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2KRA

Solution structure of Bv8

2KRA の概要
エントリーDOI10.2210/pdb2kra/pdb
NMR情報BMRB: 16633
分子名称Prokineticin Bv8 (1 entity in total)
機能のキーワードbeta strands, beta turn, helix, disulfide bond, secreted, contractile protein
由来する生物種Bombina variegata (Yellow-bellied toad)
細胞内の位置Secreted: Q9PW66
タンパク質・核酸の鎖数1
化学式量合計8042.23
構造登録者
Daly, N.L.,Craik, D.J.,Mobli, M. (登録日: 2009-12-14, 公開日: 2010-08-11, 最終更新日: 2014-04-23)
主引用文献Morales, R.A.V.,Daly, N.L.,Vetter, I.,Mobli, M.,Napier, I.A.,Craik, D.J.,Lewis, R.J.,Christie, M.J.,King, G.F.,Alewood, P.F.,Durek, T.
Chemical synthesis and structure of the prokineticin Bv8
CHEMBIOCHEM, 11:1882-1888, 2010
Cited by
PubMed Abstract: Bv8, a 77-residue protein isolated from frogs, is the prototypic member of the prokineticin family of cytokines. Prokineticins (PKs) have only recently been identified in vertebrates (including humans), and they are believed to be involved in a number of key physiological processes, such as angiogenesis, neurogenesis, nociception, and tissue development. We used a combination of Boc solid-phase peptide synthesis, native chemical ligation, and in vitro protein folding to establish robust chemical access to this molecule. Synthetic Bv8 was obtained in good yield and exhibited full activity in a human neuroblastoma cell line and rat dorsal root ganglion (DRG) neurons. The 3D structure of the synthetic protein was determined by using NMR spectroscopy and it was found to be homologous with that of mamba intestinal toxin 1, which is the only other known prokineticin structure. Analysis of a truncated mutant lacking five residues at the N terminus that are critical for receptor binding and activation showed no perturbation to the core protein structure. Together with the functional data, this suggests that receptor binding is likely to be a highly cooperative process possibly involving major allosterically driven structural rearrangements. The facile and efficient synthesis presented here will enable preparation of unique chemical analogues of prokineticins, which should be powerful tools for modulating the structure and function of prokineticins and their receptors, and studying the many physiological processes that have been linked to them.
PubMed: 20677202
DOI: 10.1002/cbic.201000330
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2kra
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2024-10-30に公開中

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