Loading
PDBj
メニューPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

1BD6

7-FE FERREDOXIN FROM BACILLUS SCHLEGELII, NMR, MINIMIZED AVERAGE STRUCTURE

1BD6 の概要
エントリーDOI10.2210/pdb1bd6/pdb
NMR情報BMRB: 4268
分子名称7-FE FERREDOXIN, FE3-S4 CLUSTER, IRON/SULFUR CLUSTER (3 entities in total)
機能のキーワードelectron transport, iron-sulfur
由来する生物種Bacillus schlegelii
タンパク質・核酸の鎖数1
化学式量合計9398.26
構造登録者
Aono, S.,Bentrop, D.,Bertini, I.,Donaire, A.,Luchinat, C.,Niikura, Y.,Rosato, A. (登録日: 1998-05-06, 公開日: 1998-06-17, 最終更新日: 2024-05-22)
主引用文献Aono, S.,Bentrop, D.,Bertini, I.,Donaire, A.,Luchinat, C.,Niikura, Y.,Rosato, A.
Solution structure of the oxidized Fe7S8 ferredoxin from the thermophilic bacterium Bacillus schlegelii by 1H NMR spectroscopy.
Biochemistry, 37:9812-9826, 1998
Cited by
PubMed Abstract: The solution structure of the paramagnetic seven-iron ferredoxin from Bacillus schlegelii in its oxidized form has been determined by 1H NMR. The protein, which contains 77 amino acids, is thermostable. Seventy-two residues and 79% of all theoretically expected proton resonances have been assigned. The structure has been determined through torsion angle dynamics calculations with the program DYANA, using 966 meaningful NOEs (from a total of 1305), hydrogen bond constraints, and NMR derived dihedral angle constraints for the cluster ligating cysteines, and by using crystallographic information to build up the two clusters. Afterwards, restrained energy minimization and restrained molecular dynamics were applied to each conformer of the family. The final family of 20 structures has RMSD values from the mean structure of 0.68 A for the backbone atoms and of 1.16 A for all heavy atoms. The contributions to the thermal stability of the B. schlegelii ferredoxin are discussed by comparing the present structure to that of the less stable Azotobacter vinelandii ferredoxin I which is the only other available structure of a bacterial seven-iron ferredoxin. It is proposed that the hydrophobic interactions and the hydrogen bond network linking the N-terminus and the C-terminus together and a high number of salt bridges contribute to the stability.
PubMed: 9657695
DOI: 10.1021/bi972818b
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 1bd6
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

PDB statisticsPDBj update infoContact PDBjnumon