228 (Reactome)
TTC21BR-HSA-5617829 (Reactome)
TTC26R-HSA-5617820 (Reactome)
TTC30R-HSA-5617820 (Reactome)
TTC8R-HSA-5624125 (Reactome)
Tectonic-like complexR-HSA-5626681 (Reactome)
UNC119B:myristoylated ciliary cargoArrowR-HSA-5624131 (Reactome)
UNC119B:myristoylated ciliary cargoArrowR-HSA-5624132 (Reactome)
UNC119B:myristoylated ciliary cargoR-HSA-5624132 (Reactome)
UNC119B:myristoylated ciliary cargoR-HSA-5624133 (Reactome)
UNC119BArrowR-HSA-5638016 (Reactome)
UNC119BR-HSA-5624131 (Reactome)
VxPx-containing

ciliary membrane

proteins
ArrowR-HSA-5623527 (Reactome)
VxPx-containing

ciliary membrane

proteins
R-HSA-5620914 (Reactome)
WDR19R-HSA-5617829 (Reactome)
WDR35R-HSA-5617829 (Reactome)
acetylated microtubuleArrowR-HSA-5618328 (Reactome)
acetylated microtubuleArrowR-HSA-5625421 (Reactome)
acetylated microtubuleArrowR-HSA-5625424 (Reactome)
acetylated microtubuleR-HSA-5618331 (Reactome)
active dynein-2 motorsR-HSA-5624952 (Reactome)
active kinesin-2 motorsR-HSA-5624949 (Reactome)
anterograde IFT trainsArrowR-HSA-5624949 (Reactome)
anterograde IFT trainsArrowR-HSA-5625416 (Reactome)
anterograde IFT trainsR-HSA-5625416 (Reactome)
anterograde IFT trainsR-HSA-5625421 (Reactome)
basal

body:transition zone

proteins:RAB3IP:RAB11A:GTP:Golgi-derived vesicle
ArrowR-HSA-5638009 (Reactome)
basal

body:transition zone

proteins:RAB3IP:RAB11A:GTP:Golgi-derived vesicle
mim-catalysisR-HSA-5617816 (Reactome)
basal

body:transition

zone proteins
ArrowR-HSA-5626681 (Reactome)
basal

body:transition

zone proteins
R-HSA-5638009 (Reactome)
basal bodyArrowR-HSA-5626227 (Reactome)
basal bodyR-HSA-5626681 (Reactome)
centrosome:C2CD2:distal appendage proteins:TTBK2:MARK4ArrowR-HSA-5626699 (Reactome)
centrosome:C2CD2:distal appendage proteins:TTBK2:MARK4R-HSA-5626227 (Reactome)
dynein-2ArrowR-HSA-5625421 (Reactome)
dynein-2ArrowR-HSA-5625424 (Reactome)
dynein-2R-HSA-5624949 (Reactome)
exocyst complex:RAB8A:GTP:RAB3IP:RAB11:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsArrowR-HSA-5623524 (Reactome)
exocyst complex:RAB8A:GTP:RAB3IP:RAB11:GTP:RAB11FIP3 dimer:ASAP1 dimer:VxPx-containing ciliary membrane proteinsR-HSA-5623527 (Reactome)
exocyst complexR-HSA-5623524 (Reactome)
microtubuleArrowR-HSA-5618331 (Reactome)
microtubuleR-HSA-5618328 (Reactome)
mother centriole:C2CD3ArrowR-HSA-5626220 (Reactome)
mother centriole:C2CD3R-HSA-5626223 (Reactome)
mother centrioleR-HSA-5626220 (Reactome)
myristoylated ciliary cargoR-HSA-5624131 (Reactome)
myristoylated ciliary proteinsArrowR-HSA-5624130 (Reactome)
retrograde IFT trainsArrowR-HSA-5624952 (Reactome)
retrograde IFT trainsArrowR-HSA-5625426 (Reactome)
retrograde IFT trainsR-HSA-5625424 (Reactome)
retrograde IFT trainsR-HSA-5625426 (Reactome)
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