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3B4F

Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with twelve mammalian isoforms: kinetic and X-Ray crystallographic studies

Summary for 3B4F
Entry DOI10.2210/pdb3b4f/pdb
DescriptorCarbonic anhydrase 2, ZINC ION, MERCURY (II) ION, ... (5 entities in total)
Functional Keywordscarbonic anhydrase, inhibitors, sulfonamide, acetylation, cytoplasm, disease mutation, lyase, metal-binding, polymorphism, zinc, lyase(oxo-acid)
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm : P00918
Total number of polymer chains1
Total formula weight29885.42
Authors
Guzel, o.,Temperini, c.,Innocenti, a.,Scozzafava, A.,Salman, a.,Supuran, c.t. (deposition date: 2007-10-24, release date: 2008-01-22, Last modification date: 2023-08-30)
Primary citationGuzel, O.,Temperini, C.,Innocenti, A.,Scozzafava, A.,Salman, A.,Supuran, C.T.
Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with 12 mammalian isoforms: kinetic and X-ray crystallographic studies.
Bioorg.Med.Chem.Lett., 18:152-158, 2008
Cited by
PubMed: 18024029
DOI: 10.1016/j.bmcl.2007.10.110
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.89 Å)
Structure validation

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