Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage Cell Signaling Technology
PhosphoSitePlus
HomeAbout PhosphoSiteUsing PhosphoSiteCuration ProcessContact
NIH-logos NIGMS Logo NIAAA Logo NCI Logo NIH Logo
Protein Page:
TOMM7 (human)
p Phosphorylation
ac Acetylation
me Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
ub Ubiquitination
sm Sumoylation
ne Neddylation
gl O-GlcNAc
ga O-GalNAc
pa Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage
sc Succinylation

Overview
TOMM7 Required for assembly and stability of the TOM complex. Belongs to the Tom7 family. Note: This description may include information from UniProtKB.
Protein type: Mitochondrial; Membrane protein, integral
Cellular Component: mitochondrion; mitochondrial outer membrane translocase complex; integral to membrane
Molecular Function: protein binding; protein transmembrane transporter activity
Biological Process: protein import into mitochondrial matrix; cellular protein metabolic process; protein targeting to mitochondrion
Reference #:  Q9P0U1 (UniProtKB)
Alt. Names/Synonyms: 6.2 kd protein; homolog of Tom7; Mitochondrial import receptor subunit TOM7 homolog; TOM7; TOMM07; TOMM7; Translocase of outer membrane 7 kDa subunit homolog; translocase of outer mitochondrial membrane 7 homolog (yeast)
Gene Symbols: TOMM7
Molecular weight: 6,248 Da
Basal Isoelectric point: 10.28  Predict pI for various phosphorylation states
Select Structure to View Below

TOMM7

Protein Structure Not Found.


STRING  |  Reactome  |  neXtProt  |  Protein Atlas  |  BioGPS  |  Scansite  |  Pfam  |  Phospho.ELM  |  Source  |  GeneCards  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene  |  InnateDB


Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 23 K17-ub QRLQQLFkGsQFAIR
0 1 S19-p LQQLFkGsQFAIRWG
  mouse

 
K17-ub QRLQQLFkGGQFAIR
G19 LQQLFkGGQFAIRWG
Home  |  Curator Login With enhanced literature mining using Linguamatics I2E I2E Logo Produced by 3rd Millennium  |  Design by Digizyme
©2003-2013 Cell Signaling Technology, Inc.