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Qi Zhang - Publications

Affiliations: 
Chemistry Fudan university, Shanghai, Shanghai Shi, China 
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40 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Ma S, Zhang Q. Linaridin natural products. Natural Product Reports. PMID 32484193 DOI: 10.1039/C9Np00074G  0.308
2020 Ding W, Ji X, Zhong Y, Xu K, Zhang Q. Adenosylation reactions catalyzed by the radical S-adenosylmethionine superfamily enzymes. Current Opinion in Chemical Biology. 55: 86-95. PMID 32086168 DOI: 10.1016/J.Cbpa.2020.01.007  0.38
2020 Ji W, Ji X, Zhang Q, Mandalapu D, Deng Z, Ding W, Sun P, Zhang Q. Sulfonium-based Homolytic Substitution Observed for the Radical SAM Enzyme HemN. Angewandte Chemie (International Ed. in English). PMID 32065719 DOI: 10.1002/Anie.202000812  0.405
2020 Zhao J, Ji W, Ji X, Zhang Q. Biochemical Characterization of an Arginine 2,3‐aminomutase with Dual Substrate Specificity Chinese Journal of Chemistry. 38: 959-962. DOI: 10.1002/Cjoc.202000119  0.3
2019 Zhu X, Su M, Zhang Q, Li Y, Bao H. Cu-Catalyzed Alkylarylation of Vinylarenes with Masked Alkyl Electrophiles. Organic Letters. PMID 31855441 DOI: 10.1021/Acs.Orglett.9B04392  0.308
2019 Liu L, Chan S, Mo T, Ding W, Yu S, Zhang Q, Yuan S. Movements of the Substrate-Binding Clamp of Cypemycin Decarboxylase CypD. Journal of Chemical Information and Modeling. PMID 31033286 DOI: 10.1021/Acs.Jcim.9B00156  0.351
2019 Ji X, Mo T, Liu WQ, Ding W, Deng Z, Zhang Q. Revisiting the mechanism of anaerobic coproporphyrinogen III oxidases, a radical SAM enzyme involved in heme biosynthesis. Angewandte Chemie (International Ed. in English). PMID 30884058 DOI: 10.1002/Anie.201814708  0.4
2018 Wu Y, Wu R, Mandalapu D, Ji X, Chen T, Ding W, Zhang Q. Radical SAM-dependent adenosylation catalyzed by l-tyrosine lyases. Organic & Biomolecular Chemistry. PMID 30520933 DOI: 10.1039/C8Ob02906G  0.436
2018 Mandalapu D, Ji X, Zhang Q. Reductive cleavage of sulfoxide and sulfone by two radical S-adenosyl-L-methionine enzymes. Biochemistry. PMID 30398855 DOI: 10.1021/Acs.Biochem.8B00844  0.387
2018 Ding W, Mo T, Mandalapu D, Zhang Q. Substrate specificity of the cypemycin decarboxylase CypD. Synthetic and Systems Biotechnology. 3: 159-162. PMID 30345401 DOI: 10.1016/J.Synbio.2018.09.002  0.321
2018 Zhang Q, Ji X, Mandalapu D, Chen J. Expanded chemistry of the class C radical SAM methyltransferase NosN by using an allyl analogue of SAM. Angewandte Chemie (International Ed. in English). PMID 29603551 DOI: 10.1002/Anie.201712224  0.415
2018 Zhang Q, Chen S, Wang H, Yu H. Exquisite Enzyme-Fenton Biomimetic Catalysts for Hydroxyl Radical Production by Mimicking an Enzyme Cascade. Acs Applied Materials & Interfaces. PMID 29457453 DOI: 10.1021/acsami.7b18690  0.414
2018 Gan XC, Zhang Q, Jia XS, Yin L. Asymmetric Construction of Fluoroalkyl Tertiary Alcohols through a Three-Component Reaction of (Bpin)2, 1,3-Enynes, and Fluoroalkyl Ketones Catalyzed by a Copper(I) Complex. Organic Letters. PMID 29419304 DOI: 10.1021/Acs.Orglett.7B04039  0.374
2018 Mandalapu D, Ji X, Chen J, Guo C, Liu WQ, Ding W, Zhou J, Zhang Q. Thioesterase-mediated synthesis of teixobactin analogues: mechanism and substrate specificity. The Journal of Organic Chemistry. PMID 29357665 DOI: 10.1021/Acs.Joc.7B02462  0.401
2018 Liu WQ, Amara P, Mouesca JM, Ji X, Renoux O, Martin L, Zhang C, Zhang Q, Nicolet Y. 1,2-diol dehydration by the radical SAM enzyme AprD4 - a matter of proton circulation and substrate flexibility. Journal of the American Chemical Society. PMID 29300094 DOI: 10.1021/Jacs.7B10501  0.409
2017 Ding W, Ji W, Wu Y, Wu R, Liu WQ, Mo T, Zhao J, Ma X, Zhang W, Xu P, Deng Z, Tang B, Yu Y, Zhang Q. Biosynthesis of the nosiheptide indole side ring centers on a cryptic carrier protein NosJ. Nature Communications. 8: 437. PMID 28874663 DOI: 10.1038/S41467-017-00439-1  0.362
2017 Liu L, Ji X, Li Y, Ji W, Mo T, Ding W, Zhang Q. A mechanistic study of the non-oxidative decarboxylation catalyzed by the radical S-adenosyl-l-methionine enzyme BlsE involved in blasticidin S biosynthesis. Chemical Communications (Cambridge, England). PMID 28671210 DOI: 10.1039/C7Cc04286H  0.703
2017 Ding W, Wu Y, Ji X, Qianzhu H, Chen F, Deng Z, Yu Y, Zhang Q. Nucleoside-linked shunt products in the reaction catalyzed by the class C radical S-adenosylmethionine methyltransferase NosN. Chemical Communications (Cambridge, England). PMID 28443932 DOI: 10.1039/C7Cc02162C  0.387
2017 Ding W, Li Y, Zhao J, Ji X, Mo T, Qianzhu H, Tu T, Deng Z, Yu Y, Chen F, Zhang Q. The Catalytic Mechanism of the Class C radical S-Adenosylmethionine Methyltransferase NosN. Angewandte Chemie (International Ed. in English). PMID 28112859 DOI: 10.1002/Anie.201609948  0.682
2016 Qianzhu H, Ji W, Ji X, Chu L, Guo C, Lu W, Ding W, Gao J, Zhang Q. Reactivity of the nitrogen-centered tryptophanyl radical in the catalysis by the radical SAM enzyme NosL. Chemical Communications (Cambridge, England). PMID 27929146 DOI: 10.1039/C6Cc08869D  0.38
2016 Ji X, Li Y, Xie L, Lu H, Ding W, Zhang Q. Expanding Radical SAM Chemistry by Using Radical Addition Reactions and SAM Analogues. Angewandte Chemie (International Ed. in English). PMID 27573794 DOI: 10.1002/Anie.201605917  0.679
2016 Ji X, Liu WQ, Yuan S, Yin Y, Ding W, Zhang Q. Mechanistic study of the radical SAM-dependent amine dehydrogenation reactions. Chemical Communications (Cambridge, England). PMID 27492649 DOI: 10.1039/C6Cc05661J  0.366
2016 Ding W, Ji X, Li Y, Zhang Q. Catalytic Promiscuity of the Radical S-adenosyl-L-methionine Enzyme NosL. Frontiers in Chemistry. 4: 27. PMID 27446906 DOI: 10.3389/Fchem.2016.00027  0.688
2016 Lv M, Ji X, Zhao J, Li Y, Zhang C, Su L, Ding W, Deng Z, Yu Y, Zhang Q. Characterization of a C3 deoxygenation pathway reveals a key branch point in aminoglycoside biosynthesis. Journal of the American Chemical Society. PMID 27120352 DOI: 10.1021/Jacs.6B02221  0.661
2016 Ding W, Li Q, Jia Y, Ji X, Qianzhu H, Zhang Q. Emerging diversity of the cobalamin-dependent methyltransferases involving radical-based mechanisms. Chembiochem : a European Journal of Chemical Biology. PMID 27028019 DOI: 10.1002/Cbic.201600107  0.341
2016 Ding W, Liu WQ, Jia Y, Li Y, van der Donk WA, Zhang Q. Biosynthetic investigation of phomopsins reveals a widespread pathway for ribosomal natural products in Ascomycetes. Proceedings of the National Academy of Sciences of the United States of America. PMID 26979951 DOI: 10.1073/pnas.1522907113  0.568
2016 Ji X, Li Y, Jia Y, Ding W, Zhang Q. Mechanistic Insights into the Radical S-adenosyl-l-methionine Enzyme NosL From a Substrate Analogue and the Shunt Products. Angewandte Chemie (International Ed. in English). PMID 26837062 DOI: 10.1002/Anie.201509900  0.704
2015 Ji X, Li Y, Ding W, Zhang Q. Substrate-Tuned Catalysis of the Radical S-Adenosyl-L-Methionine Enzyme NosL Involved in Nosiheptide Biosynthesis. Angewandte Chemie (International Ed. in English). PMID 26138750 DOI: 10.1002/Anie.201503976  0.697
2015 Ding W, Li Y, Zhang Q. Substrate-Controlled Stereochemistry in Natural Product Biosynthesis. Acs Chemical Biology. 10: 1590-8. PMID 25844528 DOI: 10.1021/Acschembio.5B00104  0.666
2015 Liu G, Zhang M, Chen X, Zhang W, Ding W, Zhang Q. Evolution of threonine aldolases, a diverse family involved in the second pathway of glycine biosynthesis. Journal of Molecular Evolution. 80: 102-7. PMID 25644973 DOI: 10.1007/S00239-015-9667-Y  0.347
2013 Zhang Q, Pang B, Ding W, Liu W. Aromatic polyketides produced by bacterial iterative type i polyketide synthases Acs Catalysis. 3: 1439-1447. DOI: 10.1021/Cs400211X  0.324
2012 Chen D, Zhang Q, Zhang Q, Cen P, Xu Z, Liu W. Improvement of FK506 production in Streptomyces tsukubaensis by genetic enhancement of the supply of unusual polyketide extender units via utilization of two distinct site-specific recombination systems. Applied and Environmental Microbiology. 78: 5093-103. PMID 22582065 DOI: 10.1128/Aem.00450-12  0.304
2012 Zhang Q, Yu Y. Thioether crosslinkages created by a radical SAM enzyme. Chembiochem. 13: 1097-1099. PMID 22556103 DOI: 10.1002/Cbic.201200196  0.329
2011 Zhang Q, Liu W. Complex biotransformations catalyzed by radical S-adenosylmethionine enzymes Journal of Biological Chemistry. 286: 30245-30252. PMID 21771780 DOI: 10.1074/Jbc.R111.272690  0.335
2011 Zhang Q, Chen D, Lin J, Liao R, Tong W, Xu Z, Liu W. Characterization of NocL involved in thiopeptide nocathiacin I biosynthesis: a [4Fe-4S] cluster and the catalysis of a radical S-adenosylmethionine enzyme. The Journal of Biological Chemistry. 286: 21287-94. PMID 21454624 DOI: 10.1074/Jbc.M111.224832  0.341
2011 Zhang Q, Li Y, Chen D, Yu Y, Duan L, Shen B, Liu W. Radical-mediated enzymatic carbon chain fragmentation-recombination. Nature Chemical Biology. 7: 154-60. PMID 21240261 DOI: 10.1038/Nchembio.512  0.392
2010 Ding W, Deng W, Tang M, Zhang Q, Tang G, Bi Y, Liu W. Biosynthesis of 3-methoxy-5-methyl naphthoic acid and its incorporation into the antitumor antibiotic azinomycin B Molecular Biosystems. 6: 1071-1081. PMID 20485749 DOI: 10.1039/B926358F  0.319
2009 Yu Y, Duan L, Zhang Q, Liao R, Ding Y, Pan H, Wendt-Pienkowski E, Tang G, Shen B, Liu W. Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework. Acs Chemical Biology. 4: 855-64. PMID 19678698 DOI: 10.1021/Cb900133X  0.333
2009 Liao R, Duan L, Lei C, Pan H, Ding Y, Zhang Q, Chen D, Shen B, Yu Y, Liu W. Thiopeptide biosynthesis featuring ribosomally synthesized precursor peptides and conserved posttranslational modifications. Chemistry & Biology. 16: 141-7. PMID 19246004 DOI: 10.1016/J.Chembiol.2009.01.007  0.304
2008 Fang J, Zhang Y, Huang L, Jia X, Zhang Q, Zhang X, Tang G, Liu W. Cloning and characterization of the tetrocarcin A gene cluster from Micromonospora chalcea NRRL 11289 reveals a highly conserved strategy for tetronate biosynthesis in spirotetronate antibiotics. Journal of Bacteriology. 190: 6014-25. PMID 18586939 DOI: 10.1128/Jb.00533-08  0.335
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