IFT57_HUMAN - dbPTM
IFT57_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID IFT57_HUMAN
UniProt AC Q9NWB7
Protein Name Intraflagellar transport protein 57 homolog
Gene Name IFT57
Organism Homo sapiens (Human).
Sequence Length 429
Subcellular Localization Cytoplasm, cytoskeleton, cilium basal body. Concentrates within the inner segment of cilia..
Protein Description Required for the formation of cilia. Plays an indirect role in sonic hedgehog signaling, cilia being required for all activity of the hedgehog pathway (By similarity). Has pro-apoptotic function via its interaction with HIP1, leading to recruit caspase-8 (CASP8) and trigger apoptosis. Has the ability to bind DNA sequence motif 5'-AAAGACATG-3' present in the promoter of caspase genes such as CASP1, CASP8 and CASP10, suggesting that it may act as a transcription regulator; however the relevance of such function remains unclear..
Protein Sequence MTAALAVVTTSGLEDGVPRSRGEGTGEVVLERGPGAAYHMFVVMEDLVEKLKLLRYEEEFLRKSNLKAPSRHYFALPTNPGEQFYMFCTLAAWLINKAGRPFEQPQEYDDPNATISNILSELRSFGRTADFPPSKLKSGYGEHVCYVLDCFAEEALKYIGFTWKRPIYPVEELEEESVAEDDAELTLNKVDEEFVEEETDNEENFIDLNVLKAQTYHLDMNETAKQEDILESTTDAAEWSLEVERVLPQLKVTIRTDNKDWRIHVDQMHQHRSGIESALKETKGFLDKLHNEITRTLEKISSREKYINNQLENLVQEYRAAQAQLSEAKERYQQGNGGVTERTRLLSEVMEELEKVKQEMEEKGSSMTDGAPLVKIKQSLTKLKQETVEMDIRIGIVEHTLLQSKLKEKSNMTRNMHATVIPEPATGFY
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
168PhosphorylationFTWKRPIYPVEELEE
CEECCCEEEHHHHCC
12.1526471730
177PhosphorylationVEELEEESVAEDDAE
HHHHCCCCCCCCCHH
29.8826471730
199PhosphorylationEEFVEEETDNEENFI
HHHHHHHCCCCCCEE
47.6122496350
232PhosphorylationKQEDILESTTDAAEW
CHHHHHHHCCCHHHH
32.91-
233PhosphorylationQEDILESTTDAAEWS
HHHHHHHCCCHHHHH
21.22-
234PhosphorylationEDILESTTDAAEWSL
HHHHHHCCCHHHHHH
32.68-
253PhosphorylationVLPQLKVTIRTDNKD
HHCCCEEEEECCCCC
11.8024719451
299UbiquitinationEITRTLEKISSREKY
HHHHHHHHHHHHHHH
51.5029967540
305UbiquitinationEKISSREKYINNQLE
HHHHHHHHHHHHHHH
50.7721906983
329UbiquitinationQAQLSEAKERYQQGN
HHHHHHHHHHHHHCC
38.3821906983
343PhosphorylationNGGVTERTRLLSEVM
CCCHHHHHHHHHHHH
21.3128102081
347PhosphorylationTERTRLLSEVMEELE
HHHHHHHHHHHHHHH
32.5125106551
365PhosphorylationQEMEEKGSSMTDGAP
HHHHHHCCCCCCCCC
28.18-
366PhosphorylationEMEEKGSSMTDGAPL
HHHHHCCCCCCCCCH
34.08-
368PhosphorylationEEKGSSMTDGAPLVK
HHHCCCCCCCCCHHH
32.98-
379PhosphorylationPLVKIKQSLTKLKQE
CHHHHHHHHHHHHHH
32.7629083192
381PhosphorylationVKIKQSLTKLKQETV
HHHHHHHHHHHHHHH
39.3129083192
384UbiquitinationKQSLTKLKQETVEMD
HHHHHHHHHHHHHHH
47.87-
387PhosphorylationLTKLKQETVEMDIRI
HHHHHHHHHHHHHHH
21.1929083192

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 IFT57_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of IFT57_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 IFT57_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
HIP1_HUMANHIP1physical
11788820
CASP8_HUMANCASP8physical
11788820
BFAR_HUMANBFARphysical
14502241
IF172_HUMANIFT172physical
26186194
IFT56_HUMANTTC26physical
26186194
IFT81_HUMANIFT81physical
26186194
MIPT3_HUMANTRAF3IP1physical
26186194
EHBP1_HUMANEHBP1physical
26186194
SYNE1_HUMANSYNE1physical
26186194
CLUA1_HUMANCLUAP1physical
26186194
IFT46_HUMANIFT46physical
26186194
HOME1_HUMANHOMER1physical
26186194
HOME2_HUMANHOMER2physical
26186194
HOME3_HUMANHOMER3physical
26186194
IFT88_HUMANIFT88physical
26186194
STX18_HUMANSTX18physical
26186194
COG6_HUMANCOG6physical
26186194
RABE2_HUMANRABEP2physical
26186194
IFT74_HUMANIFT74physical
26186194
EXOC7_HUMANEXOC7physical
26186194
TT30B_HUMANTTC30Bphysical
26186194
TT30A_HUMANTTC30Aphysical
26186194
SPAG5_HUMANSPAG5physical
26186194
IFT20_HUMANIFT20physical
26186194
TRAF7_HUMANTRAF7physical
26186194
IFT52_HUMANIFT52physical
26186194
IFT80_HUMANIFT80physical
26186194
CENPH_HUMANCENPHphysical
26186194
CDR2_HUMANCDR2physical
26186194
HOOK3_HUMANHOOK3physical
26186194
HSBP1_HUMANHSBP1physical
26186194
CCD22_HUMANCCDC22physical
26186194
SKAP_HUMANKNSTRNphysical
26186194
IFT22_HUMANIFT22physical
26186194
COR1A_HUMANCORO1Aphysical
26186194
SEC20_HUMANBNIP1physical
26186194
POC1A_HUMANPOC1Aphysical
26186194
COR1B_HUMANCORO1Bphysical
26186194
NEDD1_HUMANNEDD1physical
26186194
ATP9A_HUMANATP9Aphysical
26186194
TRPM4_HUMANTRPM4physical
26186194
UBX10_HUMANUBXN10physical
26389662
TT30A_HUMANTTC30Aphysical
28514442
COR1A_HUMANCORO1Aphysical
28514442
TT30B_HUMANTTC30Bphysical
28514442
IFT80_HUMANIFT80physical
28514442
MIPT3_HUMANTRAF3IP1physical
28514442
IFT88_HUMANIFT88physical
28514442
SYNE1_HUMANSYNE1physical
28514442
IFT20_HUMANIFT20physical
28514442
COG6_HUMANCOG6physical
28514442
IF172_HUMANIFT172physical
28514442
HOME1_HUMANHOMER1physical
28514442
IFT81_HUMANIFT81physical
28514442
IFT46_HUMANIFT46physical
28514442
IFT22_HUMANIFT22physical
28514442
SPAG5_HUMANSPAG5physical
28514442
IFT52_HUMANIFT52physical
28514442
IFT74_HUMANIFT74physical
28514442
HOME2_HUMANHOMER2physical
28514442
HSBP1_HUMANHSBP1physical
28514442
RABE2_HUMANRABEP2physical
28514442
CLUA1_HUMANCLUAP1physical
28514442
TRPM4_HUMANTRPM4physical
28514442
EHBP1_HUMANEHBP1physical
28514442
POC1A_HUMANPOC1Aphysical
28514442
TRAF7_HUMANTRAF7physical
28514442
SKAP_HUMANKNSTRNphysical
28514442
CENPH_HUMANCENPHphysical
28514442
HOME3_HUMANHOMER3physical
28514442
NEDD1_HUMANNEDD1physical
28514442
ATP9A_HUMANATP9Aphysical
28514442
CDR2_HUMANCDR2physical
28514442
HOOK3_HUMANHOOK3physical
28514442
STX18_HUMANSTX18physical
28514442
EXOC7_HUMANEXOC7physical
28514442
SGF29_HUMANCCDC101physical
28514442
SEC20_HUMANBNIP1physical
28514442
IFT56_HUMANTTC26physical
28514442
IF172_HUMANIFT172physical
27173435
IFT74_HUMANIFT74physical
27173435
IFT46_HUMANIFT46physical
27173435

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
There are no disease associations of PTM sites.
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of IFT57_HUMAN

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Related Literatures of Post-Translational Modification

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