FATE1_HUMAN - dbPTM
FATE1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID FATE1_HUMAN
UniProt AC Q969F0
Protein Name Fetal and adult testis-expressed transcript protein
Gene Name FATE1
Organism Homo sapiens (Human).
Sequence Length 183
Subcellular Localization Mitochondrion . Mitochondrion outer membrane . Endoplasmic reticulum membrane
Single-pass membrane protein
Cytoplasmic side . Localized to specific membrane structures termed mitochondria-associated membranes (MAMs) which connect the endoplasmic
Protein Description Involved in the regulation of endoplasmic reticulum (ER)-mitochondria coupling. Negatively regulates the ER-mitochondria distance and Ca(2+) transfer from ER to mitochondria possibly implicating it in the regulation of apoptosis. [PubMed: 27402544 May collaborate with RNF183 to restrain BIK protein levels thus regulating apoptotic signaling]
Protein Sequence MAGGPPNTKAEMEMSLAEELNHGRQGENQEHLVIAEMMELGSRSRGASQKKQKLEQKAAGSASAKRVWNMTATRPKKMGSQLPKPRMLRESGHGDAHLQEYAGNFQGIRFHYDRNPGTDAVAQTSLEEFNVLEMEVMRRQLYAVNRRLRALEEQGATWRHRETLIIAVLVSASIANLWLWMNQ
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

Oops, there are no PTM records of FATE1_HUMAN !!

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 FATE1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of FATE1_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 FATE1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
RN183_HUMANRNF183physical
16189514
SNP47_HUMANSNAP47physical
25416956
SYNPR_HUMANSYNPRphysical
25416956
NRSN1_HUMANNRSN1physical
25416956
NRG4_HUMANNRG4physical
25416956
KASH5_HUMANCCDC155physical
25416956
TMM74_HUMANTMEM74physical
25416956
SYNE4_HUMANSYNE4physical
25416956
SNG2_HUMANSYNGR2physical
21516116

Drug and Disease Associations
Kegg Drug
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of FATE1_HUMAN

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Related Literatures of Post-Translational Modification

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