Homo sapiens Protein: ABCC3
Summary
InnateDB Protein IDBP-381780.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ABCC3
Protein Name ATP-binding cassette, sub-family C (CFTR/MRP), member 3
Synonyms ABC31; cMOAT2; EST90757; MLP2; MOAT-D; MRP3;
Species Homo sapiens
Ensembl Protein ENSP00000395160
InnateDB Gene IDBG-59146 (ABCC3)
Protein Structure
UniProt Annotation
Function May act as an inducible transporter in the biliary and intestinal excretion of organic anions. Acts as an alternative route for the export of bile acids and glucuronides from cholestatic hepatocytes (By similarity). {ECO:0000250}.
Subcellular Localization Membrane; Multi-pass membrane protein.
Disease Associations
Tissue Specificity Mainly expressed in the liver. Also expressed in small intestine, colon, prostate, testis, brain and at a lower level in the kidney.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 2 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005524 ATP binding
GO:0008514 organic anion transmembrane transporter activity
GO:0042626 ATPase activity, coupled to transmembrane movement of substances
Biological Process
GO:0006200 ATP catabolic process
GO:0006810 transport
GO:0008206 bile acid metabolic process
GO:0015721 bile acid and bile salt transport
GO:0044281 small molecule metabolic process
GO:0055085 transmembrane transport
Cellular Component
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR001140 ABC transporter, transmembrane domain
IPR011527 ABC transporter type 1, transmembrane domain
PFAM PF00664
PF13748
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O15438
PhosphoSite PhosphoSite-O15438
TrEMBL Q2M3C9
UniProt Splice Variant
Entrez Gene 8714
UniGene Hs.685104
RefSeq NP_001137542
HUGO HGNC:54
OMIM 604323
CCDS CCDS45739
HPRD 06826
IMGT
EMBL AB010887 AC004590 AC005921 AF009670 AF083552 AF085690 AF085691 AF085692 AF104943 AF154001 BC046126 BC104952 BC137347 BC137348 CH471109 U83659 Y17151
GenPept AAB71756 AAC34668 AAD01430 AAD02845 AAD02846 AAD02847 AAD04170 AAD38185 AAH46126 AAI04953 AAI37348 AAI37349 BAA28146 CAA76658 EAW94590 EAW94592 EAW94593