3MCO

Crystal Structure of the 6-hyroxymethyl-7,8-dihydropterin pyrophosphokinase dihydropteroate synthase bifunctional enzyme from Francisella tularensis

3MCO の概要

• エントリーDOI: 10.2210/pdb3mco/pdb
• 関連するPDBエントリー: 3MCM 3MCN
• 分子名称: 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase/dihydropteroate synthase, 2-AMINO-6-HYDROXYMETHYL-7,8-DIHYDRO-3H-PTERIDIN-4-ONE, DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER, ... (5 entities in total)
• 機能のキーワード: folate, tim barrel, kinase, synthase, hppk, dhps, pterin, transferase
• 由来する生物種: Francisella tularensis subsp. holarctica
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 103062.86

構造登録者

Pemble IV, C.W.,Mehta, P.K.,Mehra, S.,Li, Z.,Lee, R.E.,White, S.W. (登録日: 2010-03-29, 公開日: 2010-12-22, 最終更新日: 2023-09-06)

主引用文献

Pemble, C.W.,Mehta, P.K.,Mehra, S.,Li, Z.,Nourse, A.,Lee, R.E.,White, S.W.
Crystal structure of the 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase.dihydropteroate synthase bifunctional enzyme from Francisella tularensis.
Plos One, 5:e14165-e14165, 2010

PubMed Abstract: The 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase (HPPK) and dihydropteroate synthase (DHPS) enzymes catalyze sequential metabolic reactions in the folate biosynthetic pathway of bacteria and lower eukaryotes. Both enzymes represent validated targets for the development of novel anti-microbial therapies. We report herein that the genes which encode FtHPPK and FtDHPS from the biowarfare agent Francisella tularensis are fused into a single polypeptide. The potential of simultaneously targeting both modules with pterin binding inhibitors prompted us to characterize the molecular details of the multifunctional complex. Our high resolution crystallographic analyses reveal the structural organization between FtHPPK and FtDHPS which are tethered together by a short linker. Additional structural analyses of substrate complexes reveal that the active sites of each module are virtually indistinguishable from those of the monofunctional enzymes. The fused bifunctional enzyme therefore represents an excellent vehicle for finding inhibitors that engage the pterin binding pockets of both modules that have entirely different architectures. To demonstrate that this approach has the potential of producing novel two-hit inhibitors of the folate pathway, we identify and structurally characterize a fragment-like molecule that simultaneously engages both active sites. Our study provides a molecular framework to study the enzyme mechanisms of HPPK and DHPS, and to design novel and much needed therapeutic compounds to treat infectious diseases.

PubMed: 21152407
DOI: 10.1371/journal.pone.0014165

実験手法

X-RAY DIFFRACTION (2.3 Å)