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1QKB

OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KVK

1QKB の概要
エントリーDOI10.2210/pdb1qkb/pdb
関連するPDBエントリー1B05 1B0H 1B1H 1B2H 1B32 1B3F 1B3G 1B3H 1B3L 1B40 1B46 1B4H 1B4Z 1B51 1B52 1B58 1B5H 1B5I 1B5J 1B6H 1B7H 1B9J 1JET 1JEU 1JEV 1OLA 1OLC 1QKA 1RKM 2OLB 2RKM
分子名称PERIPLASMIC OLIGOPEPTIDE-BINDING PROTEIN, PEPTIDE LYS-VAL-LYS, URANYL (VI) ION, ... (5 entities in total)
機能のキーワードprotein transport, complex (peptide transport-peptide), peptide transport
由来する生物種SALMONELLA TYPHIMURIUM
詳細
細胞内の位置Periplasm: P06202
タンパク質・核酸の鎖数2
化学式量合計61828.02
構造登録者
Tame, J.R.H.,Sleigh, S.H.,Wilkinson, A.J. (登録日: 1999-07-14, 公開日: 1999-09-09, 最終更新日: 2024-10-23)
主引用文献Sleigh, S.H.,Seavers, P.R.,Wilkinson, A.J.,Ladbury, J.E.,Tame, J.R.H.
Crystallographic and Calorimetric Analysis of Peptide Binding to Oppa Protein
J.Mol.Biol., 291:393-, 1999
Cited by
PubMed Abstract: Isothermal titration calorimetry has been used to study the binding of 20 different peptides to the peptide binding protein OppA, and the crystal structures of the ligand complexes have been refined. This periplasmic binding protein, part of the oligopeptide permease system of Gram negative bacteria, has evolved to bind and enclose small peptides of widely varying sequences. The peptides used in this study have the sequence Lys-X-Lys, where X is any of the 20 commonly occurring amino acids. The various side-chains found at position 2 on the ligand fit into a hydrated pocket. The majority of side-chains are restrained to particular conformations within the pocket. Water molecules act as flexible adapters, matching the hydrogen-bonding requirements of the protein and ligand and shielding charges on the buried ligand. This use of water by OppA to broaden the repertoire of its binding site is not unique, but contrasts sharply with other proteins which use water to help bind ligands highly selectively. Predicting the thermodynamics of binding from the structure of the complexes is highly complicated by the influence of water on the system.
PubMed: 10438628
DOI: 10.1006/JMBI.1999.2929
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 1qkb
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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