Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | hypothetical protein |
| MTBC0 PGAP re-annotation | ribosome-associated translation inhibitor RaiA |
| Revised (this work) | Ribosome-associated translation inhibitor RaiA. Pfam: Ribosomal_S30AE (PF02482.26), Ribosom_S30AE_C (PF16321.11). |
Auto-curated: this verdict and function were generated by rules from
PGAP + Pfam + Foldseek and have not been hand-reviewed.
Curated reference (UniProt)
| UniProt |
O05886
SwissProt · reviewed
· Evidence at protein level
|
| UniProt name | Ribosome hibernation promotion factor |
| Curated function | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase; 100S ribosomes are translationally inactive and sometimes present during exponential growth. |
Functional vocabulary (eggNOG-mapper, orthology transfer)
| COG category |
J Translation, ribosomal structure and biogenesis
|
| Preferred name | hpf |
| eggNOG description | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase |
| Orthologous group | COG1544 |
| KEGG orthology |
K05808
|
| Gene Ontology (64) |
GO:0003674, GO:0005488, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0005840, GO:0006417, GO:0006448, GO:0008150, GO:0009889 +52 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 |
0.484 · purifying
|
| Polymorphic sites (≥ 0.1% of strains) |
2 synonymous, 3 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)
| Pfam | Accession | i-Evalue | Residues | Description |
Ribosomal_S30AE | PF02482.26 |
1.0e-19 | 16–112 |
Sigma 54 modulation protein / S30EA ribosomal protein |
Ribosom_S30AE_C | PF16321.11 |
1.8e-26 | 155–210 |
Sigma 54 modulation/S30EA ribosomal protein C terminus |
Functional interaction network (STRING v12, guilt-by-association)
| Partner | Product | Score | No text-mining | Channels (≥400) |
Rv0053 rpsF |
30S ribosomal protein S6 |
999 |
999 |
experimental:999 |
Rv3442c rpsI |
30S ribosomal protein S9 |
998 |
999 |
experimental:997 database:540 |
Rv0707 rpsC |
30S ribosomal protein S3 |
998 |
999 |
experimental:997 database:540 |
Rv2785c rpsO |
30S ribosomal protein S15 |
943 |
941 |
experimental:870 database:540 |
Rv0721 rpsE |
30S ribosomal protein S5 |
943 |
939 |
experimental:870 database:540 |
Rv0705 rpsS |
30S ribosomal protein S19 |
940 |
938 |
experimental:870 database:540 |
Rv0710 rpsQ |
30S ribosomal protein S17 |
940 |
938 |
experimental:870 database:540 |
Rv0683 rpsG |
30S ribosomal protein S7 |
939 |
938 |
experimental:870 database:540 |
Rv3459c rpsK |
30S ribosomal protein S11 |
938 |
938 |
experimental:870 database:540 |
Rv0055 rpsR1 |
30S ribosomal protein S18 |
937 |
938 |
experimental:870 database:540 |
Rv0718 rpsH |
30S ribosomal protein S8 |
937 |
938 |
experimental:870 database:540 |
Rv2890c rpsB |
30S ribosomal protein S2 |
937 |
938 |
experimental:870 database:540 |
Rv2055c rpsR2 |
30S ribosomal protein S18 |
937 |
938 |
experimental:870 database:540 |
Rv0709 rpmC |
50S ribosomal protein L29 |
925 |
918 |
experimental:870 |
Rv1630 rpsA |
30S ribosomal protein S1 |
914 |
911 |
experimental:806 database:540 |
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: ribosome-associated translation inhibitor RaiA
- Pfam (hmmscan --cut_ga): Ribosomal_S30AE PF02482.26 (E=1e-19), Ribosom_S30AE_C PF16321.11 (E=2e-26)
- (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_217758.3)
- Domains: Pfam-A via hmmscan --cut_ga — Ribosomal_S30AE (PF02482.26), Ribosom_S30AE_C (PF16321.11)
- 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
COG1544
- Curated reference: UniProt
O05886
(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 —
106 functional partner(s)
- Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_003449|Rv3241c|raiA
MDSGQVLAEPKSNAEIVFKGRNVEIPDHFRIYVSQKLARLERFDRTIYLFDVELDHERNRRQRKSCQRVEITARGRGPVVRGEACADSFYAALESAVVKLESRLRRGKDRRKVHYGDKTPVSLAEATAVVPAPENGFNTRPAEAHDHDGAVVEREPGRIVRTKEHPAKPMSVDDALYQMELVGHDFFLFYDKDTERPSVVYRRHAYDYGLIRLA
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