2cdn Citations

The crystal structure of Mycobacterium tuberculosis adenylate kinase in complex with two molecules of ADP and Mg2+ supports an associative mechanism for phosphoryl transfer.

Protein Sci 15 1489-93 (2006)
Cited: 24 times
EuropePMC logo PMID: 16672241

Abstract

The crystal structure of Mycobacterium tuberculosis adenylate kinase (MtAK) in complex with two ADP molecules and Mg2+ has been determined at 1.9 A resolution. Comparison with the solution structure of the enzyme, obtained in the absence of substrates, shows significant conformational changes of the LID and NMP-binding domains upon substrate binding. The ternary complex represents the state of the enzyme at the start of the backward reaction (ATP synthesis). The structure is consistent with a direct nucleophilic attack of a terminal oxygen from the acceptor ADP molecule on the beta-phosphate from the donor substrate, and both the geometry and the distribution of positive charge in the active site support the hypothesis of an associative mechanism for phosphoryl transfer.

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Articles - 2cdn mentioned but not cited (9)

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  12. Adenylate Kinase-Catalyzed Reactions of AMP in Pieces: Specificity for Catalysis at the Nucleoside Activator and Dianion Catalytic Sites. Fernandez PL, Richard JP. Biochemistry 61 2766-2775 (2022)
  13. Triple resonance EPR spectroscopy determines the Mn2+ coordination to ATP. Litvinov A, Feintuch A, Un S, Goldfarb D. J Magn Reson 294 143-152 (2018)
  14. Protective efficacy of six recombinant proteins as vaccine candidates against Echinococcus granulosus in dogs. Shao G, Hua R, Song H, Chen Y, Zhu X, Hou W, Li S, Yang A, Yang G. PLoS Negl Trop Dis 17 e0011709 (2023)