IFT52_HUMAN - dbPTM
IFT52_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID IFT52_HUMAN
UniProt AC Q9Y366
Protein Name Intraflagellar transport protein 52 homolog
Gene Name IFT52
Organism Homo sapiens (Human).
Sequence Length 437
Subcellular Localization Cell projection, cilium .
Protein Description Involved in ciliogenesis as part of a complex involved in intraflagellar transport (IFT), the bi-directional movement of particles required for the assembly, maintenance and functioning of primary cilia. [PubMed: 27466190 Required for the anterograde transport of IFT88]
Protein Sequence MEKELRSTILFNAYKKEIFTTNNGYKSMQKKLRSNWKIQSLKDEITSEKLNGVKLWITAGPREKFTAAEFEILKKYLDTGGDVFVMLGEGGESRFDTNINFLLEEYGIMVNNDAVVRNVYHKYFHPKEALVSSGVLNREISRAAGKAVPGIIDEESSGNNAQALTFVYPFGATLSVMKPAVAVLSTGSVCFPLNRPILAFYHSKNQGGKLAVLGSCHMFSDQYLDKEENSKIMDVVFQWLTTGDIHLNQIDAEDPEISDYMMLPYTATLSKRNRECLQESDEIPRDFTTLFDLSIFQLDTTSFHSVIEAHEQLNVKHEPLQLIQPQFETPLPTLQPAVFPPSFRELPPPPLELFDLDETFSSEKARLAQITNKCTEEDLEFYVRKCGDILGVTSKLPKDQQDAKHILEHVFFQVVEFKKLNQEHDIDTSETAFQNNF
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
3Ubiquitination-----MEKELRSTIL
-----CCHHHHHHHH
61.83-
20PhosphorylationAYKKEIFTTNNGYKS
HHHCEEEECCCHHHH
33.9923403867
21PhosphorylationYKKEIFTTNNGYKSM
HHCEEEECCCHHHHH
18.8823403867
25PhosphorylationIFTTNNGYKSMQKKL
EEECCCHHHHHHHHH
11.3023403867
27PhosphorylationTTNNGYKSMQKKLRS
ECCCHHHHHHHHHHC
20.2623403867
37UbiquitinationKKLRSNWKIQSLKDE
HHHHCCCCCCHHHHH
34.8122817900
42UbiquitinationNWKIQSLKDEITSEK
CCCCCHHHHHHHHHH
59.5722817900
49UbiquitinationKDEITSEKLNGVKLW
HHHHHHHHHCCEEEE
47.20-
64UbiquitinationITAGPREKFTAAEFE
EEECCHHHCCHHHHH
49.66-
66PhosphorylationAGPREKFTAAEFEIL
ECCHHHCCHHHHHHH
35.7123532336
93PhosphorylationMLGEGGESRFDTNIN
EECCCCCCCCHHCHH
41.33-
122UbiquitinationVVRNVYHKYFHPKEA
HHHHHHHHHCCHHHH
31.74-
123PhosphorylationVRNVYHKYFHPKEAL
HHHHHHHHCCHHHHH
8.2022210691
127UbiquitinationYHKYFHPKEALVSSG
HHHHCCHHHHHHHCC
47.2329967540
132PhosphorylationHPKEALVSSGVLNRE
CHHHHHHHCCCCCHH
23.4022210691
133PhosphorylationPKEALVSSGVLNREI
HHHHHHHCCCCCHHH
25.9922210691
209UbiquitinationHSKNQGGKLAVLGSC
ECCCCCCCEEEEEEC
39.8529967540
226UbiquitinationFSDQYLDKEENSKIM
CCHHHCCHHHHCCHH
65.42-
241PhosphorylationDVVFQWLTTGDIHLN
HHHHHHHHHCCCCCC
26.27-
364UbiquitinationDETFSSEKARLAQIT
CCCCCCHHHHHHHHH
40.5329967540
373UbiquitinationRLAQITNKCTEEDLE
HHHHHHCCCCHHHHH
33.6129967540
385UbiquitinationDLEFYVRKCGDILGV
HHHHHHHHHHHHHCC
32.3129967540
428PhosphorylationNQEHDIDTSETAFQN
CCCCCCCHHHHHHHH
28.8827732954
429PhosphorylationQEHDIDTSETAFQNN
CCCCCCHHHHHHHHC
29.2429214152
431PhosphorylationHDIDTSETAFQNNF-
CCCCHHHHHHHHCC-
32.3227732954

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 IFT52_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of IFT52_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 IFT52_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
UBX10_HUMANUBXN10physical
26389662
IFT46_HUMANIFT46physical
27173435
IFT74_HUMANIFT74physical
27173435
IF172_HUMANIFT172physical
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 IFT52_HUMAN

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Related Literatures of Post-Translational Modification

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