3IIG
Crystal structure of mouse Bcl-xl mutant (F105A) at pH 5.0
3IIG の概要
エントリーDOI | 10.2210/pdb3iig/pdb |
関連するPDBエントリー | 3IHC 3IHD 3IHE 3IHF 3IIH |
分子名称 | Bcl-2-like protein 1 (2 entities in total) |
機能のキーワード | apoptosis, bh3 domain, bcl-2, membrane, mitochondrion, transmembrane |
由来する生物種 | Mus musculus (mouse) |
細胞内の位置 | Mitochondrion membrane; Single-pass membrane protein. Isoform Bcl-X(L): Mitochondrion inner membrane. Isoform Bcl-X(delta-TM): Cytoplasm: Q64373 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 21980.11 |
構造登録者 | |
主引用文献 | Priyadarshi, A.,Roy, A.,Kim, K.S.,Kim, E.E.,Hwang, K.Y. Structural insights into mouse anti-apoptotic Bcl-xl reveal affinity for Beclin 1 and gossypol. Biochem.Biophys.Res.Commun., 394:515-521, 2010 Cited by PubMed Abstract: This study reports the crystal structures of Bcl-xl wild type and three Bcl-xl mutants (Y101A, F105A, and R139A) with amino acid substitutions in the hydrophobic groove of the Bcl-xl BH3 domain. An additional 12 ordered residues were observed in a highly flexible loop between the alpha1 and alpha2 helices, and were recognized as an important deamidation site for the regulation of apoptosis. The autophagy-effector protein, Beclin 1, contains a novel BH3 domain (residues 101-125), which binds to the surface cleft of Bcl-xl, as confirmed by nuclear magnetic resonance (NMR) spectroscopy and analytical gel-filtration results. Gossypol, a potent inhibitor of Bcl-xl, had a K(d) value of 0.9 microM. In addition, the structural and biochemical analysis of five Bcl-xl substitution mutants will provide structural insights into the design and development of anti-cancer drugs. PubMed: 20206602DOI: 10.1016/j.bbrc.2010.03.002 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.3 Å) |
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