Family Search for PF01933 (CofD)
April 2024: See Interactive Tools for Functional Annotation of Bacterial Genomes for advice on using these tools.
Running HMMer for PF01933
PF01933 hits 43 sequences in PaperBLAST's database above the trusted cutoff. Showing all hits. Or show only hits to curated sequences or try another family.
GNGF_BACSU / O06974 Gluconeogenesis factor from Bacillus subtilis (strain 168) (see 2 papers)
BSU34760 gluconeogenesis factor from Bacillus subtilis subsp. subtilis str. 168
NP_391356 gluconeogenesis morphogenetic factor (UDP-sugar binding) from Bacillus subtilis subsp. subtilis str. 168
Aligns to 7:293 / 317 (90.5%), covers 99.7% of PF01933, 405.1 bits
- function: Required for morphogenesis under gluconeogenic growth conditions. Required, in gluconeogenic growth conditions, for the correct localization of PBP1 and hence for displaying a normal rod shape.
disruption phenotype: Deletion leads to growth defects when cells are grown on minimal medium containing ribose, gluconate, citrate, fumarate or succinate, but does not affect growth and morphology on minimal medium containing glycolytic substrates such as glucose, sucrose or glycerol. Mutants exhibit media-dependent filamentous or L-shape-like aberrant morphologies. - The Blueprint of a Minimal Cell: MiniBacillus
Reuß, Microbiology and molecular biology reviews : MMBR 2016 - “...3ZIH 4UG3 B. subtilis B. subtilis B. subtilis yvcK BSU34760 No 2HZB B. halodurans BSU34750 No 3HYI T. maritima BSU15420 No 2WUJ B. subtilis minC BSU28000 No...”
- YvcK of Bacillus subtilis is required for a normal cell shape and for growth on Krebs cycle intermediates and substrates of the pentose phosphate pathway.
Görke, Microbiology (Reading, England) 2005 (PubMed)- GeneRIF: important role in carbon metabolism, probably in gluconeogenesis required for the synthesis of cell wall precursor molecules
alr2298 hypothetical protein from Nostoc sp. PCC 7120
Aligns to 139:426 / 456 (63.2%), covers 99.7% of PF01933, 404.7 bits
sll0154 hypothetical 35.6 kD protein from Synechocystis sp. PCC 6803
Aligns to 149:435 / 462 (62.1%), covers 100.0% of PF01933, 404.1 bits
- Identification of the key functional genes in salt-stress tolerance of Cyanobacterium Phormidium tenue using in silico analysis
Shahbazi, 3 Biotech 2021 - “...sll0821 hypothetical protein, ssr3188 mrgA, slr1894 cruE, sll0154 lspA, slr1366 pbpD, sll1167 fdp, slr0952 cbiO, sll0385 putative peptidase, sll1369 nrsB,...”
- The Biosynthetic pathway for synechoxanthin, an aromatic carotenoid synthesized by the euryhaline, unicellular cyanobacterium Synechococcus sp. strain PCC 7002
Graham, Journal of bacteriology 2008 - “...and that in Synechocystis sp. strain PCC 6803 is sll0154. CruE sequences resemble the CrtU sequences of green sulfur bacteria by having a Rieske iron/sulfur...”
- Use of transposon Tn5367 mutagenesis and a nitroimidazopyran-based selection system to demonstrate a requirement for fbiA and fbiB in coenzyme F(420) biosynthesis by Mycobacterium bovis BCG
Choi, Journal of bacteriology 2001 - “...against Synechocystis alone, a weak hit was obtained with SLL0154 (score 44; E 105). The -Blast analysis also revealed a homolog from a Nostoc sp. (also known...”
- “...MJ1256 (Methanococcus) Vng1429c (Halobacterium) MTH1018 (Methanobacterium) SLL0154 (Synechocystis) AAC03105 (Anabaena) Score 575 450 315 126 112 96 83...”
BH3568 hypothetical protein from Bacillus halodurans C-125
Aligns to 6:292 / 322 (89.1%), covers 99.7% of PF01933, 403.4 bits
- Molecular insights into the biosynthesis of the F420 coenzyme
Forouhar, The Journal of biological chemistry 2008 - “...M. jannaschii, and M. tuberculosis, as well as the BH3568 protein from B. gen) and eluted in lysis buffer conhalodurans. The secondary structure elements are...”
- “...nonF420-producing CofD homologs have been determined, including the BH3568 protein from Bacillus halodurans (PDB entries 2HZB and 2O2Z, 24% sequence identity to...”
2o2zA / Q9K706 Crystal structure of a protein member of the upf0052 family (bh3568) from bacillus halodurans at 2.60 a resolution
Aligns to 7:292 / 310 (92.3%), covers 99.7% of PF01933, 400.1 bits
- Ligand: nicotinamide-adenine-dinucleotide (2o2zA)
BC5155 hypothetical Cytosolic Protein from Bacillus cereus ATCC 14579
Aligns to 9:295 / 317 (90.5%), covers 99.0% of PF01933, 384.7 bits
USA300HOU_0795 hypothetical protein from Staphylococcus aureus subsp. aureus USA300_TCH1516
SA0721 hypothetical protein from Staphylococcus aureus subsp. aureus N315
SAOUHSC_00788 hypothetical protein from Staphylococcus aureus subsp. aureus NCTC 8325
SAUSA300_0749 hypothetical protein from Staphylococcus aureus subsp. aureus USA300_FPR3757
SAR0821 conserved hypothetical protein from Staphylococcus aureus subsp. aureus MRSA252
SACOL0831 hypothetical protein from Staphylococcus aureus subsp. aureus COL
Aligns to 6:291 / 331 (86.4%), covers 98.3% of PF01933, 380.1 bits
- Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification
Bianco, Frontiers in cellular and infection microbiology 2023 - “...USA300HOU_0191 (202764) , intergenic (265666) , USA300HOU_0397 (424978) , argS (670365) , intergenic (835434) , USA300HOU_0795 (850349) vwb (876702) , USA300HOU_0938 (982790) , oppD1 (990291) , ebh (1488257) , rluB (1611873) , comGA (1657533) , alaS (1723795) , tyrS (1843158) , USA300HOU_1746) 1877551) , intergenic (1978879)...”
- Insights Into the Impact of Small RNA SprC on the Metabolism and Virulence of Staphylococcus aureus
Zhou, Frontiers in cellular and infection microbiology 2022 - “...rsbV -67.3 SAOUHSC_02881 SA2351 -85.3 SAOUHSC_00871 dltc -66.1 SAOUHSC_01452 ald -84.9 SAOUHSC_03045 cspB -65.7 SAOUHSC_00788 SA0721 -84.4 SAOUHSC_03055 rpmH -61 SAOUHSC_01955 lukE -83.7 SAOUHSC_02853 SA2331 -59.8 SAOUHSC_01424 murG -83.6 SAOUHSC_01336 SA1176 -54.4 SAOUHSC_02329 thiM -82.9 All the mRNAs transcribed by DEGs with defined functions were predicted...”
- Characterizing the effects of inorganic acid and alkaline shock on the Staphylococcus aureus transcriptome and messenger RNA turnover
Anderson, FEMS immunology and medical microbiology 2010 - “...SA0653 hypothetical protein sa_c7835s10216_x_at 4.2 2.5 2.5 SA0654 hypothetical protein sa_c8905s7823_a_at * 6.5 2.5 2.5 SA0721 hypothetical protein sa_c8928s7841_a_at * 4.5 2.5 2.5 SA0755 hypothetical protein sa_c8934s7849_a_at 7.5 2.5 2.5 SA0767 hypothetical protein sa_c8196s7173_a_at 12.2 2.5 stable SA0768 hypothetical protein sa_c8228s7205_a_at * 3.6 2.5 30 SA0777...”
- “...SA0703 hypothetical protein sa_c8013s6998_a_at 26.8 2.5 2.5 SA0711 hypothetical protein sa_c8905s7823_a_at * 2.5 2.5 2.5 SA0721 hypothetical protein sa_c8079s7064_a_at 2.4 2.5 5 SA0734 hypothetical protein sa_c8131s7116_a_at 2.1 2.5 2.5 SA0749 hypothetical protein sa_c8147s7131_a_at 2.6 2.5 2.5 SA0752 hypothetical protein sa_c8151s7135_at 2.2 2.5 ND SA0753 hypothetical protein...”
- Insights Into the Impact of Small RNA SprC on the Metabolism and Virulence of Staphylococcus aureus
Zhou, Frontiers in cellular and infection microbiology 2022 - “...SAOUHSC_02300 rsbV -67.3 SAOUHSC_02881 SA2351 -85.3 SAOUHSC_00871 dltc -66.1 SAOUHSC_01452 ald -84.9 SAOUHSC_03045 cspB -65.7 SAOUHSC_00788 SA0721 -84.4 SAOUHSC_03055 rpmH -61 SAOUHSC_01955 lukE -83.7 SAOUHSC_02853 SA2331 -59.8 SAOUHSC_01424 murG -83.6 SAOUHSC_01336 SA1176 -54.4 SAOUHSC_02329 thiM -82.9 All the mRNAs transcribed by DEGs with defined functions were...”
- A new platform for ultra-high density Staphylococcus aureus transposon libraries
Santiago, BMC genomics 2015 - “...ruvA [ 31 - 34 ] Unknown SAOUHSC_00760 hypothetical protein [ 33 , 34 ] SAOUHSC_00788 hypothetical protein [ 31 , 33 , 34 ] * mprF aiso annotated as fmtC, and lcpA also annotated as msrR. Figure 6 Genes that influence fitness at high temperature....”
- Novel Pathways for Ameliorating the Fitness Cost of Gentamicin Resistant Small Colony Variants
Vestergaard, Frontiers in microbiology 2016 - “...compensation via membrane potential restoration was suppressed, however, selected for secondary mutations in fusA and SAUSA300_0749 . This study is the first to describe fitness compensatory events in SCVs with deletion mutations and adaptation of SCVs to continued exposure to gentamicin. Staphylococcus aureus evolution gentamicin resistance...”
- “...the presence of gentamicin. All of the seven lineages contained mutations in either fusA and/or SAUSA300_0749 , while none of the lineages evolved without gentamicin contained mutations in these genes ( Figure 5 ). The gene fusA encodes the elongation factor G (EF-G) and mutations were...”
- The Staphylococcus aureus response to unsaturated long chain free fatty acids: survival mechanisms and virulence implications
Kenny, PloS one 2009 - “...protein 2.29 4.39E-03 SAR0733 conserved hypothetical protein 3.04 1.99E-03 SAR0734 conserved hypothetical protein 2.23 1.59E-03 SAR0821 conserved hypothetical protein 3.19 6.54E-03 SAR0825 conserved hypothetical protein 5.06 1.86E-03 SAR0840 putative membrane protein 5.25 2.63E-03 SAR0849 hypothetical protein 2.81 6.05E-03 SAR0850 hypothetical protein 2.94 6.81E-04 SAR0854 hypothetical protein...”
- Transcriptomic Adjustments of Staphylococcus aureus COL (MRSA) Forming Biofilms Under Acidic and Alkaline Conditions
Efthimiou, Frontiers in microbiology 2019 - “...| BAB83937.11 SepA multidrug resistance efflux pump 3.38 0.0023 General functions [transporters, DNA-RNA, general] ybhK SACOL0831 pir| B90736 probable structural protein 4.08 0.0340 not found ref | NP_337929.l| phosphate transport system regulator PhoU-related protein 3.35 0.0016 mdlB SACOL2430 502776-1 Predicted CDS, ABC transporter with ABC transporter...”
Eab7_2247 YvcK family protein from Exiguobacterium antarcticum B7
Aligns to 7:294 / 332 (86.7%), covers 99.7% of PF01933, 377.8 bits
lp_0780 unknown from Lactobacillus plantarum WCFS1
Aligns to 13:304 / 333 (87.7%), covers 100.0% of PF01933, 358.8 bits
lmo2473 conserved hypothetical protein from Listeria monocytogenes EGD-e
Aligns to 9:292 / 322 (88.2%), covers 100.0% of PF01933, 358.1 bits
- Vying for the control of inflammasomes: The cytosolic frontier of enteric bacterial pathogen-host interactions
Sanchez-Garrido, Cellular microbiology 2020 - “...release of its DNA and direct activation of the AIM2 inflammasome. A mutant lacking the lmo2473 gene lyses more in the cytosol of infected macrophages and hyperactivates the AIM2ASCcaspase1 inflammasome pathway (Sauer et al., 2010 ). AIM2 expression requires type I IFN signalling, consistent with which,...”
- AIM2 in health and disease: Inflammasome and beyond
Kumari, Immunological reviews 2020 - “...release or by suppressing the priming signals ( 134 137 ). Mutation in L. monocytogenes lmo2473 enhances bacterial lysis in the cytosol thus leading to increased AIM2 activation.( 138 ) Mtb has been reported to inhibit AIM2 inflammasome activation via its type VII secretion system ESX-1-mediated...”
- Evasion of inflammasome activation by microbial pathogens
Ulland, The Journal of clinical investigation 2015 - “...associated induction of host cell death. Mutation of lmo2473, a gene that encodes a protein of unknown function, resulted in L. monocytogenes that...”
- “...linked to impaired cell wall integrity of the lmo2473 mutant, driving an increase in its intracellular lysis. Enhanced bacterial lysis resulted in an increase...”
- Listeria monocytogenes is resistant to lysozyme through the regulation, not the acquisition, of cell wall-modifying enzymes
Burke, Journal of bacteriology 2014 - “...lmo2515 lmo0290 lmo0971 lmo0973 lmo1741 lmo1745 lmo1746 lmo2219 lmo2473 lmo2768 pgdA pbpX rli31 degU walI dltD dltB virS virR Peptidoglycan deacetylase Putative...”
- “...resistance or to the cell wall was unknown. lmo2473 encodes an uncharacterized protein that has been hypothesized to function in the synthesis of peptidoglycan...”
- Listeria monocytogenes induces IFNβ expression through an IFI16-, cGAS- and STING-dependent pathway
Hansen, The EMBO journal 2014 - “...infection with a L. monocytogenes mutant lacking the lmo2473 gene, and which lyses with increased frequency in the macrophage cytosol (Sauer et al, 2010),...”
- Listeria monocytogenes MDR transporters are involved in LTA synthesis and triggering of innate immunity during infection
Tadmor, Frontiers in cellular and infection microbiology 2014 - “...regulator spx family Regulation LMRG_01692.6 lmo2555 Glycosyl transferase LTA LMRG_01693.6 lmo2554 Galactosyl transferase LTA LMRG_01775.6 lmo2473 N/A unknown LMRG_01983.6 lmo2713 Cell wall bound protein, contains 1 GW-repeat Cell surface proteins LMRG_02415.6 lmo0170 Hypothetical protein Unknown LMRG_02642.6 lmo0220 Highly similar to cell division protein ftsH Cell division...”
- PrkC-mediated phosphorylation of overexpressed YvcK protein regulates PBP1 protein localization in Bacillus subtilis mreB mutant cells
Foulquier, The Journal of biological chemistry 2014 - “...essential (15). In Listeria monocytogenes, a mutation in lmo2473, the gene encoding the Rv1422 homolog, causes pyroptosis, followed by bacterial lysis in the...”
- Listeria monocytogenes triggers AIM2-mediated pyroptosis upon infrequent bacteriolysis in the macrophage cytosol
Sauer, Cell host & microbe 2010 - “...identify Listeria monocytogenes mutants that induced altered levels of host cell death. A mutation in lmo2473 resulted in hyper-stimulation of host cell death and IL-1 secretion (pyroptosis) following bacteriolysis in the macrophage cytosol. In addition, strains engineered to lyse in the cytosol by expression of both...”
- “...death. The mutant with the most robust phenotype was identified as a transposon insertion in lmo2473 . Deletion of lmo2473 resulted in mutant bacteria that hyper-induced pyroptosis. Bacterial cell lysis caused either by the loss of lmo2473 , expression of bacteriophage holin and lysin or treatment...”
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LMOSA_4390 YvcK family protein from Listeria monocytogenes str. Scott A
Aligns to 9:292 / 322 (88.2%), covers 100.0% of PF01933, 356.9 bits
LGG_00928 extracellular lipase/esterase precursor from Lactobacillus rhamnosus GG
DU507_04840, LGG_00928 uridine diphosphate-N-acetylglucosamine-binding protein YvcK from Lacticaseibacillus rhamnosus GG
Aligns to 18:311 / 342 (86.0%), covers 100.0% of PF01933, 354.6 bits
stu0832 hypothetical protein from Streptococcus thermophilus LMG 18311
Aligns to 6:298 / 324 (90.4%), covers 100.0% of PF01933, 351.2 bits
SPy0653, SPy_0653 conserved hypothetical protein from Streptococcus pyogenes M1 GAS
Aligns to 6:298 / 325 (90.2%), covers 99.0% of PF01933, 344.5 bits
- Global Analysis and Comparison of the Transcriptomes and Proteomes of Group A Streptococcus Biofilms
Freiberg, mSystems 2016 - “...Hypothetical protein Spy0652 1.4 1.38 2.17 2.14 1.46 1.82 1.79 1.11 Predicted flavin-nucleotide-binding protein R Spy0653 czcD 3.04 2.94 1.82 3.18 3.08 1.96 2.53 2.43 1.31 Cobalt-zinc-cadmium resistance protein P Spy0716 3.93 3.98 2.6 2.5 2.55 1.17 2.15 2.19 0.82 Hypothetical protein Spy0787 1.02 0.95 1.05...”
- Mechanisms of group A Streptococcus resistance to reactive oxygen species
Henningham, FEMS microbiology reviews 2015 - “...etal. , 2011 ), demonstrated that mutants in a putative Zn 2+ efflux/activator system, czcD (Spy_0653) and gzcA (Spy_0654) resulted in increased susceptibility to Zn 2+ and clearance by innate immune cells in vitro and in a mouse model of soft-tissue infection (Ong etal. , 2014...”
- An antimicrobial role for zinc in innate immune defense against group A streptococcus
Ong, The Journal of infectious diseases 2014 (PubMed)- “...mutants were constructed with deletions in the czcD gene (Spy0653; which encodes a putative zinc efflux pump) and adjacent gczA gene (Spy0654; which encodes a...”
- “...addition to zinc uptake systems, GAS possesses czcD (Spy0653), which encodes a cation diffusion facilitator that is associated with resistance of cobalt, zinc,...”
spr1423 Conserved hypothetical protein from Streptococcus pneumoniae R6
Aligns to 6:299 / 325 (90.5%), covers 100.0% of PF01933, 326.8 bits
MXAN_3230 hypothetical protein from Myxococcus xanthus DK 1622
Aligns to 7:300 / 325 (90.5%), covers 99.7% of PF01933, 319.3 bits
YbhK / b0780 putative transferase YbhK from Escherichia coli K-12 substr. MG1655 (see 3 papers)
b0780 predicted transferase with NAD(P)-binding Rossmann-fold domain from Escherichia coli str. K-12 substr. MG1655
Aligns to 12:300 / 302 (95.7%), covers 95.5% of PF01933, 280.1 bits
c0861 Hypothetical protein ybhK from Escherichia coli CFT073
Aligns to 32:320 / 322 (89.8%), covers 95.2% of PF01933, 279.6 bits
VV1197 conserved hypothetical protein from Vibrio vulnificus YJ016
Aligns to 9:294 / 296 (96.6%), covers 95.5% of PF01933, 272.1 bits
- Genome-wide SNP-genotyping array to study the evolution of the human pathogen Vibrio vulnificus biotype 3
Raz, PloS one 2014 - “...lysA, pntA, pyrC and tnaA ) [26] , five conserved hypothetical genes (VV0048, VV0178, VV0415, VV1197 and VV1483) [27] , the 16S rRNA gene [56] , and seven newly selected genes ( S3 Table ). PCRs, sequencing and result analyses of selected loci were performed as...”
STM0801 putative cytoplasmic protein from Salmonella typhimurium LT2
Aligns to 12:300 / 302 (95.7%), covers 95.5% of PF01933, 270.1 bits
KPNIH1_08215 uridine diphosphate-N-acetylglucosamine-binding protein YvcK from Klebsiella pneumoniae subsp. pneumoniae KPNIH1
Aligns to 12:298 / 301 (95.3%), covers 94.5% of PF01933, 268.1 bits
SCO1951 hypothetical protein from Streptomyces coelicolor A3(2)
Aligns to 48:334 / 363 (79.1%), covers 89.0% of PF01933, 248.7 bits
GNGF_MYCTU / P9WMU5 Putative gluconeogenesis factor from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see paper)
NP_215938 hypothetical protein from Mycobacterium tuberculosis H37Rv
Rv1422 hypothetical protein from Mycobacterium tuberculosis H37Rv
WP_003407352 carbon utilization/virulence protein CuvA from Mycobacterium tuberculosis
Aligns to 5:297 / 342 (85.7%), covers 94.1% of PF01933, 247.8 bits
- function: Required for morphogenesis under gluconeogenic growth conditions.
- Mycobacterial gene cuvA is required for optimal nutrient utilization and virulence.
Mir, Infection and immunity 2014 - GeneRIF: Authors name this gene cuvA (carbon utilization and virulence protein A) and suggest a model in which deletion of cuvA leads to changes in nutrient uptake and/or metabolism that affect cell wall structure, morphology, and virulence.
- A proposed carbon-utilization and virulence protein A, CuvA (Rv1422), from Mycobacterium tuberculosis H37Rv: crystallization, X-ray diffraction analysis and ligand binding
Jeong, Acta crystallographica. Section F, Structural biology communications 2020 - “...protein A, CuvA (Rv1422), from Mycobacterium tuberculosis H37Rv: crystallization, X-ray diffraction analysis and ligand binding Yoon Chae Jeong and Ki Seog Lee*...”
- “...of Korea Keywords: Mycobacterium tuberculosis; CuvA (Rv1422); bacterial adaptation; nutrient utilization; cell-wall precursor components. Department of Clinical...”
- Mycobacterial gene cuvA is required for optimal nutrient utilization and virulence
Mir, Infection and immunity 2014 - “...nutrient utilization and alterations in growth rate. M. tuberculosis Rv1422 is a conserved gene of unknown function that was found in a genetic screen to...”
- “...interact with the mce4 cholesterol uptake locus. The Rv1422 protein is phosphorylated by the M. tuberculosis Ser/Thr kinases PknA and PknB, which regulate cell...”
- PrkC-mediated phosphorylation of overexpressed YvcK protein regulates PBP1 protein localization in Bacillus subtilis mreB mutant cells
Foulquier, The Journal of biological chemistry 2014 - “...shape and cell division (12). Interestingly, PknB phosphorylates Rv1422, a protein present in many bacteria, at the single yet non-conserved Thr-325 residue in...”
- “...important functions. For example, in Staphylococcus aureus, the Rv1422 homolog is essential (15). In Listeria monocytogenes, a mutation in lmo2473, the gene...”
- Whole genome sequencing of Mycobacterium tuberculosis reveals slow growth and low mutation rates during latent infections in humans
Colangeli, PloS one 2014 - “...- - G Rv3586 - - - A A - - - - - G Rv1422 - - T - - - - - - - C lldD2 T - - - T T T T T T C fadE21 G - - - G G...”
- Mycobacterium tuberculosis Serine/Threonine Protein Kinases
Prisic, Microbiology spectrum 2014 - “...inhibits protein interactions ( 55 ) Rv0681 Transcriptional regulator In vitro (PknH) ( 116 ) Rv1422 Cell wall synthesis? In vitro (PknA and PknB), in vivo ( 17 ) Rvl747 ABC-transporter? Virulence factor In vitro (multiple kinases), in vivo, FHA domain interacts with kinases, activates (...”
- Eukaryote-like serine/threonine kinases and phosphatases in bacteria
Pereira, Microbiology and molecular biology reviews : MMBR 2011 - “...FtsZ GlmU GroEL1 KasA KasB MabA MurD PknB Rv1422 Wag31 Cell division Cell wall synthesis MurC PknB Cell division eSTK Pathogenesis Transaldolase; central...”
- “...sigma factor; oxidative stress PBPA PknA RshA Rv0020c Rv1422 Rv1747 SigH Putative ABC transporter Mycolic acid biosynthesis Mycolic acid synthesis, cell wall...”
- Extensive phosphorylation with overlapping specificity by Mycobacterium tuberculosis serine/threonine protein kinases
Prisic, Proceedings of the National Academy of Sciences of the United States of America 2010 - “...defined M. tuberculosis phosphoproteins, including four STPKs, GarA, Rv1422, and FhaA (4, 8, 10). The MS/MS search algorithms that we used can identify the...”
- “...at least two M. tuberculosis STPK substrates, GarA and Rv1422 (4, 23). The other implication is that other factors must contribute to in vivo substrate...”
- Phthiocerol dimycocerosate transport is required for resisting interferon-gamma-independent immunity
Murry, The Journal of infectious diseases 2009 - “...increased growth in iNOS / mice relative to wild-type mice at 4 weeks (Rv1224, Rv0326, Rv1422, and Rv3864; figure 1 ). None of these mutants was significantly overrepresented in iNOS / mice relative to wild-type mice at 3 weeks. The differences observed at these time points...”
- “...to the stringent requirements used to identify reproducible attenuation and rescue. For example, mutations in Rv1422 consistently caused attenuation in mice and increased replication in iNOS / mice at 4 weeks but were not statistically significant at 3 weeks ( P =.055). Similarly, mutations in pstP...”
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- A proposed carbon-utilization and virulence protein A, CuvA (Rv1422), from Mycobacterium tuberculosis H37Rv: crystallization, X-ray diffraction analysis and ligand binding.
Jeong, Acta crystallographica. Section F, Structural biology communications 2020 - GeneRIF: A proposed carbon-utilization and virulence protein A, CuvA (Rv1422), from Mycobacterium tuberculosis H37Rv: crystallization, X-ray diffraction analysis and ligand binding.
Mb1457 CONSERVED HYPOTHETICAL PROTEIN from Mycobacterium bovis AF2122/97
Aligns to 5:297 / 342 (85.7%), covers 94.1% of PF01933, 246.7 bits
MSMEG_3080 hypothetical protein from Mycobacterium smegmatis str. MC2 155
Aligns to 5:296 / 354 (82.5%), covers 92.4% of PF01933, 244.1 bits
- Mycobacterial gene cuvA is required for optimal nutrient utilization and virulence
Mir, Infection and immunity 2014 - “...and M. tuberculosis cuvA deletion strains. To delete cuvA (MSMEG_3080) from M. smegmatis, a 1,008bp region (L arm) 5= to MSMEG_3080, including 6 codons of...”
- “...Similarly, a 1,040-bp region (R arm) 3= to MSMEG_3080, including 100 bp of the MSMEG_3080 gene, was PCR amplified using primers MSMEG3080-cond-3 and...”
- LpqM, a mycobacterial lipoprotein-metalloproteinase, is required for conjugal DNA transfer in Mycobacterium smegmatis
Nguyen, Journal of bacteriology 2009 - “...had insertions in msmeg_0033, msmeg_1435, msmeg_1455, msmeg_3080, msmeg_4913, and msmeg_6128. Notably, four independent insertions were isolated in msmeg_4913,...”
CPS_2836 hypothetical protein from Colwellia psychrerythraea 34H
Aligns to 8:294 / 304 (94.4%), covers 95.5% of PF01933, 243.4 bits
FQ188_04305 2-phospho-L-lactate transferase from Rhodococcus sp. ANT_H53B
Aligns to 3:319 / 324 (97.8%), covers 88.3% of PF01933, 208.8 bits
6uw3B / A0QTG2 The crystal structure of fbia from mycobacterium smegmatis, gdp bound form (see paper)
Aligns to 3:317 / 326 (96.6%), covers 87.6% of PF01933, 204.7 bits
- Ligands: guanosine-5'-diphosphate; calcium ion (6uw3B)
MSMEG_1830 lppg:fo 2-phospho-l-lactate transferase from Mycobacterium smegmatis str. MC2 155
Aligns to 3:317 / 327 (96.3%), covers 87.6% of PF01933, 204.7 bits
- Cellular and Structural Basis of Synthesis of the Unique Intermediate Dehydro-F420-0 in Mycobacteria
Grinter, mSystems 2020 - “...that the strains were otherwise isogenic. MSMEG_1829 ( fbiB ), MSMEG_2392 ( fbiD ), and MSMEG_1830 ( fbiA ) deletion mutants were generated by using the same methods used for MSMEG_5126, using gene-specific primer combinations ( TableS3 ). Individual deletion mutants of fbiA , fbiB ,...”
- Unexpected abundance of coenzyme F(420)-dependent enzymes in Mycobacterium tuberculosis and other actinobacteria
Selengut, Journal of bacteriology 2010 - “...the biosynthetic genes for CofC (MSMEG_2393), CofD (fbiA; MSMEG_1830), CofE (fbiB; MSMEG_1829), and the fusion protein CofGH (fbiC; MSMEG_5126), 62 of the top...”
fbiA / P9WP81 phosphoenolpyruvate transferase (EC 2.7.8.28) from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see 2 papers)
FBIA_MYCTU / P9WP81 Phosphoenolpyruvate transferase; EPPG:FO PEP transferase; EC 2.7.8.28 from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see 3 papers)
Rv3261 PROBABLE F420 BIOSYNTHESIS PROTEIN FBIA from Mycobacterium tuberculosis H37Rv
Aligns to 3:318 / 331 (95.5%), covers 87.2% of PF01933, 198.8 bits
- function: Catalyzes the transfer of the phosphoenolpyruvate moiety from enoylpyruvoyl-2-diphospho-5'-guanosine (EPPG) to 7,8-didemethyl-8- hydroxy-5-deazariboflavin (FO) with the formation of dehydro coenzyme F420-0 and GMP.
catalytic activity: 7,8-didemethyl-8-hydroxy-5-deazariboflavin + enolpyruvoyl-2- diphospho-5'-guanosine = dehydro coenzyme F420-0 + GMP + H(+) (RHEA:27510)
cofactor: Mg(2+)
subunit: Homodimer. - Refined understanding of the impact of the Mycobacterium tuberculosis complex diversity on the intrinsic susceptibility to pretomanid
Rupasinghe, Microbiology spectrum 2024 (no snippet) - Designing molecular diagnostics for current tuberculosis drug regimens
Georghiou, Emerging microbes & infections 2023 - “...F 420 pathway enzymes, including ddn ( Rv3547 ), fgd1 ( Rv0407 ), fbiA ( Rv3261 ), fbiB ( Rv3262 ), and fbiC ( Rv1173 ), is expected to result in cross-resistance [ 5053 ]. However, 10-17% of phenotypically pretomanid-resistant isolates have no mutations in these...”
- Mechanism of Action, Resistance, Synergism, and Clinical Implications of Delamanid Against Multidrug-Resistant Mycobacterium tuberculosis
Khoshnood, Frontiers in microbiology 2021 - “...glucose-6-phosphate dehydrogenase (G6PD; FGD1, Rv0407), as well as four coenzymes, Fbi A (Rv3361), Fbi B (Rv3261), Fbi C (Rv1173), and Rv0132c ( Bashiri et al., 2010 ; Hartkoorn et al., 2014 ). All of these genes and coenzymes are involved in the synthesis and recycling of...”
- Recombinant Rv3261 protein of Mycobacterium tuberculosis induces apoptosis through a mitochondrion-dependent pathway in macrophages and inhibits intracellular bacterial growth
Lee, Cellular immunology 2020 (PubMed)- “...Rv3261 protein of Mycobacterium tuberculosis induces apoptosis through a mitochondrion-dependent pathway in macrophages and inhibits intracellular bacterial growth Cellular Immunology Journal fla 00088749 354 104145...”
- “...understood. In this study, we investigated protein Rv3261, isolated from an Mtb culture filtrate, for its apoptotic potential using multidimensional...”
- Adduct Formation of Delamanid with NAD in Mycobacteria
Hayashi, Antimicrobial agents and chemotherapy 2020 (secret) - Whole Genome Sequencing for the Analysis of Drug Resistant Strains of Mycobacterium tuberculosis: A Systematic Review for Bedaquiline and Delamanid
Nieto, Antibiotics (Basel, Switzerland) 2020 - “...to BDQ resistance [ 9 ]. Similarly, off-target mutations at ddn (Rv3547), fgd1 (Rv0407), fbiA (Rv3261), fbiB (Rv3262), and fbiC (Rv1173) were associated to DLM resistance [ 6 , 10 , 11 ]. Resistance mechanisms for BDQ and DLM can be found in previous reviews [...”
- “...them naturally resistant to DLM and pretomanid [ 57 ]. In the same sense, fbiA (Rv3261), fbiB (Rv3262), and fbiC (Rv1173) are essential for the mycobacterial F 420 synthesis that together with the glucose-6-phosphate dehydrogenase encoded by fgd1 (Rv0407) complete the conversion of DLM to its...”
- Characterization of Genomic Variants Associated with Resistance to Bedaquiline and Delamanid in Naive Mycobacterium tuberculosis Clinical Strains
Battaglia, Journal of clinical microbiology 2020 (secret) - Integrating informatics tools and portable sequencing technology for rapid detection of resistance to anti-tuberculous drugs
Phelan, Genome medicine 2019 - “...Bedaquiline Rv0678 Rv0678 5 (0) 2 (1) Clofazimine Rv0678 Rv0678 5 (0) 2 (1) Delamanid Rv3261 fbiA 1 (0) 0 (0) Drugs which are new to the library are bolded; indels insertions and deletions, FQ fluoroquinolones, PAS para-aminosalicylic acid. *Number of mutations observed in the ~17k...”
- More
ML0759 conserved hypothetical protein from Mycobacterium leprae TN
Aligns to 49:353 / 379 (80.5%), covers 87.2% of PF01933, 197.2 bits
MAP_RS17350 2-phospho-L-lactate transferase from Mycobacterium avium subsp. paratuberculosis K-10
Aligns to 3:325 / 337 (95.8%), covers 86.9% of PF01933, 191.2 bits
- Diagnostic Sequences That Distinguish M. avium Subspecies Strains
Bannantine, Frontiers in veterinary science 2020 - “...PCR and Taq-based PCR. This gene encodes a hypothetical protein and is immediately upstream of MAP_RS17350 in Map K-10, but with a significant 27-amino acid overlap in these coding sequences. MAP_RS17350 is annotated as a frameshifted non-functional protein that contains several internal stop codons. The primers...”
- “...MAP_RS22905 coding sequence while the reverse primer binds within the coding sequence that overlaps with MAP_RS17350. In the non- Map strains (as well as other Map strains) there is a single protein that is functional and encompasses the sequence that corresponds to MAP_RS22905 and MAP_RS17350. Therefore,...”
MAP3374 hypothetical protein from Mycobacterium avium subsp. paratuberculosis str. k10
Aligns to 9:331 / 343 (94.2%), covers 86.9% of PF01933, 191.1 bits
cofD / Q58653 LPPG:Fo 2-phospho-L-lactate transferase subunit (EC 2.7.8.28) from Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) (see 3 papers)
COFD_METJA / Q58653 2-phospho-L-lactate transferase; LPPG:FO 2-phospho-L-lactate transferase; EC 2.7.8.28 from Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) (Methanococcus jannaschii) (see paper)
Q58653 2-phospho-L-lactate transferase (EC 2.7.8.28) from Methanocaldococcus jannaschii (see paper)
MJ1256 conserved hypothetical protein from Methanocaldococcus jannaschii DSM 2661
Aligns to 5:300 / 311 (95.2%), covers 88.6% of PF01933, 171.4 bits
AF0917 conserved hypothetical protein from Archaeoglobus fulgidus DSM 4304
Aligns to 1:293 / 296 (99.0%), covers 91.0% of PF01933, 169.9 bits
Q8PVT6 2-phospho-L-lactate transferase (EC 2.7.8.28) from Methanosarcina mazei (see paper)
Aligns to 1:299 / 303 (98.7%), covers 87.9% of PF01933, 162.3 bits
3c3dA / Q8PVT6 Crystal structure of 2-phospho-(s)-lactate transferase from methanosarcina mazei in complex with fo and phosphate. Northeast structural genomics consortium target mar46 (see paper)
Aligns to 1:302 / 306 (98.7%), covers 88.3% of PF01933, 162.3 bits
- Ligands: phosphate ion; 1-deoxy-1-(8-hydroxy-2,4-dioxo-3,4-dihydropyrimido[4,5-b]quinolin-10(2h)-yl)-d-ribitol (3c3dA)
cofD / E5ASS0 3-phospho-(R)-glycerate transferase (EC 2.7.8.28) from Mycetohabitans rhizoxinica (strain DSM 19002 / CIP 109453 / HKI 454) (see paper)
Aligns to 4:304 / 328 (91.8%), covers 90.3% of PF01933, 154.7 bits
YNB1_YEAST / P53980 Uncharacterized protein YNL011C from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see paper)
YNL011C Putative protein of unknown function; YNL011C is not an essential gene from Saccharomyces cerevisiae
Aligns to 3:440 / 444 (98.6%), covers 94.1% of PF01933, 145.3 bits
- Systematic profiling of ale yeast protein dynamics across fermentation and repitching
Garge, G3 (Bethesda, Md.) 2024 (no snippet) - A widespread inversion polymorphism conserved among Saccharomyces species is caused by recurrent homogenization of a sporulation gene family
Salzberg, PLoS genetics 2022 - “...in spores [ 63 , 64 ]. We integrated these markers into the non-essential gene YNL011C , which is located between the FF region and the centromere of chromosome XIV, to make parental base strains LS022 ( MAT a ynl011c :: P DIT1 -GFP ) and...”
- Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease
Vignogna, eLife 2022 - “...we observe multiple independent mutations in the known SEC53 -interactors RPN5 , SRP1 , and YNL011C in sec53 populations, which could have positive genetic interactions with sec53 ( Figure 2 ). We find a high probability that the mutational spectrum of PGM1 (five missense mutations, 0...”
- A Genome-Wide Screen for Genes Affecting Spontaneous Direct-Repeat Recombination in Saccharomyces cerevisiae
Novarina, G3 (Bethesda, Md.) 2020 - “...8.3 YEL014C 22.9 RAD55 29.2 BUD20 32.1 BDF1 11.1 CDC40 23.1 SNO1 29.2 RPS16A 32.6 YNL011C 12.5 MDM34 23.4 SPE2 29.2 SWI6 12.8 OST4 23.5 SPT21 29.2 URA1 13.2 YOL013W-B 24.0 TCD1 29.2 YGR272C 13.2 YCK1 24.3 TPM1 29.2 BUD19 13.3 KNH1 25.0 YDR157W 29.2 UGO1...”
- Genetic Networks Required to Coordinate Chromosome Replication by DNA Polymerases α, δ, and ε in Saccharomyces cerevisiae
Dubarry, G3 (Bethesda, Md.) 2015 - “...:: :MRC1 Pol CFD1 GPI15 INO2 PKR1 PMR1 PRE8 PRI1 RAD51 RAD54 RAD55 RFC5 RMI1 YNL011C Pol AIM4 ARC18 ARP4 ARP6 ATG21 ATO2 AZF1 BEM1 BET3 BFA1 BPH1 BRE2 BUB2 BUD27 CAT5 CDC21 CDC33 CHK1 CHS5 CKB1 CKB2 CLB2 CLB5 DCC1 DCR2 DEG1 DFG16 DIA2 DPB11...”
- Most, but not all, yeast strains in the deletion library contain the [PIN(+)] prion
Manogaran, Yeast (Chichester, England) 2010 - “...] cells YBL107C YDR491C YIL041W (GVP36) YMR307W (GAS1) YBR001C ( NTH2 ) YDR506C YIL073C (SPO22) YNL011C YBR010W ( HHT1 ) YDR552C ( SPS2 ) YJL003W (COX16) YNL109W YBR044C ( TCM62 ) YER141W ( COX15 ) YJL007C YNL141W (AAH1) YBR114W ( RAD16 ) YFL033C ( RIM15 )...”
- Combining chemical genomics screens in yeast to reveal spectrum of effects of chemical inhibition of sphingolipid biosynthesis
Kemmer, BMC microbiology 2009 - “...PRP11 SIR2 2.04 1.72 NST1 RHO2 2.03 3.02 SDS22 ACP1 3.09 1.71 1.95 2.60 SPO1 YNL011C YNL010W IDP3 ASI3 3.88 2.15 3.11 YHR162W SOL3 DNA2 2.92 2.99 YML081W DUS1 YML079W CPR3 1.75 2.81 EBS1 UME6 MSS4 YDR210W 2.35 2.43 Syntenic regions enriched after treatment with motuporamines....”
- Cumulative mutations affecting sterol biosynthesis in the yeast Saccharomyces cerevisiae result in synthetic lethality that is suppressed by alterations in sphingolipid profiles
Valachovic, Genetics 2006 - “...HDA3 RPN9 IES1 SSN2 BCK2 RDN25-1 RDN37-1 TAR1 YNL011C YNL010W M2-7A: erg2upc2ecm22 M6-3B: erg6upc2ecm22 MH1-3B: hap1upc2ecm22 M28-2D: erg28upc2ecm22 1 1 -- -- 1...”
HVO_2479 LPPG:Fo 2-phospho-L-lactate transferase from Haloferax volcanii DS2
Aligns to 2:325 / 330 (98.2%), covers 86.9% of PF01933, 143.3 bits
A9WAV7 Gluconeogenesis factor from Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl)
Aligns to 152:329 / 391 (45.5%), covers 54.8% of PF01933, 139.2 bits
- Deciphering the functional role of hypothetical proteins from Chloroflexus aurantiacs J-10-f1 using bioinformatics approach
Thakur, Molecular biology research communications 2020 - “...protein M like A9WEQ6 Carbohydrate binding domain containing protein Cthe_2159 A9WAF1 O antigen ligase related A9WAV7 LPPG:FO 2 phospho L lactate transferaseCofD/UPF0052 A9WBQ0 Glycoside hydrolase family 30 A9WBU0 Glycoside hydrolase superfamily A9WCD7 Peptidase C11, clostripain A9WCF4 PDZ superfamily A9WD37 Putative zincin peptidase A9WD59 4Fe4S_Fe-S-bd, NarG like...”
- “...4 22015 20.02 stable 95.06 0.208 A9WAF1 511 58050.12 10.05 125820 45.72 unstable 121.14 0.683 A9WAV7 391 43267.39 6.16 37485 40.53 unstable 119.67 0.225 A9WBQ0 461 50401.05 4.59 92485 42.22 unstable 88.29 0.005 A9WCD7 907 97634.61 4.58 99615 39.74 stable 98.29 0.009 A9WCF4 511 57752.24 5.23...”
An14g06550 uncharacterized protein from Aspergillus niger
Aligns to 11:446 / 509 (85.7%), covers 82.4% of PF01933, 137.9 bits
AT2G34090 MEE18 (maternal effect embryo arrest 18) from Arabidopsis thaliana
Aligns to 54:421 / 445 (82.7%), covers 94.8% of PF01933, 136.4 bits
Or search for genetic data about PF01933 in the Fitness Browser
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory