Chenna Bala Chandra, Shinkre Bidhan A, King Jason R, Lucius Aaron L, Narayana Sthanam V L, Velu Sadanandan E
Department of Chemistry, University of Alabama at Birmingham, 901 14th Street South, Birmingham, AL 35294, USA.
Bioorg Med Chem Lett. 2008 Jan 1;18(1):380-5. doi: 10.1016/j.bmcl.2007.10.051. Epub 2007 Oct 18.
In-silico virtual screening of bacterial surface enzyme Staphylococcus aureus Sortase A against commercial compound libraries using FlexX software package has led to the identification of novel inhibitors. Inhibition of enzyme catalytic activity was determined by monitoring the steady state cleavage of a model peptide substrate. Preliminary structure activity relationship studies on the lead compound resulted in the identification of compounds with improved activity. The most active compound has an IC50 value of 58 microM against the enzyme.
使用FlexX软件包对金黄色葡萄球菌分选酶A这一细菌表面酶针对商业化合物文库进行计算机虚拟筛选,已鉴定出新型抑制剂。通过监测模型肽底物的稳态裂解来确定酶催化活性的抑制情况。对先导化合物进行的初步构效关系研究已鉴定出活性有所提高的化合物。最具活性的化合物对该酶的IC50值为58微摩尔。