| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 2050866 | FEBS Letters | 2008 | 6 Pages | 
Abstract
												Very long-chain fatty acids are produced through a four-step cycle. However, the 3-hydroxyacyl-CoA dehydratase catalyzing the third step in mammals has remained unidentified. Mammals have four candidates, HACD1–4, based on sequence similarities to the recently identified yeast Phs1, although HACD3 and HACD4 share relatively weak similarity. We demonstrate that all four of these human proteins are indeed 3-hydroxyacyl-CoA dehydratases, in growth suppression experiments using a PHS1-shut off yeast strain and/or in vitro 3-hydroxypalmitoyl-CoA dehydratase assays. HACD proteins exhibit distinct tissue-expression patterns. We also establish that HACD proteins interact with the condensation enzymes ELOVL1–7, with some preferences.
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											Authors
												Mika Ikeda, Yuki Kanao, Masao Yamanaka, Hiroko Sakuraba, Yukiko Mizutani, Yasuyuki Igarashi, Akio Kihara, 
											