Year |
Citation |
Score |
2020 |
Dong M, Lauro ML, Koblish TJ, Bahnson BJ. Conformational sampling and kinetics changes across a non-Arrhenius break point in the enzyme thermolysin. Structural Dynamics (Melville, N.Y.). 7: 014101. PMID 32095489 DOI: 10.1063/1.5130582 |
0.635 |
|
2020 |
Herbert D, Gibbs S, Riddick A, Conway M, Dong M. Crystal structure of an oxidized mutant of human mitochondrial branched-chain aminotransferase. Acta Crystallographica. Section F, Structural Biology Communications. 76: 14-19. PMID 31929181 DOI: 10.1107/S2053230X19016480 |
0.343 |
|
2017 |
Dong M, Gonzalez TD, Klems MM, Steinberg LM, Chen W, Papoutsakis ET, Bahnson BJ. In vitro methanol production from methyl coenzyme M using the Methanosarcina barkeri MtaABC protein complex. Biotechnology Progress. PMID 28556629 DOI: 10.1002/Btpr.2503 |
0.565 |
|
2013 |
Schaefer SA, Dong M, Rubenstein RP, Wilkie WA, Bahnson BJ, Thorpe C, Rozovsky S. (77)Se enrichment of proteins expands the biological NMR toolbox. Journal of Molecular Biology. 425: 222-31. PMID 23159557 DOI: 10.1016/J.Jmb.2012.11.011 |
0.642 |
|
2013 |
Aron Schaefer S, Dong M, Bahnson B, Thorpe C, Rozovsky S. Conversion of the Sulfhydryl Oxidase Augmenter of Liver Regeneration into a Selenoprotein Biophysical Journal. 104: 396a. DOI: 10.1016/J.Bpj.2012.11.2208 |
0.665 |
|
2012 |
Nagel ZD, Meadows CW, Dong M, Bahnson BJ, Klinman JP. Active site hydrophobic residues impact hydrogen tunneling differently in a thermophilic alcohol dehydrogenase at optimal versus nonoptimal temperatures Biochemistry. 51: 4147-4156. PMID 22568562 DOI: 10.1021/Bi3001352 |
0.697 |
|
2011 |
Nagel ZD, Dong M, Bahnson BJ, Klinman JP. Impaired protein conformational landscapes as revealed in anomalous Arrhenius prefactors Proceedings of the National Academy of Sciences of the United States of America. 108: 10520-10525. PMID 21670258 DOI: 10.1073/Pnas.1104989108 |
0.696 |
|
2010 |
Daithankar VN, Schaefer SA, Dong M, Bahnson BJ, Thorpe C. Structure of the human sulfhydryl oxidase augmenter of liver regeneration and characterization of a human mutation causing an autosomal recessive myopathy . Biochemistry. 49: 6737-45. PMID 20593814 DOI: 10.1021/Bi100912M |
0.65 |
|
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