6H34
The crystal structure of human carbonic anhydrase II in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
Summary for 6H34
Entry DOI | 10.2210/pdb6h34/pdb |
Related | 6H2Z 6H33 |
Descriptor | Carbonic anhydrase 2, ZINC ION, 4-[4-[(4-fluorophenyl)methyl]piperazin-1-yl]carbonylbenzenesulfonamide, ... (5 entities in total) |
Functional Keywords | protein-inhibitor binding, benzenesulfonamide, lyase |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 30012.24 |
Authors | Buemi, M.R.,Di Fiore, A.,De Luca, L.,Ferro, S.,Mancuso, F.,Monti, S.M.,Buonanno, M.,Angeli, A.,Russo, E.,De Sarro, G.,Supuran, C.T.,De Simone, G.,Gitto, R. (deposition date: 2018-07-17, release date: 2018-12-19, Last modification date: 2024-01-17) |
Primary citation | Buemi, M.R.,Di Fiore, A.,De Luca, L.,Angeli, A.,Mancuso, F.,Ferro, S.,Monti, S.M.,Buonanno, M.,Russo, E.,De Sarro, G.,De Simone, G.,Supuran, C.T.,Gitto, R. Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety. Eur J Med Chem, 163:443-452, 2018 Cited by PubMed: 30530195DOI: 10.1016/j.ejmech.2018.11.073 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.55 Å) |
Structure validation
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