Jiahai Zhou
Affiliations: | University of Michigan, Ann Arbor, Ann Arbor, MI |
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"Jiahai Zhou"Mean distance: 20.6 (cluster 32) | S | N | B | C | P |
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Publications
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| Dong Q, Yuan S, Wu L, et al. (2020) Structure-guided engineering of a Thermobifida fusca cutinase for enhanced hydrolysis on natural polyester substrate Bioresources and Bioprocessing. 7: 1-9 |
| Cai Y, Hai Y, Ohashi M, et al. (2019) Structural basis for stereoselective dehydration and hydrogen-bonding catalysis by the SAM-dependent pericyclase LepI. Nature Chemistry |
| Cen Y, Singh W, Arkin M, et al. (2019) Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution. Nature Communications. 10: 3198 |
| Xu J, Cen Y, Singh W, et al. (2019) Stereodivergent Protein Engineering of a Lipase to Access All Possible Stereoisomers of Chiral Esters with Two Stereo-centers. Journal of the American Chemical Society |
| Zhou J, Wang Y, Xu G, et al. (2018) Structural Insight into Enantioselective Inversion of an Alcohol Dehydrogenase Reveals a "Polar Gate" in Stereorecognition of Diaryl Ketones. Journal of the American Chemical Society |
| Li F, Kong X, Chen Q, et al. (2018) Regioselectivity Engineering of Epoxide Hydrolase: Near-Perfect Enantioconvergence through a Single Site Mutation Acs Catalysis. 8: 8314-8317 |
| Sun Z, Wu L, Bocola M, et al. (2017) Structural and Computational Insight into the Catalytic Mechanism of Limonene Epoxide Hydrolase Mutants in Stereoselective Transformations. Journal of the American Chemical Society |
| Yuan H, Zhang J, Cai Y, et al. (2017) GyrI-like proteins catalyze cyclopropanoid hydrolysis to confer cellular protection. Nature Communications. 8: 1485 |
| Li M, Zhang ZJ, Kong XD, et al. (2017) Engineering Streptomyces coelicolor carbonyl reductase for efficient synthesis of atorvastatin precursor. Applied and Environmental Microbiology |
| Zhou J, Wu F, Yang W, et al. (2016) The Mass Loss and Humification of Stumps and Roots in Masson Pine Plantations Based on Log File Records. Plos One. 11: e0160913 |