Homo sapiens Protein: SLC25A42
Summary
InnateDB Protein IDBP-39338.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC25A42
Protein Name solute carrier family 25, member 42
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000326693
InnateDB Gene IDBG-39334 (SLC25A42)
Protein Structure
UniProt Annotation
Function Mitochondrial carrier mediating the transport of coenzyme A (CoA) in mitochondria in exchange for intramitochondrial (deoxy)adenine nucleotides and adenosine 3',5'- diphosphate. {ECO:0000269PubMed:19429682}.
Subcellular Localization Mitochondrion inner membrane {ECO:0000269PubMed:19429682}; Multi-pass membrane protein {ECO:0000269PubMed:19429682}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005347 ATP transmembrane transporter activity
GO:0015217 ADP transmembrane transporter activity
GO:0015228 coenzyme A transmembrane transporter activity
GO:0043262 adenosine-diphosphatase activity
GO:0080122 AMP transmembrane transporter activity
Biological Process
GO:0008152 metabolic process
GO:0015866 ADP transport
GO:0015867 ATP transport
GO:0035349 coenzyme A transmembrane transport
GO:0080121 AMP transport
Cellular Component
GO:0005634 nucleus
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR002067 Mitochondrial carrier protein
IPR002167 Graves disease carrier protein
IPR018108 Mitochondrial substrate/solute carrier
IPR023395 Mitochondrial carrier domain
PFAM PF00153
PRINTS PR00926
PR00928
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q86VD7
PhosphoSite PhosphoSite-Q86VD7
TrEMBL A0A024R7K2
UniProt Splice Variant
Entrez Gene 284439
UniGene Hs.638088
RefSeq NP_848621
HUGO HGNC:28380
OMIM 610823
CCDS CCDS32966
HPRD 17523
IMGT
EMBL AC002126 AC004143 BC045598 CH471106 FN356975
GenPept AAB86983 AAC02758 AAH45598 CAX94853 EAW84777 EAW84778