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 Metagenomic sequencing of prokaryotic 16S rRNA present in feces from naive mice an

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

4 exo- and endoribonuclease RNase J, the only prokaryotic 5'->3' ribonuclease that is commonly present

5 reveal conserved dynamical behaviors in four prokaryotic actin homologs: MreB, FtsA, ParM, and crenac

6 e majority of the conformational dynamics of prokaryotic actins can be explained by treating the four

7 ymerization dependencies of the structure of prokaryotic actins, suggesting mechanisms for how these

8 CRISPR-Cas is a prokaryotic adaptive immune system that functions by inc

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

10 Prokaryotic adaptive immune systems use Clustered Regula

11 -associated (Cas) genes, a diverse family of prokaryotic adaptive immune systems, have emerged as a b

12 in (Ago2), reminiscent of an active state in prokaryotic Ago(4,5).

13 sight for understanding the evolution of the prokaryotic aldehyde dehydrogenase superfamily and their

14 Cyanobacteria are unicellular prokaryotic algae that perform oxygenic photosynthesis,

15 vation of conservative NOS architecture from prokaryotic ancestors.

16 embrane protein by comparing the shapes of a prokaryotic and a eukaryotic sodium/proton antiporter ho

17 Prokaryotic and archaeal chromosomes encode a diversity

18 In prokaryotic and eukaryotic cells alike, Acs activity is

19 ute compatible with the physiologies of both prokaryotic and eukaryotic cells and is widely synthesiz

20 ted the effect of DNA extracted from diverse prokaryotic and eukaryotic cells in tau misfolding and a

21 d utility of this approach to eliminate both prokaryotic and eukaryotic cells was demonstrated by pai

22 ning proteins execute essential functions in prokaryotic and eukaryotic cells, but their biogenesis i

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

24 ides (CDNs) are secondary messengers used by prokaryotic and eukaryotic cells.

25 ious biological processes, occurring in both prokaryotic and eukaryotic cells.

26 alogous motifs have been observed in several prokaryotic and eukaryotic channels.

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

28 GenBank currently has automatic prokaryotic and eukaryotic genome annotation pipelines b

29 A third of the genes in prokaryotic and eukaryotic genomes encode membrane prote

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

31 spurious protein "families" across multiple prokaryotic and eukaryotic genomes.

32 could be recombinantly expressed by diverse prokaryotic and eukaryotic hosts and was found to co-sed

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

34 Nine different prokaryotic and eukaryotic membrane proteins were used a

35 ingdom communication that is conserved among prokaryotic and eukaryotic microbes.

36 The prokaryotic and eukaryotic microorganisms that drive the

37 t is home to a vibrant, diverse ecosystem of prokaryotic and eukaryotic microorganisms.

38 rovide a unified view of TA elements in both prokaryotic and eukaryotic organisms and highlight their

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

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

41 Prokaryotic and eukaryotic pathogens are represented in

42 divergence in the binding interface between prokaryotic and eukaryotic PC4-like proteins.

43 machine that delivers effector proteins into prokaryotic and eukaryotic preys.

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

45 suggests a general mechanism by which other prokaryotic and eukaryotic regulatory proteins can be co

46 and significant differences between how the prokaryotic and eukaryotic ribosomes recognize the UBP,

47 ave impacted past host range studies in both prokaryotic and eukaryotic systems.

48 hs) proteins as toxic effectors against both prokaryotic and eukaryotic target cells.

49 Drug discrimination by prokaryotic and eukaryotic topoisomerases is vital to th

50 utionary conserved mode of recognition among prokaryotic and eukaryotic transcription factors.

51 This missing link between prokaryotic and eukaryotic transcription regulation prov

52 method can be applied for precise mapping of prokaryotic and eukaryotic type II topoisomerases cleava

53 host specificity, IMG/VR v.2.0 now separates prokaryotic and eukaryotic viruses, utilizes known proph

54 ata on the diversity of microorganisms, both prokaryotic and eukaryotic, is lacking.

55 Structural comparisons with prokaryotic and evolutionarily older PRKs revealed that

56 er individual subunits, can be produced from prokaryotic and human expression platforms, can employ a

57 anslational control of CRISPR-Cas systems in prokaryotic and mammalian cells, organisms and ecosystem

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

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

60 Complexity Regions (LCRs) in more than 1500 prokaryotic and phage proteomes.

61 utionary classifications, we have added more prokaryotic and plant genomes to the phylogenetic gene t

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

63 nd messengers are increasingly implicated in prokaryotic anti-viral defence systems.

64 Prokaryotic Argonaute proteins acquire guide strands der

65 Unlike eukaryotic proteins, several prokaryotic Argonaute proteins use small DNA guides to c

66 Prokaryotic Argonautes (pAgos) are much more diverse tha

67 rsatile and high-throughput method to evolve prokaryotic aTF specificity and transfer functions in a

68 ading to a meltwater system that accumulates prokaryotic biota as it travels downstream.

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

70 al process of in vivo protein synthesis in a prokaryotic cell containing several thousand unique mRNA

71 Although the major events in prokaryotic cell cycle progression are likely to be coor

72 potentially useful system to investigate the prokaryotic cell cycle.

73 , there is growing interest in nonanimal and prokaryotic cell interfacing.

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

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

76 cognized by the DNA replication machinery in prokaryotic cells and reveal that Ada contributes to mut

77 l (phage) infection, a small fraction of the prokaryotic cells are able to integrate a small sequence

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

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

80 Most prokaryotic cells are encased in a surface layer (S-laye

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

82 volutionary transitions, during which simple prokaryotic cells gave rise to complex eukaryotic cells.

83 determinants", which provide specificity for prokaryotic cells over eukaryotic cells.

84 nd lack of membrane-based DNA encapsulation, prokaryotic cells still organize and scale their nucleoi

85 ar vesicles (EVs) secreted by eukaryotic and prokaryotic cells to transport lipids, proteins, and nuc

86 In prokaryotic cells, a single-input-module motif with one

87 nce space, performing disparate functions in prokaryotic cells, including cellular defense, cell-shap

88 ere between 47%-96%, representing >99.98% of prokaryotic cells.

89 chanism to distribute sizeable cargos within prokaryotic cells.

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

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

92 Using the prokaryotic channel, NaChBac, we found some similarity a

93 ecies as well as genetically programming new prokaryotic chassis for a suite of fundamental and biote

94 , and are functional when ported back into a prokaryotic chassis.

95 The prokaryotic chemotaxis system is arguably the best-under

96 vidence of multiple modes of organization in prokaryotic chromosomes and yield insights into the evol

97 the bulk of Earth's bacterial and archaeal ("prokaryotic") clades and to estimate their overall globa

98 , FUS, and alpha-synuclein toxicity, whereas prokaryotic ClpB and hyperactive variants were ineffecti

99 Prokaryotic ClpG reduced TDP-43, FUS, and alpha-synuclei

100 The prokaryotic clustered regularly interspaced short palind

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

102 Differences in the rumen prokaryotic communities disappear later in life when all

103 evaluated the structure and diversity of the prokaryotic communities from a range of highly saline so

104 Salinity had a secondary role in shaping prokaryotic communities in these highly saline samples s

105 cons to elucidate the attached and suspended prokaryotic community dynamics within three nonchlorinat

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

107 elected across plant genetic groups: 3.7% of prokaryotic community members and 4.9% of fungal communi

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

109 tripartite SMC-kleisin complexes, including prokaryotic condensin, eukaryotic cohesin, and eukaryoti

110 We isolated a novel bacterial strain from a prokaryotic consortium associated to the psychrophilic m

111 are functionally interchangeable with their prokaryotic counterpart, TIG1 was not able to complement

112 o those of eukaryotes than to those of their prokaryotic cousins, the bacteria.

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

114 Unlike prokaryotic cysteine desulfurases, the SDA structure ado

115 Overall, we unravel the function of a prokaryotic cytoskeletal constituent that is widespread

116 ut only recently discovered filaments of the prokaryotic cytoskeleton.

117 Here, using a global prokaryotic dataset, we find that maximal growth rate at

118 vation of a functional cGAS-STING pathway in prokaryotic defence against bacteriophages.

119 l functional STING homologues encoded within prokaryotic defence islands, as well as a conserved mech

120 the recognition of foreign nucleic acids by prokaryotic defence systems involves common principles.

121 hensive defense systems database to organize prokaryotic defense gene datasets.

122 nsive resource to accelerate the research of prokaryotic defense systems.

123 Here, we mined prokaryotic diversity to establish a synthetic platform

124 Prokaryotic DNA contains three types of methylation: N6-

125 ircRNA immunity has considerable parallel to prokaryotic DNA restriction modification system that tra

126 Similarly, the rep genes of prokaryotic DNA viruses appear to have evolved from HUH

127 f the first assembly intermediate of certain prokaryotic dsRNA viruses.

128 unlabeled membrane-reconstituted Glt(Ph), a prokaryotic EAAT homologue, with millisecond temporal re

129 Lastly, prokaryotic encapsulins may be more common and diverse t

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

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

132 carboxylase and appears to have evolved from prokaryotic enzymes that bind negatively charged substra

133 ong the >120 modified ribonucleosides in the prokaryotic epitranscriptome, many tRNA modifications ar

134 Here, we present prokaryotic expression profiling by tagging RNA in situ

135 r is unlike those of all other characterized prokaryotic ferritins and instead resembles an animal H-

136 Our results expand the repertoire of known prokaryotic filament-forming CCRPs and demonstrate that

137 tion to the factors discussed should improve prokaryotic gene detection and the comparability of ribo

138 elix bundles which possibly originate due to prokaryotic gene duplication.

139 e AssessORF, a new approach for benchmarking prokaryotic gene predictions based on evidence from prot

140 FttA resolves the dichotomy of a prokaryotic gene structure (operons and polarity) and eu

141 and consequent selection and fixation of the prokaryotic genes in the new eukaryotic setting are larg

142 eukaryotic microbes to promote adaptation of prokaryotic genes to their new environment.

143 graphy, Assembly, RefSeq, viral genomes, the prokaryotic genome annotation pipeline, Genome Workbench

144 of error introduced during the annotation of prokaryotic genome assemblies.

145 lt, very few simulators are adapted to model prokaryotic genome evolution while accounting for recomb

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

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

148 accurately and automatically annotate ISs in prokaryotic genome sequences.

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

150 ias is a universal feature of eukaryotic and prokaryotic genomes and plays an important role in regul

151 this problem by reconstructing 60,664 draft prokaryotic genomes from 3,810 faecal metagenomes, from

152 However, the automated annotation of prokaryotic genomes is imperfect, and errors due to frag

153 Population-level comparisons of prokaryotic genomes must take into account the substanti

154 of new spacers during CRISPR adaptation, and prokaryotic genomes that encode Ago nucleases are enrich

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

156 MC, Bookshelf, genome data viewer, Assembly, prokaryotic genomes, Genome, BioProject, dbSNP, dbVar, B

157 l insights into the SD sequence variation in prokaryotic genomes, identifies a simple design principl

158 earches in 101 mycobacterial and ~4500 other prokaryotic genomes, we assessed the relative conservati

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

160 genomic datasets constructed using sequenced prokaryotic genomes.

161 I toxin-antitoxins systems are widespread in prokaryotic genomes.

162 Due to their prokaryotic heritage, chloroplast outer membranes contai

163 es iron homeostasis in eukaryotes, while the prokaryotic homolog from Novosphingobium aromaticivorans

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

165 Here we present crystal structures of a prokaryotic homolog of the mammalian transporters in com

166 of ZIP2 that was based on the structure of a prokaryotic homolog, Bordetella bronchiseptica ZrT/Irt-l

167 of function, as previously reported for the prokaryotic homolog, the Erwinia chrysanthemi ligand-gat

168 ubstituted compounds with human DMT1 and its prokaryotic homologue EcoDMT.

169 corporating them into the CRISPR loci of the prokaryotic host genome.

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

171 free and can be produced in high yields in a prokaryotic host, such as Escherichia coli In conclusion

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

173 his tradeoff implies an optimal size for the prokaryotic immune repertoire in the observational range

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

175 Type III CRISPR-Cas prokaryotic immune systems provide anti-viral and anti-p

176 palindromic repeats (CRISPR) machineries are prokaryotic immune systems that have been adapted as ver

177 Cultured Asgard archaea are typically prokaryotic in both size and internal morphology, albeit

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

179 s notable evolutionary conservation with the prokaryotic insertases(4,5), suggests that eukaryotic TM

180 ertain eukaryotic intermediary processes and prokaryotic intermediary or biodegradative metabolism.

181 KirBac1.1 is a prokaryotic inward-rectifier K(+) channel from Burkholde

182 KirBac1.1 is a prokaryotic Kir channel that shares homology with human

183 The emergence of eukaryotes from ancient prokaryotic lineages embodied a remarkable increase in c

184 is entirely synthesized in the chloroplast (prokaryotic lipids).

185 vious studies suggest that most, if not all, prokaryotic LRS membrane proteins serve as inhibitors of

186 GNIP1Aa is unique in being a prokaryotic MACPF member to have both its structure and

187 The magnetic minerals identified in prokaryotic magnetosomes are magnetite (Fe(3) O(4) ) and

188 eukaryotic diatoms, less is known for small, prokaryotic marine picocyanobacteria.

189 for diverging transport mechanisms within a prokaryotic MATE subfamily.

190 at is distinct from previously characterized prokaryotic mechanisms.

191 Prokaryotic mechanosensitive (MS) channels open by sensi

192 These results indicate that RaxX is a prokaryotic member of a previously unclassified and unde

193 heds light on protein structures involved in prokaryotic membrane fusion.

194 well as discovery of chemicals that inhibit prokaryotic membrane transport.

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

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

197 short-term (within-day) thermal responses of prokaryotic metabolic rates are typically more sensitive

198 Hydrogen sulfide (H(2)S) participates in prokaryotic metabolism and is associated with several ph

199 icability of both tools, we analyzed the 139 prokaryotic metagenomes of TARA Oceans and revealed the

200 Prokaryotic microbial assemblages were dominated by Prot

201 Although applications to prokaryotic microbial systems are emphasized, this proto

202 eptococcus pneumoniae NADPH oxidase (NOX), a prokaryotic model system for exploring structure and fun

203 arch on Na(+)/H(+) exchange has been done in prokaryotic models, mainly on the NhaA Na(+)/H(+)-exchan

204 d demonstrate that elements key to anaerobic prokaryotic molecular nanomachines, including Fe, V, Ni,

205 Shine-Dalgarno sequences (SD) in prokaryotic mRNA facilitate protein translation by pairi

206 Here, we used the same strategy on another prokaryotic Na(V) channel, Na(V)Sp1, to test whether equ

207 A crystal structure of Na(V)Ms, a prokaryotic Na(V) channel, suggests that the S4-S5 linke

208 Prokaryotic Na(V) channels are tetramers and eukaryotic

209 New prokaryotic Na(v) structures by Wisedchaisri et al. have

210 The prokaryotic NAD synthetase enzyme NadE catalyzes the las

211 We used the prokaryotic NavMs sodium channel, which has been shown t

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

213 ecruitment of UvrA, the initiating enzyme of prokaryotic NER, to an alkyl lesion by ATL.

214 Here we report the X-ray structure of the prokaryotic NSS member, LeuT, in a Na(+)/substrate-bound

215 These prokaryotic NulOs are similar in structure to Neu5Ac but

216 From this data set, we recovered 739,880 prokaryotic operational taxonomic units (OTUs, 16S-V4 ge

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

218 channels and transporters in eukaryotic and prokaryotic organisms by responding to ions or nucleotid

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

220 site-specific programmable transposition in prokaryotic organisms.

221 tic physiology, but much less is known about prokaryotic organisms.

222 the first proteinaceous plasmin inhibitor of prokaryotic origin described to date.

223 Chloroplasts are of prokaryotic origin with a double-membrane envelope separ

224 We identify distinct 6mA sensor domains of prokaryotic origin within the MPND deubiquitinase and AS

225 FAMIN and its prokaryotic orthologs additionally have adenosine deamin

226 Currently, only prokaryotic orthologs have been kinetically and structur

227 t there exist globally about 0.8-1.6 million prokaryotic OTUs, of which we recovered somewhere betwee

228 nt predictions that there exist trillions of prokaryotic OTUs.

229 Because uncharacterized proteins involved in prokaryotic oxidative stress response are rare, we sough

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

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

232 assembly was enhanced at the expense of the prokaryotic pathway.

233 from the genome in a manner identical to the prokaryotic pattern by incising 7 nt 5' and 3 or 4 nt 3'

234 sDNA-binding property different from YdbC, a prokaryotic PC4-like protein from Lactococcus lactis, bu

235 cyanobacteria opens the possibility of using prokaryotic photosynthetic cells in biotechnological app

236 6 per thousand), and those typical of modern prokaryotic phototrophs (-25 +/- 10 per thousand).

237 al role in the metabolism of C(i) throughout prokaryotic phyla.

238 assembling molecules with important roles in prokaryotic physiology with marked potential for synthet

239 eticulum membrane or the SecY channel in the prokaryotic plasma membrane(1,2).

240 ryotic endoplasmic reticulum membrane or the prokaryotic plasma membrane.

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

242 In conclusion, prokaryotic polyphosphates disturb multiple macrophage f

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

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

245 models are predominately based on studies of prokaryotic proteins.

246 as an invaluable blueprint for comprehensive prokaryotic proteomics.

247 pable of Q de novo synthesis, salvage of the prokaryotic Q precursors preQ(0) and preQ(1) also occurs

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

249 In contrast, the function of prokaryotic rhomboids has remained enigmatic.

250 Here, we report a class of de novo-designed prokaryotic riboregulators that provide ultraspecific RN

251 RNase H (RNH) nascent chains stalled on the prokaryotic ribosome in vitro We found that ribosome-sta

252 differential impact of m(4)C methylation on prokaryotic ribosomes and eukaryotic mitochondrial ribos

253 Type III-A CRISPR-Cas systems are prokaryotic RNA-guided adaptive immune systems that use

254 Cas9 is a prokaryotic RNA-guided DNA endonuclease that binds subst

255 also found in bacteria and archaea; whether prokaryotic Rqc2 has an RQC-related function has remaine

256 cing (PETRI-seq)-a low-cost, high-throughput prokaryotic scRNA-seq pipeline that overcomes these tech

257 Although conceptually similar, prokaryotic segregation systems and the eukaryotic kinet

258 istidine protein kinases (HKs) are prevalent prokaryotic sensor kinases that are central to phosphotr

259 unrecognized, but widely conserved class of prokaryotic sensory system that we refer to as the LytTR

260 r arose de novo via fusion of eukaryotic and prokaryotic sequences.

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

262 The characterization of prokaryotic serine/threonine protein kinases in bacteria

263 d for metal-responsive regulation of several prokaryotic single-component metalloregulators, and we b

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

265 We concluded that for prokaryotic sodium channels, a fine balance among filter

266 ntinuous cultivation alters the structure of prokaryotic soil microbiota after soil domestication, in

267 This report of sterol essentiality in a prokaryotic species advances our understanding of sterol

268 l for pan-genome analysis of closely related prokaryotic species or strains.

269 een as a crucial process in the evolution of prokaryotic species, but until recently it was thought t

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

271 an occur among genomes belonging to the same prokaryotic species, with only a fraction of genes being

272 e in the coordination of cell behavior among prokaryotic species.

273 r loop cysteine and FXN binding, and why the prokaryotic system does not require a similar FXN-based

274 ry histories with proteins involved in a few prokaryotic systems and a multitude of eukaryotic proces

275 Spatially organized molecular components in prokaryotic systems imply compartmentalization without t

276 In prokaryotic systems, the translation initiation of many,

277 resolved, genome phylogeny-based and digital prokaryotic taxonomy.

278 o the suicidal THI4 pathway: (i) nonsuicidal prokaryotic THI4s that lack the active-site Cys residue

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

280 activated by MtPrpR, a member of a family of prokaryotic transcription factors whose structures and m

281 Prokaryotic transcription is one of the most studied bio

282 mmation describes the composition of a model prokaryotic transcriptome.

283 foundly impact the evolution and function of prokaryotic translation initiation and other RNA-mediate

284 ners with potent inhibitory activity against prokaryotic translation initiation.

285 otency and selectivity for the inhibition of prokaryotic translation.

286 monstrated selectivity for the inhibition of prokaryotic translation.

287 Glimmer and Prodigal on genomes spanning the prokaryotic tree of life.

288 on of an iron-dependent mechanism regulating prokaryotic tryptophan biosynthesis that may indicate th

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

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

291 -incision patterns have been discovered: the prokaryotic type, which removes the damage in 11-13-nucl

292 defensin) protein; and the first report of a prokaryotic-type ribosomal protein in a eukaryotic virus

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

294 or antimicrobial drug discovery if issues of prokaryotic versus eukaryotic selectivity and antibiotic

295 dy, deep sequencing was used to characterize prokaryotic viral communities associated with honey bees

296 The vast majority of the prokaryotic viral populations are novel at the genus lev

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

298 Many prokaryotic viruses also carry CRISPR mini-arrays, some

299 roteins are commonly found in eukaryotic and prokaryotic viruses, where they play important roles in

300 fold centred around Emc3 that resembles the prokaryotic YidC insertase and that delineates a largely