7PAF
Streptococcus pneumoniae choline importer LicB in lipid nanodiscs
7PAF の概要
| エントリーDOI | 10.2210/pdb7paf/pdb |
| EMDBエントリー | 13268 |
| 分子名称 | Nanobody, LicB protein, (1S)-2-{[{[(2R)-2,3-DIHYDROXYPROPYL]OXY}(HYDROXY)PHOSPHORYL]OXY}-1-[(PALMITOYLOXY)METHYL]ETHYL STEARATE (3 entities in total) |
| 機能のキーワード | importer, choline, nanodisc, nanobody, transport protein |
| 由来する生物種 | synthetic construct 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 97651.01 |
| 構造登録者 | |
| 主引用文献 | Barland, N.,Rueff, A.S.,Cebrero, G.,Hutter, C.A.J.,Seeger, M.A.,Veening, J.W.,Perez, C. Mechanistic basis of choline import involved in teichoic acids and lipopolysaccharide modification. Sci Adv, 8:eabm1122-eabm1122, 2022 Cited by PubMed Abstract: Phosphocholine molecules decorating bacterial cell wall teichoic acids and outer-membrane lipopolysaccharide have fundamental roles in adhesion to host cells, immune evasion, and persistence. Bacteria carrying the operon that performs phosphocholine decoration synthesize phosphocholine after uptake of the choline precursor by LicB, a conserved transporter among divergent species. is a prominent pathogen where phosphocholine decoration plays a fundamental role in virulence. Here, we present cryo-electron microscopy and crystal structures of LicB, revealing distinct conformational states and describing architectural and mechanistic elements essential to choline import. Together with in vitro and in vivo functional characterization, we found that LicB displays proton-coupled import activity and promiscuous selectivity involved in adaptation to choline deprivation conditions, and describe LicB inhibition by synthetic nanobodies (sybodies). Our results provide previously unknown insights into the molecular mechanism of a key transporter involved in bacterial pathogenesis and establish a basis for inhibition of the phosphocholine modification pathway across bacterial phyla. PubMed: 35235350DOI: 10.1126/sciadv.abm1122 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.75 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






