6TTH
PKM2 in complex with L-threonine
Summary for 6TTH
Entry DOI | 10.2210/pdb6tth/pdb |
EMDB information | 10575 10576 |
Descriptor | Pyruvate kinase PKM, 1,6-di-O-phosphono-beta-D-fructofuranose, THREONINE, ... (4 entities in total) |
Functional Keywords | pkm2, fbdd, l-threonine, cytosolic protein |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 4 |
Total formula weight | 241164.22 |
Authors | Saur, M.,Hartshorn, M.J.,Dong, J.,Reeks, J.,Bunkoczi, G.,Jhoti, H.,Williams, P.A. (deposition date: 2019-12-27, release date: 2020-01-15, Last modification date: 2024-05-22) |
Primary citation | Saur, M.,Hartshorn, M.J.,Dong, J.,Reeks, J.,Bunkoczi, G.,Jhoti, H.,Williams, P.A. Fragment-based drug discovery using cryo-EM. Drug Discov Today, 25:485-490, 2020 Cited by PubMed Abstract: Recent advances in electron cryo-microscopy (cryo-EM) structure determination have pushed the resolutions obtainable by the method into the range widely considered to be of utility for drug discovery. Here, we review the use of cryo-EM in fragment-based drug discovery (FBDD) based on in-house method development. We demonstrate not only that cryo-EM can reveal details of the molecular interactions between fragments and a protein, but also that the current reproducibility, quality, and throughput are compatible with FBDD. We exemplify this using the test system β-galactosidase (Bgal) and the oncology target pyruvate kinase 2 (PKM2). PubMed: 31877353DOI: 10.1016/j.drudis.2019.12.006 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.6 Å) |
Structure validation
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