Defining the active site of cytochrome P-450: the crystal and molecular structure of an inhibitor, SKF-525A.
Defining the active site of cytochrome P-450: the crystal and molecular structure of an inhibitor, SKF-525A.
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定义细胞色素 P-450 的活性位点:抑制剂 SKF-525A 的晶体和分子结构。
DOI:
10.1093/carcin/8.7.881
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发表时间:
1987
期刊:
影响因子:
4.7
通讯作者:
Callahan,T
中科院分区:
文献类型:
--
作者:
Rossi,M;Markovitz,S;Callahan,T
The crystal and molecular structure of the cytochrome P-450 inhibitor, SKF-525A [2-(diethy1amino)ethyl 2,2diphenylpentenoate; proadifen hydrochloride] is described. Proadifen hydrochloride crystallized from an ethyl acetate and acetic acid mixture in the space group P21/cwith one molecule in the asymmetric unit. Cell constants area= 18.716(4),b= 8.906(1),c= 14.201(3), β = 109.41(1)°. The structure was solved using directmethods and was refined to anRvalue of 0.047; weightedRof 0.061 using 3757 reflections. From the crystal and molecular structure, it is seen that SKF-525A has two principal modes of complementary interactions with the enzyme available: polar and non-polar. Polar interactions that principally involve the chloride anion, the quaternary nitrogen atom and the carbonyl oxygen atom. In particular, there are two-strong hydrogen bonds, one between Cl . . . HN, 3.090(1) Å, the other between O2 . . ..H-C111 (one of the ethyl hydrogen atoms) at 3.411(2) Å. The other is thrortgh non-polar interactions involving the phenyl and alkyl groups. Comparisons between proadifen hydrochloride and other inhibitors whose atomic coordinates are available reveal common features which correlate with their function. These include groups to provide necessary intermolecular contacts and bulk, such as a pheyl group and a hydrogen bond acceptor, as well as a tetrahedral atom, which allows for substrate flexibility