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6UC5

Fab397 in complex with NPNA peptide

6UC5 の概要
エントリーDOI10.2210/pdb6uc5/pdb
分子名称Fab397 heavy chain, Fab397 light chain, NPNA peptide, ... (4 entities in total)
機能のキーワードantibody, malaria, circumsporozoite protein, csp, nanp, nanp repeats, plasmodium, plasmodium falciparum, immune system
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数3
化学式量合計48565.27
構造登録者
Pholcharee, T.,Oyen, D.,Wilson, I.A. (登録日: 2019-09-13, 公開日: 2020-01-08, 最終更新日: 2024-10-23)
主引用文献Pholcharee, T.,Oyen, D.,Torres, J.L.,Flores-Garcia, Y.,Martin, G.M.,Gonzalez-Paez, G.E.,Emerling, D.,Volkmuth, W.,Locke, E.,King, C.R.,Zavala, F.,Ward, A.B.,Wilson, I.A.
Diverse Antibody Responses to Conserved Structural Motifs in Plasmodium falciparum Circumsporozoite Protein.
J.Mol.Biol., 432:1048-1063, 2020
Cited by
PubMed Abstract: Malaria vaccine candidate RTS,S/AS01 is based on the central and C-terminal regions of the circumsporozoite protein (CSP) of P. falciparum. mAb397 was isolated from a volunteer in an RTS,S/AS01 clinical trial, and it protects mice from infection by malaria sporozoites. However, mAb397 originates from the less commonly used VH3-15 germline gene compared to the VH3-30/33 antibodies generally elicited by RTS,S to the central NANP repeat region of CSP. The crystal structure of mAb397 with an NPNA peptide shows that the central NPNA forms a type I β-turn and is the main recognition motif. In most anti-NANP antibodies studied to date, a germline-encoded Trp is used to engage the Pro in NPNA β-turns, but here the Trp interacts with the first Asn. This "conserved" Trp, however, can arise from different germline genes and be located in the heavy or the light chain. Variation in the terminal ψ angles of the NPNA β-turns results in different dispositions of the subsequent NPNA and, hence, different stoichiometries and modes of antibody binding to rsCSP. Diverse protective antibodies against NANP repeats are therefore not limited to a single germline gene response or mode of binding.
PubMed: 31883801
DOI: 10.1016/j.jmb.2019.12.029
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.75 Å)
構造検証レポート
Validation report summary of 6uc5
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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