Rv2319c Resolved · high auto-curated

H37Rv Rv2319c · MTBC0 mtbc0_002467 · 292 aa · 2616597–2617475 (-) · RefSeq NP_216835.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)universal stress protein
MTBC0 PGAP re-annotationuniversal stress protein
Revised (this work)Universal stress protein. Pfam: Usp (PF00582.33).

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

Curated reference (UniProt)

UniProt P9WLB5 SwissProt · reviewed · Evidence at protein level
UniProt nameUniversal stress protein Rv2319c

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category T Signal transduction mechanisms
Preferred nameuspA4
eggNOG descriptionUniversal stress protein
Orthologous groupCOG0589
Gene Ontology (2) GO:0008150, GO:0040007

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) pseudogene candidate

pN/pS 0.871 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 7 missense, 0 nonsense, 1 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 17.63% of strains (25598) · 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
UspPF00582.33 2.3e-202–140 Universal stress protein family

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

Closest characterised functional partner: rocE (cationic amino acid transporter permease RocE), high confidence from genomic context alone (score 975 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2320c rocE cationic amino acid transporter permease RocE 983 975 ctx neighborhood:800 coexpression:861
Rv2323c hyp hypothetical protein 978 963 ctx neighborhood:780 coexpression:840 textmining:433
Rv2322c rocD1 Rv2322c, (MTCY3G12.12), len: 221 aa. Probable rocD1,ornithine aminotransferase, highly similar to N-terminal region of other ornithine amino 962 961 ctx neighborhood:783 coexpression:826
Rv2321c rocD2 Rv2321c, (MTCY3G12.13), len: 181 aa. Probable rocD2,ornithine aminotransferase, highly similar to C-terminal region of other ornithine amino 984 954 ctx neighborhood:783 coexpression:797 textmining:667
Rv2324 AsnC family transcriptional regulator 713 615 ctx neighborhood:613
Rv1921c lppF lipoprotein LppF 531 531 ctx cooccurence:529
Rv0295c stf0 hyp hypothetical protein 460 460 ctx cooccurence:460
Rv1288 hyp hypothetical protein 463 444 ctx cooccurence:440
Rv3882c eccE1 ESX-1 secretion system protein EccE1 443 443 ctx cooccurence:443
Rv2226 hyp hypothetical protein 438 438 ctx cooccurence:421
Rv1316c ogt methylated-DNA--protein-cysteine methyltransferase 424 424 coexpression:415
Rv3637 Possible transposase; Rv3637, (MTCY15C10.15c), len: 166 aa. Possible transposase. C-terminal end highly similar to Q9RLQ9|ISTA putative tran 413 413
Rv3636 Possible transposase; Rv3636, (MTCY15C10.16c), len: 115 aa. Possible transposase, weakly similar to others e.g. O69924|SC3C8.12 putative tra 410 410
Rv3314c deoA thymidine phosphorylase 409 409 coexpression:406
Rv0049 hyp hypothetical protein 734 229 textmining:670

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: universal stress protein
  • MTBC0 PGAP product: universal stress protein
  • Pfam (hmmscan --cut_ga): Usp PF00582.33 (E=2e-20)
  • (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_216835.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Usp (PF00582.33)
  • 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 COG0589
  • Curated reference: UniProt P9WLB5 (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)
  • Interaction network: STRING v12.0 (Szklarczyk et al. 2023, doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 — 21 functional partner(s); context anchor rocE
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002467|Rv2319c|
MTIVVGYLAGKVGPSALHLAVRVARMHKTSLTVATIVRRHWPTPSLARVDAEYELWSEQLAAASAREAQRYLRRLADGIEVSYHHRAHRSVSAGLLDVVEELEAEVLVLGSFPSGRRARVLIGSTADRLLHSSPVPVAITPRRYRCYTDRLTRLSCGYSATSGSVDVVRRCGHLASRYGVPMRVITFAVRGRTMYPPEVGLHAEASVLEAWAAQARELLEKLRINGVVSEDVVLQVVTGNGWAQALDAADWQDGEILALGTSPFGDVARVFLGSWSGKIIRYSPVPVLVLPG