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Volumn 17, Issue 8, 2007, Pages 2210-2215

Phosph(on)ate as a zinc-binding group in metalloenzyme inhibitors: X-ray crystal structure of the antiviral drug foscarnet complexed to human carbonic anhydrase I

Author keywords

Carbonic anhydrase; Enzyme activator; Enzyme inhibitor; Foscarnet; Isozymes; X ray crystallography; Zinc binding group

Indexed keywords

ANTIVIRUS AGENT; CARBONATE DEHYDRATASE; CARBONATE DEHYDRATASE I; ENZYME INHIBITOR; FOSCARNET; ISOENZYME; PHOSPHONIC ACID DERIVATIVE; ZINC;

EID: 33947690287     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.01.113     Document Type: Article
Times cited : (48)

References (60)
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    • 2 concentrations ranged from 1.7 to 17 mM for the determination of the kinetic parameters and inhibition constants. For each inhibitor concentration at least six traces of the initial 5-10% of the reaction have been used for determining the initial velocity. The uncatalyzed rates were determined in the same manner and subtracted from the total observed rates. Stock solutions of inhibitors were prepared at a concentration of 10-50 mM (in water) and dilutions up to 0.1 μM done with the assay buffer mentioned above. Inhibitor and enzyme solutions were preincubated together for 15 min at room temperature prior to assay (or as otherwise indicated)
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    • note
    • 23 Coordinates and structure factors have been deposited within the Protein Data Bank (accession code 2IT4). Crystallographic parameters and refinement statistics are summarized in Table 2.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.