1by6: Difference between revisions
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{{STRUCTURE_1by6| PDB=1by6 | SCENE= }} | {{STRUCTURE_1by6| PDB=1by6 | SCENE= }} | ||
===Peptide of human apolipoprotein C-II=== | |||
{{ABSTRACT_PUBMED_10903476}} | |||
=== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/APOC2_HUMAN APOC2_HUMAN]] Defects in APOC2 are the cause of hyperlipoproteinemia type 1B (HLPP1B) [MIM:[http://omim.org/entry/207750 207750]]. It is an autosomal recessive trait characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis.<ref>PMID:8323539</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/APOC2_HUMAN APOC2_HUMAN]] Component of the very low density lipoprotein (VLDL) fraction in plasma, and is an activator of several triacylglycerol lipases. The association of APOC2 with plasma chylomicrons, VLDL, and HDL is reversible, a function of the secretion and catabolism of triglyceride-rich lipoproteins, and changes rapidly. | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:010903476</ref><references group="xtra"/> | <ref group="xtra">PMID:010903476</ref><references group="xtra"/><references/> | ||
[[Category: Cushley, R J.]] | [[Category: Cushley, R J.]] | ||
[[Category: Rozek, A.]] | [[Category: Rozek, A.]] | ||
Revision as of 21:39, 24 March 2013
Peptide of human apolipoprotein C-IIPeptide of human apolipoprotein C-II
Template:ABSTRACT PUBMED 10903476
DiseaseDisease
[APOC2_HUMAN] Defects in APOC2 are the cause of hyperlipoproteinemia type 1B (HLPP1B) [MIM:207750]. It is an autosomal recessive trait characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis.[1]
FunctionFunction
[APOC2_HUMAN] Component of the very low density lipoprotein (VLDL) fraction in plasma, and is an activator of several triacylglycerol lipases. The association of APOC2 with plasma chylomicrons, VLDL, and HDL is reversible, a function of the secretion and catabolism of triglyceride-rich lipoproteins, and changes rapidly.
About this StructureAbout this Structure
1by6 is a 1 chain structure. Full experimental information is available from OCA.
ReferenceReference
- ↑ Inadera H, Hibino A, Kobayashi J, Kanzaki T, Shirai K, Yukawa S, Saito Y, Yoshida S. A missense mutation (Trp 26-->Arg) in exon 3 of the apolipoprotein CII gene in a patient with apolipoprotein CII deficiency (apo CII-Wakayama). Biochem Biophys Res Commun. 1993 Jun 30;193(3):1174-83. PMID:8323539 doi:http://dx.doi.org/S0006-291X(83)71749-3