Homo sapiens Protein: GRPEL2
Summary
InnateDB Protein IDBP-52871.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GRPEL2
Protein Name GrpE-like 2, mitochondrial (E. coli)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000329558
InnateDB Gene IDBG-52869 (GRPEL2)
Protein Structure
UniProt Annotation
Function Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. Seems to control the nucleotide-dependent binding of mitochondrial HSP70 to substrate proteins. Stimulates ATPase activity of mt-HSP70. May also serve to modulate the interconversion of oligomeric (inactive) and monomeric (active) forms of mt-HSP70 (By similarity). {ECO:0000250}.
Subcellular Localization Mitochondrion matrix {ECO:0000250}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0000774 adenyl-nucleotide exchange factor activity
GO:0042803 protein homodimerization activity
GO:0051082 unfolded protein binding
GO:0051087 chaperone binding
Biological Process
GO:0006457 protein folding
GO:0006626 protein targeting to mitochondrion
GO:0044267 cellular protein metabolic process
GO:0050790 regulation of catalytic activity
Cellular Component
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005759 mitochondrial matrix
Protein Structure and Domains
PDB ID
InterPro IPR000740 GrpE nucleotide exchange factor
IPR009012 GrpE nucleotide exchange factor, head
PFAM PF01025
PRINTS PR00773
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8TAA5
PhosphoSite PhosphoSite-Q8TAA5
TrEMBL Q8N3S0
UniProt Splice Variant
Entrez Gene 134266
UniGene Hs.619552
RefSeq NP_689620
HUGO HGNC:21060
OMIM
CCDS CCDS4295
HPRD 17079
IMGT
EMBL AK074293 AL832325 BC036678 BC070090
GenPept AAH36678 AAH70090 BAB85040 CAD38619