Homo sapiens Protein: CAPN10 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-84779.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | CAPN10 | ||||||||||||||||||
Protein Name | calpain 10 | ||||||||||||||||||
Synonyms | CANP10; NIDDM1; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000349556 | ||||||||||||||||||
InnateDB Gene | IDBG-84773 (CAPN10) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Calcium-regulated non-lysosomal thiol-protease which catalyze limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. May play a role in insulin-stimulated glucose uptake. {ECO:0000269PubMed:17572128}. | ||||||||||||||||||
Subcellular Localization | |||||||||||||||||||
Disease Associations | Diabetes mellitus, non-insulin-dependent, 1 (NIDDM1) [MIM:601283]: A multifactorial disorder of glucose homeostasis caused by a lack of sensitivity to the body's own insulin. Affected individuals usually have an obese body habitus and manifestations of a metabolic syndrome characterized by diabetes, insulin resistance, hypertension and hypertriglyceridemia. The disease results in long-term complications that affect the eyes, kidneys, nerves, and blood vessels. {ECO:0000269PubMed:11017071, ECO:0000269PubMed:16721485}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Detected in primary skeletal muscle cells (at protein level). Ubiquitous. {ECO:0000269PubMed:17572128}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 4 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 |
IPR001300
Peptidase C2, calpain, catalytic domain IPR022682 Peptidase C2, calpain, large subunit, domain III IPR022683 Peptidase C2, calpain, domain III IPR022684 Peptidase C2, calpain family |
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PFAM |
PF00648
PF01067 |
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PRINTS |
PR00704
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PIRSF | |||||||||||||||||||
SMART |
SM00230
SM00720 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9HC96 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9HC96 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 11132 | ||||||||||||||||||
UniGene | Hs.728234 | ||||||||||||||||||
RefSeq | |||||||||||||||||||
HUGO | HGNC:1477 | ||||||||||||||||||
OMIM | 605286 | ||||||||||||||||||
CCDS | |||||||||||||||||||
HPRD | 05595 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB058748 AC124862 AF089088 AF089090 AF089091 AF089092 AF089093 AF089094 AF089095 AF089096 AK074807 BC004260 BC007553 | ||||||||||||||||||
GenPept | AAG17966 AAG17968 AAG17969 AAG17970 AAG17971 AAG17972 AAG17973 AAG17974 AAH04260 AAH07553 AAX88944 BAB47474 BAC11220 | ||||||||||||||||||