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3VBD

Complex of human carbonic anhydrase II with 4-(6-methoxy-3,4-dihydroisoquinolin-1-yl)benzenesulfonamide

Summary for 3VBD
Entry DOI10.2210/pdb3vbd/pdb
Related3V7X
DescriptorCarbonic anhydrase 2, ZINC ION, 4-(6-methoxy-3,4-dihydroisoquinolin-1-yl)benzenesulfonamide, ... (6 entities in total)
Functional Keywordslyase-lyase inhibitor complex, lyase/lyase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P00918
Total number of polymer chains1
Total formula weight30367.24
Authors
Mader, P.,Brynda, J.,Rezacova, P. (deposition date: 2012-01-02, release date: 2012-04-04, Last modification date: 2024-02-28)
Primary citationGitto, R.,Damiano, F.M.,Mader, P.,De Luca, L.,Ferro, S.,Supuran, C.T.,Vullo, D.,Brynda, J.,Rezacova, P.,Chimirri, A.
Synthesis, Structure-Activity Relationship Studies, and X-ray Crystallographic Analysis of Arylsulfonamides as Potent Carbonic Anhydrase Inhibitors.
J.Med.Chem., 55:3891-3899, 2012
Cited by
PubMed: 22443141
DOI: 10.1021/jm300112w
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.05 Å)
Structure validation

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