phosphatidate phosphatase LPIN2; lipin-2 (LPIN2, KIAA0249)
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Function
- roles in controlling metabolism of fatty acids at differents levels
- Mg+2-dependent phosphatidate phosphatase enzyme
- catalyzes conversion of phosphatidic acid to diacylglycerol during triglyceride, phosphatidylcholine & phosphatidylethanolamine biosynthesis in the endoplasmic reticulum membrane
- nuclear transcriptional coactivator for PPARGC1A to modulate lipid metabolism (putative)
- inhibited by N-ethylmaleimide (putative)
Structure
- contains 1 Asp-Xaa-Asp-Xaa-Thr (DXDXT) motif, a catalytic motif known to be essential for phosphatidate phosphatase activity
- contains one Leu-Xaa-Xaa-Ile-Leu (LXXIL) motif, a motif known to be a transcriptional binding motif (putative)
- belongs to the lipin family
Compartment
- nucleus (putative)
- cytoplasm, cytosol (putative)
- endoplasmic reticulum membrane
- translocates to endoplasmic reticulum membrane with increasing levels of oleate (putative)
Expression
- expressed in liver, lung, kidney, placenta, spleen, thymus, lymph node, prostate, testes, small intestine, & colon
Pathology
- defects in LPIN2 are the cause of Majeed syndrome
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/Q92539.html
- ↑ INFEVERS; Note: repertory of FMF & hereditary autoinflammatory disorders mutations http://fmf.igh.cnrs.fr/ISSAID/infevers/disease_menu.php?n=7
- ↑ OMIM https://mirror.omim.org/entry/605519