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4Q6D

Crystal structure of human carbonic anhydrase isozyme II with 4-[(Z)-azepan-1-yldiazenyl]benzenesulfonamide

Summary for 4Q6D
Entry DOI10.2210/pdb4q6d/pdb
Related4Q6E
DescriptorCarbonic anhydrase 2, ZINC ION, DIMETHYL SULFOXIDE, ... (6 entities in total)
Functional Keywordsdrug design, carbonic anhydrase, benzenesulfonamide, metal-binding, lyase-lyase inhibitor complex, lyase/lyase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm : P00918
Total number of polymer chains1
Total formula weight29878.14
Authors
Smirnov, A.,Manakova, E.,Grazulis, S. (deposition date: 2014-04-22, release date: 2014-11-26, Last modification date: 2023-09-20)
Primary citationRutkauskas, K.,Zubriene, A.,Tumosiene, I.,Kantminiene, K.,Kazemekaite, M.,Smirnov, A.,Kazokaite, J.,Morkunaite, V.,Capkauskaite, E.,Manakova, E.,Grazulis, S.,Beresnevicius, Z.J.,Matulis, D.
4-Amino-substituted Benzenesulfonamides as Inhibitors of Human Carbonic Anhydrases.
Molecules, 19:17356-17380, 2014
Cited by
PubMed: 25353386
DOI: 10.3390/molecules191117356
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.12 Å)
Structure validation

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