PDB ID: 3M5E
Hetero Atom Contents
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| Code | Name | Style | Show | Link | |
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| DMS | Dimethyl sulfoxide | PoSSuM | |||
| JDR | 4-({[6-chloro-5-formyl-2-(methylsulfanyl)pyrimidin-4-yl]amino}methyl)benzenesulfonamide | PoSSuM | |||
| ZN | Zinc ion | PoSSuM |
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Download interaction data: 3M5E
Structure summary
| Code : | 3M5E 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]methyl}benzenesulfonamide | ||||||||||||
| Release Data : | 2010-10-20 | ||||||||||||
| Compound : |
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| Authors : | Grazulis, S., Manakova, E., Golovenko, D. | ||||||||||||
| Keywords : | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR complex | ||||||||||||
| Exp. method : | X-RAY DIFFRACTION ( 1.700 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 |
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