tsf Resolved · high auto-curated

H37Rv Rv2889c · MTBC0 mtbc0_003071 · 271 aa · 3219121–3219936 (-) · RefSeq NP_217405.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)elongation factor EF-Ts
MTBC0 PGAP re-annotationtranslation elongation factor Ts
Revised (this work)Translation elongation factor Ts. Pfam: EF_TS (PF00889.26).

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

Curated reference (UniProt)

UniProt P9WNM1 SwissProt · reviewed · Evidence at protein level
UniProt nameElongation factor Ts
Curated functionAssociates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF-Tu.GTP complex up to the GTP hydrolysis stage on the ribosome (By similarity).

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category J Translation, ribosomal structure and biogenesis
Preferred nametsf
eggNOG descriptionAssociates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome
Orthologous groupCOG0264
KEGG orthology K02357
Gene Ontology (49) GO:0003674, GO:0003676, GO:0003723, GO:0003746, GO:0005488, GO:0005575, GO:0005618, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0005886 +37 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 0.347 · purifying
Polymorphic sites (≥ 0.1% of strains) 4 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.

Domains (Pfam, hmmscan --cut_ga)

PfamAccessioni-EvalueResiduesDescription
EF_TSPF00889.26 1.5e-6175–270 Elongation factor TS

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

Closest characterised functional partner: rpsB (30S ribosomal protein S2), high confidence from genomic context alone (score 998 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv0685 tuf elongation factor Tu 999 1000 coexpression:861 experimental:999 database:664 textmining:771
Rv2890c rpsB 30S ribosomal protein S2 999 998 ctx neighborhood:876 coexpression:964 textmining:622
Rv1307 atpH ATP synthase subunit b/delta 997 995 coexpression:994 textmining:453
Rv3442c rpsI 30S ribosomal protein S9 989 975 coexpression:957 database:404 textmining:587
Rv2882c frr ribosome recycling factor 984 960 ctx cooccurence:491 coexpression:860 textmining:618
Rv3443c rplM 50S ribosomal protein L13 977 948 coexpression:915 textmining:591
Rv1643 rplT 50S ribosomal protein L20 975 944 coexpression:858 database:404 textmining:583
Rv0652 rplL 50S ribosomal protein L7/L12 978 939 coexpression:885 database:404 textmining:670
Rv0056 rplI 50S ribosomal protein L9 953 939 coexpression:882 database:404
Rv0702 rplD 50S ribosomal protein L4 973 938 coexpression:883 textmining:583
Rv0641 rplA 50S ribosomal protein L1 969 933 coexpression:863 textmining:562
Rv1630 rpsA 30S ribosomal protein S1 955 930 coexpression:862 experimental:474
Rv2909c rpsP 30S ribosomal protein S16 946 930 coexpression:881 database:404
Rv2888c amiC amidase AmiC 930 930 ctx neighborhood:882
Rv0715 rplX 50S ribosomal protein L24 937 928 coexpression:860

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: elongation factor EF-Ts
  • MTBC0 PGAP product: translation elongation factor Ts
  • Pfam (hmmscan --cut_ga): EF_TS PF00889.26 (E=2e-61)
  • (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_217405.1)
  • Domains: Pfam-A via hmmscan --cut_ga — EF_TS (PF00889.26)
  • 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 COG0264
  • Curated reference: UniProt P9WNM1 (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 — 221 functional partner(s); context anchor rpsB
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003071|Rv2889c|tsf
MANFTAADVKRLRELTGAGMLACKNALAETDGDFDKAVEALRIKGAKDVGKRAERATAEGLVAAKDGALIELNCETDFVAKNAEFQTLADQVVAAAAAAKPADVDALKGASIGDKTVEQAIAELSAKIGEKLELRRVAIFDGTVEAYLHRRSADLPPAVGVLVEYRGDDAAAAHAVALQIAALRARYLSRDDVPEDIVASERRIAEETARAEGKPEQALPKIVEGRLNGFFKDAVLLEQASVSDNKKTVKALLDVAGVTVTRFVRFEVGQA