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4HU1

Crystal structure of human carbonic anhydrase isozyme XIII with the inhibitor.

Summary for 4HU1
Entry DOI10.2210/pdb4hu1/pdb
Related4HT0 4HT2
DescriptorCarbonic anhydrase 13, ZINC ION, 2,3,5,6-tetrafluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide, ... (6 entities in total)
Functional Keywordsdrug design, carbonic anhydrase, benzenesulfonamide, metal-binding, lyase-lyase inhibitor complex, carbonate dehydratase activity, carbon-oxygen lyase activity, lyase/lyase inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight60572.59
Authors
Smirnov, A.,Manakova, E.,Grazulis, S. (deposition date: 2012-11-02, release date: 2013-04-10, Last modification date: 2023-09-20)
Primary citationDudutiene, V.,Zubriene, A.,Smirnov, A.,Gylyte, J.,Timm, D.,Manakova, E.,Grazulis, S.,Matulis, D.
4-Substituted-2,3,5,6-tetrafluorobenzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, XII, and XIII.
Bioorg.Med.Chem., 21:2093-2106, 2013
Cited by
PubMed: 23394791
DOI: 10.1016/j.bmc.2013.01.008
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

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