ermJ encodes an Erm-family 23S rRNA adenine-N6 methyltransferase in Bacillus anthracis. UniProt/CARD identify this entry as a macrolide-lincosamide-streptogramin resistance determinant; methylation of 23S rRNA alters the macrolide binding site on the large ribosomal subunit. UniProt names the protein 'rRNA adenine N-6-methyltransferase' (accession Q04720).
| GO Term | Evidence | Action | Reason |
|---|---|---|---|
|
GO:0000154
rRNA modification
|
IEA
GO_REF:0000002 |
ACCEPT |
Summary: The rRNA modification/methylation process is consistent with an Erm-family 23S rRNA methyltransferase.
Reason: Erm enzymes confer resistance by methylating 23S rRNA; this process annotation is biologically appropriate.
Supporting Evidence:
file:genes/BACAN/ermJ/ermJ-uniprot.txt
CC -!- FUNCTION: Involved in erythromycin resistance.
|
|
GO:0000179
rRNA (adenine-N6,N6-)-dimethyltransferase activity
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: The existing dimethyltransferase term is retained as the more specific molecular function for this Erm-family enzyme.
Reason: GO:0000179 is a child of the broader rRNA adenine-N6 methyltransferase activity and captures the N6,N6-dimethylation activity expected for Erm-mediated macrolide-lincosamide-streptogramin resistance.
Supporting Evidence:
file:genes/BACAN/ermJ/ermJ-uniprot.txt
CC -!- FUNCTION: Involved in erythromycin resistance.
|
|
GO:0031167
rRNA methylation
|
IEA
GO_REF:0000118 |
ACCEPT |
Summary: The rRNA modification/methylation process is consistent with an Erm-family 23S rRNA methyltransferase.
Reason: Erm enzymes confer resistance by methylating 23S rRNA; this process annotation is biologically appropriate.
Supporting Evidence:
file:genes/BACAN/ermJ/ermJ-uniprot.txt
CC -!- FUNCTION: Involved in erythromycin resistance.
|
|
GO:0046677
response to antibiotic
|
RCA
file:projects/ANTIMICROBIAL_RESISTANCE/aro2go.sssom.yaml |
NEW |
Summary: NEW process annotation: ermJ is an AMR determinant involved in antibiotic response/resistance.
Reason: CARD/ARO identity places this gene in an antimicrobial-resistance determinant family; response to antibiotic is the appropriate high-level GO biological process for the resistance role.
Supporting Evidence:
file:genes/BACAN/ermJ/ermJ-uniprot.txt
DR CARD; ARO:3000495; ErmD; ARO:0001001; antibiotic target alteration.
|
Q: Is the ARO-derived rRNA (adenine-N6-)-methyltransferase activity annotation sufficiently specific for ermJ, or is a narrower substrate/site-specific GO term warranted?
Experiment: Biochemically assay purified ermJ against representative antibiotic substrates for the inferred AMR family and measure loss of drug activity or target modification.
Type: in vitro enzyme assay
Focused AMR batch review. UniProt accession: Q04720. Source organism: Bacillus anthracis.
DR CARD; ARO:3000495; ErmD; ARO:0001001; antibiotic target alteration.projects/ANTIMICROBIAL_RESISTANCE/data/candidate_new_annotations.tsv and projects/ANTIMICROBIAL_RESISTANCE/aro2go.sssom.yaml.id: Q04720
gene_symbol: ermJ
product_type: PROTEIN
status: DRAFT
taxon:
id: NCBITaxon:1392
label: Bacillus anthracis
description: ermJ encodes an Erm-family 23S rRNA adenine-N6 methyltransferase in Bacillus anthracis. UniProt/CARD identify this entry as a macrolide-lincosamide-streptogramin resistance determinant; methylation of 23S rRNA alters the macrolide binding site on the large ribosomal subunit. UniProt names the protein 'rRNA adenine N-6-methyltransferase' (accession Q04720).
existing_annotations:
- term:
id: GO:0000154
label: rRNA modification
evidence_type: IEA
original_reference_id: GO_REF:0000002
qualifier: involved_in
review:
summary: The rRNA modification/methylation process is consistent with an Erm-family 23S rRNA methyltransferase.
action: ACCEPT
reason: Erm enzymes confer resistance by methylating 23S rRNA; this process annotation is biologically appropriate.
supported_by:
- reference_id: file:genes/BACAN/ermJ/ermJ-uniprot.txt
supporting_text: 'CC -!- FUNCTION: Involved in erythromycin resistance.'
- term:
id: GO:0000179
label: rRNA (adenine-N6,N6-)-dimethyltransferase activity
evidence_type: IEA
original_reference_id: GO_REF:0000120
qualifier: enables
review:
summary: The existing dimethyltransferase term is retained as the more specific molecular function for this Erm-family enzyme.
action: ACCEPT
reason: GO:0000179 is a child of the broader rRNA adenine-N6 methyltransferase activity and captures the N6,N6-dimethylation activity expected for Erm-mediated macrolide-lincosamide-streptogramin resistance.
supported_by:
- reference_id: file:genes/BACAN/ermJ/ermJ-uniprot.txt
supporting_text: 'CC -!- FUNCTION: Involved in erythromycin resistance.'
- term:
id: GO:0031167
label: rRNA methylation
evidence_type: IEA
original_reference_id: GO_REF:0000118
qualifier: involved_in
review:
summary: The rRNA modification/methylation process is consistent with an Erm-family 23S rRNA methyltransferase.
action: ACCEPT
reason: Erm enzymes confer resistance by methylating 23S rRNA; this process annotation is biologically appropriate.
supported_by:
- reference_id: file:genes/BACAN/ermJ/ermJ-uniprot.txt
supporting_text: 'CC -!- FUNCTION: Involved in erythromycin resistance.'
- term:
id: GO:0046677
label: response to antibiotic
evidence_type: RCA
original_reference_id: file:projects/ANTIMICROBIAL_RESISTANCE/aro2go.sssom.yaml
qualifier: involved_in
review:
summary: 'NEW process annotation: ermJ is an AMR determinant involved in antibiotic response/resistance.'
action: NEW
reason: CARD/ARO identity places this gene in an antimicrobial-resistance determinant family; response to antibiotic is the appropriate high-level GO biological process for the resistance role.
additional_reference_ids:
- file:genes/BACAN/ermJ/ermJ-uniprot.txt
supported_by:
- reference_id: file:genes/BACAN/ermJ/ermJ-uniprot.txt
supporting_text: DR CARD; ARO:3000495; ErmD; ARO:0001001; antibiotic target alteration.
references:
- id: GO_REF:0000002
title: Gene Ontology annotation through association of InterPro records with GO terms
findings: []
- id: GO_REF:0000118
title: TreeGrafter-generated GO annotations
findings: []
- id: GO_REF:0000120
title: Combined Automated Annotation using Multiple IEA Methods
findings: []
- id: file:genes/BACAN/ermJ/ermJ-uniprot.txt
title: UniProt flat file for ermJ (Q04720)
findings:
- statement: UniProt/CARD identity and protein naming for ermJ.
supporting_text: 'CC -!- FUNCTION: Involved in erythromycin resistance.'
- id: file:projects/ANTIMICROBIAL_RESISTANCE/aro2go.sssom.yaml
title: Curated ARO to GO mapping set for AMR gene families
findings:
- statement: Manual ARO-to-GO mappings used to identify focused AMR annotation gains.
supporting_text: 'mapping_set_title: ARO to GO mapping (AMR gene families and resistance mechanisms)'
- id: file:projects/ANTIMICROBIAL_RESISTANCE/data/candidate_new_annotations.tsv
title: Annotation-gain candidates from ARO to GO mappings
findings:
- statement: Candidate GO annotations projected from the ARO-to-GO mapping set.
supporting_text: Candidate GO annotations that UniProtKB entries with a CARD cross-reference would gain from the
core_functions:
- description: ermJ methylates adenine N6 in 23S rRNA, modifying the antibiotic target site in the large ribosomal subunit and contributing to macrolide/lincosamide/streptogramin resistance.
molecular_function:
id: GO:0000179
label: rRNA (adenine-N6,N6-)-dimethyltransferase activity
directly_involved_in:
- id: GO:0046677
label: response to antibiotic
supported_by:
- reference_id: file:genes/BACAN/ermJ/ermJ-uniprot.txt
supporting_text: 'CC -!- FUNCTION: Involved in erythromycin resistance.'
suggested_questions:
- question: Is the ARO-derived rRNA (adenine-N6-)-methyltransferase activity annotation sufficiently specific for ermJ, or is a narrower substrate/site-specific GO term warranted?
experts: []
suggested_experiments:
- description: Biochemically assay purified ermJ against representative antibiotic substrates for the inferred AMR family and measure loss of drug activity or target modification.
experiment_type: in vitro enzyme assay