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

1ZUG

STRUCTURE OF PHAGE 434 CRO PROTEIN, NMR, 20 STRUCTURES

1ZUG の概要
エントリーDOI10.2210/pdb1zug/pdb
分子名称PHAGE 434 CRO PROTEIN (1 entity in total)
機能のキーワードgene regulating protein, transcription regulation
由来する生物種Phage 434
タンパク質・核酸の鎖数1
化学式量合計8076.62
構造登録者
Padmanabhan, S.,Jimenez, M.A.,Gonzalez, C.,Sanz, J.M.,Gimenez-Gallego, G.,Rico, M. (登録日: 1997-03-14, 公開日: 1997-07-07, 最終更新日: 2024-05-22)
主引用文献Padmanabhan, S.,Jimenez, M.A.,Gonzalez, C.,Sanz, J.M.,Gimenez-Gallego, G.,Rico, M.
Three-dimensional solution structure and stability of phage 434 Cro protein.
Biochemistry, 36:6424-6436, 1997
Cited by
PubMed Abstract: 1H NMR resonances of the phage 434 Cro protein were assigned using standard 2D NMR methods, and its solution structure determined using 867 distance constraints in distance geometry (DIANA) calculations ultimately refined by restrained molecular dynamics (GROMOS). In the 20 best NMR structures, the average pairwise backbone and heavy atom RMSDs are 0.63 +/- 0.14 and 1.53 +/- 0.15 A, respectively, for the structurally well-defined residues 4-65. Residues 1-3 and 66-71 at the N- and C-termini are structurally disordered. The region 4-65 includes five alpha-helices and tight turns which define the hydrophobic core of the protein. The backbone and heavy atom RMSDs for residues 4-65 are 0.92 +/- 0.12 and 1.99 +/- 0.12 A, respectively, for the NMR versus the crystal structures, but there are significant differences in the side-chain conformations and solvent accessibilities for some core residues. Analytical ultracentrifugation experiments confirm that 434 Cro is monomeric even at the high NMR concentrations. 434 Cro folding under NMR solution conditions is two-state as indicated by coincident urea denaturation curves from circular dichroism and intrinsic fluorescence measurements. They yield values for 434 Cro stability which show good correspondence to the free energy for global unfolding determined by NMR hydrogen exchange measurements for the slowest exchanging amide protons.
PubMed: 9174359
DOI: 10.1021/bi970085p
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 1zug
検証レポート(詳細版)ダウンロードをダウンロード

252456

件を2026-04-22に公開中

PDB statisticsPDBj update infoContact PDBjnumon