首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Structure of the T109S mutant of Escherichia coli dihydroorotase complexed with the inhibitor 5-­fluoroorotate: catalytic activity is reflected by the crystal form
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Structure of the T109S mutant of Escherichia coli dihydroorotase complexed with the inhibitor 5-­fluoroorotate: catalytic activity is reflected by the crystal form

机译:与抑制剂5- di氟乳清酸盐复合的大肠杆菌二氢乳清酶T109S突变体的结构:催化活性通过晶体形式反映

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摘要

Crystals of a single-point mutant (T109S) of Escherichia coli dihydroorotase (DHOase) with diminished activity grown in the presence of l-dihydroorotate (l-DHO) are tetragonal, with a monomer in the asymmetric unit. These crystals are extremely unstable and disintegrate shortly after formation, which is followed by the growth of orthorhombic crystals from the remnants of the tetragonal crystals or at new nucleation sites. Orthorhombic crystals, for which a structure has previously been reported [Thoden et al. (2001), Biochemistry, >40, 6989–6997; Lee et al. (2005), J. Mol. Biol. >348, 523–533], contain a dimer of DHOase in the asymmetric unit; the active site of one monomer contains the substrate N-carbamyl-l-aspartate (l-CA-asp) and the active site of the other monomer contains the product of the reaction, l-DHO. In the subunit with l-­DHO in the active site, a surface loop (residues 105–115) is ‘open’. In the other subunit, with l-CA-asp in the active site, the loop folds inwards, forming specific hydrogen bonds from the loop to the l-CA-asp. The tetragonal crystal form can be stabilized by crystallization in the presence of the inhibitor 5-fluoroorotate (FOA), a product (l-DHO) mimic. Crystals of the complex of T109S DHOase with FOA are tetragonal, space group P41212, with unit-cell parameters a = b = 72.6, c = 176.1 Å. The structure has been refined to R and R free values of 0.218 and 0.257, despite severe anisotropy of the diffraction. In this structure, the flexible loops are both in the ‘open’ conformation, which is consistent with FOA, like l-­DHO, binding at both sites. The behaviour of the T109S mutant crystals of DHOase in the presence of l-DHO is explained by initial binding of l-DHO to both subunits, followed by slow conversion to l-CA-asp, with consequent movement of the flexible loop and dissolution of the crystals. Orthorhombic crystals are then able to grow in the presence of l-DHO and l-CA-asp.
机译:在1-二氢乳清酸酯(1-DHO)存在下生长的活性减弱的大肠杆菌二氢乳清酶(DHOase)的单点突变体(T109S)的晶体是四方晶的,单体位于不对称单元中。这些晶体极不稳定并在形成后立即崩解,随后正交晶体的晶体从四方晶体的残余物或在新的成核位置生长。正交晶体,其结构先前已有报道[Thoden等。 (2001),生物化学,> 40 ,6989–6997; Lee等。 (2005),J.Mol。生物学> 348 ,523-533],在不对称单元中包含DHOase的二聚体;一个单体的活性位点包含底物N-氨甲酰基-1-天门冬氨酸(1-CA-asp),另一种单体的活性位点包含反应产物1-DHO。在活动位点具有1-DHO的亚基中,表面环(残基105-115)是“开放的”。在活性位点具有1-CA-asp的另一个亚基中,环向内折叠,形成从环到1-CA-asp的特定氢键。在抑制剂5-氟乳清酸酯(FOA)(一种模拟产物(1-DHO))的存在下,可以通过结晶来稳定四方晶型。 T109S DHOase与FOA的复合物的晶体为四边形,空间群P41212,其晶胞参数a = b = 72.6,c = 176.1。尽管衍射存在严重的各向异性,但该结构已精炼到R和R free值分别为0.218和0.257。在这种结构中,柔性环均处于“开放”构型,这与FOA(如l-­DHO)在两个位点的结合一致。在存在1-DHO的情况下,DHOase的T109S突变体晶体的行为可通过1-DHO与两个亚基的初始结合,随后缓慢转化为1-CA-asp以及随后的柔性环移动和DNA的溶解来解释。晶体。斜方晶体然后能够在1-DHO和1-CA-asp存在下生长。

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