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4I26

2.20 Angstroms X-ray crystal structure of 2-aminomuconate 6-semialdehyde dehydrogenase from Pseudomonas fluorescens

Summary for 4I26
Entry DOI10.2210/pdb4i26/pdb
Related4I1W 4I25 4I2R
Descriptor2-aminomuconate 6-semialdehyde dehydrogenase, 1,2-ETHANEDIOL, SODIUM ION, ... (4 entities in total)
Functional Keywordsaldehyde dehydrogenase, dehydrogenase, oxidoreductase
Biological sourcePseudomonas fluorescens
Total number of polymer chains4
Total formula weight216282.03
Authors
Davis, I.,Huo, L.,Chen, L.,Liu, A. (deposition date: 2012-11-21, release date: 2014-05-21, Last modification date: 2023-09-20)
Primary citationHuo, L.,Davis, I.,Liu, F.,Andi, B.,Esaki, S.,Iwaki, H.,Hasegawa, Y.,Orville, A.M.,Liu, A.
Crystallographic and spectroscopic snapshots reveal a dehydrogenase in action.
Nat Commun, 6:5935-5935, 2015
Cited by
PubMed Abstract: Aldehydes are ubiquitous intermediates in metabolic pathways and their innate reactivity can often make them quite unstable. There are several aldehydic intermediates in the metabolic pathway for tryptophan degradation that can decay into neuroactive compounds that have been associated with numerous neurological diseases. An enzyme of this pathway, 2-aminomuconate-6-semialdehyde dehydrogenase, is responsible for 'disarming' the final aldehydic intermediate. Here we show the crystal structures of a bacterial analogue enzyme in five catalytically relevant forms: resting state, one binary and two ternary complexes, and a covalent, thioacyl intermediate. We also report the crystal structures of a tetrahedral, thiohemiacetal intermediate, a thioacyl intermediate and an NAD(+)-bound complex from an active site mutant. These covalent intermediates are characterized by single-crystal and solution-state electronic absorption spectroscopy. The crystal structures reveal that the substrate undergoes an E/Z isomerization at the enzyme active site before an sp(3)-to-sp(2) transition during enzyme-mediated oxidation.
PubMed: 25565451
DOI: 10.1038/ncomms6935
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.204 Å)
Structure validation

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数据于2024-11-06公开中

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