Homo sapiens Protein: CORIN | |||||||||||||||||||
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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 |
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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.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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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 |
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PFAM |
PF00089
PF00057 PF01392 |
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PRINTS |
PR00722
PR00261 |
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PIRSF |
PIRSF036376
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SMART |
SM00020
SM00192 SM00202 SM00063 |
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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 | ||||||||||||||||||