Rv1775 Family assigned · medium auto-curated

H37Rv Rv1775 · MTBC0 mtbc0_001889 · 272 aa · 2027183–2028001 (+) · RefSeq NP_216291.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationhypothetical protein
Revised (this work)Contains DAPG_hydrolase (PF18089.8) domain(s); putative function inferred from the domain architecture.

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

Curated reference (UniProt)

UniProt O33178 TrEMBL · unreviewed · Inferred from homology
UniProt nameDAPG hydrolase PhiG domain-containing protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

Orthologous group2DBDZ

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 1.846 · diversifying/relaxed
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 5 missense, 1 nonsense, 3 frameshift
Disruption 4 distinct premature-stop/frameshift site(s); most common in 24.09% of strains (34986) · convergent

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
DAPG_hydrolasePF18089.8 3.5e-5649–267 DAPG hydrolase PhiG domain

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

Closest characterised functional partner: Rv1774 (oxidoreductase), high confidence from genomic context alone (score 921 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv1774 oxidoreductase 989 921 ctx neighborhood:882 textmining:870
Rv1773c transcriptional regulator 825 825 ctx neighborhood:742
Rv3903c cpnT hyp hypothetical protein 765 765 ctx cooccurence:764
Rv0538 membrane protein 761 762 ctx cooccurence:761
Rv2113 integral membrane protein 740 741 ctx cooccurence:740
Rv1937 oxygenase 725 726 ctx cooccurence:724
Rv2761c hsdS type I restriction/modification system specificity determinant HsdS 714 714 ctx cooccurence:711
Rv3788 hyp hypothetical protein 713 713 ctx cooccurence:713
Rv0493c hyp hypothetical protein 700 700 ctx cooccurence:699
Rv1963c mce3R transcriptional repressor Mce3R 639 640 ctx cooccurence:638
Rv2939 papA5 phthiocerol/phthiodiolone dimycocerosyl transferase 634 634 ctx cooccurence:633
Rv1024 membrane protein 628 629 ctx cooccurence:627
Rv2843 hyp hypothetical protein 619 619 ctx cooccurence:619
Rv2164c hyp hypothetical protein 616 616 ctx cooccurence:614
Rv3732 hyp hypothetical protein 591 592 ctx cooccurence:589

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: hypothetical protein
  • Pfam (hmmscan --cut_ga): DAPG_hydrolase PF18089.8 (E=3e-56)
  • (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_216291.1)
  • Domains: Pfam-A via hmmscan --cut_ga — DAPG_hydrolase (PF18089.8)
  • 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 2DBDZ
  • Curated reference: UniProt O33178 (TrEMBL, unreviewed; Inferred from homology)
  • 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 — 50 functional partner(s); context anchor Rv1774
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001889|Rv1775|
MASDLYLGYRNDDADTPFGKFFKPEMAPLPQHVVVALQHGPQAGMALLAFDDAASIVDEGYQQTENGYGILGDGSMQVSVRTDMPGVTPAMWAWWFGWHGSDTRRYKLWHPRAHLSARWKDGDQDSGAGRRGAQRYVGRWSMISEYIGSTKLGAAIQFVEPAAMGLPDDSDDTVSICARLGSADAPVDAGWFVHQVRSTPGGSEMRSRFWMGGPHIAVRKAPEVASKAVRPIASKLIGVSESTARNLLVYCAQEMNHLAGFLADLWESFGDE