PDB ID: 3MHO
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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DMS | Dimethyl sulfoxide | PoSSuM | |||
J43 | 4-{[6-chloro-5-formyl-2-(methylsulfanyl)pyrimidin-4-yl]amino}benzenesulfonamide | PoSSuM | |||
UNL | Unknown ligand | PoSSuM | |||
ZN | Zinc ion | PoSSuM |
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Download interaction data: 3MHO
Structure summary
Code : | 3MHO PDBj RCSB PDB PDBe | ||||||||||||
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Header : | LYASE/LYASE INHIBITOR | ||||||||||||
Title : | Crystal structure of human carbonic anhydrase isozyme II with 4-[N-(6-chloro-5-formyl-2-methylthiopyrimidin-4-yl)amino]benzenesulfonamide | ||||||||||||
Release Data : | 2010-10-20 | ||||||||||||
Compound : |
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Authors : | Grazulis, S., Manakova, E., Golovenko, D., Sukackaite, R. | ||||||||||||
Keywords : | drug design, carbonic anhydrase, sulfonamide, LYASE-LYASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.150 Å ) | ||||||||||||
Citation : |
4-[N-(Substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII
Sudzius, J.,Baranauskiene, L.,Golovenko, D.
et al.
PubMed: 20889345 |
Reaction
Chain : | A | ||||||||||||
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UniProt : | P00918 (CAH2_HUMAN) | ||||||||||||
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