4M2T

Corrected Structure of Mouse P-glycoprotein bound to QZ59-SSS

4M2T の概要

• エントリーDOI: 10.2210/pdb4m2t/pdb
• 関連するPDBエントリー: 3G5U 3G60 3G61 4M1M 4M2S
• 分子名称: Multidrug resistance protein 1A, (4S,11S,18S)-4,11,18-tri(propan-2-yl)-6,13,20-triselena-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1~5,8~.1~12,15~]tetracosa-1(21),5(24),7,12(23),14,19(22)-hexaene-2,9,16-trione (2 entities in total)
• 機能のキーワード: atp-binding cassette transporter, multidrug efflux, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
• 由来する生物種: Mus musculus (mouse)
• 細胞内の位置: Cell membrane; Multi-pass membrane protein: P21447
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 286105.03

構造登録者

Li, J.,Jaimes, K.F.,Aller, S.G. (登録日: 2013-08-05, 公開日: 2013-11-13, 最終更新日: 2024-02-28)

主引用文献

Li, J.,Jaimes, K.F.,Aller, S.G.
Refined structures of mouse P-glycoprotein.
Protein Sci., 23:34-46, 2014

PubMed Abstract: The recently determined C. elegans P-glycoprotein (Pgp) structure revealed significant deviations compared to the original mouse Pgp structure, which suggested possible misinterpretations in the latter model. To address this concern, we generated an experimental electron density map from single-wavelength anomalous dispersion phasing of an original mouse Pgp dataset to 3.8 Å resolution. The map exhibited significantly more detail compared to the original MAD map and revealed several regions of the structure that required de novo model building. The improved drug-free structure was refined to 3.8 Å resolution with a 9.4 and 8.1% decrease in R(work) and R(free), respectively, (R(work)  = 21.2%, R(free) = 26.6%) and a significant improvement in protein geometry. The improved mouse Pgp model contains ∼95% of residues in the favorable Ramachandran region compared to only 57% for the original model. The registry of six transmembrane helices was corrected, revealing amino acid residues involved in drug binding that were previously unrecognized. Registry shifts (rotations and translations) for three transmembrane (TM)4 and TM5 and the addition of three N-terminal residues were necessary, and were validated with new mercury labeling and anomalous Fourier density. The corrected position of TM4, which forms the frame of a portal for drug entry, had backbone atoms shifted >6 Å from their original positions. The drug translocation pathway of mouse Pgp is 96% identical to human Pgp and is enriched in aromatic residues that likely play a collective role in allowing a high degree of polyspecific substrate recognition.

PubMed: 24155053
DOI: 10.1002/pro.2387

実験手法

X-RAY DIFFRACTION (4.35 Å)