mupP encodes the MurNAc-6-phosphate phosphatase that completes the Pseudomonas anabolic peptidoglycan recycling pathway. It converts MurNAc-6P to MurNAc, supports UDP-MurNAc precursor salvage, and contributes to intrinsic fosfomycin resistance.
Definition: Catalysis of the dephosphorylation of N-acetyl-D-muramate 6-phosphate to N-acetyl-D-muramate and phosphate.
Justification: MupP has a biochemically characterized MurNAc-6P phosphatase activity, but the review is forced to use the overly broad phosphatase activity term.
Parent term: phosphatase activity
Supporting Evidence:
| GO Term | Evidence | Action | Reason |
|---|---|---|---|
| GO:0005829 cytosol | IEA GO_REF:0000118 | ACCEPT | Summary: MupP acts on MurNAc-6-phosphate in the cytosolic recycling pathway. Reason: Full-text fractionation analysis directly tested the PP_1764 deletion mutant and detected recycling intermediates in its cytosolic fraction. Supporting Evidence: PMID:28351914 whether recycling intermediates accumulate specifically in the cytosolic fractions of ΞmupP (Ξpp_1764) mutant cells |
| GO:0006281 DNA repair | IEA GO_REF:0000118 | REMOVE | Summary: DNA repair is not supported for MupP; this appears to be an over-transfer from HAD phosphatase family context. Reason: MupP is characterized as a MurNAc-6P phosphatase in peptidoglycan recycling, not a DNA repair protein. Supporting Evidence: file:PSEPK/mupP/mupP-uniprot.txt Specifically catalyzes the dephosphorylation of N- |
| GO:0008967 phosphoglycolate phosphatase activity | IEA GO_REF:0000118 | REMOVE | Summary: Phosphoglycolate phosphatase activity is not the characterized substrate specificity of MupP. Reason: The characterized substrate is MurNAc-6P, with narrow substrate specificity. Supporting Evidence: file:PSEPK/mupP/mupP-uniprot.txt Shows a very low activity on GlcNAc-6P |
| GO:0016791 phosphatase activity | IEA GO_REF:0000117 | ACCEPT | Summary: MupP is a phosphatase, but GO lacks a specific MurNAc-6P phosphatase term in these annotations. Reason: Retain the broad phosphatase term and propose a more specific ontology term. Supporting Evidence: file:PSEPK/mupP/mupP-uniprot.txt Reaction=N-acetyl-D-muramate 6-phosphate + H2O |
| GO:0009254 peptidoglycan turnover | IEA GO_REF:0000041 | ACCEPT | Summary: MupP is directly involved in peptidoglycan recycling/turnover. Reason: Retain the peptidoglycan turnover annotation. Supporting Evidence: file:PSEPK/mupP/mupP-uniprot.txt PATHWAY: Cell wall biogenesis; peptidoglycan recycling. |
| GO:0009254 peptidoglycan turnover | IMP PMID:28351914 The N-Acetylmuramic acid 6-phosphate phosphatase MupP comple... | ACCEPT | Summary: MupP is directly involved in peptidoglycan recycling/turnover. Reason: Retain the peptidoglycan turnover annotation. Supporting Evidence: file:PSEPK/mupP/mupP-uniprot.txt PATHWAY: Cell wall biogenesis; peptidoglycan recycling. |
| GO:0016791 phosphatase activity | IDA PMID:28351914 The N-Acetylmuramic acid 6-phosphate phosphatase MupP comple... | ACCEPT | Summary: MupP is a phosphatase, but GO lacks a specific MurNAc-6P phosphatase term in these annotations. Reason: Retain the broad phosphatase term and propose a more specific ontology term. Supporting Evidence: file:PSEPK/mupP/mupP-uniprot.txt Reaction=N-acetyl-D-muramate 6-phosphate + H2O |
| GO:0097172 N-acetylmuramic acid metabolic process | IDA PMID:28351914 The N-Acetylmuramic acid 6-phosphate phosphatase MupP comple... | ACCEPT | Summary: MupP acts on N-acetylmuramate 6-phosphate in the MurNAc recycling pathway. Reason: Retain the N-acetylmuramic acid metabolic process annotation. Supporting Evidence: PMID:28351914 specifically converts MurNAc 6-phosphate to MurNAc |
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Download this section (compressed HTML)Q: How broadly is MupP-dependent anabolic peptidoglycan recycling used across non-enterobacterial Gram-negative lineages lacking MurQ?
Suggested experts: Peptidoglycan recycling and bacterial cell-wall metabolism experts
Experiment: Compare MurNAc-6P, MurNAc, UDP-MurNAc, and fosfomycin susceptibility in mupP, amgK, and murU mutants across Pseudomonas growth phases.
Type: cell-wall precursor metabolomics and antibiotic susceptibility assay
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