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

1HXT

OMPF PORIN MUTANT NQAAA

1HXT の概要
エントリーDOI10.2210/pdb1hxt/pdb
関連するPDBエントリー1HXU 1HXX 2OMF
分子名称OUTER MEMBRANE PROTEIN F, (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE (3 entities in total)
機能のキーワードporin, beta barrel, membrane protein
由来する生物種Escherichia coli
細胞内の位置Cell outer membrane ; Multi-pass membrane protein : P02931
タンパク質・核酸の鎖数1
化学式量合計39918.31
構造登録者
Phale, P.S.,Philippsen, A.,Widmer, C.,Phale, V.P.,Rosenbusch, J.P.,Schirmer, T. (登録日: 2001-01-17, 公開日: 2001-06-06, 最終更新日: 2024-02-07)
主引用文献Phale, P.S.,Philippsen, A.,Widmer, C.,Phale, V.P.,Rosenbusch, J.P.,Schirmer, T.
Role of charged residues at the OmpF porin channel constriction probed by mutagenesis and simulation.
Biochemistry, 40:6319-6325, 2001
Cited by
PubMed Abstract: The channel constriction of OmpF porin, a pore protein in the bacterial outer membrane, is highly charged due to the presence of three arginines (R42, R82, and R132) and two acidic residues (D113 and E117). The influence of these charges on ion conductance, ion selectivity, and voltage gating has been studied with mutants D113N/E117Q, R42A/R82A/R132A/D113N/E117Q, and V18K/G131K, which were designed to remove or add protein charge at the channel constriction. The crystal structures revealed no or only local changes compared to wild-type OmpF, thus allowing a comparative study. The single-channel conductance of the isosteric D113N/E117Q variant was found to be 2-fold reduced, and that of the pentuple mutant was 70% of the wild-type value, despite a considerably larger pore cross section. Ion selectivity was drastically altered by the mutations with cation/anion permeability ratios ranging from 1 to 12. Ion flow through these and eight other mutants, which have been characterized previously, was simulated by Brownian dynamics based on the detailed crystal structures. The calculated ion selectivity and relative channel conductance values agree well with the experimental data. This demonstrates that ion translocation through porin is mainly governed by pore geometry and charge, the two factors that are properly represented in the simulations.
PubMed: 11371193
DOI: 10.1021/bi010046k
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.4 Å)
構造検証レポート
Validation report summary of 1hxt
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