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Crystallization Of An Atypical Short-Chain Dehydrogenase From Vibrio Vulnificus Lacking The Conserved Catalytic Tetrad.

Acta Crystallogr Sect F Struct Biol Cryst Commun.. 2012-07;  68(Pt 7):771 - 4
Buysschaert G, Verstraete K, Savvides SN, Vergauwen B. Unit for Structural Biology, Laboratory for Protein Biochemistry and Biomolecular Engineering, Unit for Structural Biology, Ghent University, K. L. Ledeganckstraat 35, B-9000 Ghent, Belgium.
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摘要

Short-chain dehydrogenases/reductases (SDRs) are a rapidly expanding superfamily of enzymes that are found in all kingdoms of life. Hallmarked by a highly conserved Asn-Ser-Tyr-Lys catalytic tetrad, SDRs have a broad substrate spectrum and play diverse roles in key metabolic processes. Locus tag VVA1599 in Vibrio vulnificus encodes a short-chain dehydrogenase (hereafter referred to as SDRvv) which lacks the signature catalytic tetrad of SDR members. Structure-based protein sequence alignments have suggested that SDRvv may harbour a unique binding site for its nicotinamide cofactor. To date, structural studies of SDRs with altered catalytic centres are underrepresented in the scientific literature, thus limiting... More

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