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7BU2

Structure of alcohol dehydrogenase YjgB from Escherichia coli

Summary for 7BU2
Entry DOI10.2210/pdb7bu2/pdb
DescriptorAlcohol dehydrogenase, NITRATE ION, GLYCEROL, ... (5 entities in total)
Functional Keywordsalcohol dehydrogenase, oxidoreductase
Biological sourceEscherichia coli
Total number of polymer chains2
Total formula weight76075.96
Authors
Nguyen, G.T.,Kim, Y.-G.,Ahn, J.-W.,Chang, J.H. (deposition date: 2020-04-03, release date: 2020-05-13, Last modification date: 2023-11-29)
Primary citationNguyen, G.T.,Kim, Y.G.,Ahn, J.W.,Chang, J.H.
Structural Basis for Broad Substrate Selectivity of Alcohol Dehydrogenase YjgB from Escherichia coli .
Molecules, 25:-, 2020
Cited by
PubMed Abstract: In metabolic engineering and synthetic biology fields, there have been efforts to produce variable bioalcohol fuels, such as isobutanol and 2-phenylethanol, in order to meet industrial demands. YjgB is an aldehyde dehydrogenase from Escherichia coli that shows nicotinamide adenine dinucleotide phosphate (NADP)-dependent broad selectivity for aldehyde derivatives with an aromatic ring or small aliphatic chain. This could contribute to the design of industrial synthetic pathways. We determined the crystal structures of YjgB for both its apo-form and NADP-complexed form at resolutions of 1.55 and 2.00 Å, respectively, in order to understand the mechanism of broad substrate selectivity. The hydrophobic pocket of the active site and the nicotinamide ring of NADP(H) are both involved in conferring its broad specificity toward aldehyde substrates. In addition, based on docking-simulation data, we inferred that π-π stacking between substrates and aromatic side chains might play a crucial role in recognizing substrates. Our structural analysis of YjgB might provide insights into establishing frameworks to understand its broad substrate specificity and develop engineered enzymes for industrial biofuel synthesis.
PubMed: 32455802
DOI: 10.3390/molecules25102404
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.553 Å)
Structure validation

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