Reaction: HRASLS transfer acyl group from PC to PE to form NAPE
- in pathway: Acyl chain remodelling of PE
The H-RAS-like suppressor (HRASLS) subfamily consists of five enzymes (1–5) in humans that share sequence homology with lecithin:retinol acyltransferase (LRAT). All HRASLS members possess in vitro phospholipid metabolizing abilities including phospholipase A1/2 (PLA1/2) activities and O-acyltransferase activities for the remodeling of glycerophospholipid acyl chains (Golczak et al. 2012), as well as N-acyltransferase activities for the production of N-acylphosphatidylethanolamines (Mardian et al. 2015). Acyl chain remodelling can play a key role in regulating triglyceride accumulation and energy expenditure in adipocytes, making this process a potential target for treatment of metabolic disorders causing obesity. The example here describes the N-acyltransferase activity of HRASLSs for the production of N-acylphosphatidylethanolamines (NAPEs) (Uyama et al. 2012).
Reaction - small molecule participants:
NAPE [endoplasmic reticulum membrane]
LysoPtdCho [endoplasmic reticulum membrane]
PC [endoplasmic reticulum membrane]
PE [endoplasmic reticulum membrane]
Reactome.org reaction link: R-HSA-8858298
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Reaction input - small molecules:
1,2-diacyl-sn-glycero-3-phosphocholine
phosphatidylethanolamine zwitterion
Reaction output - small molecules:
N-acylphosphatidylethanolamine
1-O-acyl-sn-glycero-3-phosphocholine
Reactome.org link: R-HSA-8858298