1CHZ

A NEW NEUROTOXIN FROM BUTHUS MARTENSII KARSCH

1CHZ の概要

• エントリーDOI: 10.2210/pdb1chz/pdb
• 分子名称: PROTEIN (BMK M2), CHLORIDE ION (3 entities in total)
• 機能のキーワード: neurotoxin, scorpion, toxin
• 由来する生物種: Mesobuthus martensii (Chinese scorpion)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 7257.69

構造登録者

He, X.L.,Deng, J.P.,Li, H.M.,Wang, D.C. (登録日: 1999-03-31, 公開日: 2000-03-31, 最終更新日: 2024-11-06)

主引用文献

He, X.L.,Deng, J.P.,Wang, M.,Zhang, Y.,Wang, D.C.
Structure of a new neurotoxin from the scorpion Buthus martensii Karsch at 1.76 A.
Acta Crystallogr.,Sect.D, 56:25-33, 2000

PubMed Abstract: A new neurotoxin BmK M2, toxic to both mammals and insects, with the strongest toxicity in the BmK toxin series, has been purified from the Chinese scorpion Buthus martensii Karsch and crystallized with MPD at pH 7.5. The crystals are orthorhombic, belonging to space group P2(1)2(1)2(1), with unit-cell parameters a = 36.64, b = 36.95, c = 37.23 A. The structure was solved by molecular replacement and refined to R = 0.186 for all reflections to a resolution of 1.76 A. The whole sequence (64 residues) of BmK M2 was determined by crystallographic analysis based on high-resolution data and the homologous model of BmK M8. The refined BmK M2 structure shows a non-proline cis peptide bond between Pro9 and His10 which enables the C-terminal segment to adopt a conformation different to that of the weak toxin BmK M8. Recently, a mutation analysis had suggested that both the tenth residue and the C-terminus play key roles in receptor binding. Therefore, these features may be related to the binding selectivity of the group III alpha-like toxins. The charge changes of residues 8, 10, 18, 28, 55 and 59 from neutral or negative to positive or neutral, which leads to a positive electrostatic potential surface, may be responsible for the high toxicity of BmK M2.

PubMed: 10666623
DOI: 10.1107/S0907444999014614

実験手法

X-RAY DIFFRACTION (1.76 Å)