Purification, characterization and primary structure of a chymotrypsin inhibitor from Naja atra venom
Data(s) |
2004
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Resumo |
A chymotrypsin inhibitor, designated NA-CI, was isolated from the venom of the Chinese cobra Naja atra by three-step chromatography. It inhibited bovine (x-chymotrypsin with a K-i of 25 nM. The molecular mass of NA-CI was determined to be 6403.8 Da by matrix-assisted laser-desorption ionization time-of-flight (MALDI-TOF) analysis. The complete amino acid sequence was determined after digestion of S-carboxymethylated inhibitor with Staphylococcus aureus V8 protease and porcine trypsin. NA-CI was a single polypeptide chain composed of 57 amino acid residues. The main contact site with the protease (PI) has a Phe, showing the specificity of the inhibitor. NA-CI shared great similarity with the chymotrypsin inhibitor from Naja naja venom (identities = 89.5%) and other snake venom protease inhibitors. (C) 2003 Elsevier Inc. All rights reserved. |
Identificador | |
Direitos |
Purification, characterization and primary structure of a chymotrypsin inhibitor from Naja atra venom |
Fonte |
Zhou, XD; Jin, Y; Lua, QM; Lia, DS; Zhu, SW; Wang, WY; Xiong, YL.Purification, characterization and primary structure of a chymotrypsin inhibitor from Naja atra venom,137,219-224 ,(SCI-E ): |
Palavras-Chave | #Biochemistry & Molecular Biology; Zoology |
Tipo |
期刊论文 |