CDA1b
naturalproductmech:mibig-c9928f3f0b MINTED SEEDED
What these status tags mean
Curation status describes a workflow state. SEEDED means the record entered through the source-seeding workflow; it does not imply that no later curation occurred. PROPOSED marks an addition awaiting review; REVIEWED records curator sign-off on identity, structure, filing class and producer claims; DEPRECATED retains a superseded or out-of-scope record. These are workflow decisions, not independently verified human review. Agent-assisted contributions may appear in the record history.
Grounding describes the identifier mapping: EXACT uses an ontology identity asserted by the source; MINTED keeps a local identifier when no defensible ontology identity is available; REVIEW_NEEDED flags an exact structure whose ontology identity needs adjudication. The grounding note retains any unresolved alternatives. These tags do not establish the strength of producer or activity evidence.
Structure
| Standard InChIKey | LUYIOBWFMDELAR-NMJWYASFSA-N |
|---|---|
| SMILES | O=C(N[C@@H](CC(O)=O)C(N[C@H](C1=CC=C(O)C=C1)C(N[C@@H](CC(O)=O)C(NCC(N[C@@H](C(N[C@@H](CCC(O)=O)C(N[C@@H](CC2=CNC3=C2C=CC=C3)C(O[C@H](C)[C@@H]4NC([C@H](CO)NC(C(O5)C5CCC)=O)=O)=O)=O)=O)[C@H](OP(O)(O)=O)C(N)=O)=O)=O)=O)=O)[C@H](CC(O)=O)NC([C@@H](CC6=CNC7=C6C=CC=C7)NC4=O)=O |
| Stereochemistry | undefined stereocentres — the InChIKey does not distinguish this compound from its stereoisomers |
Filing pathway
Unclassified — computed by NPClassifier npclassifier.gnps2.org@2026-09-07, which is why it is pinned rather than recomputed. The gene cluster's asserted class is nrps, from MIBiG.
Producer organisms 1
A claim that this taxon makes the compound. The basis says what the evidence addressed — a knockout and a database assertion are not the same claim.
| Taxon | Basis | Cluster | Evidence |
|---|---|---|---|
| Streptomyces coelicolor A3(2) NCBITaxon:100226 |
BGC_CHARACTERIZED | mibig:BGC0000315 | PMID:12445768 |
Occurrences 4
Somebody found the compound in this organism and cited it. That is not a claim that the organism makes it, and nothing here promotes one to the other.
| Taxon | Source | Reference |
|---|---|---|
| Streptomyces albidoflavus NCBITaxon:1886 |
LOTUS | DOI:10.1002/ANIE.199704981 |
| Streptomyces albidoflavus NCBITaxon:1886 |
LOTUS | DOI:10.1016/S1074-5521(02)00252-1 |
| Streptomyces coelicolor NCBITaxon:1902 |
LOTUS | DOI:10.1002/ANIE.199704981 |
| Streptomyces coelicolor NCBITaxon:1902 |
LOTUS | DOI:10.1016/S1074-5521(02)00252-1 |
Biosynthetic gene clusters 1
| Accession | Host | Locus evidence | Genome |
|---|---|---|---|
| mibig:BGC0000315 | Streptomyces coelicolor A3(2) NCBITaxon:100226 |
CLUSTER_DEMONSTRATED | genbank:AL645882.2 |
A locus claim and a taxon claim are different questions. Heterologous expression settles the first and leaves the second where the isolation report left it.
Biosynthesis curated
Written by a curator with claim-level evidence on each step; not derived from a source. This is what the rest of the record exists to support.
| Step | Enzyme | Reaction | Substrate → product | Evidence |
|---|---|---|---|---|
| 1 | HmaS 4-hydroxymandelate synthase UniProtKB:Q9Z4X7 |
CHEBI:15999 → CHEBI:17210 | DOI:10.1016/S1074-5521(02)00252-1 |
Step 1: SCO3229/HmaS is curated as the 4-hydroxymandelate synthase that supplies the L-4-hydroxyphenylglycine branch of CDA1b biosynthesis. HmaS sits at the first step of the pathway from 4-hydroxyphenylpyruvate to 4-hydroxyphenylglycine; the exact SCO3229 4-hydroxyphenylpyruvate to (S)-4-hydroxymandelate reaction is inferred from the HmaS assignment and therefore kept proposed.
Mechanism & Biosynthesis Overview
Causal graph — biosynthesis 4 nodes, 3 edges
Partial Streptomyces coelicolor CDA1b biosynthesis graph for HmaS-dependent 4-hydroxyphenylglycine precursor supply.
| Subject | Predicate | Object | Notes | Evidence |
|---|---|---|---|---|
| 4-hydroxyphenylpyruvic acid | is proposed to be oxidatively decarboxylated by | HmaS | The direct 4-hydroxyphenylpyruvate to (S)-4-hydroxymandelate assignment is inferred for SCO3229/HmaS. | DOI:10.1016/S1074-5521(02)00252-1 |
| HmaS | is proposed to form | (S)-4-hydroxymandelate | HmaS is curated as the entry enzyme for the CDA 4-hydroxyphenylglycine precursor pathway. | DOI:10.1016/S1074-5521(02)00252-1 |
| HmaS | is genetically required for biosynthesis of | CDA1b | Deletion of hmaS abolished CDA production, and exogenous 4-hydroxymandelate or downstream pathway intermediates restored it. | DOI:10.1016/S1074-5521(02)00252-1 |
Every edge carries its own citation; an uncited edge is refused by the corpus tests.
Explore across X-Mech
Provenance
| Source concept | Source | Version |
|---|---|---|
| BGC0000315 | MIBIG | 5 |
This page is generated from data/natural_products/unclassified/cda1b.yaml, which is generated from the committed inventories. Neither is edited by hand.