1 234 in the presumptive active site of JIP60
are conserved in 815 plant RIPs in the Pfam database tha
2 inear epitope sequences targeted by the LFIA
were conserved in 98% of 954 B. pertussis isolates colle
3 deficiency and enhanced herbivory resistance
is conserved in a diversity of plants, including crops.
4 Lys-149
is conserved in a narrow part of branch B, and Trp-112 i
5 Further, the antitumoral effect of miR-28
is conserved in a primary murine in vivo model of BL.
6 Residue C373 in K14, which
is conserved in a subset of keratins, is revealed as a n
7 ed in a narrow part of branch B, and Trp-112
is conserved in a wider group within branch B.
8 Moreover, Ile-48 and the phiX(D/E) motif
are conserved in A55 orthologues from other poxviruses,
9 We find that the activation trajectory
is conserved in aged cells, and we develop effective mac
10 Melanoma antigen (MAGE) genes
are conserved in all eukaryotes and encode for proteins
11 MAGE genes
are conserved in all eukaryotes and have expanded from a
12 Mitogen-activated protein kinase cascades
are conserved in all eukaryotes.
13 These cysteine residues
are conserved in all four desmoglein family members.
14 well gH-gL and the fusion protein gB, which
are conserved in all herpesviruses.
15 nt proteins from herpes simplex virus 1 that
are conserved in all herpesviruses: pUL7 and pUL51.
16 ncident with the emergence of the Hyaenidae,
being conserved in all extant hyena species.
17 The finger
is conserved in all algal septin sequences, suggesting a
18 We identify an auxin-degradation operon that
is conserved in all available genomes of Variovorax and
19 The bifunctional AdhE enzyme
is conserved in all bacterial kingdoms but also in more
20 The receptor-interacting site
is conserved in all coronavirus S glycoproteins that eng
21 includes eight families among which the RidA
is conserved in all domains of life.
22 the pathway of two tapetal-bHLH subfamilies
is conserved in all land plants, and likely was establis
23 hybridization and immunohistochemistry, and
is conserved in all Mabuya species tested, spanning over
24 mutates a cytoplasmic arginine residue that
is conserved in all neuroligins.
25 ylation at an adjacent residue (N102), which
is conserved in all NLGNs.
26 The I2 protein
is conserved in all poxviruses that infect vertebrates,
27 m(1)G37 methyltransferase enzyme TrmD, which
is conserved in all three domains of life as a tight 3',
28 e analysis, the beta-bracelet motif of delta
is conserved in all three nematode viruses and could acc
29 The overall structure of thyroglobulin
is conserved in all vertebrates.
30 n, fibrinogen, into a polymeric fibrin clot,
is conserved in all vertebrates.
31 olidated in a single organ, the liver, which
is conserved in all vertebrates.
32 this non-neural origin of pineal progenitors
is conserved in amniotes.
33 igate whether inhibition by divalent cations
is conserved in an invertebrate SLO2 channel we cloned t
34 signaling to division-specific PG synthesis
is conserved in another alpha-proteobacterium, Agrobacte
35 This immunosuppressive ability
is conserved in another nudivirus, suggesting that the T
36 ent named conoid protein hub 1 (CPH1), which
is conserved in apicomplexan parasites.
37 porting that the essential function of CBL10
is conserved in Arabidopsis and tomato.
38 nslation of the psbJ ORF, that this function
is conserved in Arabidopsis LPE1, and that an additional
39 Cyanobacterial TM protein localization
was conserved in Arabidopsis (Arabidopsis thaliana) chlo
40 PINA
is conserved in archaea and vital for S. islandicus viab
41 This mechanism
is conserved in at least two rodents and humans, making
42 This novel LOTUS domain-RNA interaction
is conserved in bacteria, plants and animals, comprising
43 We find that only some TADs
are conserved in both cell lines, whereas the rest are c
44 and a putative catalytic glutamic acid that
is conserved in both bacterial TIR NAD(+)-cleaving enzym
45 uitos implying that the requirement for ERI3
is conserved in both DENV hosts.
46 genous chromophore supply, and this response
is conserved in both human and mouse retinas.
47 eases the deacylation rate, but this residue
is conserved in both KPC-2 and non-carbapenemase beta-la
48 us Nedd8 binding sequence, L(X7)R(X5)F(X)ALQ
is conserved in both Smurfs.
49 that BMP signaling-based germ cell induction
is conserved in both the mouse Mus musculus and the cric
50 We found that only 14% of their BSs
were conserved in both species and that these contained
51 dies suggested that the roles of VRN1 and FT
are conserved in Brachypodium distachyon yet identified
52 es a Cdc4 phosphodegron (CPD) in LIN-45 that
is conserved in BRAF.
53 gical techniques to show that autoinhibition
is conserved in budding yeast, and plays a key role in c
54 ing and EutR-dependent regulation of the LEE
are conserved in C. rodentium Moreover, during infection
55 Moreover, tyrosine fragmentation
is conserved in C. elegans.
56 hydrophobic surface on the Hrr25 N-lobe that
is conserved in CK1delta-family kinases, suggesting a ro
57 omplementation indicates that MrfAB function
is conserved in closely related species.
58 pecies indicated that the repressive element
is conserved in closely related species.
59 A pair of histidine residues, which
are conserved in coronavirus spike proteins, are predict
60 This TCP/HD-ZIP genetic module seems to
be conserved in dicot and monocotyledonous species to pr
61 asic gene network controlling fruit ripening
is conserved in different Solanaceae clades, and that cl
62 found that the properties of the excitation
were conserved in different brain areas.
63 feedback inhibition by NAD(+) This mechanism
is conserved in distantly related bacteria.
64 Ngs1
is conserved in diverse fungi that have GlcNAc catabolic
65 ost-transcriptional control of miR171 levels
is conserved in diverse rice species.
66 rthologs on misfolded proteins were found to
be conserved in Drosophila and mammalian cells.
67 This mechanism was shown to
be conserved in Drosophila cells.
68 This phospho-dependent binding interaction
is conserved in Drosophila and facilitates the stable in
69 Moreover, this relationship
was conserved in each clinical subgroup, despite the het
70 ins putative cytokinin response elements and
is conserved in eight more legume species.
71 Vps13 proteins
are conserved in eukaryotes, but their molecular functio
72 Putative orthologs of Arabidopsis DGS1
are conserved in eukaryotes, including the Nuclear Contr
73 The enzyme
is conserved in eukaryotes and also found in some prokar
74 The core elements of the CDK control system
are conserved in eukaryotic cells, which contain multipl
75 vivo, suggesting that our in vitro findings
are conserved in evolution.
76 hesis of de novo proteasomes is a trait that
is conserved in evolution and is found in organisms rang
77 of viral RNA, and show that this interaction
is conserved in evolutionarily distant influenza viruses
78 We show that this mechanism
is conserved in evolutionary very distant species.
79 Here we quantify how that diversity
is conserved in ex situ collections across the world's b
80 constraining octane for omega-hydroxylation
are conserved in family 4 P450s.
81 l tRNAs showed reduced aminoacylation, which
was conserved in fasted mice.
82 egrity of its binding motif His-X-Asp, which
is conserved in Fe-dependent dioxygenases(3).
83 This gene
is conserved in fishes as well as tetrapods.
84 Although similar structures appear to
be conserved in fission yeast, computational modeling an
85 SK1 and BSK2, two close paralogs of SSP that
are conserved in flowering plants, are involved in sever
86 er to AtPIN1, Sister-of-PIN1 (SoPIN1), which
is conserved in flowering plants.
87 ive role of IRE1alpha under genotoxic stress
is conserved in fly and mouse.
88 factor attachment protein receptors (SNAREs)
are conserved in fungi, plants and animals.
89 Although these polyploid genomes
are conserved in gene content and synteny, they have div
90 sponsible for transcription, RNA polymerase,
is conserved in general architecture and catalytic funct
91 Serine-rich repeat glycoproteins (SRRPs)
are conserved in Gram-positive bacteria.
92 Thus, IDE1 seems to
be conserved in grass and nongrass species.
93 n sites are conserved and that a fourth site
is conserved in H3N2 IAVs.
94 Core stabilising structures
are conserved in herpesviruses suggesting their ancestra
95 to a previously uncharacterized family that
is conserved in heterokont algae.
96 The protein
is conserved in higher plants and bryophytes but absent
97 This tyrosine
is conserved in homomeric GABA(A)Rs and in the Erwinia c
98 Notably, IFNbeta effects
are conserved in human adipocytes and detection of the t
99 ay, regulate the onset of FIA reactions, and
are conserved in human intestine.
100 Brg1-regulated pathways
are conserved in human Shh-type medulloblastoma, and Brg
101 he transcriptional activation of WNT by AP-1
is conserved in human cancer cells.
102 HP-1 homolog CHORDC1 during EGFR trafficking
is conserved in human cells.
103 turity and neurotransmitter uptake function,
is conserved in human development, and is disrupted by n
104 Here, we show that this cell heterogeneity
is conserved in human epicardium, regulated by BNC1 and
105 narily young LINE-1 elements, a pattern that
is conserved in human ESCs.
106 Proton leak-mediated NGSIS
is conserved in human islets and is stimulated by exposu
107 erse correlation between DACH1 and ATF6/PLAT
is conserved in human liver.
108 The extent to which local protein synthesis
is conserved in human neurons is unknown.
109 ke receptors on T cells, and this regulation
is conserved in human T cells.
110 this architecture of the CENP-H/I/K complex
is conserved in human.
111 DPR-dependent SAP sampling of food allergens
was conserved in human intestinal organoids.
112 Our observations in the mouse models
were conserved in human cells.
113 d that markers of heart and lung ECs in mice
were conserved in human fetal heart and lung ECs.
114 These functional relationships
were conserved in human GBM.
115 HSC, however only 17 underwent changes that
were conserved in human HSC.
116 cers and showed that most epigenetic changes
are conserved in humans and mice.
117 Most circRNAs
are conserved in humans and specific ones are deregulate
118 Key macaque types
are conserved in humans, allowing mapping of cell-type a
119 44 novel candidate CA proteins, of which 13
are conserved in humans.
120 urface of its TPR domain using residues that
are conserved in humans.
121 effects of 1,25(OH)(2)D(3) observed in mice
are conserved in humans.
122 clock, suggesting that this oscillator might
be conserved in humans(3).
123 We explored whether this distinction would
be conserved in humans.
124 ion of Gal-9, indicating these processes may
be conserved in humans.
125 ulator of glial progenitor proliferation may
be conserved in humans.
126 tonic structure of the rodent MFC has mostly
been conserved in humans, it is a long-standing question
127 We show the prevalence of complex LSVs
is conserved in humans and identify hundreds of LSVs tha
128 t the transcriptionally discrete border zone
is conserved in humans, and led to the identification of
129 r, it is controversial whether BCO2 function
is conserved in humans, because of a 4-amino acid long i
130 gon-like peptide-1 system defined in rodents
is conserved in humans, highlighting the translational i
131 This pathway
is conserved in humans, suggesting that it may be a viab
132 ase expression, indicating that this pathway
is conserved in humans.
133 This ChREBP/G6PC signaling axis
is conserved in humans.
134 cry and has a motif near the N terminus that
is conserved in IkappaBalpha, beta-catenin, HIV Vpu, and
135 The upward growth direction
is conserved in indica and japonica rice varieties, sugg
136 However, Fam20 kinases
are conserved in invertebrates lacking bone and enamel,
137 major mechanisms of voltage-dependent gating
are conserved in K(V)10.2 channels.
138 ides, we show that the ligand/receptor model
is conserved in K(V)10.2, suggesting that this model is
139 nts revealed impaired autophagic flux, which
was conserved in kidney epithelial cells derived from bo
140 one another into a secondary structure that
is conserved in lincRNA-p21 among primates.
141 the FPs of 3 different lineages of beta-CoVs
are conserved in location within the S glycoproteins and
142 to damage repair and regeneration in mammals
are conserved in lower organisms, indicating that it is
143 TDP-43-mediated impairments
are conserved in mammalian cells, and, importantly, the
144 Poxins
are conserved in mammalian poxviruses.
145 Because the N-terminal RDs
are conserved in mammalian Pumilio orthologs, the result
146 ex and provide evidence that this regulation
is conserved in mammalian cells.
147 The hybrid cilium
is conserved in mammalian multiciliated cells, originate
148 As TSP-12 and TSP-14
are conserved in mammals, our findings suggest that the
149 Some of these mechanisms are now known to
be conserved in mammals.
150 s1 in spermatogenesis, a function that could
be conserved in mammals.
151 her this represents an uptake mechanism that
is conserved in mammals and how these cells affect funct
152 Umbilical vessel dimorphism
is conserved in mammals, suggesting that differential pr
153 NA damage-induced nuclear Dicer accumulation
is conserved in mammals.
154 sion of two genes, HIST2H2AA3 and HIST1H2BC,
is conserved in mammals.
155 parallel topology, is thermally stable, and
is conserved in mammals.
156 These kinases
are conserved in many eukaryotes including humans, sugge
157 nments show that the lipid-interaction sites
are conserved in many family members but less so in thos
158 duced by other metabolism, and AcuI and PrpE
are conserved in many organisms across all domains of li
159 We found that CrsR
is conserved in many aquatic proteobacteria, and most of
160 d methionine, producing the 25 kDa form that
is conserved in many bacteria and protozoans.
161 The gene pair encoding PsXEG1 and PsXLP1
is conserved in many Phytophthora species, and the P. pa
162 ition and formation of this membrane network
is conserved in maturing primitive and definitive erythr
163 ases (GT4) and contains an E-X7-E motif that
is conserved in members of GT4 and two other GT families
164 fficient for replication initiation in vitro
is conserved in metazoa.
165 lapping a known Ptf1a enhancer region, which
is conserved in mice and humans.
166 This effect
is conserved in mice and is independent of the different
167 of epigenetic aging, and this role seems to
be conserved in model organisms.
168 ing motifs for various transcription factors
are conserved in monkeys and humans.
169 hese data confirm that health benefits of CR
are conserved in monkeys and suggest that CR mechanisms
170 ls cellular survival, surface BCR expression
is conserved in most mature B-cell lymphomas.
171 ons of present day higher plant's Rca, which
is conserved in most species seem to have evolved in cha
172 Moreover, some of the human motifs appear to
be conserved in mouse and fruit fly.
173 endent SHISA3 regulation was demonstrated to
be conserved in mouse and human models.
174 The transcriptomic signature of c-KIT(+) ECs
was conserved in mouse and human lungs and enriched in F
175 This mechanism
is conserved in murine hearts in which cardiomyocyte pro
176 rtantly, the CR-independent membrane binding
was conserved in murine and canine muscles.
177 We show that the AtZAR1 immune pathway
is conserved in N. benthamiana and identify AtZAR1 domai
178 acquired residues (e.g. Pro(52) and Asp(55))
are conserved in naturally efficient CMs, but most of th
179 Here, we show that this vulnerability
is conserved in non-small cell lung cancer (NSCLC), wher
180 In rabbits, we find that expression of Satb2
is conserved in On-Off DSGCs; however, it has evolved to
181 case core and several auxiliary domains that
are conserved in orthologs of the enzyme.
182 better understand whether these differences
are conserved in other CYP3A5 structures and how they re
183 ement; however, only three subfamily members
are conserved in other fungi.
184 thesis, and that the interfaces mediating it
are conserved in other members of Mononegavirales Finall
185 We show that these genome release stages
are conserved in other mimiviruses.
186 for stem cell-mediated regeneration that may
be conserved in other adult stem cell niches.
187 This model could
be conserved in other bacteria, including the pathogenic
188 This protective mechanism might
be conserved in other differentiating cyanobacteria as H
189 Furthermore, this ATR system appears to
be conserved in other Gram-negative bacteria.
190 is consistent between mice and rats and may
be conserved in other species.
191 ostasis in anticipation of fertilization may
be conserved in other species.
192 tecture and synaptic physiology, which could
be conserved in other species.
193 The E-loop may
be conserved in other systems in order to play similar r
194 NsdD's role in repressing conidiation
is conserved in other aspergilli, as deleting nsdD cause
195 uring MHV68 infection and that this activity
is conserved in other herpesviral protein kinase homolog
196 iors in Drosophila This phosphorylation site
is conserved in other insects, including mosquitoes, ind
197 ations in Kir1.1 suggest that this mechanism
is conserved in other Kir channels.
198 We show that myomaker function
is conserved in other mammalian orthologs; however, rela
199 S551 of SIK3
is conserved in other members of the SIK family, such as
200 t the regulatory function of MYB31 and MYB42
is conserved in other monocots, specifically in sorghum
201 cle and that this pattern of gene expression
is conserved in other Plasmodium species.
202 translational RNA contains a C residue that
is conserved in other S-box RNAs that are predicted to r
203 ial genomes, it is unknown if this mechanism
is conserved in other species.
204 switch that mediates androgen signaling and
is conserved in other steroid hormone receptors.
205 Moreover, this rank
is conserved in other zebrafish embryonic assays and Dro
206 lid structure that folds over the substrate
are conserved in P4H-TM, whereas the extensive loop stru
207 involved in (R)-16 binding to SARS-3CL(pro)
are conserved in PEDV-3CL(pro); however, the sequence va
208 governing circadian activator stability that
are conserved in perhaps all eukaryotes, and suggest tha
209 s involved in potassium homeostasis seems to
be conserved in phylogenetically related bacteria.
210 is revealed that a majority of these modules
are conserved in Picea abies The high spatial resolution
211 /Rhodospirillaceae-like phosphatases (RLPHs)
are conserved in plants and several other eukaryotes, bu
212 enes belong to the Argonaute gene family and
are conserved in plants, animals and humans.
213 show that the TOR-LARP1-5'TOP signaling axis
is conserved in plants and regulates expression of a cor
214 ction in the maturation of FeS proteins that
is conserved in plants, and is closely allied to the fun
215 of Pol epsilon in replicative stress sensing
is conserved in plants, and provide, to our knowledge, t
216 A1 observed in recombinant fragments of VWF
are conserved in plasma-derived VWF.
217 dentified in essential germline proteins and
are conserved in prokaryotes and eukaryotes.
218 mals remains unknown, although TRH receptors
are conserved in proto- and deuterostomians.
219 PstSCR1 homologs were found to
be conserved in Pst, and in its closest relatives, Pucci
220 hat condensin-dependent chromatin compaction
is conserved in quiescent human fibroblasts.
221 neven distribution of Aii signals to ON CBCs
is conserved in rabbit, including one class entirely lac
222 ating decision-making in the multistage task
are conserved in rats and humans.
223 Hooft anomaly matching condition: anomalies
are conserved in renormalization group flow.
224 Finally, we demonstrate that this phenomenon
is conserved in rice (Oryza sativa) and wheat (Triticum
225 cord injury, we asked if the S1 CST response
is conserved in rodents.
226 erizes and demonstrate that this interaction
is conserved in Salvador's mammalian homolog.
227 ong them, the Lsr (LuxS-regulated) QS system
is conserved in scores of bacteria, and its signal molec
228 target sites fall within two domains, which
are conserved in sequence/structure indicating their imp
229 cific to the targeted gene's sequence, which
is conserved in several bacterial genera, and the oligom
230 siveness of His73 methylation, which we find
is conserved in several model animals and plants, its fu
231 ptor binding region of the HN protein, which
is conserved in several paramyxoviruses.IMPORTANCE Oncol
232 the chemotactic signal transduction pathway
is conserved in Shewanella, and histidine kinase and fla
233 of flies and fish but whether this activity
is conserved in somatic human cells is not known.
234 nding motif, but not the degradation signal,
is conserved in SREBP1.
235 ain in which point mutation of residues that
are conserved in staphylococci and major truncations abo
236 higher eukaryotes, since the key components
are conserved in structure and function throughout evolu
237 veground species, while "disordered" domains
were conserved in subterranean organisms, and confirmed
238 cal exposures from other mechanisms that may
be conserved in TDS.
239 e also show that native protein conformation
is conserved in TENG-ESI, and that patterned ion deposit
240 Moreover, the HIV-1 and SIV Vif proteins
are conserved in terms of their interactions with HIV-1
241 ecies, whereas threonine (serine in rodents)
is conserved in terrestrial vertebrate MR.
242 folding mechanisms of WT- and D76N-beta(2)m
are conserved in that both proteins fold slowly via an I
243 and olfactory receptor (Or) genes of MP-OSNs
are conserved in the agricultural pest D. suzukii.
244 ne whether renal primary ciliogenic programs
are conserved in the eye, and to characterize the functi
245 summary, we show that ciliogenesis programs
are conserved in the kidneys and eyes of zebrafish and m
246 wo clades and found 151 candidate genes that
are conserved in the Listeria sensu stricto species.
247 Key proteins involved in the pathway
are conserved in the model photosynthetic microalga Chla
248 Although six MCU gene homologs
are conserved in the model plant Arabidopsis (Arabidopsi
249 een Ascaris and Parascaris, whereas only 10%
are conserved in the more divergent T. canis.
250 n BPV-1 and HPV-31 E2, 8 of the 11 tyrosines
are conserved in the N-terminal domain, suggesting that
251 how that the dual functions of EspE and EspF
are conserved in the orthologous proteins from M. tuberc
252 Moreover, PHR-tail interactions
are conserved in the paralog CRY2 and reduced when eithe
253 kinase PKA, except the catalytic aspartate,
are conserved in the PKDs of GC-A and GC-B.
254 gest that allosteric pathways for activation
are conserved in the TRPV family.
255 These architectural features
are conserved in the yeast and bacterial Mre11/Rad50 com
256 ults show that major trunk lymphatic vessels
are conserved in the zebrafish, and provide a thorough a
257 It
is conserved in the alphabaculoviruses and expressed at
258 f a novel PCNA interacting protein NreA that
is conserved in the archaea and that has a PIP motif at
259 We demonstrate that the ogc cluster
is conserved in the Burkholderia genus, and we confirm t
260 The site of methylation on PP2Ac
is conserved in the catalytic subunits of PP4 and PP6, a
261 The gene encoding AceI
is conserved in the core genome of A. baumannii, suggest
262 demonstrated that the role of YAP signaling
is conserved in the developing human esophagus by utiliz
263 The transcription factor EutR
is conserved in the Enterobacteriaceae and is required f
264 This role
is conserved in the fungus Sordaria However, functional
265 approach is that the solution-phase labeling
is conserved in the gas phase prior to precursor fragmen
266 This residue
is conserved in the GT-C superfamily.
267 The fusogenic activity of Minion
is conserved in the human orthologue, and co-expression
268 n of HERV-K to a CGG-containing element that
is conserved in the LTRs of HERV-K-10, -K-11, and -K-20,
269 n essential lipid A biosynthetic enzyme that
is conserved in the majority of gram-negative bacteria.
270 investigate whether this barotactic response
is conserved in the more primitive model organism Dictyo
271 ratase (GMD) and GDP-L-fucose synthase (FS),
is conserved in the parasite genome, but the importance
272 The recognition of H4K16ac
is conserved in the PHD7 finger of paralogous MLL3.
273 SAL1 for activation of chloroplast signaling
is conserved in the plant kingdom, and the plant protein
274 The FSE-arch
is conserved in the related MERS-CoV and is under purify
275 /ZP-C linker that is not observed in ZP2 but
is conserved in the sequence of deafness/Crohn's disease
276 o find that the Ser5 sensitivity to glycoGag
is conserved in the SERINC family.
277 Here, we show that this relationship
is conserved in the simple eukaryote Dictyostelium and e
278 -dependent but IRF3-independent process that
is conserved in the STING S365A mice.
279 This pattern
is conserved in the tetrasaccharide, showing that linkag
280 cated within an Alu element in a region that
was conserved in the murine B1 element.
281 Nevertheless, many antigens
were conserved in the core genome, and strains' antigeni
282 e contacts with haemagglutinin residues that
were conserved in the great majority of 2016-2017 H7N9 i
283 Few of the loci were found to
be conserved in two other legume species (chickpea [Cice
284 evealed by SUMO E1 structures are thought to
be conserved in Ub E1, there is currently a lack of stru
285 n the capture of the TRIM21 substrate lysine
are conserved in ubiquitin-conjugating E2s, whereas resi
286 ns of the TL and Gre factors in RNA cleavage
are conserved in various species, with important variati
287 The RNAi machinery
is conserved in vertebrate cells, yet whether antiviral
288 ming and stem-cell-based translational study-
is conserved in vertebrate embryos(6-8).
289 ytokine that belongs to the IL-17 family and
is conserved in vertebrates and invertebrates.
290 We show that this key role
is conserved in vertebrates, because "crispant" zebrafis
291 The RNAP-LuxR interaction domain
is conserved in Vibrio cholerae HapR and is required for
292 This antiviral mechanism
is conserved in virtually all cell types, except for emb
293 This Metformin-mediated effect
was conserved in vivo; Metformin-treatment significantly
294 mains: the acidic region, the WUS-box, which
is conserved in WUS-related HOMEOBOX family members, and
295 activity is related to a loop structure that
is conserved in yeast and forms a distinct penultimate (
296 that Dbp5 helicase activity of mRNA release
is conserved in yeast and humans.
297 zed WRDPLVDID domain (residues 637-645) that
is conserved in yeast, mice, and humans.
298 f CTD Ser2 residues at 5' ends of genes that
is conserved in yeast.
299 Although circadian rhythms of Vo2
were conserved in young lean CT-1(-/-) mice (2 mo), CT-1
300 a negatively charged RLDP motif in NS3 that
is conserved in ZIKV strains of African and Asian lineag