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-Structure paper
タイトル | Discovery of a Regulatory Subunit of the Yeast Fatty Acid Synthase. |
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ジャーナル・号・ページ | Cell, Vol. 180, Issue 6, Page 1130-1143.e20, Year 2020 |
掲載日 | 2020年3月19日 |
著者 | Kashish Singh / Benjamin Graf / Andreas Linden / Viktor Sautner / Henning Urlaub / Kai Tittmann / Holger Stark / Ashwin Chari / |
PubMed 要旨 | Fatty acid synthases (FASs) are central to metabolism but are also of biotechnological interest for the production of fine chemicals and biofuels from renewable resources. During fatty acid ...Fatty acid synthases (FASs) are central to metabolism but are also of biotechnological interest for the production of fine chemicals and biofuels from renewable resources. During fatty acid synthesis, the growing fatty acid chain is thought to be shuttled by the dynamic acyl carrier protein domain to several enzyme active sites. Here, we report the discovery of a γ subunit of the 2.6 megadalton α-βS. cerevisiae FAS, which is shown by high-resolution structures to stabilize a rotated FAS conformation and rearrange ACP domains from equatorial to axial positions. The γ subunit spans the length of the FAS inner cavity, impeding reductase activities of FAS, regulating NADPH turnover by kinetic hysteresis at the ketoreductase, and suppressing off-pathway reactions at the enoylreductase. The γ subunit delineates the functional compartment within FAS. As a scaffold, it may be exploited to incorporate natural and designed enzymatic activities that are not present in natural FAS. |
リンク | Cell / PubMed:32160528 |
手法 | EM (単粒子) / X線回折 |
解像度 | 2.8 - 4.6 Å |
構造データ | EMDB-4577, PDB-6ql5: EMDB-4578, PDB-6ql6: PDB-6ql7: PDB-6ql9: |
化合物 | ChemComp-PNS: ChemComp-FMN: ChemComp-J8T: ChemComp-EDO: ChemComp-NA: ChemComp-A2P: ChemComp-ACT: ChemComp-PGE: ChemComp-MLI: ChemComp-HOH: |
由来 |
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キーワード | TRANSFERASE / Fatty acid synthase / Acyl carrier protein / Ketosynthase / Ketoreductase / Enoyl reductase / Dehydratase / Malonyl/palmitoyl transferase / Acetyl transferase / Phosphopantetheine transferase |