Homo sapiens Protein: GPX7 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-98649.5 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | GPX7 | ||||||||||||||||||
Protein Name | glutathione peroxidase 7 | ||||||||||||||||||
Synonyms | CL683; GPx-7; GPX6; GSHPx-7; NPGPx; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000354677 | ||||||||||||||||||
InnateDB Gene | IDBG-98647 (GPX7) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | It protects esophageal epithelia from hydrogen peroxide- induced oxidative stress. It suppresses acidic bile acid-induced reactive oxigen species (ROS) and protects against oxidative DNA damage and double-strand breaks. {ECO:0000269PubMed:22157330}. | ||||||||||||||||||
Subcellular Localization | Secreted {ECO:0000305}. | ||||||||||||||||||
Disease Associations | Barrett esophagus (BE) [MIM:614266]: A condition characterized by a metaplastic change in which normal esophageal squamous epithelium is replaced by a columnar and intestinal-type epithelium. Patients with Barrett esophagus have an increased risk of esophageal adenocarcinoma. The main cause of Barrett esophagus is gastroesophageal reflux. The retrograde movement of acid and bile salts from the stomach into the esophagus causes prolonged injury to the esophageal epithelium and induces chronic esophagitis, which in turn is believed to trigger the pathologic changes. {ECO:0000269PubMed:22157330}. Note=The disease is caused by mutations affecting the gene represented in this entry. The pathologic mechanisms leading to Barrett esophagus involve GPX7 dysfunction that results in higher levels of hydrogen peroxide and ROS-induced oxidative stress and DNA damage in esophageal cells. | ||||||||||||||||||
Tissue Specificity | Expressed in esophageal epithelial cells; expression is up-regulated after exposure to acidic bile acids. {ECO:0000269PubMed:22157330}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 10 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 |
IPR000866
Alkyl hydroperoxide reductase subunit C/ Thiol specific antioxidant IPR000889 Glutathione peroxidase IPR012336 Thioredoxin-like fold IPR013376 Glutathione peroxidase Gpx7, putative |
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PFAM |
PF00578
PF00255 PF13098 PF13192 PF13462 PF13905 |
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PRINTS |
PR01011
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PIRSF |
PIRSF000303
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SMART | |||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q96SL4 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q96SL4 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 2882 | ||||||||||||||||||
UniGene | Hs.43728 | ||||||||||||||||||
RefSeq | NP_056511 | ||||||||||||||||||
HUGO | HGNC:4559 | ||||||||||||||||||
OMIM | 615784 | ||||||||||||||||||
CCDS | CCDS569 | ||||||||||||||||||
HPRD | 13606 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF091092 AF320068 AK027683 AL356976 AY358402 BC032788 DQ096732 | ||||||||||||||||||
GenPept | AAC72961 AAH32788 AAN76501 AAQ88768 AAY88741 BAB55294 CAI22476 | ||||||||||||||||||