Rv3837c Family assigned · medium auto-curated

H37Rv Rv3837c · MTBC0 mtbc0_004067 · 232 aa · 4335120–4335818 (-) · RefSeq NP_218354.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)phosphoglycerate mutase
MTBC0 PGAP re-annotationhistidine phosphatase family protein
Revised (this work)Histidine phosphatase family protein. Pfam: His_Phos_1 (PF00300.28).

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

Curated reference (UniProt)

UniProt P96241 TrEMBL · unreviewed · Evidence at protein level
UniProt nameProbable phosphoglycerate mutase

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category G Carbohydrate transport and metabolism
Preferred namepgmB
eggNOG descriptionBelongs to the phosphoglycerate mutase family
Orthologous groupCOG0406

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 0.34 · purifying
Polymorphic sites (≥ 0.1% of strains) 4 synonymous, 3 missense, 1 nonsense, 1 frameshift
Disruption 2 distinct premature-stop/frameshift site(s); most common in 0.26% of strains (380) · 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
His_Phos_1PF00300.28 1.1e-335–202 Histidine phosphatase superfamily (branch 1)

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

Closest characterised functional partner: pheA (prephenate dehydratase), high confidence from genomic context alone (score 884 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv3838c pheA prephenate dehydratase 884 884 ctx neighborhood:882
Rv0563 htpX protease HtpX 811 812 coexpression:806
Rv3839 hyp hypothetical protein 783 782 ctx neighborhood:781
Rv0983 pepD serine protease PepD 760 761 coexpression:757
Rv3840 transcriptional regulator 538 538 ctx neighborhood:532
Rv2066 cobIJ bifunctional S-adenosyl-L-methionine-precorrin-2 methyl transferase/precorrin-3 methylase 540 520 coexpression:459
Rv1437 pgk phosphoglycerate kinase 639 512 database:500
Rv1023 eno enolase 749 504 database:500 textmining:515
Rv2743c hyp hypothetical protein 470 471
Rv2373c dnaJ2 chaperone protein DnaJ 459 460
Rv2609c membrane protein 437 438
Rv0255c cobQ1 cobyric acid synthase 456 431 coexpression:412
Rv2869c rip zinc metalloprotease 416 416
Rv1747 ABC transporter ATP-binding protein/permease 409 410
Rv3214 gpm2 phosphoglycerate mutase 693 361 textmining: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: phosphoglycerate mutase
  • MTBC0 PGAP product: histidine phosphatase family protein
  • Pfam (hmmscan --cut_ga): His_Phos_1 PF00300.28 (E=1e-33)
  • (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_218354.1)
  • Domains: Pfam-A via hmmscan --cut_ga — His_Phos_1 (PF00300.28)
  • 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 COG0406
  • Curated reference: UniProt P96241 (TrEMBL, unreviewed; 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 — 27 functional partner(s); context anchor pheA
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_004067|Rv3837c|
MSGRLVLLRHGQSYGNVERRLDTLPPGTALTPLGRDQARAFARSGCRRPALLAHSVAIRAYQTAAVVAAELDMVAHEVAGIHEVQVGELENRNDDEAVAEFNATYSRWHRGELDVPLPGGETANDVLDRYLPVLADLRMRYLDDGDWDGDIVVVSHSAAIRLAAAVLAGVDGNFVLDNHLENVESVVLAPITDGRWSCVQWGLRKPPFCPDPAEAAASPVTHAVTSSTDPMG