Rv0925c Family assigned · medium auto-curated

H37Rv Rv0925c · MTBC0 mtbc0_000983 · 245 aa · 1035113–1035850 (-) · RefSeq NP_215440.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationflavodoxin family protein
Revised (this work)Flavodoxin family protein. Pfam: FMN_red (PF03358.21).

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

Curated reference (UniProt)

UniProt I6Y946 TrEMBL · unreviewed · Evidence at protein level
UniProt nameConserved protein

UniProt still lists this protein as Conserved protein; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
eggNOG descriptionNADPH-dependent FMN reductase
Orthologous groupCOG0655

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 0.315 · purifying
Polymorphic sites (≥ 0.1% of strains) 2 synonymous, 2 missense, 0 nonsense, 1 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.11% of strains (156) · clonal

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.

Domains (Pfam, hmmscan --cut_ga)

PfamAccessioni-EvalueResiduesDescription
FMN_redPF03358.21 2.5e-0821–169 NADPH-dependent FMN reductase

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

Closest characterised functional partner: mntH (divalent metal cation transporter MntH), high confidence from genomic context alone (score 722 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv0924c mntH divalent metal cation transporter MntH 722 722 ctx neighborhood:708
Rv0923c hyp hypothetical protein 710 710 ctx neighborhood:708
Rv0007 membrane protein 660 648 coexpression:648
Rv0926c hyp hypothetical protein 637 637 ctx neighborhood:613
Rv0927c oxidoreductase 537 534 ctx neighborhood:511
Rv1884c rpfC resuscitation-promoting factor RpfC 472 447 coexpression:446
Rv3701c egtD histidine-specific methyltransferase EtgD 444 445 ctx cooccurence:411
Rv2450c rpfE resuscitation-promoting factor RpfE 466 441 coexpression:440
Rv1449c tkt transketolase 457 436 coexpression:426
Rv0867c rpfA resuscitation-promoting factor RpfA 446 424 coexpression:424
Rv2389c rpfD resuscitation-promoting factor RpfD 444 422 coexpression:422
Rv1448c tal transaldolase 418 418 coexpression:406
Rv0432 sodC superoxide dismutase 442 415 coexpression:409
Rv1954A Rv1954A, len: 100 aa. Hypothetical unknown protein. 412 413 coexpression:413
Rv3372 otsB2 trehalose 6-phosphate phosphatase 411 412 coexpression:412

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 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: hypothetical protein
  • MTBC0 PGAP product: flavodoxin family protein
  • Pfam (hmmscan --cut_ga): FMN_red PF03358.21 (E=2e-08)
  • (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_215440.1)
  • Domains: Pfam-A via hmmscan --cut_ga — FMN_red (PF03358.21)
  • 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 COG0655
  • Curated reference: UniProt I6Y946 (TrEMBL, unreviewed; 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)
  • Interaction network: STRING v12.0 (Szklarczyk et al. 2023, doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 — 23 functional partner(s); context anchor mntH
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000983|Rv0925c|
MTTTSDQNAAAPPRFDGLRALFINATLKRSPELSHTDGLIERSSGIMREHGVQVDTLRAVDHDIATGVWPDMTEHGWATDEWPALYRRVLDAHILVLCGPIWLGDNSSVMKRVIERLYACSSLLNEDGQYAYYGRAGGCLITGNEDGVKHCAMNVLYSLQHLGYTIPPQADAGWIGEAGPGPSYLDPGSGGPENDFTNRNTTFMTFNLMHIAQMLRVAGGIPAYGNQRTKWDAGCRPDFANPDYR