VPP3_HUMAN - dbPTM
VPP3_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID VPP3_HUMAN
UniProt AC Q13488
Protein Name V-type proton ATPase 116 kDa subunit a isoform 3
Gene Name TCIRG1
Organism Homo sapiens (Human).
Sequence Length 830
Subcellular Localization Membrane
Multi-pass membrane protein.
Protein Description Part of the proton channel of V-ATPases (By similarity). Seems to be directly involved in T-cell activation..
Protein Sequence MGSMFRSEEVALVQLFLPTAAAYTCVSRLGELGLVEFRDLNASVSAFQRRFVVDVRRCEELEKTFTFLQEEVRRAGLVLPPPKGRLPAPPPRDLLRIQEETERLAQELRDVRGNQQALRAQLHQLQLHAAVLRQGHEPQLAAAHTDGASERTPLLQAPGGPHQDLRVNFVAGAVEPHKAPALERLLWRACRGFLIASFRELEQPLEHPVTGEPATWMTFLISYWGEQIGQKIRKITDCFHCHVFPFLQQEEARLGALQQLQQQSQELQEVLGETERFLSQVLGRVLQLLPPGQVQVHKMKAVYLALNQCSVSTTHKCLIAEAWCSVRDLPALQEALRDSSMEEGVSAVAHRIPCRDMPPTLIRTNRFTASFQGIVDAYGVGRYQEVNPAPYTIITFPFLFAVMFGDVGHGLLMFLFALAMVLAENRPAVKAAQNEIWQTFFRGRYLLLLMGLFSIYTGFIYNECFSRATSIFPSGWSVAAMANQSGWSDAFLAQHTMLTLDPNVTGVFLGPYPFGIDPIWSLAANHLSFLNSFKMKMSVILGVVHMAFGVVLGVFNHVHFGQRHRLLLETLPELTFLLGLFGYLVFLVIYKWLCVWAARAASAPSILIHFINMFLFSHSPSNRLLYPRQEVVQATLVVLALAMVPILLLGTPLHLLHRHRRRLRRRPADRQEENKAGLLDLPDASVNGWSSDEEKAGGLDDEEEAELVPSEVLMHQAIHTIEFCLGCVSNTASYLRLWALSLAHAQLSEVLWAMVMRIGLGLGREVGVAAVVLVPIFAAFAVMTVAILLVMEGLSAFLHALRLHWVEFQNKFYSGTGYKLSPFTFAATDD
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
3Phosphorylation-----MGSMFRSEEV
-----CCCCCCCHHH
17.2824043423
7Phosphorylation-MGSMFRSEEVALVQ
-CCCCCCCHHHHHHH
27.1824043423
19PhosphorylationLVQLFLPTAAAYTCV
HHHHHHHHHHHHHHH
30.9524043423
23PhosphorylationFLPTAAAYTCVSRLG
HHHHHHHHHHHHHHH
8.9224043423
24PhosphorylationLPTAAAYTCVSRLGE
HHHHHHHHHHHHHHH
11.1624043423
27PhosphorylationAAAYTCVSRLGELGL
HHHHHHHHHHHHCCC
24.7624043423
45PhosphorylationRDLNASVSAFQRRFV
ECCCCCCHHHHHHHE
22.3721964256
152PhosphorylationTDGASERTPLLQAPG
CCCCCCCCCCCCCCC
17.7828674419
178UbiquitinationAGAVEPHKAPALERL
EECCCCCCCHHHHHH
67.7721906983
178 (in isoform 1)Ubiquitination-67.7721906983
218PhosphorylationGEPATWMTFLISYWG
CCCCHHHHHHHHHHH
13.5724043423
222PhosphorylationTWMTFLISYWGEQIG
HHHHHHHHHHHHHHH
19.5824043423
223PhosphorylationWMTFLISYWGEQIGQ
HHHHHHHHHHHHHHH
15.5024043423
303PhosphorylationVHKMKAVYLALNQCS
HHHHHHHHHHHHCCC
7.36-
368PhosphorylationLIRTNRFTASFQGIV
EEECCCCEECCCCCH
20.3924043423
370PhosphorylationRTNRFTASFQGIVDA
ECCCCEECCCCCHHH
18.2924043423
378PhosphorylationFQGIVDAYGVGRYQE
CCCCHHHHCCCCCCC
14.1024043423
459 (in isoform 2)Ubiquitination-4.0621906983
675UbiquitinationADRQEENKAGLLDLP
CCHHHHHCCCCCCCC
47.302190698
675 (in isoform 1)Ubiquitination-47.3021906983
685PhosphorylationLLDLPDASVNGWSSD
CCCCCCCCCCCCCCH
24.4025627689
690PhosphorylationDASVNGWSSDEEKAG
CCCCCCCCCHHHHCC
29.3430108239
691PhosphorylationASVNGWSSDEEKAGG
CCCCCCCCHHHHCCC
42.4029507054
819UbiquitinationFYSGTGYKLSPFTFA
CCCCCCCCCCCEEEE
43.78-

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 VPP3_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of VPP3_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 VPP3_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
ZNT5_HUMANSLC30A5physical
22939629
TERF1_HUMANTERF1physical
21988832

Drug and Disease Associations
Kegg Disease
H00436 Osteopetrosis, including: Osteopetrosis, severe neonatal or infantile forms; Osteopetrosis, intermed
OMIM Disease
259700Osteopetrosis, autosomal recessive 1 (OPTB1)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of VPP3_HUMAN

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Related Literatures of Post-Translational Modification

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