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A propeptide‐independent protease from Tannerella sp.6_1_58FAA_CT1 displays trypsin‐like specificity
Author(s) -
Song Qitao,
Zhang Xiaoyue,
Li Na,
Shen Jie,
Cheng Jiansong
Publication year - 2017
Publication title -
journal of basic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.58
H-Index - 54
eISSN - 1521-4028
pISSN - 0233-111X
DOI - 10.1002/jobm.201600486
Subject(s) - proteases , trypsin , biochemistry , protein precursor , porphyromonas gingivalis , protease , chemistry , tannerella forsythia , serine protease , subtilisin , biology , microbiology and biotechnology , enzyme , bacteria , medicine , honeysuckle , alternative medicine , traditional chinese medicine , pathology , genetics
Despite the absence of any homologs of Tannerella forsythia KLIKK proteases in Tannerella sp.6_1_58FAA_CT1, the strain possesses a putative cysteine protease (G9S4N1) closely related to RgpB of Porphyromonas gingivalis . G9S4N1 lacks obvious propeptide that behaves as inhibitor of proteases and was proven to be a propeptide‐independent protease. Unlike RgpB, which exclusively cleaves ArgXaa bonds, G9S4N1 exhibits both arginine‐ and citrulline‐specific activities. Mutations of Asp177, a potential P1‐Arg binding site, to uncharged or positively charged residues did not alter the substrate specificity of G9S4N1 significantly. Moreover, a group of arginine‐specific proteases from different species including porcine trypsin, bovine thrombin, and a trypsin‐like serine protease of dengue 2 virus CF40‐Gly‐NS3pro185 also display different specificity toward citrulline residue, suggesting that citrulline‐modified protein might have different roles and destiny in biological processes involving various proteases.

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