deaD Resolved · high auto-curated

H37Rv Rv1253 · MTBC0 mtbc0_001342 · 563 aa · 1408414–1410105 MTBC0 (+) · RefSeq NP_215769.1

Genomic neighbourhood (genome browser)

Open in full genome browser →

This gene (outlined) in its genomic context; arrows are neighbouring genes coloured by verdict. Click any gene to navigate. Pan and zoom in the full browser.

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)ATP-dependent RNA helicase DeaD
MTBC0 PGAP re-annotationDEAD/DEAH box helicase
Revised (this work)DEAD/DEAH box helicase. Pfam: DEAD (PF00270.36), Helicase_C (PF00271.38), DeaD_dimer (PF25399.2), DbpA (PF03880.22).
Functional category (TubercuList)information pathways

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

In the literature (TB corpus sweep) 743 publications

743 TB publications mention this gene. 743 publication(s) discuss this gene (592 in a M. tuberculosis context, 108 in other mycobacteria — M. smegmatis (14), M. leprae (11), M. abscessus (8), M. marinum (5)).

Most recent 5 of 743.
PublicationDate
High-throughput screening system for antimycobacterial compounds using in vitro infected cells: construction and application to compounds in the Ōmura Natural Compound Library. doi:10.1128/spectrum.00484-26 2026
Elucidation of the Antimycobacterial Activity of D-Form Human Lactoferricin 1-11 (D-Form hLF 1-11) Against Mycobacterium smegmatis Through Proteomics and Imaging Analysis. doi:10.3390/antibiotics15060607 2026
Immortal genome assumption significantly underestimates replication and death rates of Mycobacterium tuberculosis in mice and monkeys. doi:10.1128/spectrum.03020-25 2026
Radiological Anatomy of the Pelvis and Hind Limb of the Southern Giant Pouched Rat (Cricetomys ansorgei). doi:10.1111/ahe.70142 2026
Autopsy-Based Insights Into Maternal Mortality: A Retrospective Study From a Tertiary Care Center in North India. doi:10.7759/cureus.108077 2026

This layer CITES the literature and adds context; it does not change the verdict or the function stated elsewhere in this fiche. This distinguishes a gene that is dark because nobody has looked from one that is dark despite having been studied. Source: PubMed (whole): H37Rv locus tag + GENE NAME + ortholog identifiers (Mb…, MMAR_…, MSMEG_…, ML…, MAB_…), under a mycobacterial context filter; hits verified against the abstract text. Species-context counts distinguish M. tuberculosis literature from literature on other mycobacteria. phase76/phase77, 2026-07-13.

Genomic-neighbour overlap (structural caveat) co-directional · 0 % of gene

NeighbourRv1254 (Rv1254, + strand)
Overlap4 bp, 0 % of this gene's length

co-directional overlap: ordinary (e.g. shared stop/start codons in an operon), not the Rv2438A-type artefact P20.1, derived from GFF3 gene coordinates, 2026-08-03.

CRISPRi vulnerability

Vulnerability index 0.65 (95% CI -2.26 to 4.45). A more negative index = more vulnerable to knockdown (better drug-target quality); indicative threshold VI ≤ -6 = highly vulnerable.

Quantitative CRISPRi knockdown, graded (finer than binary Tn-seq essentiality). Source: CRISPRi vulnerability index (Bosch 2021, pebble.rockefeller.edu).

Legacy record & comparison (Mycobrowser)

Mycobrowser functionHas a helix-destabilizing activity
Mycobrowser EC 3.6.4.13 · agrees with the atlas

The legacy Mycobrowser record is shown for verification. Mycobrowser is no longer maintained; its EC numbers predate recent nomenclature revisions, so a class change usually reflects re-numbering, not a conflict.

Orthologues (reciprocal best hits across mycobacteria)

M. bovis Mb1285 · 99.8% identity
M. marinum MMAR_4189 · 83.4% identity
M. smegmatis MSMEG_5042 · 75.2% identity
M. orygis RJtmp_001319 · 99.8% identity
M. abscessus MAB_1403 · 75.0% identity

Reciprocal-best-hit orthologues (DIAMOND) against the Mycobrowser reference proteomes. A missing species is informative: e.g. a gene absent from M. leprae was likely lost in its reductive genome evolution. Locus tags link to Mycobrowser.

Curated reference (UniProt)

UniProt P9WH05 SwissProt · reviewed · Evidence at protein level
UniProt nameATP-dependent RNA helicase DeaD
EC (curated) EC 3.6.4.13
Curated functionDEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category J Translation, ribosomal structure and biogenesis
K Transcription
L Replication, recombination and repair
Preferred namedeaD
eggNOG descriptionDEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation
Orthologous groupCOG0513
EC number EC 3.6.4.13
KEGG orthology K05592, K11927
KEGG pathways map03018
Gene Ontology (43) GO:0003674, GO:0003724, GO:0003824, GO:0004004, GO:0004386, GO:0005575, GO:0005618, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0006139 +31 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 1.181 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 10 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.

Outgroup conservation (beyond the MTBC) Bacteria

M. canettii dN/dS (deep-divergence selection) 0.266 · 16 consensus substitution(s)
under purifying selection vs M. canettii (deep divergence; dN/dS=0.266) — a real, constrained gene predating the MTBC clonal expansion
Genus-wide presence (~53 non-MTBC Mycobacterium) present in 53/53 (100%) · mean identity 78.8% · 4/4 closest MTBAP relatives
conserved across the genus (present in 53/53 non-MTBC Mycobacterium genomes, incl. distant relatives) — an ancient core gene predating the genus radiation
Phylostratum (deepest detected homolog) MTBC-specific Mycobacterium Mycobacteriaceae Corynebacteriales Actinomycetia Bacteria
detected in 13/13 non-Mycobacterium reference genomes (down to Bacteria) · mean identity 56.0%
detected down to outside the phylum (Proteobacteria/Firmicutes controls) — a universally conserved, ancient bacterial gene

Two orthogonal outgroup signals. M. canettii (the immediate outgroup) gives a deep-divergence dN/dS (a low value confirms a constrained, real gene; shown as confident only at ≥8 substitutions, else flagged low-power). Genus-wide presence/absence (tblastn vs assembled non-MTBC genomes) places the gene on the ancient-core ↔ MTBC-specific axis: a gene absent even from the closest MTBAP relatives is a candidate MTBC-specific innovation (possible host-adaptation factor, to confirm by synteny). The phylostratum extends that axis outside the genus (tblastn vs 13 reference genomes spanning Mycobacteriaceae → Corynebacteriales → Actinomycetia → outside the phylum): it is the deepest clade in which a homolog is still detected, i.e. a proxy for gene age. Read it with the null model in mind: a shallow (young) stratum can also reflect homology-detection failure for short or fast-evolving ORFs, so it is a descriptive axis, not a proof of novelty.

Essentiality (transposon mutagenesis)

DeJesus 2017 callNE · non-essential
What the call meansnon-essential
TA sites (Himar1) 35 in the ORF — 0 in the essential state, 0 growth-defect, 35 non-essential, 0 growth-advantage. Saturation 0.829, mean read count 70.5862068966. A region of the protein devoid of TA sites is invisible to this assay: nothing can be inferred about it, in either direction.

Genome-wide Himar1 transposon essentiality in H37Rv (DeJesus 2017). An essential call (ES/ESD/GD) is strong, independent evidence that a "hypothetical" locus encodes a functional, selectively required gene — orthogonal to intra-species conservation.

Mutant phenotypes (conditional Tn-seq, MtbTnDB)

Conditionlog2FCqEffect
fitness after prolonged in vitro passage (in vitro passage) -2.080.0 required

Conditional fitness of transposon-disruption mutants across 1 significant condition(s) (|log2FC|≥1, q≤0.05), from the standardized MtbTnDB compendium. A negative log2FC means the mutant is depleted — the gene contributes to fitness in that condition. An in-vivo defect for a "hypothetical" is strong evidence it matters for infection, even without a known molecular function. Disruption (Tn insertion), not a clean deletion; genetic-interaction screens excluded.

Proteomics (mass spectrometry) detected

MS detectiondetected in 14 of 16 independent MS datasets
Integrated abundance27.2 ppm · rank 2127/3519 (39.6th percentile)

Detection by mass spectrometry is direct, experimental evidence that the protein product exists — orthogonal to sequence conservation and to Tn-seq essentiality, and especially decisive for a "hypothetical" locus. Reproducible detection across several independent datasets (PaxDb) makes the existence claim robust; the integrated abundance places the protein in the proteome's dynamic range.

Physico-chemical properties (computed, ProtParam)

Length563 aa
Molecular weight61.4 kDa
Theoretical pI9.34
GRAVY-0.168 (hydrophilic)
Aliphatic index95.2
Aromaticity0.055
Instability index40.4 (unstable)

Computed from the ancestral MTBC0 sequence with the ExPASy ProtParam method (Biopython). Descriptive biophysical context: a positive GRAVY flags a hydrophobic (often membrane) protein, a high instability index (>40) predicts a short in-vitro half-life, an extreme pI hints at compartment or binding partner.

Domains (Pfam, hmmscan --cut_ga)

PfamAccessioni-EvalueResiduesDescription
DEADPF00270.36 1.1e-4737–202 DEAD/DEAH box helicase
Helicase_CPF00271.38 1.5e-30237–345 Helicase conserved C-terminal domain
DeaD_dimerPF25399.2 1.7e-22379–444 RNA helicase DeaD dimerization domain
DbpAPF03880.22 9.6e-21471–540 DbpA RNA binding domain

Structural search (AlphaFold DB model, Foldseek vs PDB — genome-wide) pLDDT 85.0

PDB hitprobTM-scoreE-valueDescription
7pli-assembly3_I 1.00 0.78 7.2e-43 sig 7pli-assembly3_I DEAD-box helicase DbpA bound to single stranded RNA and ADP/BeF3
7pli-assembly1_B 1.00 0.77 2.6e-42 sig 7pli-assembly1_B DEAD-box helicase DbpA bound to single stranded RNA and ADP/BeF3
8enk-assembly1_A 1.00 0.94 2.0e-37 sig 8enk-assembly1_A Crystal structure of UAP56 in complex with Tho1, the yeast homolog of human SARNP
7pli-assembly2_F 1.00 0.77 1.9e-41 sig 7pli-assembly2_F DEAD-box helicase DbpA bound to single stranded RNA and ADP/BeF3
8c6j-assembly1_7 1.00 0.94 1.2e-37 sig 8c6j-assembly1_7 Human spliceosomal PM5 C* complex

Foldseek search of the AlphaFold DB model (mean pLDDT 85.0, gated at 70) against the PDB — a genome-wide extension of the ESMFold dark-gene search that also covers proteins beyond the single-sequence length limit. Confident structural neighbours (E < 0.01) shown.

Genomic context (neighbours & predicted operon) operon of 2

Upstream (5' on genome)lprE (- strand, 65 bp gap)
Downstream (3' on genome)Rv1254 (+ strand, -4 bp gap)
Predicted operon deaD · Rv1254

Neighbours from the H37Rv annotation (+ strand). The operon is predicted by co-directional intergenic distance (same strand, gaps ≤50 bp) — a transcription-unit hypothesis, not a mapped TSS. For a "hypothetical", co-transcription with a characterised operon is a concrete functional lead (complements the STRING neighborhood channel below).

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

Explore full network →

Node colour = verdict, dashed = hypothetical; edge colour = evidence (green experimental, orange genomic-context, grey co-expression), width ∝ score. Click a partner to open its page; "Explore full network" to walk the graph.

Closest characterised functional partner: Rv1254 (acyltransferase), high confidence from genomic context alone (score 884 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv3433c nnr exp bifunctional ADP-dependent (S)-NAD(P)H-hydrate dehydratase/NAD(P)H-hydrate epimerase 933 926 experimental:781 database:659
Rv0702 rplD exp 50S ribosomal protein L4 920 912 coexpression:404 experimental:722 database:508
Rv3443c rplM exp 50S ribosomal protein L13 897 889 experimental:798
Rv1254 acyltransferase 884 884 ctx neighborhood:881
Rv0701 rplC exp 50S ribosomal protein L3 891 877 coexpression:423 experimental:796
Rv0120c fusA2 exp elongation factor G 872 861 experimental:597 database:626
Rv0684 fusA1 exp elongation factor G 872 861 experimental:597 database:626
Rv3458c rpsD exp 30S ribosomal protein S4 874 859 database:662
Rv0009 ppiA exp iron-regulated peptidyl-prolyl cis-trans isomerase PpiA 861 853 experimental:473 database:626
Rv2582 ppiB exp peptidyl-prolyl cis-trans isomerase B 856 848 experimental:473 database:626
Rv2101 helZ exp helicase HelZ 844 824 experimental:434 database:621
Rv0715 rplX exp 50S ribosomal protein L24 843 824 experimental:814
Rv0721 rpsE exp 30S ribosomal protein S5 829 812 database:662
Rv2783c gpsI exp bifunctional guanosine pentaphosphate synthetase/polyribonucleotide nucleotidyltransferase 881 810 coexpression:405 experimental:676 textmining:403
Rv0714 rplN exp 50S ribosomal protein L14 810 810 experimental:783

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 exp badge marks an experimentally-supported partner (measured interaction, experimental/database channel ≥400) as opposed to a purely predicted one — but note that the M. tuberculosis experimental interactome is dominated by a noisy bacterial-two-hybrid screen, so a strong measured link that contradicts the operon/localisation context is likely a false positive. 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: ATP-dependent RNA helicase DeaD
  • MTBC0 PGAP product: DEAD/DEAH box helicase
  • Pfam (hmmscan --cut_ga): DEAD PF00270.36 (E=1e-47), Helicase_C PF00271.38 (E=1e-30), DeaD_dimer PF25399.2 (E=2e-22), DbpA PF03880.22 (E=1e-20)
  • (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_215769.1)
  • Domains: Pfam-A via hmmscan --cut_ga — DEAD (PF00270.36), Helicase_C (PF00271.38), DeaD_dimer (PF25399.2), DbpA (PF03880.22)
  • 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 COG0513
  • Curated reference: UniProt P9WH05 (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)
  • Genome-wide structure: AlphaFold DB model (Jumper et al. 2021, doi:10.1038/s41586-021-03819-2; Varadi et al. 2024, doi:10.1093/nar/gkad1011) searched vs PDB with Foldseek (mean pLDDT 85.0)
  • Interaction network: STRING v12.0 (Szklarczyk et al. 2023, doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 — 166 functional partner(s); context anchor Rv1254
  • Essentiality: genome-wide transposon mutagenesis in H37Rv — DeJesus et al. 2017 (mBio, doi:10.1128/mBio.02133-16, CC BY)
  • Proteomics: integrated mass-spectrometry abundance from PaxDb 5.0 (Huang et al. 2023, doi:10.1016/j.mcpro.2023.100640), taxon 83332 — weighted average of 16 datasets, incl. Schubert et al. 2013 (doi:10.1016/j.chom.2013.04.008) and Albrethsen et al. 2013 (doi:10.1074/mcp.M112.018846)
  • Functional category: TubercuList scheme (Cole et al. 1998, doi:10.1038/31159), via Mycobrowser (Kapopoulou et al. 2011, doi:10.1016/j.tube.2010.09.006)
  • Orthologues: reciprocal best hits (DIAMOND, Buchfink et al. 2021, doi:10.1038/s41592-021-01101-x) against Mycobrowser release 5 reference proteomes
  • Genomic context / operon: H37Rv annotation; operon predicted by co-directional intergenic distance (Salgado et al. 2000, doi:10.1073/pnas.030539397)
  • Mutant phenotypes: standardized Tn-seq compendium MtbTnDB (Jinich et al. 2025, doi:10.1111/mmi.15370), aggregating many primary Tn-seq studies across conditions
  • Physico-chemical properties: ExPASy ProtParam method via Biopython (Gasteiger et al. 2005), computed from the MTBC0 sequence
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001342|Rv1253|deaD
MAFPEYSPAASAATFADLQIHPRVLRAIGDVGYESPTAIQAATIPALMAGSDVVGLAQTGTGKTAAFAIPMLSKIDITSKVPQALVLVPTRELALQVAEAFGRYGAYLSQLNVLPIYGGSSYAVQLAGLRRGAQVVVGTPGRVIDHLERATLDLSRVDFLVLDEADEMLTMGFADDVERILSETPEYKQVALFSATMPPAIRKLSAKYLHDPFEVTCKAKTAVAENISQSYIQVARKMDALTRVLEVEPFEAMIVFVRTKQATEEIAEKLRARGFSAAAISGDVPQAQRERTITALRDGDIDILVATDVAARGLDVERISHVLNYDIPHDTESYVHRIGRTGRAGRSGAALIFVSPRELHLLKAIEKATRQTLTEAQLPTVEDVNTQRVAKFADSITNALGGPGIELFRRLVEEYEREHDVPMADIAAALAVQCRGGEAFLMAPDPPLSRRNRDQRRDRPQRPKRRPDLTTYRVAVGKRHKIGPGAIVGAIANEGGLHRSDFGQIRIGPDFSLVELPAKLPRATLKKLAQTRISGVLIDLRPYRPPDAARRHNGGKPRRKHVG