<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carter MS</submitter><funding>NIGMS NIH HHS</funding><pagination>696-705</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6435334</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(7)</volume><pubmed_abstract>Colocation of the genes encoding ABC, TRAP, and TCT transport systems and catabolic pathways for the transported ligand provides a strategy for discovering novel microbial enzymes and pathways. We screened solute-binding proteins (SBPs) for ABC transport systems and identified three that bind D-apiose, a branched pentose in the cell walls of higher plants. Guided by sequence similarity networks (SSNs) and genome neighborhood networks (GNNs), the identities of the SBPs enabled the discovery of four catabolic pathways for D-apiose with eleven previously unknown reactions. The new enzymes include D-apionate oxidoisomerase, which catalyzes hydroxymethyl group migration, as well as 3-oxo-isoapionate-4-phosphate decarboxylase and 3-oxo-isoapionate-4-phosphate transcarboxylase/hydrolase, which ar</pubmed_abstract><journal>Nature chemical biology</journal><pubmed_title>Functional assignment of multiple catabolic pathways for D-apiose.</pubmed_title><pmcid>PMC6435334</pmcid><funding_grant_id>P01 GM118303</funding_grant_id><funding_grant_id>U54 GM093342</funding_grant_id><pubmed_authors>Al-Obaidi N</pubmed_authors><pubmed_authors>Ghosh A</pubmed_authors><pubmed_authors>Gerlt JA</pubmed_authors><pubmed_authors>Vetting MW</pubmed_authors><pubmed_authors>Bonanno JB</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Carter MS</pubmed_authors><pubmed_authors>Almo SC</pubmed_authors><pubmed_authors>Bouvier JT</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zallot RG</pubmed_authors><pubmed_authors>Andersen HM</pubmed_authors><pubmed_authors>Francisco BS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional assignment of multiple catabolic pathways for D-apiose.</name><description>Colocation of the genes encoding ABC, TRAP, and TCT transport systems and catabolic pathways for the transported ligand provides a strategy for discovering novel microbial enzymes and pathways. We screened solute-binding proteins (SBPs) for ABC transport systems and identified three that bind D-apiose, a branched pentose in the cell walls of higher plants. Guided by sequence similarity networks (SSNs) and genome neighborhood networks (GNNs), the identities of the SBPs enabled the discovery of four catabolic pathways for D-apiose with eleven previously unknown reactions. The new enzymes include D-apionate oxidoisomerase, which catalyzes hydroxymethyl group migration, as well as 3-oxo-isoapionate-4-phosphate decarboxylase and 3-oxo-isoapionate-4-phosphate transcarboxylase/hydrolase, which ar</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jul</publication><modification>2026-05-03T12:19:13.867Z</modification><creation>2019-06-06T21:03:04Z</creation></dates><accession>S-EPMC6435334</accession><cross_references><pubmed>29867142</pubmed><doi>10.1038/s41589-018-0067-7</doi></cross_references></HashMap>