8QAG

X-ray crystal structure of a de novo designed single-chain parallel coiled-coil alpha-helical barrel with 6 inner helices, sc-CC-6-95

8QAG の概要

• エントリーDOI: 10.2210/pdb8qag/pdb
• 分子名称: sc-CC-6-95, DI(HYDROXYETHYL)ETHER, TETRAETHYLENE GLYCOL, ... (4 entities in total)
• 機能のキーワード: coiled coil, alpha-helical barrel, de novo protein design, de novo protein
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 67531.68

構造登録者

Petrenas, R.,Albanese, K.I.,Woolfson, D.N. (登録日: 2023-08-22, 公開日: 2024-07-03, 最終更新日: 2024-08-07)

主引用文献

Albanese, K.I.,Petrenas, R.,Pirro, F.,Naudin, E.A.,Borucu, U.,Dawson, W.M.,Scott, D.A.,Leggett, G.J.,Weiner, O.D.,Oliver, T.A.A.,Woolfson, D.N.
Rationally seeded computational protein design of ɑ-helical barrels.
Nat.Chem.Biol., 20:991-999, 2024

PubMed Abstract: Computational protein design is advancing rapidly. Here we describe efficient routes starting from validated parallel and antiparallel peptide assemblies to design two families of α-helical barrel proteins with central channels that bind small molecules. Computational designs are seeded by the sequences and structures of defined de novo oligomeric barrel-forming peptides, and adjacent helices are connected by loop building. For targets with antiparallel helices, short loops are sufficient. However, targets with parallel helices require longer connectors; namely, an outer layer of helix-turn-helix-turn-helix motifs that are packed onto the barrels. Throughout these computational pipelines, residues that define open states of the barrels are maintained. This minimizes sequence sampling, accelerating the design process. For each of six targets, just two to six synthetic genes are made for expression in Escherichia coli. On average, 70% of these genes express to give soluble monomeric proteins that are fully characterized, including high-resolution structures for most targets that match the design models with high accuracy.

PubMed: 38902458
DOI: 10.1038/s41589-024-01642-0

実験手法

X-RAY DIFFRACTION (2.8 Å)