Homo sapiens Protein: CTSF | |||||||
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Summary | |||||||
InnateDB Protein | IDBP-59420.6 | ||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
Gene Symbol | CTSF | ||||||
Protein Name | cathepsin F | ||||||
Synonyms | CATSF; CLN13; | ||||||
Species | Homo sapiens | ||||||
Ensembl Protein | ENSP00000310832 | ||||||
InnateDB Gene | IDBG-59418 (CTSF) | ||||||
Protein Structure |
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UniProt Annotation | |||||||
Function | Thiol protease which is believed to participate in intracellular degradation and turnover of proteins. Has also been implicated in tumor invasion and metastasis. | ||||||
Subcellular Localization | Lysosome. | ||||||
Disease Associations | Ceroid lipofuscinosis, neuronal, 13 (CLN13) [MIM:615362]: A form of neuronal ceroid lipofuscinosis characterized by adult onset of progressive cognitive decline and motor dysfunction leading to dementia and often early death. Some patients develop seizures. Neuronal ceroid lipofuscinoses are progressive neurodegenerative, lysosomal storage diseases characterized by intracellular accumulation of autofluorescent liposomal material. {ECO:0000269PubMed:23297359}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||
Tissue Specificity | High expression levels in heart, skeletal muscle, brain, testis and ovary; moderate levels in prostate, placenta, liver and colon; and no detectable expression in peripheral leukocytes and thymus. | ||||||
Comments | |||||||
Interactions | |||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 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 |
IPR000668
Peptidase C1A, papain C-terminal IPR013201 Proteinase inhibitor I29, cathepsin propeptide |
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PFAM |
PF00112
PF08246 |
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PRINTS |
PR00705
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PIRSF | |||||||
SMART |
SM00645
SM00848 |
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TIGRFAMs | |||||||
Post-translational Modifications | |||||||
Modification | |||||||
Cross-References | |||||||
SwissProt | Q9UBX1 | ||||||
PhosphoSite | PhosphoSite-Q9UBX1 | ||||||
TrEMBL | E9PSC2 | ||||||
UniProt Splice Variant | |||||||
Entrez Gene | 8722 | ||||||
UniGene | Hs.11590 | ||||||
RefSeq | NP_003784 | ||||||
HUGO | HGNC:2531 | ||||||
OMIM | 603539 | ||||||
CCDS | CCDS8144 | ||||||
HPRD | 04643 | ||||||
IMGT | |||||||
EMBL | AF071748 AF071749 AF088886 AF132894 AF136279 AJ007331 AK313657 AL137742 AP002748 BC011682 BC036451 CH471076 | ||||||
GenPept | AAC78838 AAC78839 AAD26616 AAD41790 AAF13146 AAH11682 AAH36451 BAG36411 CAB42883 CAB70900 EAW74547 EAW74548 | ||||||