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9M3T

Crystal structure of human pyruvate dehydrogenase kinase isoform 2 in complex with ATP competitive inhibitor 22

This is a non-PDB format compatible entry.
Summary for 9M3T
Entry DOI10.2210/pdb9m3t/pdb
Related9M3O
Descriptor[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial, N-(2-AMINOETHYL)-2-{3-CHLORO-4-[(4-ISOPROPYLBENZYL)OXY]PHENYL} ACETAMIDE, 2-chloranyl-4-[[(3R)-1-[(3S)-7-(ethylamino)-5-fluoranyl-3-methyl-2-oxidanylidene-1H-indol-3-yl]piperidin-3-yl]amino]benzoic acid, ... (5 entities in total)
Functional Keywordsghkl atpase/kinase family, pyruvate dehydrogenase complex, mitochondrial kinase, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight42699.68
Authors
Xu, Z.H.,Chen, S. (deposition date: 2025-03-03, release date: 2025-06-11)
Primary citationXu, H.,Ding, D.,Han, X.,Miao, K.,Liang, C.,Yun, H.,Zhu, W.,Dey, F.,Zhao, D.,Wu, Y.,Reutlinger, M.,Yang, J.,Zhai, G.,Lin, Z.,Li, C.,Wu, W.,Xu, B.,Han, L.,Chen, S.,Huang, X.,Casagrande, F.,Hilbert, M.,Strebel, Q.,Wichert, M.,Westwood, P.,Schafer, R.,Roth, D.,Heer, D.,Tian, X.,Ma, T.,Zhang, T.,Zhao, J.,Urich, E.,Xia, G.,Lassen, K.,Shen, H.C.,Zou, G.
Discovery of ATP competitive PDHK1/2 dual inhibitors.
Bioorg.Med.Chem.Lett., 122:130190-130190, 2025
Cited by
PubMed Abstract: Multiple screening approaches were carried out to identify novel chemistry starting for Pyruvate Dehydrogenase Kinases (PDHKs) inhibitors. Through hit triaging efforts and structure-based optimization, two series of ATP competitive inhibitors with single digit nanomolar enzymatic potency for PDHK1/2 and around 10-100-fold selectivity over PDHK4/3 were discovered. Approach of covalent inhibitor was explored to successfully improve the cellular target engagement to single digit micromolar range.
PubMed: 40107630
DOI: 10.1016/j.bmcl.2025.130190
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.08 Å)
Structure validation

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