Homo sapiens Protein: PLA2G7
Summary
InnateDB Protein IDBP-588989.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PLA2G7
Protein Name phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)
Synonyms LDL-PLA2; LP-PLA2; PAFAD; PAFAH;
Species Homo sapiens
Ensembl Protein ENSP00000445666
InnateDB Gene IDBG-89956 (PLA2G7)
Protein Structure
UniProt Annotation
Function Modulates the action of platelet-activating factor (PAF) by hydrolyzing the sn-2 ester bond to yield the biologically inactive lyso-PAF. Has a specificity for substrates with a short residue at the sn-2 position. It is inactive against long-chain phospholipids.
Subcellular Localization Secreted, extracellular space.
Disease Associations Platelet-activating factor acetylhydrolase deficiency (PAFAD) [MIM:614278]: An enzymatic deficiency that results in exacerbated bodily response to inflammatory agents. It can be associated with several disease states including inflammatory gastrointestinal disorders, asthma and atopy. Asthmatic individuals with PAFAD may manifest aggravated respiratory symptoms. {ECO:0000269PubMed:8675689, ECO:0000269PubMed:9245731, ECO:0000269PubMed:9412624, ECO:0000269PubMed:9472966, ECO:0000269PubMed:9759612}. Note=The disease is caused by mutations affecting the gene represented in this entry.Asthma (ASTHMA) [MIM:600807]: The most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment. It is characterized by recurrent attacks of paroxysmal dyspnea, with wheezing due to spasmodic contraction of the bronchi. {ECO:0000269PubMed:10733466}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.Atopic hypersensitivity (ATOPY) [MIM:147050]: A condition characterized by predisposition to develop hypersensitivity reactions. Atopic individuals can develop eczema, allergic rhinitis and allergic asthma. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Tissue Specificity Plasma.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003847 1-alkyl-2-acetylglycerophosphocholine esterase activity
GO:0005543 phospholipid binding
GO:0047499 calcium-independent phospholipase A2 activity
Biological Process
GO:0016042 lipid catabolic process
GO:0034374 low-density lipoprotein particle remodeling
GO:0034440 lipid oxidation
GO:0034441 plasma lipoprotein particle oxidation
GO:0044267 cellular protein metabolic process
GO:0050729 positive regulation of inflammatory response
GO:0090026 positive regulation of monocyte chemotaxis
Cellular Component
GO:0005576 extracellular region
GO:0034362 low-density lipoprotein particle
Protein Structure and Domains
PDB ID
InterPro IPR005065 Platelet-activating factor acetylhydrolase
IPR016715 Platelet-activating factor acetylhydrolase, eucaryote
IPR029058 Alpha/Beta hydrolase fold
PFAM PF03403
PRINTS
PIRSF PIRSF018169
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q13093
PhosphoSite PhosphoSite-Q13093
TrEMBL
UniProt Splice Variant
Entrez Gene 7941
UniGene Hs.584823
RefSeq NP_001161829
HUGO HGNC:9040
OMIM 601690
CCDS CCDS4917
HPRD 03407
IMGT
EMBL AL591242 BC038452 CH471081 EF568110 U20157 U24577
GenPept AAB04170 AAC50126 AAH38452 ABQ01234 CAH73907 EAX04301