6X7A
Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with inhibitor SGT572
This is a non-PDB format compatible entry.
Summary for 6X7A
Entry DOI | 10.2210/pdb6x7a/pdb |
Descriptor | N-acetyltransferase Eis, 4-(4-cyclohexyl-3,4-dihydro-2~{H}-pyridin-1-yl)-1-(4-$l^{2}-fluoranylcyclohexa-1,3,5-trien-1-yl)butan-1-one, DI(HYDROXYETHYL)ETHER, ... (7 entities in total) |
Functional Keywords | aminoglycoside, drug resistance, repurposing, acetylation, inhibitor, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) |
Total number of polymer chains | 1 |
Total formula weight | 47299.46 |
Authors | Punetha, A.,Garneau-Tsodikova, S.,Tsodikov, O.V. (deposition date: 2020-05-29, release date: 2021-06-02, Last modification date: 2023-10-18) |
Primary citation | Punetha, 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/D1MD00239BPDB entries with the same primary citation |
Experimental method |
Structure validation
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