deaD Resolved · high auto-curated
H37Rv Rv1253 · MTBC0 mtbc0_001342 ·
563 aa ·
1408414–1410105 MTBC0
(+) ·
RefSeq NP_215769.1
Genomic neighbourhood (genome browser)
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Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | ATP-dependent RNA helicase DeaD |
|---|---|
| MTBC0 PGAP re-annotation | DEAD/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)).
| Publication | Date |
|---|---|
| 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
| Neighbour | Rv1254 (Rv1254, + strand) |
|---|---|
| Overlap | 4 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 function | Has 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 name | ATP-dependent RNA helicase DeaD |
| EC (curated) |
EC 3.6.4.13
|
| Curated function | DEAD-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 biogenesisK TranscriptionL Replication, recombination and repair
|
|---|---|
| Preferred name | deaD |
| eggNOG description | DEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation |
| Orthologous group | COG0513 |
| 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 call | NE · non-essential |
|---|---|
| What the call means | non-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)
| Condition | log2FC | q | Effect |
|---|---|---|---|
| fitness after prolonged in vitro passage (in vitro passage) | -2.08 | 0.0 | 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 detection | detected in 14 of 16 independent MS datasets |
|---|---|
| Integrated abundance | 27.2 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)
| Length | 563 aa |
|---|---|
| Molecular weight | 61.4 kDa |
| Theoretical pI | 9.34 |
| GRAVY | -0.168 (hydrophilic) |
| Aliphatic index | 95.2 |
| Aromaticity | 0.055 |
| Instability index | 40.4 (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)
| Pfam | Accession | i-Evalue | Residues | Description |
|---|---|---|---|---|
DEAD | PF00270.36 | 1.1e-47 | 37–202 | DEAD/DEAH box helicase |
Helicase_C | PF00271.38 | 1.5e-30 | 237–345 | Helicase conserved C-terminal domain |
DeaD_dimer | PF25399.2 | 1.7e-22 | 379–444 | RNA helicase DeaD dimerization domain |
DbpA | PF03880.22 | 9.6e-21 | 471–540 | DbpA RNA binding domain |
Structural search (AlphaFold DB model, Foldseek vs PDB — genome-wide) pLDDT 85.0
| PDB hit | prob | TM-score | E-value | Description |
|---|---|---|---|---|
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).
| Partner | Product | Score | No text-mining | Channels (≥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
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