<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(23)</volume><submitter>Argueta C</submitter><pubmed_abstract>Consisting of more than 11,000 members distributed over five families, the tautomerase superfamily (TSF) is a large collection of proteins with diverse biological functions. While much attention has been given to individual TSF enzymes, a majority remain structurally and functionally uncharacterized. Given its large size, studying a representative member of each family offers a viable approach for extracting mechanistic insights applicable to the entire superfamily. In this study, cis-3-chloroacrylic acid dehalogenase (cis-CaaD), 5-carboxymethyl-2-hydroxymuconate isomerase (CHMI), malonate semialdehyde decarboxylase (MSAD), and 4-oxalocrotonate tautomerase (4-OT) were referenced against the well-studied macrophage migration inhibitory factor (MIF) and D-dopachrome tautomerase (D-DT) using </pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>12617</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11641302</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Conformational Flexibility of the C-Terminal Region Influences Distal Active Site Residues Across the Tautomerase Superfamily.</pubmed_title><pmcid>PMC11641302</pmcid><pubmed_authors>Argueta C</pubmed_authors><pubmed_authors>Pantouris G</pubmed_authors><pubmed_authors>Parkins A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Conformational Flexibility of the C-Terminal Region Influences Distal Active Site Residues Across the Tautomerase Superfamily.</name><description>Consisting of more than 11,000 members distributed over five families, the tautomerase superfamily (TSF) is a large collection of proteins with diverse biological functions. While much attention has been given to individual TSF enzymes, a majority remain structurally and functionally uncharacterized. Given its large size, studying a representative member of each family offers a viable approach for extracting mechanistic insights applicable to the entire superfamily. In this study, cis-3-chloroacrylic acid dehalogenase (cis-CaaD), 5-carboxymethyl-2-hydroxymuconate isomerase (CHMI), malonate semialdehyde decarboxylase (MSAD), and 4-oxalocrotonate tautomerase (4-OT) were referenced against the well-studied macrophage migration inhibitory factor (MIF) and D-dopachrome tautomerase (D-DT) using </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-04-22T03:22:02.998Z</modification><creation>2025-04-03T23:26:32.517Z</creation></dates><accession>S-EPMC11641302</accession><cross_references><pubmed>39684328</pubmed><doi>10.3390/ijms252312617</doi></cross_references></HashMap>