3V56

Re-refinement of PDB entry 1OSG - Complex between BAFF and a BR3 derived peptide presented in a beta-hairpin scaffold - reveals an additonal copy of the peptide.

3V56 の概要

• エントリーDOI: 10.2210/pdb3v56/pdb
• 分子名称: Tumor necrosis factor ligand superfamily member 13B, BR3 derived peptive, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: jelly-roll, beta hairpin, protein-peptide complex, immune system
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cell membrane; Single-pass type II membrane protein. Tumor necrosis factor ligand superfamily member 13b, soluble form: Secreted: Q9Y275
• タンパク質・核酸の鎖数: 13
• 化学式量合計: 147830.12

構造登録者

Smart, O.S.,Womack, T.O.,Flensburg, C.,Keller, P.,Sharff, A.,Paciorek, W.,Vonrhein, C.,Bricogne, G. (登録日: 2011-12-16, 公開日: 2012-03-28, 最終更新日: 2024-10-09)

主引用文献

Smart, O.S.,Womack, T.O.,Flensburg, C.,Keller, P.,Paciorek, W.,Sharff, A.,Vonrhein, C.,Bricogne, G.
Exploiting structure similarity in refinement: automated NCS and target-structure restraints in BUSTER.
Acta Crystallogr.,Sect.D, 68:368-380, 2012

PubMed Abstract: Maximum-likelihood X-ray macromolecular structure refinement in BUSTER has been extended with restraints facilitating the exploitation of structural similarity. The similarity can be between two or more chains within the structure being refined, thus favouring NCS, or to a distinct 'target' structure that remains fixed during refinement. The local structural similarity restraints (LSSR) approach considers all distances less than 5.5 Å between pairs of atoms in the chain to be restrained. For each, the difference from the distance between the corresponding atoms in the related chain is found. LSSR applies a restraint penalty on each difference. A functional form that reaches a plateau for large differences is used to avoid the restraints distorting parts of the structure that are not similar. Because LSSR are local, there is no need to separate out domains. Some restraint pruning is still necessary, but this has been automated. LSSR have been available to academic users of BUSTER since 2009 with the easy-to-use -autoncs and -target target.pdb options. The use of LSSR is illustrated in the re-refinement of PDB entries 5rnt, where -target enables the correct ligand-binding structure to be found, and 1osg, where -autoncs contributes to the location of an additional copy of the cyclic peptide ligand.

PubMed: 22505257
DOI: 10.1107/S0907444911056058

実験手法

X-RAY DIFFRACTION (3 Å)