<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fernandes PM</submitter><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><pagination>4425-4441</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7702303</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>477(22)</volume><pubmed_abstract>6-Phosphofructokinase-1-kinase (PFK) tetramers catalyse the phosphorylation of fructose 6-phosphate (F6P) to fructose 1,6-bisphosphate (F16BP). Vertebrates have three PFK isoforms (PFK-M, PFK-L, and PFK-P). This study is the first to compare the kinetics, structures, and transcript levels of recombinant human PFK isoforms. Under the conditions tested PFK-M has the highest affinities for F6P and ATP (K0.5ATP 152 µM; K0.5F6P 147 µM), PFK-P the lowest affinities (K0.5ATP 276 µM; K0.5F6P 1333 µM), and PFK-L demonstrates a mixed picture of high ATP affinity and low F6P affinity (K0.5ATP 160 µM; K0.5F6P 1360 µM). PFK-M is more resistant to ATP inhibition compared with PFK-L and PFK-P (respectively, 23%, 31%, 50% decreases in specificity constants). GTP is an alternate phospho donor. Interface 2,</pubmed_abstract><journal>The Biochemical journal</journal><pubmed_title>Biochemical and transcript level differences between the three human phosphofructokinases show optimisation of each isoform for specific metabolic niches.</pubmed_title><pmcid>PMC7702303</pmcid><funding_grant_id>MC_PC_16043</funding_grant_id><funding_grant_id>106359</funding_grant_id><pubmed_authors>Fernandes PM</pubmed_authors><pubmed_authors>Walkinshaw MD</pubmed_authors><pubmed_authors>Michels PAM</pubmed_authors><pubmed_authors>McNae I</pubmed_authors><pubmed_authors>Kinkead J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biochemical and transcript level differences between the three human phosphofructokinases show optimisation of each isoform for specific metabolic niches.</name><description>6-Phosphofructokinase-1-kinase (PFK) tetramers catalyse the phosphorylation of fructose 6-phosphate (F6P) to fructose 1,6-bisphosphate (F16BP). Vertebrates have three PFK isoforms (PFK-M, PFK-L, and PFK-P). This study is the first to compare the kinetics, structures, and transcript levels of recombinant human PFK isoforms. Under the conditions tested PFK-M has the highest affinities for F6P and ATP (K0.5ATP 152 µM; K0.5F6P 147 µM), PFK-P the lowest affinities (K0.5ATP 276 µM; K0.5F6P 1333 µM), and PFK-L demonstrates a mixed picture of high ATP affinity and low F6P affinity (K0.5ATP 160 µM; K0.5F6P 1360 µM). PFK-M is more resistant to ATP inhibition compared with PFK-L and PFK-P (respectively, 23%, 31%, 50% decreases in specificity constants). GTP is an alternate phospho donor. Interface 2,</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2026-05-08T16:24:23.07Z</modification><creation>2021-02-20T09:40:33Z</creation></dates><accession>S-EPMC7702303</accession><cross_references><pubmed>33141153</pubmed><doi>10.1042/BCJ20200656</doi></cross_references></HashMap>