Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

6SY7

Structure of Trypanosome Brucei Phosphofructokinase in complex with AMP.

Summary for 6SY7
Entry DOI10.2210/pdb6sy7/pdb
DescriptorATP-dependent 6-phosphofructokinase, BENZENE, GLYCEROL, ... (5 entities in total)
Functional Keywordsglycolysis, amp, allostery, transferase
Biological sourceTrypanosoma brucei brucei
Total number of polymer chains8
Total formula weight432886.20
Authors
McNae, I.W.,Vasquez-Valdivieso, M.G.,Walkinshaw, M.D. (deposition date: 2019-09-27, release date: 2019-12-25, Last modification date: 2024-01-24)
Primary citationFernandes, P.M.,Kinkead, J.,McNae, I.W.,Vasquez-Valdivieso, M.,Wear, M.A.,Michels, P.A.M.,Walkinshaw, M.D.
Kinetic and structural studies of Trypanosoma and Leishmania phosphofructokinases show evolutionary divergence and identify AMP as a switch regulating glycolysis versus gluconeogenesis.
Febs J., 287:2847-2861, 2020
Cited by
PubMed Abstract: Trypanosomatids possess glycosome organelles that contain much of the glycolytic machinery, including phosphofructokinase (PFK). We present kinetic and structural data for PFK from three human pathogenic trypanosomatids, illustrating intriguing differences that may reflect evolutionary adaptations to differing ecological niches. The activity of Leishmania PFK - to a much larger extent than Trypanosoma PFK - is reliant on AMP for activity regulation, with 1 mm AMP increasing the L. infantum PFK (LiPFK) kcat/K value by 10-fold, compared to only a 1.3- and 1.4-fold increase for T. cruzi and T. brucei PFK, respectively. We also show that Leishmania PFK melts at a significantly lower (> 15 °C) temperature than Trypanosoma PFKs and that addition of either AMP or ATP results in a marked stabilization of the protein. Sequence comparisons of Trypanosoma spp. and Leishmania spp. show that divergence of the two genera involved amino acid substitutions that occur in the enzyme's 'reaching arms' and 'embracing arms' that determine tetramer stability. The dramatic effects of AMP on Leishmania activity compared with the Trypanosoma PFKs may be explained by differences between the T-to-R equilibria for the two families, with the low-melting Leishmania PFK favouring the flexible inactive T-state in the absence of AMP. Sequence comparisons along with the enzymatic and structural data presented here also suggest there was a loss of AMP-dependent regulation in Trypanosoma species rather than gain of this characteristic in Leishmania species and that AMP acts as a key regulator in Leishmania governing the balance between glycolysis and gluconeogenesis.
PubMed: 31838765
DOI: 10.1111/febs.15177
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.75 Å)
Structure validation

247947

PDB entries from 2026-01-21

PDB statisticsPDBj update infoContact PDBjnumon