KdsA1 is a cytoplasmic KDO-8-phosphate synthase that condenses D-arabinose-5-phosphate with phosphoenolpyruvate to form KDO-8-phosphate. It is one of two KT2440 KdsA paralogs supplying KDO for lipopolysaccharide.
| GO Term | Evidence | Action | Reason |
|---|---|---|---|
| GO:0005737 cytoplasm | IEA GO_REF:0000120 | MODIFY | Summary: KdsA1 is a soluble cytoplasmic enzyme; cytosol is the more specific location. Reason: Correct but general. KdsA1 has no membrane-anchoring feature and belongs to the KdsA subfamily whose PAINT root node (PTN000471837) carries cytosol, seeded by direct fractionation evidence for E. coli KdsA; cytosol is the part_of descendant that fits this soluble enzyme. Proposed replacements: cytosol Supporting Evidence: file:PSEPK/kdsA1/kdsA1-uniprot.txt SUBCELLULAR LOCATION: Cytoplasm {ECO:0000255|PROSITE-ProRule:PRU01406} file:interpro/panther/PTHR21057/PTHR21057-paint.tsv PTHR21057 PTN000471837 GO:0005829 C IBD false UniProtKB:P0A715 |
| GO:0008676 3-deoxy-8-phosphooctulonate synthase activity | IEA GO_REF:0000120 | ACCEPT | Summary: KdsA1 condenses D-arabinose 5-phosphate with phosphoenolpyruvate to KDO 8-phosphate. Reason: HAMAP MF_00056, NCBIfam TIGR01362 and the PTHR21057 family, whose every tree leaf is a KdsA-type enzyme and whose root carries this activity by PAINT, agree on the exact reaction. Supporting Evidence: file:PSEPK/kdsA1/kdsA1-uniprot.txt DR HAMAP; MF_00056; KDO8P_synth; 1. file:PSEPK/kdsA1/kdsA1-uniprot.txt Reaction=D-arabinose 5-phosphate + phosphoenolpyruvate + H2O |
| GO:0009103 lipopolysaccharide biosynthetic process | IEA GO_REF:0000120 | ACCEPT | Summary: KDO 8-phosphate is the precursor of the KDO residues of the LPS inner core. Reason: KdsA1 performs a step of the pathway that makes the KDO moiety of LPS; GO:0019294 has GO:0009103 among its ancestors, so the row agrees with the core process. It is kept as ACCEPT rather than refined because lipopolysaccharide biosynthesis is itself a core process of this gene (listed in core_functions.directly_involved_in), not a too-general stand-in for KDO biosynthesis. Supporting Evidence: file:PSEPK/kdsA1/kdsA1-uniprot.txt DR HAMAP; MF_00056; KDO8P_synth; 1. PMID:10734095 KDO8P is the phosphorylated precursor of 3-deoxy-D-manno-octulosonate, an essential sugar of the lipopolysaccharide of Gram-negative bacteria |
| GO:0019294 keto-3-deoxy-D-manno-octulosonic acid biosynthetic process | IEA GO_REF:0000104 | ACCEPT | Summary: KDO 8-phosphate synthesis is the second step of KDO biosynthesis. Reason: The UniRule transfer agrees with the HAMAP KdsA family and the E. coli KdsA enzymology. Supporting Evidence: file:PSEPK/kdsA1/kdsA1-uniprot.txt 3-deoxy-D-manno-octulosonate from D-ribulose 5-phosphate |
| GO:0046394 carboxylic acid biosynthetic process | IEA GO_REF:0000117 | MODIFY | Summary: KDO is an ulosonic (carboxylic) acid; the ARBA call is true but generic. Reason: Correct but general; KDO biosynthetic process (GO:0019294), which the gene also carries, is an is_a descendant of carboxylic acid biosynthetic process. Proposed replacements: keto-3-deoxy-D-manno-octulosonic acid biosynthetic process Supporting Evidence: file:PSEPK/kdsA1/kdsA1-uniprot.txt 3-deoxy-D-manno-octulosonate from D-ribulose 5-phosphate |
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Download this section (compressed HTML)Q: Are kdsA1 and kdsA2 differentially expressed during changes in surface-polysaccharide production?
Experiment: Compare expression and CMP-KDO pools in kdsA1 and kdsA2 single mutants.
Type: transcript profiling and targeted metabolomics
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