5EJ2

Crystal structure of Carveol dehydrogenase from Mycobacterium avium in complex with NAD

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5EJ2 の概要

• エントリーDOI: 10.2210/pdb5ej2/pdb
• 分子名称: Carveol dehydrogenase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, PHOSPHATE ION, ... (5 entities in total)
• 機能のキーワード: ssgcid, carveol dehydrogenase, nad, dehydrogenase, mycobacterium avium, structural genomics, seattle structural genomics center for infectious disease, oxidoreductase
• 由来する生物種: Mycobacterium avium
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 134701.75

構造登録者

Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2015-10-31, 公開日: 2015-12-02, 最終更新日: 2023-09-27)

主引用文献

Haft, D.H.,Pierce, P.G.,Mayclin, S.J.,Sullivan, A.,Gardberg, A.S.,Abendroth, J.,Begley, D.W.,Phan, I.Q.,Staker, B.L.,Myler, P.J.,Marathias, V.M.,Lorimer, D.D.,Edwards, T.E.
Mycofactocin-associated mycobacterial dehydrogenases with non-exchangeable NAD cofactors.
Sci Rep, 7:41074-41074, 2017

PubMed Abstract: During human infection, Mycobacterium tuberculosis (Mtb) survives the normally bacteriocidal phagosome of macrophages. Mtb and related species may be able to combat this harsh acidic environment which contains reactive oxygen species due to the mycobacterial genomes encoding a large number of dehydrogenases. Typically, dehydrogenase cofactor binding sites are open to solvent, which allows NAD/NADH exchange to support multiple turnover. Interestingly, mycobacterial short chain dehydrogenases/reductases (SDRs) within family TIGR03971 contain an insertion at the NAD binding site. Here we present crystal structures of 9 mycobacterial SDRs in which the insertion buries the NAD cofactor except for a small portion of the nicotinamide ring. Line broadening and STD-NMR experiments did not show NAD or NADH exchange on the NMR timescale. STD-NMR demonstrated binding of the potential substrate carveol, the potential product carvone, the inhibitor tricyclazol, and an external redox partner 2,6-dichloroindophenol (DCIP). Therefore, these SDRs appear to contain a non-exchangeable NAD cofactor and may rely on an external redox partner, rather than cofactor exchange, for multiple turnover. Incidentally, these genes always appear in conjunction with the mftA gene, which encodes the short peptide MftA, and with other genes proposed to convert MftA into the external redox partner mycofactocin.

PubMed: 28120876
DOI: 10.1038/srep41074

実験手法

X-RAY DIFFRACTION (2.15 Å)