Rv0712 Family assigned · medium auto-curated

H37Rv Rv0712 · MTBC0 mtbc0_000754 · 299 aa · 812939–813838 (+) · RefSeq NP_215226.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationformylglycine-generating enzyme family protein
Revised (this work)Formylglycine-generating enzyme family protein. Pfam: FGE-sulfatase (PF03781.23).

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

Curated reference (UniProt)

UniProt I6Y8I5 SwissProt · reviewed · Evidence at protein level
UniProt nameFormylglycine-generating enzyme
EC (curated) EC 1.8.3.7
Curated functionOxidase that catalyzes the conversion of cysteine to 3-oxoalanine on target proteins. 3-oxoalanine modification, which is also named formylglycine (fGly), occurs in the maturation of arylsulfatases and some alkaline phosphatases that use the hydrated form of 3-oxoalanine as a catalytic nucleophile.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
Preferred namepkn1
eggNOG descriptionSulfatase-modifying factor enzyme 1
Orthologous groupCOG1262
Gene Ontology (24) GO:0003674, GO:0003824, GO:0006464, GO:0006807, GO:0008150, GO:0008152, GO:0009987, GO:0016491, GO:0016667, GO:0016670, GO:0018158, GO:0019538 +12 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 0.0 · strong purifying
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 0 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
FGE-sulfatasePF03781.23 1.3e-872–293 Sulfatase-modifying factor enzyme 1-like domain

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

Closest characterised functional partner: atsA (arylsulfatase AtsA), high confidence from genomic context alone (score 979 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv3077 hydrolase 981 982 experimental:973
Rv0711 atsA arylsulfatase AtsA 978 979 ctx neighborhood:814 cooccurence:734 experimental:430
Rv3299c atsB arylsulfatase AtsB 846 846 ctx cooccurence:721 experimental:430
Rv0296c sulfatase 844 845 ctx cooccurence:706 experimental:430
Rv0663 atsD arylsulfatase AtsD 841 841 ctx cooccurence:712 experimental:430
Rv0713 transmembrane protein 480 481 ctx neighborhood:481
Rv2378c mbtG L-lysine N6-monooxygenase 447 420 coexpression:401
Rv0709 rpmC 50S ribosomal protein L29 406 406 ctx neighborhood:404
Rv0705 rpsS 30S ribosomal protein S19 406 406 ctx neighborhood:404
Rv0708 rplP 50S ribosomal protein L16 406 406 ctx neighborhood:404
Rv0707 rpsC 30S ribosomal protein S3 406 406 ctx neighborhood:404
Rv0710 rpsQ 30S ribosomal protein S17 404 404 ctx neighborhood:404
Rv0706 rplV 50S ribosomal protein L22 404 404 ctx neighborhood:404
Rv3701c egtD histidine-specific methyltransferase EtgD 639 246 textmining:541
Rv2407 rnz ribonuclease Z 891 200 textmining:870

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: formylglycine-generating enzyme family protein
  • Pfam (hmmscan --cut_ga): FGE-sulfatase PF03781.23 (E=1e-87)
  • (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_215226.1)
  • Domains: Pfam-A via hmmscan --cut_ga — FGE-sulfatase (PF03781.23)
  • 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 COG1262
  • Curated reference: UniProt I6Y8I5 (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 — 29 functional partner(s); context anchor atsA
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000754|Rv0712|
MLTELVDLPGGSFRMGSTRFYPEEAPIHTVTVRAFAVERHPVTNAQFAEFVSATGYVTVAEQPLDPGLYPGVDAADLCPGAMVFCPTAGPVDLRDWRQWWDWVPGACWRHPFGRDSDIADRAGHPVVQVAYPDAVAYARWAGRRLPTEAEWEYAARGGTTATYAWGDQEKPGGMLMANTWQGRFPYRNDGALGWVGTSPVGRFPANGFGLLDMIGNVWEWTTTEFYPHHRIDPPSTACCAPVKLATAADPTISQTLKGGSHLCAPEYCHRYRPAARSPQSQDTATTHIGFRCVADPVSG