9DA4
Crystal structure of human DNPH1 bound to inhibitor 2b
This is a non-PDB format compatible entry.
Summary for 9DA4
| Entry DOI | 10.2210/pdb9da4/pdb |
| Related | 4P5E 8QHQ |
| Descriptor | 5-hydroxymethyl-dUMP N-hydrolase, {(3R,4R)-1-[(4-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methyl]-4-hydroxypyrrolidin-3-yl}methyl dihydrogen phosphate (3 entities in total) |
| Functional Keywords | inhibitor, complex, hydrolase, hydrolase-inhibitor complex, hydrolase/inhibitor |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 16567.52 |
| Authors | Wagner, A.G.,Schramm, V.L.,Almo, S.C.,Ghosh, A. (deposition date: 2024-08-21, release date: 2025-02-05) |
| Primary citation | Wagner, A.G.,Lang, T.B.D.,Ledingham, E.T.,Ghosh, A.,Brooks, D.,Eskandari, R.,Suthagar, K.,Almo, S.C.,Lamiable-Oulaidi, F.,Tyler, P.C.,Schramm, V.L. Transition State Analogs of Human DNPH1 Reveal Two Electrophile Migration Mechanisms. J.Med.Chem., 2025 Cited by PubMed Abstract: DNPH1 is responsible for eliminating the epigenetically modified nucleotide, 5-hydroxymethyl-2'-deoxyuridine 5'-monophosphate (hmdUMP), preventing formation of hmdUTP, a mutation-inducing nucleotide. Loss of DNPH1 activity sensitizes PARP inhibition-resistant BRCA-deficient cancers by causing incorporation of hmdUTP into DNA. Hydrolysis of hmdUMP by DNPH1 proceeds through a covalent intermediate between Glu104 and 2-deoxyribose 5-phosphate, followed by hydrolysis, a reaction cycle with two transition states. We describe synthesis and characterization of transition state mimics for both transition states of DNPH1. Both transition states prefer inhibitors with cationic charge at the anomeric center and provide a foundation for inhibitor design. Ground-state complexes show reaction coordinate nucleophiles poised 3.3-3.7 Å from the anomeric carbon while transition state analogs tighten the reaction coordinate to place the nucleophiles 2.7-2.8 Å from the anomeric carbon. Crystal structures of DNPH1 with transition state analogs reveal transition states where the electrophilic ribocation migrates between the leaving groups and attacking nucleophiles. PubMed: 39818772DOI: 10.1021/acs.jmedchem.4c02778 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.73 Å) |
Structure validation
Download full validation report
