Homo sapiens Protein: SERPINB7
Summary
InnateDB Protein IDBP-584950.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SERPINB7
Protein Name serpin peptidase inhibitor, clade B (ovalbumin), member 7
Synonyms MEGSIN; PPKN; TP55;
Species Homo sapiens
Ensembl Protein ENSP00000444861
InnateDB Gene IDBG-4531 (SERPINB7)
Protein Structure
UniProt Annotation
Function Might function as an inhibitor of Lys-specific proteases. Might influence the maturation of megakaryocytes via its action as a serpin.
Subcellular Localization Cytoplasm {ECO:0000250}.
Disease Associations Keratoderma, palmoplantar, Nagashima type (PPKN) [MIM:615598]: An autosomal recessive, non-syndromic, diffuse palmoplantar keratosis characterized by well-demarcated diffuse erythematous hyperkeratosis expanding onto the dorsal surfaces of the palms and feet and the Achilles tendon area. Hyperkeratosis is mild and non-progressive. {ECO:0000269PubMed:24207119}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Predominantly expressed in mesangial cells. Expressed in the epidermis of the whole body. {ECO:0000269PubMed:24207119}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004867 serine-type endopeptidase inhibitor activity
Biological Process
GO:0010951 negative regulation of endopeptidase activity
GO:0030162 regulation of proteolysis
Cellular Component
GO:0005615 extracellular space
GO:0005737 cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR023796 Serpin domain
PFAM PF00079
PRINTS
PIRSF
SMART SM00093
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O75635
PhosphoSite PhosphoSite-O75635
TrEMBL Q6MZG5
UniProt Splice Variant
Entrez Gene 8710
UniGene Hs.742388
RefSeq NP_001248759
HUGO HGNC:13902
OMIM 603357
CCDS CCDS11988
HPRD 04524
IMGT
EMBL AC069356 AC072051 AF027866 AK300828 BC069417 BC069442 BC069547 BC106743 BC106744 BX641156 D88575
GenPept AAC64506 AAH69417 AAH69442 AAH69547 AAI06744 AAI06745 BAA31232 BAG62480 CAE46069