6VPT

Crystal structure and mechanistic molecular modeling studies of Rv3377c: the Mycobacterium tuberculosis diterpene cyclase

6VPT の概要

• エントリーDOI: 10.2210/pdb6vpt/pdb
• 分子名称: Cyclase (2 entities in total)
• 機能のキーワード: diterpene synthase, diterpene cyclase, lyase
• 由来する生物種: Mycobacterium tuberculosis
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 55324.23

構造登録者

Zhang, T.,Prach, L.,DiMaio, F.,Siegel, J. (登録日: 2020-02-04, 公開日: 2020-12-02, 最終更新日: 2023-10-11)

主引用文献

Zhang, Y.,Prach, L.M.,O'Brien, T.E.,DiMaio, F.,Prigozhin, D.M.,Corn, J.E.,Alber, T.,Siegel, J.B.,Tantillo, D.J.
Crystal Structure and Mechanistic Molecular Modeling Studies of Mycobacterium tuberculosis Diterpene Cyclase Rv3377c.
Biochemistry, 59:4507-4515, 2020

PubMed Abstract: Terpenes make up the largest class of natural products, with extensive chemical and structural diversity. Diterpenes, mostly isolated from plants and rarely prokaryotes, exhibit a variety of important biological activities and valuable applications, including providing antitumor and antibiotic pharmaceuticals. These natural products are constructed by terpene synthases, a class of enzymes that catalyze one of the most complex chemical reactions in biology: converting simple acyclic oligo-isoprenyl diphosphate substrates to complex polycyclic products via carbocation intermediates. Here we obtained the second ever crystal structure of a class II diterpene synthase from bacteria, tuberculosinol pyrophosphate synthase (i.e., Halimadienyl diphosphate synthase, MtHPS, or Rv3377c) from (). This enzyme transforms ()-geranylgeranyl diphosphate into tuberculosinol pyrophosphate (Halimadienyl diphosphate). Rv3377c is part of the diterpene pathway along with Rv3378c, which converts tuberculosinol pyrophosphate to 1-tuberculosinyl adenosine (1-TbAd). This pathway was shown to exist only in virulent species, but not in closely related avirulent species, and was proposed to be involved in phagolysosome maturation arrest. To gain further insight into the reaction pathway and the mechanistically relevant enzyme substrate binding orientation, electronic structure calculation and docking studies of reaction intermediates were carried out. Results reveal a plausible binding mode of the substrate that can provide the information to guide future drug design and anti-infective therapies of this biosynthetic pathway.

PubMed: 33182997
DOI: 10.1021/acs.biochem.0c00762

実験手法

X-RAY DIFFRACTION (2.718 Å)