Homo sapiens Protein: CORIN
Summary
InnateDB Protein IDBP-16907.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CORIN
Protein Name corin, serine peptidase
Synonyms ATC2; CRN; Lrp4; PEE5; TMPRSS10;
Species Homo sapiens
Ensembl Protein ENSP00000273857
InnateDB Gene IDBG-16903 (CORIN)
Protein Structure
UniProt Annotation
Function Serine-type endopeptidase involved in atrial natriuretic peptide hormone (NPPA) processing. Converts through proteolytic cleavage the non-functional propeptide NPPA into the active hormone, thereby regulating blood pressure in heart and promoting natriuresis, diuresis and vasodilation. Proteolytic cleavage of pro-NPPA also plays a role in female pregnancy by promoting trophoblast invasion and spiral artery remodeling in uterus. Also acts as a regulator of sodium reabsorption in kidney. May also process pro-NPPB the B-type natriuretic peptide.Isoform 2: has weaker endopeptidase activity compared to isoform 1.
Subcellular Localization Cell membrane {ECO:0000269PubMed:19751717, ECO:0000269PubMed:21288900, ECO:0000269PubMed:21518754}; Single- pass type II membrane protein {ECO:0000269PubMed:19751717, ECO:0000269PubMed:21288900, ECO:0000269PubMed:21518754}. Note=May easily detached from the endothelial cell membrane.Isoform 2: Cell membrane; Single-pass type II membrane protein. Note=Less efficiently targeted to the cell membrane compared to isoform 1.Atrial natriuretic peptide-converting enzyme, 180 kDa soluble fragment: Secreted. Note=Soluble form produced following cleavage by ADAM10.Atrial natriuretic peptide-converting enzyme, 160 kDa soluble fragment: Secreted. Note=Soluble form produced following autocatalytic cleavage.Atrial natriuretic peptide-converting enzyme, 100 kDa soluble fragment: Secreted. Note=Soluble form produced following autocatalytic cleavage.
Disease Associations Pre-eclampsia/eclampsia 5 (PEE5) [MIM:614595]: A hypertensive disorder of pregnancy characterized by new hypertension (blood pressure 140/90 or greater) presenting after 20 weeks' gestation with clinically relevant proteinuria. It impacts 2 individuals, the mother and her child, both of whom can be severely affected. Preeclampsia is one of the causes of maternal mortality and morbidity worldwide. {ECO:0000269PubMed:22437503}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Highly expressed in heart. Expressed in heart myocytes. Also expressed in pregnant uterus. Detected in blood, in plasma as well as in serum (at protein level). {ECO:0000269PubMed:10329693, ECO:0000269PubMed:19751717, ECO:0000269PubMed:22437503}.
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 0
Protein-DNA 0
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004252 serine-type endopeptidase activity
GO:0005515 protein binding
GO:0070008 serine-type exopeptidase activity
Biological Process
GO:0003050 regulation of systemic arterial blood pressure by atrial natriuretic peptide
GO:0006508 proteolysis
GO:0007565 female pregnancy
GO:0008217 regulation of blood pressure
GO:0016486 peptide hormone processing
GO:0035813 regulation of renal sodium excretion
Cellular Component
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0009986 cell surface
GO:0016020 membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR001254 Peptidase S1
IPR001314 Peptidase S1A, chymotrypsin-type
IPR002172 Low-density lipoprotein (LDL) receptor class A repeat
IPR009003 Trypsin-like cysteine/serine peptidase domain
IPR017052 Peptidase S1A, corin
IPR017448 SRCR-like domain
IPR020067 Frizzled domain
PFAM PF00089
PF00057
PF01392
PRINTS PR00722
PR00261
PIRSF PIRSF036376
SMART SM00020
SM00192
SM00202
SM00063
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y5Q5
PhosphoSite PhosphoSite-Q9Y5Q5
TrEMBL Q8IZR7
UniProt Splice Variant
Entrez Gene 10699
UniGene Hs.604887
RefSeq NP_006578
HUGO HGNC:19012
OMIM 605236
CCDS CCDS3477
HPRD 05573
IMGT
EMBL AC092597 AC104646 AC107068 AF113248 AF133845 AF521006 BC110451 EU326305
GenPept AAD31850 AAF21966 AAI10452 AAN40016 AAY40917 AAY40991 ACA05911