7AA1

Structural comparison of cellular retinoic acid binding proteins I and II in the presence and absence of natural and synthetic ligands

これはPDB形式変換不可エントリーです。

7AA1 の概要

• エントリーDOI: 10.2210/pdb7aa1/pdb
• 関連するPDBエントリー: 7A9Y 7A9Z 7AA0
• 分子名称: Cellular retinoic acid-binding protein 2, 4-[2-(5,5,8,8-tetramethyl-6,7-dihydroquinoxalin-2-yl)ethynyl]benzoic acid (3 entities in total)
• 機能のキーワード: crabp, retinoid, retinoic acid, dc645, signaling protein
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 16047.41

構造登録者

Tomlinson, C.W.E.,Cornish, K.A.S.,Pohl, E. (登録日: 2020-09-02, 公開日: 2021-02-17, 最終更新日: 2024-01-31)

主引用文献

Tomlinson, C.W.E.,Cornish, K.A.S.,Whiting, A.,Pohl, E.
Structure-functional relationship of cellular retinoic acid-binding proteins I and II interacting with natural and synthetic ligands.
Acta Crystallogr D Struct Biol, 77:164-175, 2021

PubMed Abstract: A detailed understanding of the interactions between small-molecule ligands and their proposed binding targets is of the utmost importance for modern drug-development programs. Cellular retinoic acid-binding proteins I and II (CRABPI and CRABPII) facilitate a number of vital retinoid signalling pathways in mammalian cells and offer a gateway to manipulation of signalling that could potentially reduce phenotypes in serious diseases, including cancer and neurodegeneration. Although structurally very similar, the two proteins possess distinctly different biological functions, with their signalling influence being exerted through both genomic and nongenomic pathways. In this article, crystal structures are presented of the L29C mutant of Homo sapiens CRABPI in complex with naturally occurring fatty acids (1.64 Å resolution) and with the synthetic retinoid DC645 (2.41 Å resolution), and of CRABPII in complex with the ligands DC479 (1.80 Å resolution) and DC645 (1.71 Å resolution). DC645 and DC479 are two potential drug compounds identified in a recent synthetic retinoid development program. In particular, DC645 has recently been shown to have disease-modifying capabilities in neurodegenerative disease models by activating both genomic and nongenomic signalling pathways. These co-crystal structures demonstrate a canonical binding behaviour akin to that exhibited with all-trans-retinoic acid and help to explain how the compounds are able to exert an influence on part of the retinoid signalling cascade.

PubMed: 33559606
DOI: 10.1107/S2059798320015247

実験手法

X-RAY DIFFRACTION (1.71 Å)