Smith W W, Pattridge K A, Ludwig M L, Petsko G A, Tsernoglou D, Tanaka M, Yasunobu K T
J Mol Biol. 1983 Apr 25;165(4):737-53. doi: 10.1016/s0022-2836(83)80277-0.
The structure of oxidized flavodoxin from the cyanobacterium Anacystis nidulans has been determined at 2.5 A resolution with phases calculated from ethylmercury phosphate and dimercuriacetate derivatives. The determination of partial sequences, including a total of 85 residues, has assisted in the interpretation of the electron density. Preliminary refinement of a partial model (1072 atoms) has reduced R to 0.349 for the 10.997 reflections between 2.0 and 5.0 A with 1 greater than 2 sigma. The polypeptide backbone, which comprises 167 residues in the current model, adopts the familiar beta-alpha-beta conformation found in other flavodoxins and in the nucleotide-binding domains of the pyridine-nucleotide dehydrogenases, with five parallel strands in the central sheet. Comparison with flavodoxin from Clostridium MP (138 residues) shows that extra residues of A. nidulans flavodoxin are accommodated in a major insertion about 20 residues in length, which forms a lobe adjacent to the fifth strand of parallel sheet, and in additions to several external segments. Residues added between the fourth sheet strand and the start of the third helix alter the environment of the pyrimidine end of the flavin mononucleotide ring. The flavin mononucleotide phosphate binds to the start of helix 1, interacting with hydroxyamino acids and with main-chain amide groups. Two hydrophobic residues, both tentatively identified as Trp, enclose the isoalloxazine ring; the solvent-exposed Trp is nearly parallel to the flavin ring. The hydrophobic environment provided by these residues must be partly responsible for the pronounced vibrational resolution of the flavin spectrum near 450 nm. The flavin ring is tilted relative to its orientation in Clostridium MP flavodoxin. In addition, atoms N-3 and O-2 alpha of the isoalloxazine appear to form hydrogen bonds to the backbone at CO97 and NH99 in a conformation entirely different from that found in Clostridium MP flavodoxin but structurally analogous to Desulfovibrio vulgaris flavodoxin.
已通过从磷酸乙基汞和二巯基乙酸衍生物计算出的相位,以2.5埃分辨率确定了来自蓝细菌集胞藻6803的氧化型黄素氧还蛋白的结构。包括总共85个残基的部分序列的测定有助于对电子密度的解释。对部分模型(1072个原子)的初步精修已将2.0至5.0埃之间10997个I大于2σ的反射的R值降至0.349。当前模型中包含167个残基的多肽主链采用了在其他黄素氧还蛋白以及吡啶核苷酸脱氢酶的核苷酸结合结构域中发现的常见β-α-β构象,中央片层中有五条平行链。与来自梭菌MP的黄素氧还蛋白(138个残基)相比,集胞藻6803黄素氧还蛋白的额外残基容纳在一个约20个残基长的主要插入片段中,该插入片段形成一个与平行片层的第五条链相邻的叶,此外还有几个外部片段。在第四条片层链和第三条螺旋起点之间添加的残基改变了黄素单核苷酸环嘧啶端的环境。黄素单核苷酸磷酸结合到螺旋1的起点,与羟基氨基酸和主链酰胺基团相互作用。两个疏水残基(均暂定为色氨酸)包围异咯嗪环;溶剂暴露的色氨酸几乎与黄素环平行。这些残基提供的疏水环境必定部分导致了黄素光谱在450nm附近明显的振动分辨率。黄素环比其在梭菌MP黄素氧还蛋白中的取向倾斜。此外,异咯嗪的N-3和O-2α原子似乎以与梭菌MP黄素氧还蛋白中完全不同但在结构上类似于普通脱硫弧菌黄素氧还蛋白的构象,与主链在CO97和NH99处形成氢键。