Cer R Z, Mudunuri U, Stephens R, Lebeda F J
Advanced Biomedical Computing Center, Advanced Technology Program, SAIC-Frederick Inc., NCI-Frederick, Frederick, MD 21702, USA.
Nucleic Acids Res. 2009 Jul;37(Web Server issue):W441-5. doi: 10.1093/nar/gkp253. Epub 2009 Apr 24.
A new web-server tool estimates K(i) values from experimentally determined IC(50) values for inhibitors of enzymes and of binding reactions between macromolecules (e.g. proteins, polynucleic acids) and ligands. This converter was developed to enable end users to help gauge the quality of the underlying assumptions used in these calculations which depend on the type of mechanism of inhibitor action and the concentrations of the interacting molecular species. Additional calculations are performed for nonclassical, tightly bound inhibitors of enzyme-substrate or of macromolecule-ligand systems in which free, rather than total concentrations of the reacting species are required. Required user-defined input values include the total enzyme (or another target molecule) and substrate (or ligand) concentrations, the K(m) of the enzyme-substrate (or the K(d) of the target-ligand) reaction, and the IC(50) value. Assumptions and caveats for these calculations are discussed along with examples taken from the literature. The host database for this converter contains kinetic constants and other data for inhibitors of the proteolytic clostridial neurotoxins (http://botdb.abcc.ncifcrf.gov/toxin/kiConverter.jsp).
一种新的网络服务器工具可根据实验测定的酶抑制剂以及大分子(如蛋白质、多核酸)与配体之间结合反应的IC50值来估算Ki值。开发此转换器是为了让终端用户能够帮助评估这些计算中所使用的基本假设的质量,这些假设取决于抑制剂作用机制的类型以及相互作用分子物种的浓度。对于酶 - 底物或大分子 - 配体系统的非经典紧密结合抑制剂,还会进行额外计算,在这种情况下需要的是反应物种的游离浓度而非总浓度。用户需要定义的输入值包括总酶(或另一种靶分子)和底物(或配体)浓度、酶 - 底物反应的Km值(或靶 - 配体反应的Kd值)以及IC50值。文中结合文献中的实例讨论了这些计算的假设和注意事项。此转换器的宿主数据库包含肉毒梭菌神经毒素抑制剂的动力学常数和其他数据(http://botdb.abcc.ncifcrf.gov/toxin/kiConverter.jsp)。