6GP7
Cell division regulator, B. subtilis GpsB, in complex with peptide fragment of Penicillin Binding Protein PBP1A
6GP7 の概要
| エントリーDOI | 10.2210/pdb6gp7/pdb |
| 分子名称 | Cell cycle protein GpsB, PBP1A, MAGNESIUM ION, ... (4 entities in total) |
| 機能のキーワード | bacterial cell division regulator, peptidoglycan synthesis regulator, penicillin binding protein interaction partner, protein-peptide complex, cell cycle |
| 由来する生物種 | Bacillus subtilis subsp. subtilis str. 168 詳細 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 17275.92 |
| 構造登録者 | |
| 主引用文献 | Cleverley, R.M.,Rutter, Z.J.,Rismondo, J.,Corona, F.,Tsui, H.T.,Alatawi, F.A.,Daniel, R.A.,Halbedel, S.,Massidda, O.,Winkler, M.E.,Lewis, R.J. The cell cycle regulator GpsB functions as cytosolic adaptor for multiple cell wall enzymes. Nat Commun, 10:261-261, 2019 Cited by PubMed Abstract: Bacterial growth and cell division requires precise spatiotemporal regulation of the synthesis and remodelling of the peptidoglycan layer that surrounds the cytoplasmic membrane. GpsB is a cytosolic protein that affects cell wall synthesis by binding cytoplasmic mini-domains of peptidoglycan synthases to ensure their correct subcellular localisation. Here, we describe critical structural features for the interaction of GpsB with peptidoglycan synthases from three bacterial species (Bacillus subtilis, Listeria monocytogenes and Streptococcus pneumoniae) and suggest their importance for cell wall growth and viability in L. monocytogenes and S. pneumoniae. We use these structural motifs to identify novel partners of GpsB in B. subtilis and extend the members of the GpsB interactome in all three bacterial species. Our results support that GpsB functions as an adaptor protein that mediates the interaction between membrane proteins, scaffolding proteins, signalling proteins and enzymes to generate larger protein complexes at specific sites in a bacterial cell cycle-dependent manner. PubMed: 30651563DOI: 10.1038/s41467-018-08056-2 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.95001799213 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






