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4QTL

Crystal structure of human carbonic anhydrase isozyme II with inhibitor

Summary for 4QTL
Entry DOI10.2210/pdb4qtl/pdb
Related4QIY 4QIZ 4QJ0 4QJM 4QJO 4QJP 4QJW 4QJX
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 weight30052.26
Authors
Smirnov, A.,Manakova, E.,Grazulis, S. (deposition date: 2014-07-08, release date: 2015-04-15, Last modification date: 2023-11-08)
Primary citationDudutiene, V.,Zubriene, A.,Smirnov, A.,Timm, D.D.,Smirnoviene, J.,Kazokaite, J.,Michailoviene, V.,Zaksauskas, A.,Manakova, E.,Grazulis, S.,Matulis, D.
Functionalization of Fluorinated Benzenesulfonamides and Their Inhibitory Properties toward Carbonic Anhydrases
Chemmedchem, 10:662-687, 2015
Cited by
PubMed: 25758852
DOI: 10.1002/cmdc.201402490
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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