PDB ID: 3M2N
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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BCN | Bicine | PoSSuM | |||
DMS | Dimethyl sulfoxide | PoSSuM | |||
J74 | 4-{2-[(6-chloro-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide | PoSSuM | |||
ZN | Zinc ion | PoSSuM |
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Download interaction data: 3M2N
Structure summary
Code : | 3M2N PDBj RCSB PDB PDBe | ||||||||||||
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Header : | LYASE/LYASE INHIBITOR | ||||||||||||
Title : | Crystal structure of human carbonic anhydrase isozyme II with 4-{2-[N-(6-chloro-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide | ||||||||||||
Release Data : | 2011-02-16 | ||||||||||||
Compound : |
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Authors : | Grazulis, S., Manakova, E., Golovenko, D. | ||||||||||||
Keywords : | drug design, carbonic anhydrase, sulfonamide, Lyase, Metal-binding, LYASE-LYASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.65 Å ) | ||||||||||||
Citation : |
Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases.
Capkauskaite, E.,Zubriene, A.,Baranauskiene, L.
et al.
PubMed: 22440859 |
Reaction
Chain : | A | ||||||||||||
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UniProt : | P00918 (CAH2_HUMAN) | ||||||||||||
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