Nonato M Cristina, Widom Joanne, Clardy Jon
Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301, USA.
Bioorg Med Chem Lett. 2006 May 15;16(10):2580-3. doi: 10.1016/j.bmcl.2006.02.047. Epub 2006 Mar 15.
Human methionine aminopeptidase type 2 (hMetAP-2) was identified as the molecular target of anti-angiogenic agents such as fumagillin and its analogues. We describe here the crystal structure of hMetAP-2 in complex with l-methionine and d-methionine at 1.9 and 2.0A resolution, respectively. The comparison of the structure of the two complexes establishes the basis of enantiomer discrimination and provides some considerations for the design of selective MetAP-2 inhibitors.
人Ⅱ型甲硫氨酸氨肽酶(hMetAP-2)被确定为烟曲霉素及其类似物等抗血管生成剂的分子靶点。我们在此分别描述了hMetAP-2与L-甲硫氨酸和D-甲硫氨酸形成的复合物的晶体结构,分辨率分别为1.9埃和2.0埃。对这两种复合物结构的比较确立了对映体识别的基础,并为选择性MetAP-2抑制剂的设计提供了一些思路。