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-Structure paper
Title | Structural insights into the putative bacterial acetylcholinesterase ChoE and its substrate inhibition mechanism. |
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Journal, issue, pages | J. Biol. Chem., Vol. 295, Page 8708-8724, Year 2020 |
Publish date | Oct 21, 2019 (structure data deposition date) |
Authors | Pham, V.D. / To, T.A. / Gagne-Thivierge, C. / Couture, M. / Lague, P. / Yao, D. / Picard, M.E. / Lortie, L.A. / Attere, S.A. / Zhu, X. ...Pham, V.D. / To, T.A. / Gagne-Thivierge, C. / Couture, M. / Lague, P. / Yao, D. / Picard, M.E. / Lortie, L.A. / Attere, S.A. / Zhu, X. / Levesque, R.C. / Charette, S.J. / Shi, R. |
External links | J. Biol. Chem. / PubMed:32371400 |
Methods | X-ray diffraction |
Resolution | 1.35 - 1.85 Å |
Structure data | PDB-6uqv: PDB-6uqw: PDB-6uqx: PDB-6uqy: PDB-6uqz: PDB-6ur0: PDB-6ur1: |
Chemicals | ChemComp-MES: ChemComp-GOL: ChemComp-BUA: ChemComp-CL: ChemComp-P6G: ChemComp-HOH: ChemComp-ACT: ChemComp-ETM: ChemComp-QFJ: ChemComp-IOD: ChemComp-PPI: ChemComp-AT3: |
Source |
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Keywords | HYDROLASE / esterase / acetylcholine / prokaryotic / acetylcholinesterase |