5C3G
Crystal structure of Bcl-xl bound to BIM-MM
5C3G の概要
エントリーDOI | 10.2210/pdb5c3g/pdb |
分子名称 | Bcl-2-like protein 1,Bcl-2-like protein 1, Bcl-2-like protein 11 (3 entities in total) |
機能のキーワード | complex, bcl-2 family, bh3, stapled peptide, apoptosis |
由来する生物種 | Mus musculus (House Mouse) 詳細 |
細胞内の位置 | Isoform Bcl-X(L): Mitochondrion inner membrane : Q07817 Endomembrane system ; Peripheral membrane protein . Isoform BimEL: Mitochondrion. Isoform BimL: Mitochondrion. Isoform BimS: Mitochondrion. Isoform Bim-alpha1: Mitochondrion: O43521 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 20117.53 |
構造登録者 | Miles, J.A.,Yeo, D.J.,Rowell, P.,Rodriguez-Marin, S.,Pask, C.M.,Warriner, S.L.,Edwards, T.A.,Wilson, A.J. (登録日: 2015-06-17, 公開日: 2016-04-20, 最終更新日: 2024-01-10) |
主引用文献 | Miles, J.A.,Yeo, D.J.,Rowell, P.,Rodriguez-Marin, S.,Pask, C.M.,Warriner, S.L.,Edwards, T.A.,Wilson, A.J. Hydrocarbon constrained peptides - understanding preorganisation and binding affinity. Chem Sci, 7:3694-3702, 2016 Cited by PubMed Abstract: The development of constrained peptides represents an emerging strategy to generate peptide based probes and hits for drug-discovery that address challenging protein-protein interactions (PPIs). In this manuscript we report on the use of a novel α-alkenylglycine derived amino acid to synthesise hydrocarbon constrained BH3-family sequences (BIM and BID). Our biophysical and structural analyses illustrate that whilst the introduction of the constraint increases the population of the bioactive α-helical conformation of the peptide in solution, it does not enhance the inhibitory potency against pro-apoptotic Bcl-x and Mcl-1 PPIs. SPR analyses indicate binding occurs an induced fit mechanism whilst X-ray analyses illustrate none of the key interactions between the helix and protein are disturbed. The behaviour derives from enthalpy-entropy compensation which may be considered in terms of the ground state energies of the unbound constrained and unconstrained peptides; this has implications for the design of preorganised peptides to target protein-protein interactions. PubMed: 28970875DOI: 10.1039/c5sc04048e 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.45 Å) |
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