recG Resolved · high auto-curated

H37Rv Rv2973c · MTBC0 mtbc0_003158 · 737 aa · 3348908–3351121 MTBC0 (-) · RefSeq NP_217489.1

Genomic neighbourhood (genome browser)

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Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)ATP-dependent DNA helicase RecG
MTBC0 PGAP re-annotationATP-dependent DNA helicase RecG
Revised (this work)ATP-dependent DNA helicase RecG. Pfam: RecG_wedge (PF17191.11), ResIII (PF04851.22), DEAD (PF00270.36), Helicase_C (PF00271.38).
Functional category (TubercuList)information pathways

Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.

In the literature (TB corpus sweep) 6 publications

6 TB publications mention this gene. 6 publication(s) discuss this gene (6 in a M. tuberculosis context, 2 in other mycobacteria — M. smegmatis (1)).

Most recent 5 of 6.
PublicationDate
RecGwed : A probable novel regulator in the resolution of branched DNA structures in mycobacteria. doi:10.1002/iub.1881 2018
Expanding the Horizon of Recombination Repair in Mycobacteria: Identification and Characterization of Novel Proteins. doi:10.1096/fasebj.2018.32.1_supplement.lb1 2018
Mycobacterium tuberculosis RecG protein but not RuvAB or RecA protein is efficient at remodeling the stalled replication forks: implications for multiple mechanisms of replication restart in mycobacteria. doi:10.1074/jbc.M115.671164 2015
Effects of conserved residues and naturally occurring mutations on Mycobacterium tuberculosis RecG helicase activity. doi:10.1099/mic.0.072140-0 2014
Evidence for the role of Mycobacterium tuberculosis RecG helicase in DNA repair and recombination. doi:10.1111/febs.12208 2013

This layer CITES the literature and adds context; it does not change the verdict or the function stated elsewhere in this fiche. This distinguishes a gene that is dark because nobody has looked from one that is dark despite having been studied. Source: PubMed (whole): H37Rv locus tag + GENE NAME + ortholog identifiers (Mb…, MMAR_…, MSMEG_…, ML…, MAB_…), under a mycobacterial context filter; hits verified against the abstract text. Species-context counts distinguish M. tuberculosis literature from literature on other mycobacteria. phase76/phase77, 2026-07-13.

Genomic-neighbour overlap (structural caveat) co-directional · 0 % of gene

NeighbourRv2972c (Rv2972c, - strand)
Overlap4 bp, 0 % of this gene's length

co-directional overlap: ordinary (e.g. shared stop/start codons in an operon), not the Rv2438A-type artefact P20.1, derived from GFF3 gene coordinates, 2026-08-03.

CRISPRi vulnerability

Vulnerability index -0.52 (95% CI -2.86 to 2.99). A more negative index = more vulnerable to knockdown (better drug-target quality); indicative threshold VI ≤ -6 = highly vulnerable.

Quantitative CRISPRi knockdown, graded (finer than binary Tn-seq essentiality). Source: CRISPRi vulnerability index (Bosch 2021, pebble.rockefeller.edu).

Legacy record & comparison (Mycobrowser)

Mycobrowser functionCritical role in recombination and DNA repair. Help process holliday junction intermediates to mature products by catalysing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3' to 5' polarity. RECG unwind branched duplex DNA (Y-DNA).
Mycobrowser EC 3.6.4.12 · agrees with the atlas

The legacy Mycobrowser record is shown for verification. Mycobrowser is no longer maintained; its EC numbers predate recent nomenclature revisions, so a class change usually reflects re-numbering, not a conflict.

Orthologues (reciprocal best hits across mycobacteria)

M. bovis Mb2998c · 99.9% identity
M. leprae ML1671c · 79.5% identity
M. marinum MMAR_1742 · 85.6% identity
M. smegmatis MSMEG_2403 · 66.4% identity
M. orygis RJtmp_003068 · 99.9% identity
M. abscessus MAB_3278c · 57.2% identity

Reciprocal-best-hit orthologues (DIAMOND) against the Mycobrowser reference proteomes. A missing species is informative: e.g. a gene absent from M. leprae was likely lost in its reductive genome evolution. Locus tags link to Mycobrowser.

Curated reference (UniProt)

UniProt P9WMQ7 SwissProt · reviewed · Evidence at protein level
UniProt nameATP-dependent DNA helicase RecG
EC (curated) EC 5.6.2.3, EC 5.6.2.4
Curated functionPlays a critical role in recombination and DNA repair (Probable). Helps process Holliday junction (HJ) intermediates to mature products by catalyzing branch migration. Has replication fork regression activity, able to displace proteins bound to DNA. An ATP-dependent helicase with a preference for HJ DNA, followed by lagging strand replication forks (RF). Has DNA helicase activity in both directions in vitro. Unwinds branched DNA substrates such as HJs to flayed complexes, unwinds full RFs, R-loop and D-loops, has weak and strong unwinding activities on leading and lagging strand RFs respective.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category L Replication, recombination and repair
Preferred namerecG
eggNOG descriptionCritical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA)
Orthologous groupCOG1200
EC number EC 3.6.4.12
KEGG orthology K03655
KEGG pathways map03440
Gene Ontology (41) GO:0003674, GO:0003724, GO:0003824, GO:0004004, GO:0004386, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005886, GO:0006139, GO:0006725 +29 more

Orthology-based transfer (eggNOG 5.0.2, diamond). EC/KO/GO/CAZy are computed annotations, not manual curation; cross-check against the primary literature before treating a specific reaction as established.

Conservation & selection (intra-MTBC, 145 209 strains)

pN/pS 0.275 · purifying
Polymorphic sites (≥ 0.1% of strains) 5 synonymous, 4 missense, 0 nonsense, 0 frameshift

pN/pS from segregating SNPs (singletons removed) normalised by possible sites. Low pN/pS = purifying selection (a strong signal that a "hypothetical" is a real, constrained gene). A high pN/pS is ambiguous: relaxed constraint or positive selection (drug resistance, antigenic variation) inflate it; e.g. rpoB/katG/pncA score high here for resistance, not loss of function. A clonal disruption (one allele over a clade) suggests lineage pseudogenisation; a convergent one (many independent alleles) is typical of resistance loss-of-function.

Outgroup conservation (beyond the MTBC) Bacteria

M. canettii dN/dS (deep-divergence selection) 0.207 · 8 consensus substitution(s)
under purifying selection vs M. canettii (deep divergence; dN/dS=0.207) — a real, constrained gene predating the MTBC clonal expansion
Genus-wide presence (~53 non-MTBC Mycobacterium) present in 53/53 (100%) · mean identity 79.4% · 4/4 closest MTBAP relatives
conserved across the genus (present in 53/53 non-MTBC Mycobacterium genomes, incl. distant relatives) — an ancient core gene predating the genus radiation
Phylostratum (deepest detected homolog) MTBC-specific Mycobacterium Mycobacteriaceae Corynebacteriales Actinomycetia Bacteria
detected in 12/13 non-Mycobacterium reference genomes (down to Bacteria) · mean identity 45.1%
detected down to outside the phylum (Proteobacteria/Firmicutes controls) — a universally conserved, ancient bacterial gene

Two orthogonal outgroup signals. M. canettii (the immediate outgroup) gives a deep-divergence dN/dS (a low value confirms a constrained, real gene; shown as confident only at ≥8 substitutions, else flagged low-power). Genus-wide presence/absence (tblastn vs assembled non-MTBC genomes) places the gene on the ancient-core ↔ MTBC-specific axis: a gene absent even from the closest MTBAP relatives is a candidate MTBC-specific innovation (possible host-adaptation factor, to confirm by synteny). The phylostratum extends that axis outside the genus (tblastn vs 13 reference genomes spanning Mycobacteriaceae → Corynebacteriales → Actinomycetia → outside the phylum): it is the deepest clade in which a homolog is still detected, i.e. a proxy for gene age. Read it with the null model in mind: a shallow (young) stratum can also reflect homology-detection failure for short or fast-evolving ORFs, so it is a descriptive axis, not a proof of novelty.

Essentiality (transposon mutagenesis)

DeJesus 2017 callNE · non-essential
What the call meansnon-essential
TA sites (Himar1) 30 in the ORF — 0 in the essential state, 0 growth-defect, 30 non-essential, 0 growth-advantage. Saturation 0.933, mean read count 61.7142857143. A region of the protein devoid of TA sites is invisible to this assay: nothing can be inferred about it, in either direction.

Genome-wide Himar1 transposon essentiality in H37Rv (DeJesus 2017). An essential call (ES/ESD/GD) is strong, independent evidence that a "hypothetical" locus encodes a functional, selectively required gene — orthogonal to intra-species conservation.

Mutant phenotypes (conditional Tn-seq, MtbTnDB) in-vivo phenotype

Conditionlog2FCqEffect
fitness in mouse infection (in vivo) +1.040.011 disruption advantageous

Conditional fitness of transposon-disruption mutants across 1 significant condition(s) (|log2FC|≥1, q≤0.05), from the standardized MtbTnDB compendium. A negative log2FC means the mutant is depleted — the gene contributes to fitness in that condition. An in-vivo defect for a "hypothetical" is strong evidence it matters for infection, even without a known molecular function. Disruption (Tn insertion), not a clean deletion; genetic-interaction screens excluded.

Proteomics (mass spectrometry) detected

MS detectiondetected in 6 of 16 independent MS datasets
Integrated abundance2.61 ppm · rank 3119/3519 (11.4th percentile)

Detection by mass spectrometry is direct, experimental evidence that the protein product exists — orthogonal to sequence conservation and to Tn-seq essentiality, and especially decisive for a "hypothetical" locus. Reproducible detection across several independent datasets (PaxDb) makes the existence claim robust; the integrated abundance places the protein in the proteome's dynamic range.

Physico-chemical properties (computed, ProtParam)

Length737 aa
Molecular weight80.4 kDa
Theoretical pI6.15
GRAVY-0.117 (hydrophilic)
Aliphatic index97.3
Aromaticity0.053
Instability index33.3 (stable)

Computed from the ancestral MTBC0 sequence with the ExPASy ProtParam method (Biopython). Descriptive biophysical context: a positive GRAVY flags a hydrophobic (often membrane) protein, a high instability index (>40) predicts a short in-vitro half-life, an extreme pI hints at compartment or binding partner.

Domains (Pfam, hmmscan --cut_ga)

PfamAccessioni-EvalueResiduesDescription
RecG_wedgePF17191.11 7.6e-0720–136 RecG wedge domain
ResIIIPF04851.22 2.5e-09287–459 Type III restriction enzyme, res subunit
DEADPF00270.36 2.8e-22292–464 DEAD/DEAH box helicase
Helicase_CPF00271.38 1.9e-17548–628 Helicase conserved C-terminal domain

Structural search (AlphaFold DB model, Foldseek vs PDB — genome-wide) pLDDT 80.7

PDB hitprobTM-scoreE-valueDescription
1gm5-assembly1_A 1.00 0.60 4.8e-40 sig 1gm5-assembly1_A Structure of RecG bound to three-way DNA junction
6x50-assembly1_A 1.00 0.74 1.3e-29 sig 6x50-assembly1_A Mfd-bound E.coli RNA polymerase elongation complex - V state
6ac8-assembly2_A 1.00 0.56 4.6e-31 sig 6ac8-assembly2_A Crystal structure of Mycobacterium smegmatis Mfd at 2.75 A resolution
6acx-assembly3_B 1.00 0.58 3.8e-30 sig 6acx-assembly3_B Crystal structure of Mycobacterium smegmatis Mfd in complex with ADP + Pi at 3.5 A resolution.
6m6b-assembly1_M 1.00 0.77 3.5e-23 sig 6m6b-assembly1_M Cryo-EM structure of Thermus thermophilus Mfd in complex with RNA polymerase and ATP-gamma-S

Foldseek search of the AlphaFold DB model (mean pLDDT 80.7, gated at 70) against the PDB — a genome-wide extension of the ESMFold dark-gene search that also covers proteins beyond the single-sequence length limit. Confident structural neighbours (E < 0.01) shown.

Genomic context (neighbours & predicted operon) operon of 4

Upstream (5' on genome)Rv2972c (- strand, -4 bp gap)
Downstream (3' on genome)Rv2974c (- strand, 2 bp gap)
Predicted operon Rv2972c · recG · Rv2974c · Rv2975c

Neighbours from the H37Rv annotation (- strand). The operon is predicted by co-directional intergenic distance (same strand, gaps ≤50 bp) — a transcription-unit hypothesis, not a mapped TSS. For a "hypothetical", co-transcription with a characterised operon is a concrete functional lead (complements the STRING neighborhood channel below).

Functional interaction network (STRING v12, guilt-by-association)

Explore full network →

Node colour = verdict, dashed = hypothetical; edge colour = evidence (green experimental, orange genomic-context, grey co-expression), width ∝ score. Click a partner to open its page; "Explore full network" to walk the graph.

Closest characterised functional partner: murB (UDP-N-acetylenolpyruvoylglucosamine reductase), medium confidence from genomic context alone (score 531 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2974c hyp hypothetical protein 944 944 ctx neighborhood:800 coexpression:732
Rv2972c hyp hypothetical protein 929 929 ctx neighborhood:881 coexpression:431
Rv2975c hyp hypothetical protein 801 801 ctx neighborhood:800
Rv0482 murB UDP-N-acetylenolpyruvoylglucosamine reductase 531 531 ctx cooccurence:430
Rv2896c dprA hyp hypothetical protein 493 493 ctx cooccurence:490
Rv0720 rplR 50S ribosomal protein L18 490 490 ctx cooccurence:488
Rv2158c murE UDP-N-acetylmuramoylalanyl-D-glutamate--2,6-diaminopimelate ligase 462 463 ctx cooccurence:445
Rv2154c ftsW lipid II flippase FtsW 458 458 ctx cooccurence:430
Rv0050 ponA1 bifunctional penicillin-insensitive transglycosylase/penicillin-sensitive transpeptidase 445 446 ctx cooccurence:421
Rv3646c topA DNA topoisomerase I 656 439 textmining:413
Rv2157c murF UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase 437 437 ctx cooccurence:415
Rv1407 fmu 16S rRNA m5C967 methyltransferase 445 425
Rv3682 ponA2 bifunctional penicillin-insensitive transglycosylase/penicillin-sensitive transpeptidase 425 425
Rv2343c dnaG DNA primase 496 420 coexpression:420
Rv2710 sigB RNA polymerase sigma factor SigB 438 408

STRING combines evidence channels (neighborhood, fusion, cooccurrence, coexpression, experimental, database, text-mining) into a 0–1000 score. The ctx badge marks edges carried by the genomic-context channels (conserved neighborhood, fusion, phylogenetic co-occurrence), which are independent of orthology and structure and the strongest signal for an unknown gene. The exp badge marks an experimentally-supported partner (measured interaction, experimental/database channel ≥400) as opposed to a purely predicted one — but note that the M. tuberculosis experimental interactome is dominated by a noisy bacterial-two-hybrid screen, so a strong measured link that contradicts the operon/localisation context is likely a false positive. The no text-mining column recomputes the score from data alone, so a link that does not depend on the literature is visible. Association is a function hypothesis, not proof: corroborate with the operon context and the primary literature before assigning a function.

Evidence

  • Legacy H37Rv annotation: ATP-dependent DNA helicase RecG
  • MTBC0 PGAP product: ATP-dependent DNA helicase RecG
  • Pfam (hmmscan --cut_ga): RecG_wedge PF17191.11 (E=8e-07), ResIII PF04851.22 (E=3e-09), DEAD PF00270.36 (E=3e-22), Helicase_C PF00271.38 (E=2e-17)
  • (auto-curated by rules from PGAP + Pfam + Foldseek; not hand-reviewed)

Sources

  • Ancestral sequence & coordinates: Harrison LB et al. (2024), An imputed ancestral reference genome for the MTBC, doi:10.1101/2023.09.07.556366
  • Product annotation: NCBI PGAP on MTBC0; legacy from H37Rv NC_000962.3 (RefSeq NP_217489.1)
  • Domains: Pfam-A via hmmscan --cut_ga — RecG_wedge (PF17191.11), ResIII (PF04851.22), DEAD (PF00270.36), Helicase_C (PF00271.38)
  • Sequence-level signal: ESM Atlas (EvolutionaryScale × BioHub) — exploratory
  • Controlled vocabulary: eggNOG-mapper 2.1.12 (Cantalapiedra et al. 2021, doi:10.1093/molbev/msab293), eggNOG 5.0 DB (Huerta-Cepas et al. 2019) — OG COG1200
  • Curated reference: UniProt P9WMQ7 (SwissProt, reviewed; Evidence at protein level)
  • Intra-MTBC selection: pN/pS and disruption from SPDI variants of 145 209 MTBC strains (this work, local collection vs H37Rv NC_000962.3)
  • Genome-wide structure: AlphaFold DB model (Jumper et al. 2021, doi:10.1038/s41586-021-03819-2; Varadi et al. 2024, doi:10.1093/nar/gkad1011) searched vs PDB with Foldseek (mean pLDDT 80.7)
  • Interaction network: STRING v12.0 (Szklarczyk et al. 2023, doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 — 53 functional partner(s); context anchor murB
  • Essentiality: genome-wide transposon mutagenesis in H37Rv — DeJesus et al. 2017 (mBio, doi:10.1128/mBio.02133-16, CC BY)
  • Proteomics: integrated mass-spectrometry abundance from PaxDb 5.0 (Huang et al. 2023, doi:10.1016/j.mcpro.2023.100640), taxon 83332 — weighted average of 16 datasets, incl. Schubert et al. 2013 (doi:10.1016/j.chom.2013.04.008) and Albrethsen et al. 2013 (doi:10.1074/mcp.M112.018846)
  • Functional category: TubercuList scheme (Cole et al. 1998, doi:10.1038/31159), via Mycobrowser (Kapopoulou et al. 2011, doi:10.1016/j.tube.2010.09.006)
  • Orthologues: reciprocal best hits (DIAMOND, Buchfink et al. 2021, doi:10.1038/s41592-021-01101-x) against Mycobrowser release 5 reference proteomes
  • Genomic context / operon: H37Rv annotation; operon predicted by co-directional intergenic distance (Salgado et al. 2000, doi:10.1073/pnas.030539397)
  • Mutant phenotypes: standardized Tn-seq compendium MtbTnDB (Jinich et al. 2025, doi:10.1111/mmi.15370), aggregating many primary Tn-seq studies across conditions
  • Physico-chemical properties: ExPASy ProtParam method via Biopython (Gasteiger et al. 2005), computed from the MTBC0 sequence
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003158|Rv2973c|recG
MASLSDRLDRVLGATAADALDEQFGMRTVDDLLRHYPRSYVEGAARVGIGDARPEAGEHITIVDVITDTYSFPMKKKPNRKCLRITVGGGRNKVTATFFNADYIMRDLTKHTKVMLSGEVGYYKGAMQLTHPAFLILDSPDGKNHGTRSLKSIADASKAISGELVVEEFERRFFPIYPASTKVQSWDIFKCVRQVLDVLDRVDDPLPAELRAKHGLIPEDEALRAIHLAESQSLRERARERLTFDEAVGLQWALVARRHGELSESGPSAAWKSNGLAAELLRRLPFELTAGQREVLDVLSDGLAANRPLNRLLQGEVGSGKTIVAVLAMLQMVDAGYQCALLAPTEVLAAQHLRSIRDVLGPLAMGGQLGGAENATRVALLTGSMTAGQKKQVRAEIASGQVGIVIGTHALLQEAVDFHNLGMVVVDEQHRFGVEQRDQLRAKAPAGITPHLLVMTATPIPRTVALTVYGDLETSTLRELPLGRQPIATNVIFVKDKPAWLDRAWRRIIEEAAAGRQAYVVAPRIDESDDTDVQGGVRPSATAEGLFSRLRSAELAELRLALMHGRLSADDKDAAMAAFRAGEVDVLVCTTVIEVGVDVPNATVMLVMDADRFGISQLHQLRGRIGRGEHPSVCLLASWVPPDTPAGQRLRAVAGTMDGFALADLDLKERKEGDVLGRNQSGKAITLRLLSLAEHEEYIVAARDFCIEAYKNPTDPALALMAARFTSTDRIEYLDKS