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3WVM

The 0.88 angstrom X-ray structure of the human heart fatty acid-binding protein complexed with stearic acid

3WVM の概要
エントリーDOI10.2210/pdb3wvm/pdb
関連するPDBエントリー3wbg
分子名称Fatty acid-binding protein, heart, STEARIC ACID, HEXAETHYLENE GLYCOL, ... (4 entities in total)
機能のキーワードantiparallel beta barrel, lipid binding protein
由来する生物種Homo sapiens (human)
細胞内の位置Cytoplasm: P05413
タンパク質・核酸の鎖数1
化学式量合計15728.16
構造登録者
主引用文献Matsuoka, S.,Sugiyama, S.,Matsuoka, D.,Hirose, M.,Lethu, S.,Ano, H.,Hara, T.,Ichihara, O.,Kimura, S.R.,Murakami, S.,Ishida, H.,Mizohata, E.,Inoue, T.,Murata, M.
Water-mediated recognition of simple alkyl chains by heart-type fatty-acid-binding protein.
Angew.Chem.Int.Ed.Engl., 54:1508-1511, 2015
Cited by
PubMed Abstract: Long-chain fatty acids (FAs) with low water solubility require fatty-acid-binding proteins (FABPs) to transport them from cytoplasm to the mitochondria for energy production. However, the precise mechanism by which these proteins recognize the various lengths of simple alkyl chains of FAs with similar high affinity remains unknown. To address this question, we employed a newly developed calorimetric method for comprehensively evaluating the affinity of FAs, sub-Angstrom X-ray crystallography to accurately determine their 3D structure, and energy calculations of the coexisting water molecules using the computer program WaterMap. Our results clearly showed that the heart-type FABP (FABP3) preferentially incorporates a U-shaped FA of C10-C18 using a lipid-compatible water cluster, and excludes longer FAs using a chain-length-limiting water cluster. These mechanisms could help us gain a general understanding of how proteins recognize diverse lipids with different chain lengths.
PubMed: 25491543
DOI: 10.1002/anie.201409830
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (0.88 Å)
構造検証レポート
Validation report summary of 3wvm
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2025-12-31に公開中

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