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5UKH

Structure of TelC from Streptococcus intermedius B196

5UKH の概要
エントリーDOI10.2210/pdb5ukh/pdb
分子名称Uncharacterized protein, CALCIUM ION (3 entities in total)
機能のキーワードantibacterial effector protein, lipid ii phosphatase, type vii secretion, esx secretion, unknown function
由来する生物種Streptococcus intermedius B196
タンパク質・核酸の鎖数1
化学式量合計42055.79
構造登録者
Whitney, J.C.,Ching, M.Q.,Bryant, D.,Mougous, J.D. (登録日: 2017-01-22, 公開日: 2017-07-26, 最終更新日: 2024-10-23)
主引用文献Whitney, J.C.,Peterson, S.B.,Kim, J.,Pazos, M.,Verster, A.J.,Radey, M.C.,Kulasekara, H.D.,Ching, M.Q.,Bullen, N.P.,Bryant, D.,Goo, Y.A.,Surette, M.G.,Borenstein, E.,Vollmer, W.,Mougous, J.D.
A broadly distributed toxin family mediates contact-dependent antagonism between gram-positive bacteria.
Elife, 6:-, 2017
Cited by
PubMed Abstract: The Firmicutes are a phylum of bacteria that dominate numerous polymicrobial habitats of importance to human health and industry. Although these communities are often densely colonized, a broadly distributed contact-dependent mechanism of interbacterial antagonism utilized by Firmicutes has not been elucidated. Here we show that proteins belonging to the LXG polymorphic toxin family present in mediate cell contact- and Esx secretion pathway-dependent growth inhibition of diverse Firmicute species. The structure of one such toxin revealed a previously unobserved protein fold that we demonstrate directs the degradation of a uniquely bacterial molecule required for cell wall biosynthesis, lipid II. Consistent with our functional data linking LXG toxins to interbacterial interactions in , we show that LXG genes are prevalent in the human gut microbiome, a polymicrobial community dominated by Firmicutes. We speculate that interbacterial antagonism mediated by LXG toxins plays a critical role in shaping Firmicute-rich bacterial communities.
PubMed: 28696203
DOI: 10.7554/eLife.26938
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.98 Å)
構造検証レポート
Validation report summary of 5ukh
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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