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-Structure paper
Title | X‑ray Crystallography Reveals How Subtle Changes Control the Orientation of Substrate Binding in an Alkene Reductase |
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Journal, issue, pages | ACS CATALYSIS, Vol. 3, Page 2376-2390, Year 2013 |
Publish date | Sep 23, 2011 (structure data deposition date) |
Authors | Pompeu, Y.A. / Sullivan, B. / Stewart, J.D. |
External links | ACS CATALYSIS / Search PubMed |
Methods | X-ray diffraction |
Resolution | 1.179 - 1.7 Å |
Structure data | PDB-3txz: PDB-4gbu: PDB-4ge8: PDB-4gwe: PDB-4gxm: PDB-4h6k: PDB-4k7v: PDB-4k7y: PDB-4k8e: PDB-4k8h: |
Chemicals | ChemComp-FMN: ChemComp-07V: ChemComp-MG: ChemComp-HOH: ChemComp-0WV: ChemComp-CL: ChemComp-NA: ChemComp-1PE: ChemComp-0WU: ChemComp-PEG: ChemComp-PGE: |
Source |
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Keywords | OXIDOREDUCTASE / Enantioselectivity / Alkene Reductase / Enone reductase / OYE Old yellow enzyme / TIM Barrel / NAD(P)H Oxidoreductase / Flavin mononucleotide / Nicotinamide adenine dinucleotide / alpha/beta barrel / enenone reductase / NADPH oxidoreductase / carvone / enenatioselectivity / binding mode / dismutation / ligand / NAD(P)H oxidoreductase; alkene reductase / NAD(P)H / ENOATE REDUCTASE / SUBSTRATE FLIPPING / reductase / flipped binding / OYE / old yellow enzyme / biocatalysis / atomic resolution / enanatiocomplementarity / FMN binding domain / FMN NAD(P)H / flipped binding mode / semi rational design / NADPH dehydrogenase 1 / TIM-barrel |