LCA5_HUMAN - dbPTM
LCA5_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID LCA5_HUMAN
UniProt AC Q86VQ0
Protein Name Lebercilin
Gene Name LCA5
Organism Homo sapiens (Human).
Sequence Length 697
Subcellular Localization Cytoplasm, cytoskeleton . Cytoplasm, cytoskeleton, cilium axoneme . Cytoplasm, cytoskeleton, cilium basal body . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . In non- ciliated cells, localizes to the centrosome and its associat
Protein Description Might be involved in minus end-directed microtubule transport..
Protein Sequence MGERAGSPGTDQERKAGKHHYSYLSDFETPQSSGRSSLVSSSPASVRRKNPKRQTSDGQVHHQAPRKPSPKGLPNRKGVRVGFRSQSLNREPLRKDTDLVTKRILSARLLKINELQNEVSELQVKLAELLKENKSLKRLQYRQEKALNKFEDAENEISQLIFRHNNEITALKERLRKSQEKERATEKRVKDTESELFRTKFSLQKLKEISEARHLPERDDLAKKLVSAELKLDDTERRIKELSKNLELSTNSFQRQLLAERKRAYEAHDENKVLQKEVQRLYHKLKEKERELDIKNIYSNRLPKSSPNKEKELALRKNAACQSDFADLCTKGVQTMEDFKPEEYPLTPETIMCYENKWEEPGHLTLDLQSQKQDRHGEAGILNPIMEREEKFVTDEELHVVKQEVEKLEDEWEREELDKKQKEKASLLEREEKPEWETGRYQLGMYPIQNMDKLQGEEEERLKREMLLAKLNEIDRELQDSRNLKYPVLPLLPDFESKLHSPERSPKTYRFSESSERLFNGHHLQDISFSTPKGEGQNSGNVRSPASPNEFAFGSYVPSFAKTSERSNPFSQKSSFLDFQRNSMEKLSKDGVDLITRKEKKANLMEQLFGASGSSTISSKSSDPNSVASSKGDIDPLNFLPGNKGSRDQEHDEDEGFFLSEGRSFNPNRHRLKHADDKPAVKAADSVEDEIEEVALR
Overview of Protein Modification Sites with Functional and Structural Information
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
7Phosphorylation-MGERAGSPGTDQER
-CCCCCCCCCCHHHH
21.1225849741
10PhosphorylationERAGSPGTDQERKAG
CCCCCCCCHHHHHCC
37.5829514088
40PhosphorylationSGRSSLVSSSPASVR
CCCCCCCCCCCHHHH
30.3227732954
41PhosphorylationGRSSLVSSSPASVRR
CCCCCCCCCCHHHHC
32.6322199227
42PhosphorylationRSSLVSSSPASVRRK
CCCCCCCCCHHHHCC
19.5825849741
45PhosphorylationLVSSSPASVRRKNPK
CCCCCCHHHHCCCCC
21.3822617229
55PhosphorylationRKNPKRQTSDGQVHH
CCCCCCCCCCCCCCC
32.5827251275
56PhosphorylationKNPKRQTSDGQVHHQ
CCCCCCCCCCCCCCC
31.2627251275
85PhosphorylationGVRVGFRSQSLNREP
CCCEEEECCCCCCCC
23.1223186163
87PhosphorylationRVGFRSQSLNREPLR
CEEEECCCCCCCCCC
28.9423403867
106PhosphorylationLVTKRILSARLLKIN
HHHHHHHHHHHHHHH
14.6824719451
1312-HydroxyisobutyrylationVKLAELLKENKSLKR
HHHHHHHHHCHHHHH
72.38-
210PhosphorylationLQKLKEISEARHLPE
HHHHHHHHHHHCCCC
26.71-
265PhosphorylationLAERKRAYEAHDENK
HHHHHHHHHHCCHHH
20.06-
282PhosphorylationQKEVQRLYHKLKEKE
HHHHHHHHHHHHHHH
10.09-
481PhosphorylationIDRELQDSRNLKYPV
HHHHHHHHCCCCCCE
15.3129514088
501PhosphorylationDFESKLHSPERSPKT
CHHHHCCCCCCCCCC
38.6029514088
505PhosphorylationKLHSPERSPKTYRFS
HCCCCCCCCCCCCCC
29.1429514088
539PhosphorylationPKGEGQNSGNVRSPA
CCCCCCCCCCCCCCC
24.6923090842
544PhosphorylationQNSGNVRSPASPNEF
CCCCCCCCCCCCCCC
22.1228857561
547PhosphorylationGNVRSPASPNEFAFG
CCCCCCCCCCCCCCC
31.4827966365
555PhosphorylationPNEFAFGSYVPSFAK
CCCCCCCCCCCCCCC
19.2623090842
556PhosphorylationNEFAFGSYVPSFAKT
CCCCCCCCCCCCCCC
19.4323090842
583PhosphorylationFLDFQRNSMEKLSKD
HHHHHHHHHHHHHHH
30.4327251275
612PhosphorylationMEQLFGASGSSTISS
HHHHHCCCCCCCCCC
39.3230576142
614PhosphorylationQLFGASGSSTISSKS
HHHCCCCCCCCCCCC
23.08-
618PhosphorylationASGSSTISSKSSDPN
CCCCCCCCCCCCCCC
31.6322468782
626PhosphorylationSKSSDPNSVASSKGD
CCCCCCCCCCCCCCC
25.1730576142
630PhosphorylationDPNSVASSKGDIDPL
CCCCCCCCCCCCCCC
30.8130576142
686PhosphorylationPAVKAADSVEDEIEE
CCHHHHHCCHHHHHH
23.7627966365

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
Modified Location Modified Residue Modification Type of Upstream Proteins Gene Name of Upstream Proteins UniProt AC of Upstream Proteins Sources

Oops, there are no upstream regulatory protein records of LCA5_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of LCA5_HUMAN !!

Disease-associated PTM Sites based on SAP

* Distance = the distance between SAP position and PTM sites.

Modified Location Modification Variant Position
(Distance <= 10)
Residue Change SAP Related Disease Reference

Oops, there are no SNP-PTM records of LCA5_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
TXLNA_HUMANTXLNAphysical
25416956
CE170_HUMANCEP170physical
26638075
MOONR_HUMANKIAA0753physical
26638075
OFD1_HUMANOFD1physical
26638075
PCM1_HUMANPCM1physical
26638075
ADIP_HUMANSSX2IPphysical
26638075
IPO7_HUMANIPO7physical
26638075
P5CR1_HUMANPYCR1physical
26638075
TRI27_HUMANTRIM27physical
26638075
SPT5H_HUMANSUPT5Hphysical
26638075
CELR2_HUMANCELSR2physical
26638075
CLUA1_HUMANCLUAP1physical
26638075
DYL1_HUMANDYNLL1physical
26638075
IF172_HUMANIFT172physical
26638075
IFT20_HUMANIFT20physical
26638075
IFT46_HUMANIFT46physical
26638075
IFT57_HUMANIFT57physical
26638075
IFT74_HUMANIFT74physical
26638075
IFT80_HUMANIFT80physical
26638075
IFT81_HUMANIFT81physical
26638075
IFT88_HUMANIFT88physical
26638075
VWA8_HUMANVWA8physical
26638075
IMB1_HUMANKPNB1physical
26638075
IFT22_HUMANIFT22physical
26638075
MIPT3_HUMANTRAF3IP1physical
26638075
IFT56_HUMANTTC26physical
26638075
TT30A_HUMANTTC30Aphysical
26638075
1433E_HUMANYWHAEphysical
26638075
1433G_HUMANYWHAGphysical
26638075
1433F_HUMANYWHAHphysical
26638075
1433Z_HUMANYWHAZphysical
26638075
ZNHI1_HUMANZNHIT1physical
26638075
PGK1_HUMANPGK1physical
26638075
SAE2_HUMANUBA2physical
26638075
IPO5_HUMANIPO5physical
26638075
NP1L4_HUMANNAP1L4physical
26638075
PTCD3_HUMANPTCD3physical
26638075
1433T_HUMANYWHAQphysical
26638075
MARE1_HUMANMAPRE1physical
26638075
TRAF7_HUMANTRAF7physical
26638075
VPS35_HUMANVPS35physical
26638075
NOC4L_HUMANNOC4Lphysical
26638075
NU155_HUMANNUP155physical
26638075
RCN1_HUMANRCN1physical
26638075
BRI3B_HUMANBRI3BPphysical
26638075
KNOP1_HUMANKNOP1physical
26638075
CSN3_HUMANCOPS3physical
26638075
PYRG1_HUMANCTPS1physical
26638075
IFT27_HUMANIFT27physical
26638075
IPYR_HUMANPPA1physical
26638075
TIM13_HUMANTIMM13physical
26638075
1433B_HUMANYWHABphysical
26638075
FKBP4_HUMANFKBP4physical
26638075
SSBP_HUMANSSBP1physical
26638075
KCD12_HUMANKCTD12physical
26638075
NSUN2_HUMANNSUN2physical
26638075
PSME3_HUMANPSME3physical
26638075
UBE2O_HUMANUBE2Ophysical
26638075
XPO5_HUMANXPO5physical
26638075
CP131_HUMANCEP131physical
26638075
CAMP1_HUMANCAMSAP1physical
26638075
CE120_HUMANCEP120physical
26638075
CKAP2_HUMANCKAP2physical
26638075
DVL2_HUMANDVL2physical
26638075
DYL2_HUMANDYNLL2physical
26638075
GTSE1_HUMANGTSE1physical
26638075
HAUS3_HUMANHAUS3physical
26638075
HAUS8_HUMANHAUS8physical
26638075
IPO8_HUMANIPO8physical
26638075
C170B_HUMANCEP170Bphysical
26638075
CFA97_HUMANCFAP97physical
26638075
LUZP1_HUMANLUZP1physical
26638075
MAP7_HUMANMAP7physical
26638075
MA7D1_HUMANMAP7D1physical
26638075
MA7D2_HUMANMAP7D2physical
26638075
MA7D3_HUMANMAP7D3physical
26638075
MAP9_HUMANMAP9physical
26638075
NP1L1_HUMANNAP1L1physical
26638075
NEDD1_HUMANNEDD1physical
26638075
SDCG3_HUMANSDCCAG3physical
26638075
TDRD3_HUMANTDRD3physical
26638075
TFP11_HUMANTFIP11physical
26638075
TRIM2_HUMANTRIM2physical
26638075
TRI26_HUMANTRIM26physical
26638075
WDR62_HUMANWDR62physical
26638075
WDR83_HUMANWDR83physical
26638075
ANR28_HUMANANKRD28physical
26638075
CC138_HUMANCCDC138physical
26638075
CCD66_HUMANCCDC66physical
26638075
CE162_HUMANCEP162physical
26638075
CEP44_HUMANCEP44physical
26638075
CEP72_HUMANCEP72physical
26638075
CSPP1_HUMANCSPP1physical
26638075
DCLK1_HUMANDCLK1physical
26638075
GPTC1_HUMANGPATCH1physical
26638075
HAUS6_HUMANHAUS6physical
26638075
HAUS7_HUMANHAUS7physical
26638075
KIF14_HUMANKIF14physical
26638075
MED4_HUMANMED4physical
26638075
MKL1_HUMANMKL1physical
26638075
MTUS1_HUMANMTUS1physical
26638075
PIBF1_HUMANPIBF1physical
26638075
PLK1_HUMANPLK1physical
26638075
FTM_HUMANRPGRIP1Lphysical
26638075
SPA24_HUMANSPATA24physical
26638075
TCHP_HUMANTCHPphysical
26638075
TRI36_HUMANTRIM36physical
26638075
TBC31_HUMANTBC1D31physical
26638075
WRP73_HUMANWRAP73physical
26638075
ZN622_HUMANZNF622physical
26638075
SSNA1_HUMANSSNA1physical
28514442
ARMC8_HUMANARMC8physical
28514442

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
604537Leber congenital amaurosis 5 (LCA5)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of LCA5_HUMAN

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Related Literatures of Post-Translational Modification

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