2fov: Difference between revisions

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'''Human Carbonic Anhydrase II complexed with two-prong inhibitors'''
===Human Carbonic Anhydrase II complexed with two-prong inhibitors===




==Overview==
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The atomic-resolution crystal structures of human carbonic anhydrases I and II complexed with "two-prong" inhibitors are reported. Each inhibitor contains a benzenesulfonamide prong and a cupric iminodiacetate (IDA-Cu(2+)) prong separated by linkers of different lengths and compositions. The ionized NH(-) group of each benzenesulfonamide coordinates to the active site Zn(2+) ion; the IDA-Cu(2+) prong of the tightest-binding inhibitor, BR30, binds to H64 of CAII and H200 of CAI. This work provides the first evidence verifying the structural basis of nanomolar affinity measured for two-prong inhibitors targeting the carbonic anhydrases.
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{{ABSTRACT_PUBMED_16506782}}


==Disease==
==Disease==
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[[Category: Lyase]]
[[Category: Lyase]]
[[Category: Zinc]]
[[Category: Zinc]]
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