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1CS9

SOLUTION STRUCTURE OF CGGIRGERA IN CONTACT WITH THE MONOCLONAL ANTIBODY MAB 4X11, NMR, 7 STRUCTURES

1CS9 の概要
エントリーDOI10.2210/pdb1cs9/pdb
関連するPDBエントリー1CT6
分子名称HISTONE H3 PEPTIDE (1 entity in total)
機能のキーワードsynthetic peptide, tr-noe, antigen-antibody complex, dna binding protein
タンパク質・核酸の鎖数1
化学式量合計920.05
構造登録者
Phan Chan Du, A.,Petit, M.C.,Guichard, G.,Briand, J.P.,Muller, S.,Cung, M.T. (登録日: 1999-08-18, 公開日: 1999-09-02, 最終更新日: 2024-05-22)
主引用文献Phan-Chan-Du, A.,Petit, M.C.,Guichard, G.,Briand, J.P.,Muller, S.,Cung, M.T.
Structure of antibody-bound peptides and retro-inverso analogues. A transferred nuclear Overhauser effect spectroscopy and molecular dynamics approach.
Biochemistry, 40:5720-5727, 2001
Cited by
PubMed Abstract: The three-dimensional structures of the two L-peptides, H-CGGIRGERA-OH, called L(A), and H-CGGIRGERG-OH, called L(G), corresponding or close to the IRGERA sequence present in the C-terminal region (residues 130-135) of histone H3, and their retro-inverso analogues HO-mAreGriGGC-NH2, called RI(mA), and HO-mGreGriGGC-NH2, called RI(mG), have been studied by two-dimensional 1H NMR and molecular dynamics calculations in association with a monoclonal antibody generated against L(A). At 25 degrees C, the affinity constants of the monoclonal antibody with respect to RI(mA) and RI(mG) were 75- and 270-fold higher than those measured with the homologous L(A) and L(G) peptides, respectively. Due to the spontaneous epimerization of the mA malonic residue, RI(mA) gave rise to two sets of resonances. With regard to the NH amide region, one set was similar to that for RI(mG) while the second was similar to those for the parent L-peptides L(A) and L(G). The antibody-bound conformations of the two couples of L- and retro-inverso peptides have been analyzed using molecular modeling calculations based on the transferred NOE interproton distances. Folded structures appeared in both cases with a type II' beta-turn in the parent GGIR sequence and a type I' beta-turn in the retro-inverso reGr sequence.
PubMed: 11341837
DOI: 10.1021/bi001151h
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 1cs9
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

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