Apolipoprotein A-II
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.[5] It is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. ApoA-II regulates many steps in HDL metabolism, and its role in coronary heart disease is unclear. [6] Remarkably, defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.[7]
ApoA-II | |||||||||
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![]() structures of apolipoprotein a-ii and a lipid surrogate complex provide insights into apolipoprotein-lipid interactions | |||||||||
Identifiers | |||||||||
Symbol | ApoA-II | ||||||||
Pfam | PF04711 | ||||||||
InterPro | IPR006801 | ||||||||
SCOP2 | 1l6k / SCOPe / SUPFAM | ||||||||
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Interactions
ApoA-II has been shown to interact with phospholipid transfer protein.[8]
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles. [§ 1]
Statin pathway edit
- The interactive pathway map can be edited at WikiPathways: "Statin_Pathway_WP430".
References
External links
Further reading
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