論文

査読有り 国際誌
2015年

Roles of Ala-149 in the catalytic activity of diadenosine tetraphosphate phosphorylase from Mycobacterium tuberculosis H37Rv.

Bioscience, biotechnology, and biochemistry
  • Shigetarou Mori
  • ,
  • Hyun Kim
  • ,
  • Emiko Rimbara
  • ,
  • Yoshichika Arakawa
  • ,
  • Keigo Shibayama

79
2
開始ページ
236
終了ページ
8
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1080/09168451.2014.973364

Diadenosine 5',5'''-P(1),P(4)-tetraphosphate (Ap4A) phosphorylase from Mycobacterium tuberculosis H37Rv (MtAPA) belongs to the histidine triad motif (HIT) superfamily, but is the only member with an alanine residue at position 149 (Ala-149). Enzymatic analysis revealed that the Ala-149 deletion mutant displayed substrate specificity for diadenosine 5',5'''-P(1),P(5)-pentaphosphate and was inactive on Ap4A and other substrates that are utilized by the wild-type enzyme.

リンク情報
DOI
https://doi.org/10.1080/09168451.2014.973364
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/25348769
ID情報
  • DOI : 10.1080/09168451.2014.973364
  • ISSN : 0916-8451
  • PubMed ID : 25348769

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