Phospholipid acyltransferase
| Acyltransferase | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| Symbol | Acyltransferase | ||||||||
| Pfam | PF01553 | ||||||||
| InterPro | IPR002123 | ||||||||
| SCOP2 | 1k30 / SCOPe / SUPFAM | ||||||||
| OPM superfamily | 474 | ||||||||
| OPM protein | 5xj5 | ||||||||
| CDD | cd06551 | ||||||||
| Membranome | 741 | ||||||||
| |||||||||
This family contains acyltransferases involved in phospholipid biosynthesis and proteins of unknown function.[1] This family also includes tafazzin,[2] the Barth syndrome gene.
Subfamilies[edit]
Human proteins containing this domain[edit]
AGPAT1; AGPAT2; AGPAT3; AGPAT4; AGPAT5; AGPAT6; AGPAT7; AYTL1; AYTL2; GNPAT; GPAM; GPAT3; LYCAT; TAZ; TMEM68;
References[edit]
- ^ Neuwald AF (1997). "Barth syndrome may be due to an acyltransferase deficiency". Curr. Biol. 7 (8): R465–6. doi:10.1016/S0960-9822(06)00237-5. PMID 9259571. S2CID 2763279.
- ^ Bolhuis PA, Toniolo D, Bione S, Maestrini E, Gedeon AK, D Adamo P (1996). "A novel X-linked gene, G4.5. is responsible for Barth syndrome". Nat. Genet. 12 (4): 385–389. doi:10.1038/ng0496-385. PMID 8630491. S2CID 23539265.
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