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6X6G

Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with droperidol

This is a non-PDB format compatible entry.
Summary for 6X6G
Entry DOI10.2210/pdb6x6g/pdb
DescriptorN-acetyltransferase Eis, 3-[1-[4-(4-fluorophenyl)-4-oxidanylidene-butyl]-2,3,4,5-tetrahydropyridin-4-yl]-1~{H}-benzimidazol-2-one, GLYCEROL, ... (6 entities in total)
Functional Keywordsaminoglycoside, drug resistance, repurposing, acetylation, inhibitor, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
Total number of polymer chains1
Total formula weight47101.40
Authors
Punetha, A.,Garneau-Tsodikova, S.,Tsodikov, O.V. (deposition date: 2020-05-28, release date: 2021-06-02, Last modification date: 2023-10-18)
Primary citationPunetha, A.,Green, K.D.,Garzan, A.,Willby, M.J.,Pang, A.H.,Hou, C.,Holbrook, S.Y.L.,Krieger, K.,Posey, J.E.,Parish, T.,Tsodikov, O.V.,Garneau-Tsodikova, S.
Structure-based design of haloperidol analogues as inhibitors of acetyltransferase Eis from Mycobacterium tuberculosis to overcome kanamycin resistance
Rsc Med Chem, 12:1894-1909, 2021
Cited by
DOI: 10.1039/D1MD00239B
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.15 Å)
Structure validation

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