PDB ID: 5H4J
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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DMS | Dimethyl sulfoxide | PoSSuM | |||
FKM | N-[(1r)-1-[3-(cyclopentyloxy)-phenyl]-ethyl]-3-[(3,4-dihydro-2,4-dioxo-1(2h)-pyrimidinyl)methoxy]-1-propanesulfonamide | PoSSuM | |||
IMD | Imidazole | PoSSuM | |||
ZN | Zinc ion | PoSSuM |
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Download interaction data: 5H4J
Structure summary
Code : | 5H4J PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | Crystal structure of Human dUTPase in complex with N-[(1R)-1-[3-(Cyclopentyloxy)-phenyl]-ethyl]-3-[(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)methoxy]-1-propanesulfonamide | ||||||||||||
Release Data : | 2017-11-01 | ||||||||||||
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Authors : | Chong, K.T., Miyahara, S., Miyakoshi, H., Fukuoka, M. | ||||||||||||
Keywords : | Hydrolase, Hydrolase inhibitor, HYDROLASE-HYDROLASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.80 Å ) | ||||||||||||
Citation : |
TAS-114, a First-in-Class Dual dUTPase/DPD Inhibitor, Demonstrates Potential to Improve Therapeutic Efficacy of Fluoropyrimidine-Based Chemotherapy.
Yano, W.,Yokogawa, T.,Wakasa, T.
et al.
PubMed: 29748212 |
Reaction
Chain : | A | ||||||||
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UniProt : | P33316 (DUT_HUMAN) | ||||||||
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