| Literature DB >> 34117479 |
Laiyin Nie1,2, Tomas C Pascoa1, Ashley C W Pike1, Simon R Bushell1,3, Andrew Quigley4,5, Gian Filippo Ruda1,6, Amy Chu1,7, Victoria Cole1,8, David Speedman1, Tiago Moreira1, Leela Shrestha1, Shubhashish M M Mukhopadhyay1, Nicola A Burgess-Brown1, James D Love9,10, Paul E Brennan1,11, Elisabeth P Carpenter12,13.
Abstract
Very long chain fatty acids (VLCFAs) are essential building blocks for the synthesis of ceramides and sphingolipids. The first step in the fatty acid elongation cycle is catalyzed by the 3-keto acyl-coenzyme A (CoA) synthases (in mammals, ELOVL elongases). Although ELOVLs are implicated in common diseases, including insulin resistance, hepatic steatosis and Parkinson's, their underlying molecular mechanisms are unknown. Here we report the structure of the human ELOVL7 elongase, which comprises an inverted transmembrane barrel surrounding a 35-Å long tunnel containing a covalently attached product analogue. The structure reveals the substrate-binding sites in the narrow tunnel and an active site deep in the membrane. We demonstrate that chain elongation proceeds via an acyl-enzyme intermediate involving the second histidine in the canonical HxxHH motif. The unusual substrate-binding arrangement and chemistry suggest mechanisms for selective ELOVL inhibition, relevant for diseases where VLCFAs accumulate, such as X-linked adrenoleukodystrophy.Entities:
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Year: 2021 PMID: 34117479 PMCID: PMC7611377 DOI: 10.1038/s41594-021-00605-6
Source DB: PubMed Journal: Nat Struct Mol Biol ISSN: 1545-9985 Impact factor: 15.369