Year |
Citation |
Score |
2020 |
Zheng Q, Osunsade A, David Y. Protein arginine deiminase 4 antagonizes methylglyoxal-induced histone glycation. Nature Communications. 11: 3241. PMID 32591537 DOI: 10.1038/S41467-020-17066-Y |
0.706 |
|
2020 |
Maksimovic I, Zheng Q, Trujillo MN, Galligan JJ, David Y. An Azidoribose Probe to Track Ketoamine Adducts in Histone Ribose Glycation. Journal of the American Chemical Society. PMID 32390412 DOI: 10.1021/Jacs.0C01325 |
0.696 |
|
2020 |
Zheng Q, Maksimovic I, Upad A, David Y. Non-enzymatic covalent modifications: a new link between metabolism and epigenetics. Protein & Cell. PMID 32356279 DOI: 10.1007/S13238-020-00722-W |
0.701 |
|
2019 |
Zheng Q, Maksimovic I, Upad A, Guber D, David Y. Synthesis of an Alkynyl Methylglyoxal Probe to Investigate Non-enzymatic Histone Glycation. The Journal of Organic Chemistry. PMID 31875401 DOI: 10.1021/Acs.Joc.9B02504 |
0.701 |
|
2019 |
Maksimovic I, Ray D, Zheng Q, David Y. Utilizing intein trans-splicing for in vivo generation of site-specifically modified proteins. Methods in Enzymology. 626: 203-222. PMID 31606075 DOI: 10.1016/Bs.Mie.2019.07.015 |
0.674 |
|
2019 |
Liu J, Lin Z, Li Y, Zheng Q, Chen D, Liu W. Insights into the thioamidation of thiopeptins to enhance the understanding of the biosynthetic logic of thioamide-containing thiopeptides. Organic & Biomolecular Chemistry. PMID 30912568 DOI: 10.1039/C9Ob00402E |
0.423 |
|
2019 |
Zheng Q, Omans ND, Leicher R, Osunsade A, Agustinus AS, Finkin-Groner E, D'Ambrosio H, Liu B, Chandarlapaty S, Liu S, David Y. Reversible histone glycation is associated with disease-related changes in chromatin architecture. Nature Communications. 10: 1289. PMID 30894531 DOI: 10.1038/S41467-019-09192-Z |
0.71 |
|
2019 |
Zheng Q, Prescott NA, Maksimovic I, David Y. (de)Toxifying the Epigenetic Code. Chemical Research in Toxicology. PMID 30839196 DOI: 10.1021/Acs.Chemrestox.9B00013 |
0.715 |
|
2018 |
Zheng Q, Gong Y, Guo Y, Zhao Z, Wu Z, Zhou Z, Chen D, Pan L, Liu W. Structural Insights into a Flavin-Dependent [4 + 2] Cyclase that Catalyzes trans-Decalin Formation in Pyrroindomycin Biosynthesis. Cell Chemical Biology. PMID 29657086 DOI: 10.1016/J.Chembiol.2018.03.007 |
0.384 |
|
2017 |
Li X, Zheng Q, Yin J, Liu W, Gao S. Chemo-enzymatic synthesis of equisetin. Chemical Communications (Cambridge, England). PMID 28401214 DOI: 10.1039/C7Cc01929G |
0.456 |
|
2017 |
Zheng Q, Fang H, Liu W. Post-translational modifications involved in the biosynthesis of thiopeptide antibiotics. Organic & Biomolecular Chemistry. PMID 28358161 DOI: 10.1039/C7Ob00466D |
0.505 |
|
2016 |
Zheng Q, Wu Z, Sun P, Chen D, Tian Z, Liu W. A linear hydroxymethyl tetramate undergoes an acetylation-elimination process for exocyclic methylene formation in the biosynthetic pathway of pyrroindomycins. Organic & Biomolecular Chemistry. PMID 27942669 DOI: 10.1039/C6Ob02567F |
0.441 |
|
2016 |
Zheng Q, Wang S, Duan P, Liao R, Chen D, Liu W. An α/β-hydrolase fold protein in the biosynthesis of thiostrepton exhibits a dual activity for endopeptidyl hydrolysis and epoxide ring opening/macrocyclization. Proceedings of the National Academy of Sciences of the United States of America. PMID 27911800 DOI: 10.1073/Pnas.1612607113 |
0.499 |
|
2016 |
Zheng Q, Wang S, Liao R, Liu W. Precursor-directed Mutational Biosynthesis Facilitates the Functional Assignment of Two Cytochromes P450 in Thiostrepton Biosynthesis. Acs Chemical Biology. PMID 27560135 DOI: 10.1021/Acschembio.6B00419 |
0.433 |
|
2016 |
Zheng Q, Guo Y, Yang L, Zhao Z, Wu Z, Zhang H, Liu J, Cheng X, Wu J, Yang H, Jiang H, Pan L, Liu W. Enzyme-Dependent [4 + 2] Cycloaddition Depends on Lid-like Interaction of the N-Terminal Sequence with the Catalytic Core in PyrI4. Cell Chemical Biology. PMID 26877021 DOI: 10.1016/J.Chembiol.2016.01.005 |
0.461 |
|
2016 |
Zheng Q, Tian Z, Liu W. Recent advances in understanding the enzymatic reactions of [4+2] cycloaddition and spiroketalization. Current Opinion in Chemical Biology. 31: 95-102. PMID 26870924 DOI: 10.1016/J.Cbpa.2016.01.020 |
0.462 |
|
2016 |
Zheng Q, Liu W. Thiopeptide Antibiotics act on both Host and Microbe to Deliver Double Punch on Mycobacterial Infection Mycobacterial Diseases. 6: 1-3. DOI: 10.4172/2161-1068.1000203 |
0.365 |
|
2016 |
Duan P, Zheng Q, Lin Z, Wang S, Chen D, Liu W. Molecular engineering of thiostrepton: Via single "base"-based mutagenesis to generate side ring-derived variants Organic Chemistry Frontiers. 3: 1254-1258. DOI: 10.1039/C6Qo00320F |
0.429 |
|
2016 |
Wang S, Zheng Q, Wang J, Chen D, Yu Y, Liu W. Concurrent modifications of the C-terminus and side ring of thiostrepton and their synergistic effects with respect to improving antibacterial activities Organic Chemistry Frontiers. 3: 496-500. DOI: 10.1039/C5Qo00433K |
0.454 |
|
2015 |
Zhang L, Mori T, Zheng Q, Awakawa T, Yan Y, Liu W, Abe I. Rational Control of Polyketide Extender Units by Structure-Based Engineering of a Crotonyl-CoA Carboxylase/Reductase in Antimycin Biosynthesis. Angewandte Chemie (International Ed. in English). PMID 26356484 DOI: 10.1002/Anie.201506899 |
0.453 |
|
2015 |
Zheng Q, Wang Q, Wang S, Wu J, Gao Q, Liu W. Thiopeptide Antibiotics Exhibit a Dual Mode of Action against Intracellular Pathogens by Affecting Both Host and Microbe. Chemistry & Biology. PMID 26211364 DOI: 10.1016/J.Chembiol.2015.06.019 |
0.402 |
|
2015 |
Tian Z, Sun P, Yan Y, Wu Z, Zheng Q, Zhou S, Zhang H, Yu F, Jia X, Chen D, Mándi A, Kurtán T, Liu W. An enzymatic [4+2] cyclization cascade creates the pentacyclic core of pyrroindomycins. Nature Chemical Biology. 11: 259-65. PMID 25730548 DOI: 10.1038/Nchembio.1769 |
0.493 |
|
2015 |
Wang S, Zheng Q, Wang J, Zhao Z, Li Q, Yu Y, Wang R, Liu W. Target-oriented design and biosynthesis of thiostrepton-derived thiopeptide antibiotics with improved pharmaceutical properties Organic Chemistry Frontiers. 2: 106-109. DOI: 10.1039/C4Qo00288A |
0.414 |
|
2014 |
Guo H, Wang J, Li Y, Yu Y, Zheng Q, Wu J, Liu W. Insight into bicyclic thiopeptide biosynthesis benefited from development of a uniform approach for molecular engineering and production improvement Chemical Science. 5: 240-246. DOI: 10.1039/C3Sc52015C |
0.47 |
|
2014 |
Zheng Q, Wang S, Liu W. Discovery and efficient synthesis of a biologically active alkaloid inspired by thiostrepton biosynthesis Tetrahedron. 70: 7686-7690. DOI: 10.1016/J.Tet.2014.06.076 |
0.446 |
|
2013 |
Yan Y, Chen J, Zhang L, Zheng Q, Han Y, Zhang H, Zhang D, Awakawa T, Abe I, Liu W. Multiplexing of combinatorial chemistry in antimycin biosynthesis: Expansion of molecular diversity and utility Angewandte Chemie - International Edition. 52: 12308-12312. PMID 24123503 DOI: 10.1002/Anie.201305569 |
0.416 |
|
Show low-probability matches. |