CRYSTALLIZATION AND STRUCTURE DETERMINATION TO 2.5-A RESOLUTION OF THE OXIDIZED [FE2-S2] FERREDOXIN ISOLATED FROM ANABAENA-7120

被引:186
作者
RYPNIEWSKI, WR
BREITER, DR
BENNING, MM
WESENBERG, G
OH, BH
MARKLEY, JL
RAYMENT, I
HOLDEN, HM
机构
[1] UNIV WISCONSIN,INST ENZYME RES,MADISON,WI 53706
[2] UNIV WISCONSIN,DEPT CHEM,MADISON,WI 53706
[3] UNIV WISCONSIN,DEPT BIOCHEM,MADISON,WI 53706
关键词
D O I
10.1021/bi00231a003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The molecular structure of the oxidized form of the [2Fe-2S] ferredoxin isolated from the cyanobacterium Anabaena species strain PCC 7120 has been determined by X-ray diffraction analysis to a nominal resolution of 2.5 angstrom and refined to a crystallographic R factor of 18.7%. Crystals used in this investigation belong to the space group P2(1)2(1)2(1) with unit cell dimensions of a = 37.42 angstrom, b = 38.12 angstrom, and c = 147.12 angstrom and two molecules in the asymmetric unit. The three-dimensional structure of this ferredoxin was solved by a method that combined X-ray data from one isomorphous heavy-atom derivative with noncrystallographic symmetry averaging and solvent flattening. As in other plant-type [2Fe-2S] ferredoxins, the iron-sulfur cluster is located toward the outer edge of the molecule, and the irons are tetrahedrally coordinated by both inorganic sulfurs and sulfurs provided by protein cysteine residues. The main secondary structural elements include four strands of beta-pleated sheet and three alpha-helical regions.
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页码:4126 / 4131
页数:6
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