作者: Alexander A. Lashkov , Nadezhda E. Zhukhlistova , Azat H. Gabdoulkhakov , Alexander A. Shtil , Roman G. Efremov
DOI: 10.1107/S0907444909044175
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摘要: Uridine nucleoside phosphorylase is an important drug target for the development of anti-infective and antitumour agents. The X-ray crystal structure Salmonella typhimurium uridine (StUPh) complexed with its inhibitor 2,2′-anhydrouridine, phosphate potassium ions has been solved refined at 1.86 A resolution (Rcryst = 17.6%, Rfree 20.6%). complex human I (HUPhI) 2,2′-anhydrouridine was modelled using a computational approach. model allowed identification atomic groups in that might improve interaction future inhibitors StUPh HUPhI.