ライフサイエンスコーパス: prokaryotic

1 Prokaryotic 16 S rRNA gene was amplified and DGGE was pe

2 ially acquired during sedimentation, as many prokaryotic 16S rRNA gene sequences retrieved from the e

3 lution native MS analysis of 0.8- to 2.3-MDa prokaryotic 30S, 50S and 70S ribosome particles and the

4 ying homologs of a fungal lactamase (renamed prokaryotic 5-oxoprolinase A, pxpA) and homologs of allo

5 Prokaryotic abundance, flux and community composition wa

6 Although most prokaryotic adaptive immune systems generally target DNA

7 CRISPR-Cas are prokaryotic adaptive immune systems that provide protect

8 ossible before, thanks to a peculiar form of prokaryotic adaptive immunity mediated by clustered regu

9 e casposons and the adaptation module of the prokaryotic adaptive immunity systems.

10 l gene silencing(1), while recent studies on prokaryotic Agos hint at their role in the protection ag

11 activation enzyme classes, lipoxygenases and prokaryotic alcohol dehydrogenases.

12 ference in the lengths of the eukaryotic and prokaryotic alpha1 helix of protein uL16 that play a key

13 Toxin-antitoxin systems are ubiquitous in prokaryotic and archaeal genomes and regulate growth in

14 stem by conducting a time series analysis of prokaryotic and eukaryotic biodiversity using the V3-V4

15 c phosphate is an essential mineral for both prokaryotic and eukaryotic cell metabolism and structure

16 The intricate structure of prokaryotic and eukaryotic cells depends on the ability

17 ranslational modification important for both prokaryotic and eukaryotic cells to control a wide array

18 howed robust, ligand-dependent activation in prokaryotic and eukaryotic cells, establishing a versati

19 anslocases and insertases have been found in prokaryotic and eukaryotic cells, the Sec61 complex and

20 recombination is routinely performed in both prokaryotic and eukaryotic cells, we expect this assay w

21 esent a key aspect in the transition between prokaryotic and eukaryotic cellular forms.

22 ect of drought on the overall composition of prokaryotic and eukaryotic communities was weak, a subse

23 g antagonistic interactions with neighboring prokaryotic and eukaryotic competitors.

24 co-polymer to extract membrane proteins from prokaryotic and eukaryotic expression systems.

25 ameters and interaction energies for several prokaryotic and eukaryotic filaments indicate that biopo

26 e synthetase (SPS or SelD), conserved in all prokaryotic and eukaryotic genomes encoding selenoprotei

27 hort tandem repeats (STRs) are found in many prokaryotic and eukaryotic genomes, and are commonly use

28 f DNA transposons, exist pervasively in both prokaryotic and eukaryotic genomes, with more than 10,00

29 Prokaryotic and eukaryotic genomic DNA is comprised of t

30 Using prokaryotic and eukaryotic glutaminase sequences, we bui

31 The cytoplasmic domains of prokaryotic and eukaryotic Kir channels show similar con

32 in three popular model organisms, including prokaryotic and eukaryotic microorganisms and an animal.

33 The prokaryotic and eukaryotic microorganisms that drive the

34 vantage of key metabolic differences between prokaryotic and eukaryotic organisms, allowing easier di

35 ssential atypical protein kinases in diverse prokaryotic and eukaryotic organisms, playing significan

36 dentification of the Lon substrates in other prokaryotic and eukaryotic organisms.

37 (P)(+) :NAD(P)H redox homeostasis in various prokaryotic and eukaryotic organisms.

38 harbor a large repertoire of metabolites of prokaryotic and eukaryotic origin that play important ro

39 Prokaryotic and eukaryotic pathogens are represented in

40 Successful colonization of plants by prokaryotic and eukaryotic pathogens requires active eff

41 r the design of selective drugs against many prokaryotic and eukaryotic pathogens to which the non-me

42 Unicellular, planktonic, prokaryotic and eukaryotic photoautotrophs (phytoplankto

43 chieved by the helicases UvrB and XPD in the prokaryotic and eukaryotic processes, respectively.

44 Given their mixed prokaryotic and eukaryotic properties, we propose the te

45 Divergence between prokaryotic and eukaryotic ribosomal RNA (rRNA) and amon

46 technological applications and their role in prokaryotic and eukaryotic systems.

47 chloroplast envelope, indicating its role in prokaryotic and eukaryotic TAG biosynthesis.

48 ase in the number of sequenced genomes, both prokaryotic and eukaryotic.

49 We examined prokaryotic and fungal communities in the rhizosphere, p

50 We found that, on average, 40% of both prokaryotic and fungal DNA was extracellular or from cel

51 Extracellular DNA inflated the observed prokaryotic and fungal richness by up to 55% and caused

52 Agaves shared core prokaryotic and fungal taxa known to promote plant growt

53 ubstrate L-cysteine, a reaction catalyzed by prokaryotic and mammalian cysteinyl-tRNA synthetases (CA

54 eminated by lateral transfer between distant prokaryotic and microbial eukaryotic lineages consistent

55 Although there is no doubt that prokaryotic and organellar group II introns are evolutio

56 enetic elements have essential roles in both prokaryotic and vertebrate adaptive immune systems.

57 pparatus that injects effector proteins into prokaryotic and/or eukaryotic target cells.

58 summarizes the current status of the viral, prokaryotic, and eukaryotic branches of the RefSeq proje

59 view, we describe mechanisms by which viral, prokaryotic, and eukaryotic polypeptides have adopted al

60 statistics: k -mer frequency, 16S abundance, prokaryotic- and viral-read abundance.

61 tion system arose and diversified from these prokaryotic antecedents.

62 imilar to, or differ from, the challenges of prokaryotic antibiotic resistance.

63 ctional proteins in a pathway termed Archaeo-Prokaryotic (AP) NHEJ that facilitates DSB repair.

64 Prokaryotic Argonaute proteins acquire guide strands der

65 is issue, Swarts et al. (2017) discover that prokaryotic Argonaute proteins generate their own DNA gu

66 gh structural similarities between human and prokaryotic Argonautes are consistent with shared mechan

67 Whereas eukaryotic and prokaryotic ATP synthases are well characterized, archae

68 esponse regulator (RR) and control important prokaryotic behaviors.

69 highest abundances of many genes involved in prokaryotic C degradation, ammonification, and nitrifica

70 cterial proteins are needed for the study of prokaryotic cell biology.

71 demonstrate that the dynamic architecture of prokaryotic cell membranes is controlled by the MreB cyt

72 The functional organization of prokaryotic cell membranes, which is essential for many

73 the number of spacers in a CRISPR array of a prokaryotic cell which maximizes its protection against

74 CRISPR adaptive immunity pathways protect prokaryotic cells against foreign nucleic acids using CR

75 mbiotic relationships between eukaryotic and prokaryotic cells are common in nature.

76 Many prokaryotic cells are encapsulated by a surface layer (S

77 is a core biological process that occurs in prokaryotic cells at high speeds ( approximately 1 nucle

78 Prokaryotic cells possess CRISPR-mediated adaptive immun

79 , a basic element in the division process of prokaryotic cells such as Escherichia coli, Bacillus sub

80 btle genetic modifications in eukaryotic and prokaryotic cells without the requirement for prior gene

81 een limited to the study of relatively small prokaryotic cells.

82 chanism to distribute sizeable cargos within prokaryotic cells.

83 RNAs that require processing for maturation, prokaryotic cellular mRNAs generally follow an 'all-or-n

84 transition to the desensitized state in the prokaryotic channel GLIC.

85 oside antibiotic hygromycin B (Hyg) inhibits prokaryotic, chloroplast and mitochondrial protein synth

86 holine synthesis pathway combining conserved prokaryotic choline kinase and CTP:phosphocholine cytidy

87 sfer resulting in substantial alterations to prokaryotic chromosomes.

88 olecules and is the best-studied model for a prokaryotic circadian clock.

89 ntegrated functional annotations for defined prokaryotic clades.

90 Prokaryotic clustered regularly interspaced short palind

91 The prokaryotic clustered regularly interspaced short palind

92 The prokaryotic clustered regularly interspaced short palind

93 Selected examples of the application of prokaryotic coevolutionary analysis to the prediction of

94 etic spatial turnover (based on DNA) of soil prokaryotic communities after long-term nitrogen (N) dep

95 Metagenomic data reveals highly complex prokaryotic communities composed of chemolithoautotrophs

96 Phytoplankton and prokaryotic communities correlated better with each othe

97 of the Symbiodinium spp. communities and the prokaryotic communities did not.

98 e under low water activity by describing the prokaryotic communities from two disparate hypersaline s

99 pared the transcriptional pattern of natural prokaryotic communities grown in continuous cultures on

100 Prokaryotic communities in groundwater underpin the turn

101 c profiling revealed that the composition of prokaryotic communities was primarily determined by the

102 ransporters indicates that the heterotrophic prokaryotic community is geared toward the utilization o

103 rom daily rRNA analysis of phytoplankton and prokaryotic community members following a bloom off sout

104 In the Prokaryotic community, there was an initial enrichment o

105 ct effectors/toxins into eukaryotic hosts or prokaryotic competitors for survival and fitness.

106 been limited to the analysis of families of prokaryotic complexes for which large multiple sequence

107 bile dissolved organic carbon (DOC) preclude prokaryotic consumption of a substantial fraction of DOC

108 The prokaryotic CRISPR (clustered regularly interspaced pali

109 Prokaryotic CRISPR-Cas adaptive immune systems insert sp

110 Prokaryotic CRISPR-Cas adaptive immune systems utilize s

111 are based on the naturally occurring Type II prokaryotic CRISPR-Cas9 system.

112 By analogy with the better characterized prokaryotic Cu-ATPases, ATP7B is assumed to be a single-

113 Eukaryotic microalgae and prokaryotic cyanobacteria are the major components of th

114 Unlike prokaryotic cysteine desulfurases, the SDA structure ado

115 Similar to its eukaryotic counterpart, the prokaryotic cytoskeleton is essential for the structural

116 Two recently discovered groups of prokaryotic di-metal carboxylate proteins harbor a heter

117 We also demonstrate that prokaryotic diversity associated with stygofauna may be

118 vated A. tequilana exhibited lower levels of prokaryotic diversity compared with native agaves, altho

119 d at a larger scale could be a new source of prokaryotic diversity in groundwater ecosystems.

120 ing inactive Cas9 (dCas9) with an engineered prokaryotic DNA methyltransferase MQ1.

121 )-methyldeoxyadenosine (6mA) is a well-known prokaryotic DNA modification that has been shown to exis

122 ng lays bare a paradox in the functioning of prokaryotic (endo)symbionts.

123 s we demonstrate for the first time that the prokaryotic-enriched anionic lipid Cardiolipin (CL) play

124 s boundaries and has been a driving force in prokaryotic evolution.

125 were consistent with current knowledge about prokaryotic evolution.

126 dimensional structures of animal, plant, and prokaryotic FeLOX are available, but none of MnLOX.

127 scopy (SIMS) of 11 specimens of five taxa of prokaryotic filamentous kerogenous cellular microfossils

128 (Tfp)-exceptionally widespread and important prokaryotic filaments.

129 io in which the dual function of the ancient prokaryotic fumarase, led to its subsequent distribution

130 sted on a collection of approximately 13 000 prokaryotic gene families.

131 g retention of ancient function, we asked if prokaryotic genes could replace their essential eukaryot

132 In fast-transcribing prokaryotic genes, such as an rrn gene in Escherichia co

133 c positions in the promoters of co-expressed prokaryotic genes.

134 Thus, the new NCBI's Prokaryotic Genome Annotation Pipeline (PGAP) relies mor

135 rokaryotic genomes, which play a key role in prokaryotic genome organization and evolution.

136 ides genome quality scores for all available prokaryotic genome sequences with a user-friendly Web-in

137 accurately and automatically annotate ISs in prokaryotic genome sequences.

138 sites are significantly underrepresented in prokaryotic genomes [4-7], suggesting that the discrimin

139 ic ancestral reconstructions from 634 extant prokaryotic genomes and a novel framework for detecting

140 ias is a universal feature of eukaryotic and prokaryotic genomes and has been proposed to regulate tr

141 usage biases are found in all eukaryotic and prokaryotic genomes and have been proposed to regulate d

142 er species, and describe a new direction for prokaryotic genomes and protein name management.

143 Additionally, prokaryotic genomes are frequently deposited as incomple

144 ication to 86.5M genome pairs between 13,151 prokaryotic genomes assigned to 3032 species.

145 nd 2,704 genes, was annotated using the NCBI Prokaryotic Genomes Automatic Annotation Pipeline.

146 veral new features have been added to RefSeq prokaryotic genomes data processing pipeline including t

147 ost taxonomy from among approximately 32 000 prokaryotic genomes for 1427 virus isolate genomes whose

148 f self-DNA by RM systems as elements shaping prokaryotic genomes has not been directly detected, and

149 Our scan of hundreds of prokaryotic genomes identified previously unknown effect

150 The compactness of prokaryotic genomes is commonly perceived as evidence of

151 The analysis of 982 representative prokaryotic genomes is consistent with this pathway bein

152 Even though more than 50% of all sequenced prokaryotic genomes possess at least one chemotaxis sign

153 results suggest that the number of genes in prokaryotic genomes reflects the equilibrium between the

154 A global analysis of 65,421 prokaryotic genomes revealed 30,261 RiPP clusters, encod

155 Our large-scale analysis of >2500 prokaryotic genomes reveals the complex evolutionary his

156 Comparative analysis of prokaryotic genomes showed that the gene encoding pyrogl

157 enome evolution with comparative analysis of prokaryotic genomes to estimate the relative contributio

158 xisting IS annotation systems when tested on prokaryotic genomes with curated annotations of IS eleme

159 as defense system, present in almost half of prokaryotic genomes, proves otherwise.

160 Applying it to 2784 prokaryotic genomes, we report the global distribution o

161 abundant autonomous transposable elements in prokaryotic genomes, which play a key role in prokaryoti

162 f CRISPR molecular machines occur broadly in prokaryotic genomes, with a diversity of Cas nucleases t

163 ng solely mutational patterns extracted from prokaryotic genomes.

164 T) information for 2472 completely sequenced prokaryotic genomes.

165 ular noise in RM systems as a factor shaping prokaryotic genomes.

166 ailed insights into the genetic structure of prokaryotic genomes.

167 es 164,651 TCS proteins, from 2758 sequenced prokaryotic genomes.

168 Prokaryotic genomic data from all sources were collected

169 Among the prokaryotic genomic islands (GIs) involved in horizontal

170 y a conservative estimate of the size of the prokaryotic genomic universe, which appears to consist o

171 scherichia coli, XylEEc, the other prominent prokaryotic GLUT homolog, GlcPSe, is equipped with a con

172 of gene sequences in various closely related prokaryotic groups reveal that sequence diversity is typ

173 a position different from those observed in prokaryotic histidine kinases.

174 are ubiquitously found in eukaryotes but no prokaryotic homolog has been characterized.

175 In LeuT, a prokaryotic homolog of neurotransmitter transporters, Na

176 Thus, DJ-1 and its prokaryotic homologs constitute a major nucleotide repai

177 oupling by comparing the propensities of two prokaryotic homologs, Gloebacter and Erwinia ligand-gate

178 properties of eukaryotic Lyp1 to that of the prokaryotic homologue LysP and find that LysP has a simi

179 Here we describe the structures of two prokaryotic homologues, archaeal SaTRIC and bacterial Cp

180 CRISPR-Cas system provides its prokaryotic host with an adaptive immune defense against

181 ntegrating them into the CRISPR locus of the prokaryotic host.

182 The prokaryotic immune system CRISPR-Cas (clustered regularl

183 The adaptive prokaryotic immune system CRISPR-Cas provides RNA-mediat

184 mic repeats-CRISPR-associated proteins) is a prokaryotic immune system that destroys foreign nucleic

185 and their associated (Cas) proteins encode a prokaryotic immune system that protects against viruses

186 as a genome-editing tool to its origin as a prokaryotic immune system.

187 e conformation adopted by several classes of prokaryotic IMPDH inhibitors.

188 d colleagues have expanded the repertoire of prokaryotic influence over eukaryotic physiology to incl

189 ystematically identifies residue contacts at prokaryotic interfaces that are structurally conserved a

190 of functionally non-selective members of the prokaryotic 'inward rectifier' subfamily of K(+) channel

191 to alter gating, with most studies involving prokaryotic K(+) channels.

192 In voltage-gated K(+) channels and the prokaryotic KcsA channel, conduction is believed to resu

193 tionally equivalent residue (Arg-165) in the prokaryotic Kir channel KirBac1.1 also significantly dec

194 Prokaryotic Ligase D is a conserved DNA repair apparatus

195 Despite being one of the few prokaryotic lineages that is cosmopolitan in both the te

196 dominated by picophytoplankton including the prokaryotic lineages, Prochlorococcus and Synechococcus.

197 andidate divisions and possibly undocumented prokaryotic lineages, the hypersaline sapropels were fou

198 enetic signal affiliating them with specific prokaryotic lineages.

199 hysiology was assigned to several uncultured prokaryotic lineages; most notably, a SAR406 representat

200 CrDGTT1 was shown to prefer prokaryotic lipid substrates and probably resides in bot

201 ound that it is sufficient to permeate model prokaryotic membranes using synchrotron x-ray diffractio

202 vely bends membranes and, when inserted into prokaryotic membranes, induces the formation of cristae-

203 c nuclease containing a motif related to the prokaryotic metallo-beta-lactamase (MBL) fold.

204 mals is a forbidden area for the majority of prokaryotic microbes; however, red blood cells tropism m

205 Prokaryotic microbial assemblages were dominated by Prot

206 ation of the animal-algal pair also with its prokaryotic microbiome.

207 The prokaryotic microbiota of mosquitoes is efficiently surv

208 ct can be controlled by drug therapy as with prokaryotic microorganisms, the emergence of drug resist

209 sidency in the eukaryotic cell pressured the prokaryotic mitochondrial ancestor to strategize for int

210 y available transcriptomics data for several prokaryotic model organisms.

211 ingzhao as a high-affinity antagonist of the prokaryotic NaVs NsVBa (nonselective voltage-gated Bacil

212 s the first report of peptide antagonist for prokaryotic NaVs.

213 Stygofauna are a newly recognized prokaryotic niche in groundwater ecosystems that have th

214 LeuT, a prokaryotic NSS homolog, has been crystallized in outwar

215 Two crystal structures of another prokaryotic NSS homolog, the multihydrophobic amino acid

216 The prokaryotic NSS homologue, LeuT, represents a principal

217 LeuT, a prokaryotic NSS protein, constitutes a primary structura

218 here they have been shown to inhibit or kill prokaryotic or eukaryotic cells and are often important

219 sposon-containing plasmid DNA, it penetrates prokaryotic or eukaryotic cells and integrates the targe

220 al nanomachine used to inject effectors into prokaryotic or eukaryotic cells and is thus involved in

221 nables stable genome integration into either prokaryotic or eukaryotic cells.

222 We characterized this issue in a model prokaryotic organism that expresses two different threon

223 an acetyltransferase by autoacetylation in a prokaryotic organism.

224 Prokaryotic organisms survive under constant pressure of

225 ergence of PSII, as found today in anaerobic prokaryotic organisms that use carbon monoxide as an ene

226 and ensure pH homeostasis in eukaryotic and prokaryotic organisms.

227 roton pumps are widespread in eukaryotic and prokaryotic organisms.

228 in fused to one of cyanobacterial or another prokaryotic origin and have emerged multiple, independen

229 Extensive integration of genes of prokaryotic origin, including genes for antimicrobial pe

230 The prokaryotic origins of the actin cytoskeleton have been

231 ted eukaryotic proteases compared with their prokaryotic orthologs.

232 Our study thus uncovers a role for prokaryotic oxylipins in the physiology and pathogenicit

233 While prokaryotic pan-genomes have been shown to contain many

234 hannels in bacterial biofilms, and provide a prokaryotic paradigm for active, long-range electrical s

235 olecular interplay between the plant and the prokaryotic partner is that, at least in certain legumes

236 enzymes catalyze the first two steps of the prokaryotic pathway for glycerolipid synthesis, so we in

237 c pathway and correspondingly suppresses the prokaryotic pathway, resulting in the switch of lipid pr

238 x in both the maturation and function of the prokaryotic pentameric ligand-gated ion channels, GLIC a

239 6 per thousand), and those typical of modern prokaryotic phototrophs (-25 +/- 10 per thousand).

240 rsification to environmental adaptation in a prokaryotic phylum.

241 es of barbiturates bound to GLIC, a cationic prokaryotic pLGIC with excellent structural homology to

242 Thus, the MBP tag is useful for efficient prokaryotic production and purification of bioactive hFG

243 regions of beta, designated as beta-c1, for prokaryotic production to be used in NMR spectroscopy.

244 During the translocation step of prokaryotic protein synthesis, elongation factor G (EF-G

245 Our findings suggest that Mcc is the first prokaryotic protein with prion properties which harnesse

246 other plant species and known mammalian and prokaryotic RBSK than to all other PfkB proteins in Arab

247 We show here how the prokaryotic regulatory protein CueR both represses and a

248 ed to improved selectivity for inhibition of prokaryotic relative to cytosolic eukaryotic in vitro tr

249 ght of meiotic sex development from existing prokaryotic repair mechanisms.

250 is one of the major regulatory mechanisms of prokaryotic replication licensing.

251 Prokaryotic ribosomes evolved in six phases, sequentiall

252 otic ribosomes are significantly larger than prokaryotic ribosomes partly because of their ESs.

253 currently remove polyadenylated transcripts, prokaryotic rRNA, and eukaryotic rRNA, including those w

254 Multiple types of bacteria employ the prokaryotic second messenger cyclic di-GMP (c-di-GMP) to

255 heterotrimeric membrane protein complex, the prokaryotic SecY or eukaryotic Sec61 complex.

256 fused via an inversion linker helix, whereas prokaryotic SemiSWEETs contain only a single THB and req

257 ed that it was evolutionarily related to the prokaryotic serine palmitoyltransferase, identified in t

258 tion crystal structure of the complete NavMs prokaryotic sodium channel in a fully open conformation.

259 aracteristics and the crystal structure of a prokaryotic sodium channel, showing for the first time t

260 Here we describe the use of small prokaryotic sodium channels (BacNav) to create de novo e

261 ined organism relationships across the known prokaryotic space.

262 ed birth-death model as a null hypothesis in prokaryotic speciation studies.

263 crobial genomes has revealed that prevailing prokaryotic species assignments can be inconsistent with

264 omponent of the respiratory chain of diverse prokaryotic species, including pathogenic bacteria.

265 To simplify (13)C-MFA of different prokaryotic species, the software provides several metab

266 Like many other prokaryotic sRNAs, Pxr is predicted to fold into three s

267 nvestigation, we confirmed that both aerobic prokaryotic (Streptomyces coelicolor) and eukaryotic (Ho

268 d that ubiquitin-like modifiers evolved from prokaryotic sulphur transfer proteins it is less clear h

269 By optimizing XXT2 expression in a prokaryotic system and in vitro activity assay condition

270 f unrecognized glycation targets of DPD in a prokaryotic system.

271 y serving as a guide biogenesis pathway in a prokaryotic system.

272 Prokaryotic systematics provides the fundamental framewo

273 In prokaryotic systems, the translation initiation of many,

274 ne) to identify characters from sentences in prokaryotic taxonomic descriptions, followed by a combin

275 ion of phenotypic character information from prokaryotic taxonomic descriptions.

276 nalysis of annotation on the full breadth of prokaryotic taxonomy.

277 by auxotrophic complementation of yeast with prokaryotic, thermophilic IGPS.

278 Here, we present the crystal structure of a prokaryotic TMEM175 channel from Chamaesiphon minutus, C

279 The prokaryotic TMEM175 channel, which is present in a subse

280 crobials and more selective to inhibition of prokaryotic translation.

281 readily available tools, not for most of the prokaryotic transporters for which high-resolution struc

282 hese proteins appear to have originated from prokaryotic transposases (e.g. TN7 and Mu) and combine a

283 encode predicted proteins homologous to RCR prokaryotic transposases.

284 ribution of RiPP biosynthesis throughout the prokaryotic tree of life, and provide a platform for the

285 physiology and mutagenesis studies show that prokaryotic TRICs have similar functional properties to

286 surface of giant unilamellar vesicles by the prokaryotic tubulin homolog, FtsZ, on phase separation i

287 data support the identification of the first prokaryotic two-component protein system related to the

288 to these lipids, while plastidial lipids of prokaryotic type were characterized by the overwhelming

289 sttranslational regulatory mechanisms in the prokaryotic ubiquitin-like protein (Pup)-proteasome syst

290 posttranslational modification in which the prokaryotic ubiquitin-like protein Pup is covalently att

291 to as pupylation, the covalent attachment of prokaryotic ubiquitin-like protein Pup to lysine side ch

292 tually exclusive neighborhoods with either a prokaryotic ubiquitin-system or a HORMA domain-PCH2-like

293 ing mode similar to those reported for other prokaryotic UGMs.

294 ed with the generation of defects around the prokaryotic vector, which is retained in the unique shor

295 A natural and permanent transfer of prokaryotic viral sequences to mammals has not been repo

296 Thus, VirD5 is a prokaryotic virulence protein that interferes with mitos

297 The Prokaryotic Virus Orthologous Groups (pVOGs, formerly ca

298 ted by short "spacer" sequences derived from prokaryotic viruses and plasmids that determine the targ

299 heir virions being among the most complex of prokaryotic viruses and their potential for biocontrol a

300 als can share and exchange a larger world of prokaryotic viruses than previously envisioned.