Robbins A H, Stout C D
Department of Molecular Biology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 1989 May;86(10):3639-43. doi: 10.1073/pnas.86.10.3639.
The structure of activated pig heart aconitase [citrate(isocitrate) hydro-lyase, EC 4.2.1.3] containing a [4Fe-4S] cluster has been refined at 2.5-A resolution to a crystallographic residual of 18.2%. Comparison of this structure to the recently determined 2.1-A resolution structure of the inactive enzyme containing a [3Fe-4S] cluster, by difference Fourier analysis, shows that upon activation iron is inserted into the structure isomorphously. The common atoms of the [3Fe-4S] and [4Fe-4S] cores agree within 0.1 A; the three common cysteinyl S gamma ligand atoms agree within 0.25 A. The fourth ligand of the Fe inserted into the [3Fe-4S] cluster is a water or hydroxyl from solvent, consistent with the absence of a free cysteine ligand in the enzyme active site cleft and the isomorphism of the two structures. A water molecule occupies a similar site in the crystal structure of the inactive enzyme.
含有[4Fe-4S]簇的活化猪心脏乌头酸酶[柠檬酸(异柠檬酸)水解酶,EC 4.2.1.3]的结构已在2.5埃分辨率下精修至晶体学残余率为18.2%。通过差分傅里叶分析将该结构与最近测定的含有[3Fe-4S]簇的无活性酶的2.1埃分辨率结构进行比较,结果表明,活化时铁以同晶型方式插入结构中。[3Fe-4S]和[4Fe-4S]核心的共同原子在0.1埃范围内一致;三个共同的半胱氨酰Sγ配体原子在0.25埃范围内一致。插入[3Fe-4S]簇中的铁的第四个配体是来自溶剂的水或羟基,这与酶活性位点裂隙中不存在游离半胱氨酸配体以及两种结构的同晶型一致。一个水分子在无活性酶的晶体结构中占据类似的位置。