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TitleInhibition and binding studies of carbonic anhydrase isozymes I, II and IX with benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides
Journal, issue, pagesJ Enzyme Inhib Med Chem, Vol. 25, Page 863-870, Year 2010
Publish dateMay 27, 2009 (structure data deposition date)
AuthorsBaranauskiene, L. / Hilvo, M. / Matuliene, J. / Golovenko, D. / Manakova, E. / Dudutiene, V. / Michailoviene, V. / Torresan, J. / Jachno, J. / Parkkila, S. ...Baranauskiene, L. / Hilvo, M. / Matuliene, J. / Golovenko, D. / Manakova, E. / Dudutiene, V. / Michailoviene, V. / Torresan, J. / Jachno, J. / Parkkila, S. / Maresca, A. / Supuran, C.T. / Grazulis, S. / Matulis, D.
External linksJ Enzyme Inhib Med Chem / PubMed:20166809
MethodsX-ray diffraction
Resolution1.44 Å
Structure data

PDB-3hlj:
Crystal structure of human carbonic anhydrase isozyme II with 3-methylthiobenzimidazo[1,2-c][1,2,3]thiadiazol-7-sulfonamide
Method: X-RAY DIFFRACTION / Resolution: 1.44 Å

Chemicals

ChemComp-V21:
3-methylthiobenzimidazo[1,2-c][1,2,3]thiadiazol-7-sulfonamide

ChemComp-NA:
Unknown entry

ChemComp-UNX:
Unknown entry

ChemComp-ZN:
Unknown entry

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsLYASE / drug design / carbonic anhydrase / sulfonamide / thiadiazole / Disease mutation / Metal-binding

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