rnc Resolved · high auto-curated

H37Rv Rv2925c · MTBC0 mtbc0_003108 · 240 aa · 3260826–3261548 (-) · RefSeq NP_217441.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)ribonuclease III
MTBC0 PGAP re-annotationribonuclease III
Revised (this work)Ribonuclease III. Pfam: Ribonucleas_3_3 (PF14622.12), Ribonuclease_3 (PF00636.32), dsrm (PF00035.33).

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

Curated reference (UniProt)

UniProt P9WH03 SwissProt · reviewed · Evidence at protein level
UniProt nameRibonuclease 3
EC (curated) EC 3.1.26.3
Curated functionDigests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre-crRNA and tracrRNA of type II CRISPR loci if present in the organism (By similarity).

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category J Translation, ribosomal structure and biogenesis
Preferred namernc
eggNOG descriptionDigests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism
Orthologous groupCOG0571
EC number EC 3.1.26.3
KEGG orthology K03685
KEGG pathways map03008, map05205
Gene Ontology (40) GO:0003674, GO:0003676, GO:0003723, GO:0003725, GO:0003824, GO:0004518, GO:0004519, GO:0004521, GO:0004525, GO:0004540, GO:0005488, GO:0006139 +28 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 0.36 · purifying
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 1 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
Ribonucleas_3_3PF14622.12 9.1e-3718–144 Ribonuclease-III-like
Ribonuclease_3PF00636.32 1.6e-2241–134 Ribonuclease III domain
dsrmPF00035.33 4.9e-17162–227 Double-stranded RNA binding motif

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv2441c rpmA 50S ribosomal protein L27 955 951 coexpression:405 experimental:918
Rv0979A rpmF 50S ribosomal protein L32 947 947 experimental:917
Rv3442c rpsI 30S ribosomal protein S9 957 945 experimental:916
Rv0708 rplP 50S ribosomal protein L16 944 941 experimental:914
Rv2926c hyp hypothetical protein 992 939 ctx neighborhood:882 coexpression:505 textmining:877
Rv2904c rplS 50S ribosomal protein L19 945 938 experimental:923
Rv3443c rplM 50S ribosomal protein L13 952 937 experimental:919
Rv0706 rplV 50S ribosomal protein L22 940 936 experimental:920
Rv2785c rpsO 30S ribosomal protein S15 967 934 experimental:917 textmining:519
Rv3456c rplQ 50S ribosomal protein L17 942 934 experimental:917
Rv0682 rpsL 30S ribosomal protein S12 939 931 experimental:910
Rv2909c rpsP 30S ribosomal protein S16 937 930 experimental:916
Rv0723 rplO 50S ribosomal protein L15 934 930 experimental:916
Rv0702 rplD 50S ribosomal protein L4 936 929 experimental:910
Rv2890c rpsB 30S ribosomal protein S2 933 926 experimental:911

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: ribonuclease III
  • MTBC0 PGAP product: ribonuclease III
  • Pfam (hmmscan --cut_ga): Ribonucleas_3_3 PF14622.12 (E=9e-37), Ribonuclease_3 PF00636.32 (E=2e-22), dsrm PF00035.33 (E=5e-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_217441.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Ribonucleas_3_3 (PF14622.12), Ribonuclease_3 (PF00636.32), dsrm (PF00035.33)
  • 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 COG0571
  • Curated reference: UniProt P9WH03 (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 — 182 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003108|Rv2925c|rnc
MIRSRQPLLDALGVDLPDELLSLALTHRSYAYENGGLPTNERLEFLGDAVLGLTITDALFHRHPDRSEGDLAKLRASVVNTQALADVARRLCAEGLGVHVLLGRGEANTGGADKSSILADGMESLLGAIYLQHGMEKAREVILRLFGPLLDAAPTLGAGLDWKTSLQELTAARGLGAPSYLVTSTGPDHDKEFTAVVVVMDSEYGSGVGRSKKEAEQKAAAAAWKALEVLDNAMPGKTSA