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3ML2

Human carbonic anhydsase II in complex with an aryl sulfonamide inhibitor

Summary for 3ML2
Entry DOI10.2210/pdb3ml2/pdb
Related3MMF
DescriptorCarbonic anhydrase 2, ZINC ION, 2-(7-methoxy-2-oxo-2H-chromen-4-yl)-N-(4-sulfamoylphenyl)acetamide, ... (5 entities in total)
Functional Keywordszinc metalloenzyme, metal-binding, lyase, sulfonamide, zinc ligands, inhibitor, lyase-lyase inhibitor complex, lyase/lyase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P00918
Total number of polymer chains1
Total formula weight29834.96
Authors
Avvaru, B.S.,Wagner, J.,Robbins, A.H.,Mckenna, R. (deposition date: 2010-04-16, release date: 2011-04-20, Last modification date: 2023-09-06)
Primary citationWagner, J.,Avvaru, B.S.,Robbins, A.H.,Scozzafava, A.,Supuran, C.T.,McKenna, R.
Coumarinyl-substituted sulfonamides strongly inhibit several human carbonic anhydrase isoforms: solution and crystallographic investigations.
Bioorg.Med.Chem., 18:4873-4878, 2010
Cited by
PubMed: 20598552
DOI: 10.1016/j.bmc.2010.06.028
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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