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3T5U

Crystal structure of the human carbonic anhydrase II in complex with N-hydroxy benzenesulfonamide

Summary for 3T5U
Entry DOI10.2210/pdb3t5u/pdb
Related1CA2 2WEJ 3T5Z
DescriptorCarbonic anhydrase 2, ZINC ION, N-hydroxybenzenesulfonamide, ... (6 entities in total)
Functional Keywordsprotein-inhibitor complex, lyase-lyase inhibitor complex, lyase/lyase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P00918
Total number of polymer chains1
Total formula weight30329.83
Authors
Di Fiore, A.,Maresca, A.,Alterio, V.,Supuran, C.T.,De Simone, G. (deposition date: 2011-07-28, release date: 2012-06-20, Last modification date: 2023-09-13)
Primary citationDi Fiore, A.,Maresca, A.,Alterio, V.,Supuran, C.T.,De Simone, G.
Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of N-substituted benzenesulfonamides to human isoform II.
Chem.Commun.(Camb.), 47:11636-11638, 2011
Cited by
PubMed: 21952494
DOI: 10.1039/c1cc14575d
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

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