Function
Processes
Removes lesion-stalled RNA polymerase and recruits the Uvr machinery to the transcribed strand.
A reusable bacterial nucleotide-excision repair module in which UvrA and UvrB recognize bulky, helix-distorting DNA lesions, UvrC incises the damaged strand on both sides of the lesion, UvrD releases the damage-containing oligonucleotide, DNA polymerase I fills the resulting gap, and an NAD-dependent DNA ligase seals the nick. Mfd supplies an optional transcription-coupled entry route by removing lesion-stalled RNA polymerase and recruiting the Uvr machinery. Base-excision repair, mismatch repair, homologous-recombination repair, translesion synthesis, and eukaryotic XPD/TFIIH excision repair are outside this module.
The module is species-neutral and represents both global-genome NER and the Mfd-dependent transcription-coupled entry route. Pseudomonas putida KT2440 supplies a concrete representative for every role. Mfd is optional for the global-genome route. Cho-family alternative incision proteins and lineage-specific UvrA2 accessory paralogs are not universal requirements. PolA and LigA are shared with replication and other DNA-repair pathways. GO:0009381 describes the assembled UvrABC activity and is retained only as module-level evidence; each subunit leaf is represented by its distinguishable activity.
module.knowledge_gaps[0] · status
(0/1)module.knowledge_gaps[0] · provenance
(0/1)module.knowledge_gaps[1] · status
(0/1)module.knowledge_gaps[1] · provenance
(0/1)✗ none found
No MODULE:bacterial_nucleotide_excision_repair deep-research report alongside the module YAML.
✓ every leaf node grounds to a representative protein.
✓ every declared conforms_to bundle matches its template motif.
✓ every PRECEDES step chains, or its break is acknowledged via chaining_status.
6 complete review(s) · 3 with deep research · 8 missing review · 3 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| ligA Q88F25 | ✓ | ✓ | ✗ |
| mfd Q88KZ1 | ✓ | ✓ | ✗ |
| E. coli PolA P00582 | ✗ | — | — |
| E. coli UvrD P03018 | ✗ | — | — |
| E. coli UvrA P0A698 | ✗ | — | — |
| E. coli UvrB P0A8F8 | ✗ | — | — |
| E. coli UvrC P0A8G0 | ✗ | — | — |
| E. coli LigA P15042 | ✗ | — | — |
| E. coli Mfd P30958 | ✗ | — | — |
| PSEPK PolA Q88RK6 | ✗ | — | — |
| uvrA Q88QK7 | ✓ | ✓ | ✗ |
| uvrB Q88LF9 | ✓ | ✓ | ✓ |
| uvrC Q88FJ7 | ✓ | ✓ | ✓ |
| uvrD Q88C31 | ✓ | ✓ | ✓ |
Removes lesion-stalled RNA polymerase and recruits the Uvr machinery to the transcribed strand.
Scans duplex DNA with UvrB and initiates recognition of helix-distorting lesions.
Verifies the lesion, locally opens DNA, and forms the UvrB-DNA preincision complex.
Cleaves the damaged strand on the 3-prime and 5-prime sides of the lesion.
Unwinds the incised duplex to release the lesion-containing oligonucleotide and UvrB.
Restores the excised DNA tract using the undamaged strand as template.
Seals the remaining phosphodiester nick after repair synthesis.