2ORC

CRO REPRESSOR INSERTION MUTANT K56-[DGEVK], NMR, 32 STRUCTURES

2ORC の概要

• エントリーDOI: 10.2210/pdb2orc/pdb
• NMR情報: BMRB: 4207
• 分子名称: CRO REPRESSOR (1 entity in total)
• 機能のキーワード: gene regulating protein
• 由来する生物種: Enterobacteria phage lambda
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 7905.05

構造登録者

Mossing, M.C. (登録日: 1998-01-20, 公開日: 1998-05-27, 最終更新日: 2024-05-22)

主引用文献

Mossing, M.C.
Solution structure and dynamics of a designed monomeric variant of the lambda Cro repressor.
Protein Sci., 7:983-993, 1998

PubMed Abstract: The solution structure of a monomeric variant of the lambda Cro repressor has been determined by multidimensional NMR. Cro K56[DGEVK] differs from wild-type Cro by the insertion of five amino acids at the center of the dimer interface. 1H and 15N resonances for 70 of the 71 residues have been assigned. Thirty-two structures were calculated by hybrid distance geometry/simulated annealing methods using 463 NOE-distance restraints, 26 hydrogen-bond, and 39 dihedral-angle restraints. The root-mean-square deviation (RMSD) from the average structure for atoms in residues 3-60 is 1.03 +/- 0.44 A for the peptide backbone and 1.6 +/- 0.73 A for all nonhydrogen atoms. The overall structure conforms very well to the original design. Although the five inserted residues form a beta hairpin as expected, this engineered turn as well as other turns in the structure are not well defined by the NMR data. Dynamics studies of backbone amides reveal T1/T2 ratios of residues in the alpha2-alpha3, beta2-beta3, and engineered turn that are reflective of chemical exchange or internal motion. The solution structure and dynamics are discussed in light of the conformational variation that has been observed in other Cro structures, and the importance of flexibility in DNA recognition.

PubMed: 9568905

実験手法

SOLUTION NMR