ライフサイエンスコーパス: subfamily

1 e the activity of members of the CESA-like D subfamily.

2 t previous studies have focused on the NEDD4 subfamily.

3 block of leak channels belonging to the TASK subfamily.

4 pheromone components for species in the same subfamily.

5 Ontology (GO) terms, and PANTHER family and subfamily.

6 a divergence in grass species of the Poideae subfamily.

7 hat MbnH is most closely related to the MauG subfamily.

8 receptors (GPCRs) from the class A bioamine subfamily.

9 ansport mechanisms within a prokaryotic MATE subfamily.

10 erian unicorn' marked the extinction of this subfamily.

11 as shown by reinvention of function between subfamilies.

12 receptor-chemokine selectivity against other subfamilies.

13 ignin biosynthetic activity of canonical CAD subfamilies.

14 ligand and heterodimerize within and across subfamilies.

15 stinct channel properties of different Ca(v) subfamilies.

16 tic candidates from the TRPC, TRPM and TRPML subfamilies.

17 e provide coverage of the major class B GPCR subfamilies.

18 The nuclear receptor subfamily 0 group B member 2 (NR0B2, also called SHP) is

19 vates transient receptor potential vanilloid subfamily 1 (TRPV1) to counter high-fat diet (HFD)-induc

20 The nuclear receptor subfamily 1 group H member 4 (NR1H4, also called FXR) is

21 Here, we demonstrate that nuclear receptor subfamily 2 group E member 3 (NR2E3) plays a crucial rol

22 s dependent on serotonin 5-hydroxytryptamine subfamily 2 receptors (5-HT(2)Rs), and entry is thought

23 alysis revealed that NR2F2 (nuclear receptor subfamily 2, group F, member 2) sites were overrepresent

24 methylation in the GR gene (nuclear receptor subfamily 3, group C, member 1; NR3C1) have been associa

25 gered transient receptor potential vanilloid subfamily 4 (TRPV4) channel opening, which was responsib

26 1 and transient receptor potential vanilloid subfamily 4 (TRPV4) in acinar cells.

27 an emphasis on TGF-beta and nuclear receptor subfamily 4 group A member 1 (NR4A1) signaling.

28 iption factor Nur77 (Nr4a1 [nuclear receptor subfamily 4 group A member 1]) mediates the transition f

29 r to the region upstream of Nuclear Receptor Subfamily 4 Group A Member 3 (NR4A3) at 9q31.

30 itical region 1 (Dscr1) and Nuclear receptor subfamily 4, group A, member 3 (Nr4a3) genes.

31 shes in South and Central America with eight subfamilies, 41 genera and more than 300 valid species.

32 ola and Serratia symbiotica in the Lachninae subfamily [7-9].

33 into RA by aldehyde dehydrogenases family 1, subfamily A (ALDH1as), such as ALDH1a1, ALDH1a2 and ALDH

34 mpared with WT apoA-I) exhibited reduced ABC subfamily A member 1 (ABCA1)-dependent cholesterol accep

35 Cytochrome P450 family 102 subfamily A member 1 (CYP102A1) is a self-sufficient fla

36 overexpression of cytochrome P450 family 24 subfamily A member 1 (CYP24A1) increases lung cancer cel

37 box A1 (Hoxa1) and cytochrome P450 family 26 subfamily A member 1 (Cyp26a1) transcripts, direct RA ta

38 uctase (Hmgcr), and cytochrome P450 family 7 subfamily A member 1 (Cyp7a1), as well as cholesterol ef

39 hemical methods to identify the DnaJ homolog subfamily A member 1 (DjA1) as a novel GRASP65-binding p

40 Transient receptor potential channel subfamily A member 1 (TRPA1) is a Ca(2+)-permeable catio

41 5922 in aromatase (cytochrome P450 family 19 subfamily A member 1 [CYP19A1]).

42 associations at ABCA1 (ATP Binding Cassette Subfamily A Member 1), APOE-APOC1-APOC4-APOC2 (Apolipopr

43 ugh targeting of Abca1 (ATP-binding cassette subfamily A member 1).

44 cetin and myricetin, in ATP-binding cassette subfamily A member 4 (-/-) /retinol dehydrogenase 8 (-/-

45 on of KCNA5 (potassium voltage-gated channel subfamily A member 5; encoding Kv1.5) was increased, whe

46 ted, actin-dependent regulator of chromatin, subfamily A, member 2) to these elements.

47 The SAUR26 subfamily, a new subfamily of SAUR genes, was identified

48 h as PIN-LIKES, and the ATP-binding cassette subfamily (ABC-B/multidrug resistance/P-glycoprotein) tr

49 lation of a member of the fumarate reductase subfamily allows this enzyme to receive electrons from t

50 Marek's disease virus (MDV), a member of the subfamily Alphaherpesvirinae Like other alphaherpesvirus

51 architecture and comprise a highly conserved subfamily among fungal species.

52 age-specific contingents of TNL, CNL and RNL subfamilies and a central role in resilience to stress.

53 uman X chromosome is partitioned into repeat subfamilies and provide initial insights into centromere

54 multiple mutations representing all RGS GAP subfamilies and sampling both G protein interface and no

55 o the variable size and diversity of the RNL subfamily and a lack of data in Gymnosperms.

56 onstrates increased potency against the GRK2 subfamily and favorable pharmacokinetic parameters in mi

57 chanism of nitration by a member of the TxtE subfamily and highlight how the enzyme facilitates this

58 RRAS2 is a member of the RAS subfamily and is ubiquitously expressed.

59 signals mediated by small GTPases of the Ras subfamily and protein kinase B (Akt) to advance the deve

60 a suggest an enzymatic activity of HeR-48C12 subfamily and their possible involvement in fundamental

61 ermined the consensus HEPN motif in the Las1 subfamily and uncovered its canonical and specialized el

62 utilized by response regulators of different subfamilies, and provided insights into interactions of

63 activity of other formins, such as the mDIA subfamily, and promotes stable microtubule assembly.

64 NAs across 4 members of the gammaherpesvirus subfamily, and they identify orthologues and potential h

65 lection of conserved short peptides) of each subfamily, and thus were further used to annotate new ge

66 Focusing on Poaceae subfamilies Anomochlooideae, Pharoideae, Pueliodieae, Ba

67 The families and subfamilies are annotated with Gene Ontology (GO) terms,

68 Indeed, multiple SAS subfamilies are encoded in widespread conserved bicistro

69 gh-throughput sequencing, we show that 84 TE subfamilies are overrepresented, and distributed in a li

70 Previous relationship hypotheses among subfamilies are strongly corroborated, such as the siste

71 ry diseases, whereas IL-1alpha and the IL-36 subfamily are associated with skin diseases.

72 inct catalytic features of the Poaceae TPS-a subfamily arose early in grass evolution and the reactio

73 suggesting that the prevailing view of some subfamilies as 'basal' or 'early-diverging' with respect

74 solve extracellular loops, known in the TRPV subfamily as 'pore turrets', which are proximal to the u

75 lant cinnamyl alcohol dehydrogenase 7 (CAD7) subfamily as targets of multiple Avr3a-like effectors fr

76 age-gated potassium (Kv) channels of the Kv4 subfamily associate with Kv channel-interacting proteins

77 immunized with NOMV with overexpressed FHbp subfamily B (NOMV-FHbp), NOMV with FHbp genetically inac

78 ABC subfamily B member 1 (ABCB1) expression was reduced, and

79 The ATP-binding cassette subfamily B member 1 (ABCB1) multidrug transporter P-gly

80 inase 1 (CHIT1) and cytochrome P450 family 1 subfamily B member 1 (CYP1B1), both previously associate

81 Cytochrome P450 family 26 subfamily B member 1 (CYP26B1) regulates the concentrati

82 Cytochrome P450 family 27 subfamily B member 1 (CYP27B1) and CYP24A1 function to m

83 25(OH)(2)D(3)) via cytochrome P450 family 27 subfamily B member 1 (CYP27B1), whose gene is regulated

84 Voltage-gated potassium (K(+)) channel subfamily B member 1 (KCNB1, Kv2.1) and integrin-alpha5

85 annel Kv2.1 (potassium voltage-gated channel subfamily B member 1 or KCNB1).

86 P-glycoprotein (ABC subfamily B member 1, ABCB1) plays an important role at

87 The human cytochrome P450 family 11 subfamily B member 2 (hCYP11B2) gene encodes aldosterone

88 , and leukocyte immunoglobulin-like receptor subfamily B member 2 (LilrB2) exhibited direct binding t

89 C-1 was administered to ATP binding cassette subfamily B member 4 (Abcb4(-/-); Mdr2(-/-)) knockout (K

90 er damage in Mdr2(-/-) (ATP binding cassette subfamily B member 4 null) mice.

91 ice were crossbred with ATP binding cassette subfamily B member 4-deficient (Abcb4(-/-), alias Mdr2(-

92 ABC subfamily B member 5 (ABCB5) has been identified as a mo

93 osomal polypeptide ABC transporter TAPL (ABC subfamily B member 9, ABCB9) transports 6-59-amino-acid-

94 p ID 896 is a member of the variant group 1 (subfamily B), bound protective anti-FHbp monoclonal anti

95 f the auxin transporter ATP-BINDING CASSETTE subfamily B19 (ABCB19) by phot1 in phototropic seedlings

96 base, which groups CAZymes into families and subfamilies based on amino acid similarities, we recombi

97 ngle-pass membrane proteins are grouped into subfamilies based on the similarity of their extracellul

98 presence of the Sec7 domain, and found three subfamilies (BIG, GBF1, and cytohesins) to have been pre

99 heterodimers with GPCRs from their immediate subfamilies but not with more distantly related receptor

100 n 1 (adenosine triphosphate-binding cassette subfamily C member 1 [ABCC1]) is abundantly expressed at

101 ation in CYP2C19 (cytochrome P450, family 2, subfamily C, polypeptide 19) *2 and *3 alleles leads to

102 ng body of evidence that RTKs from different subfamilies can interact and that these diverse interact

103 Enzymes of the Dfg5 subfamily catalyze the essential transfer of GPI-anchore

104 The two major chemokine subfamilies, CC and CXC, bind distinct receptor subsets.

105 rsification of the New World buthid scorpion subfamily Centruroidinae Kraus, 1955, a clade of seven g

106 g pheromone use in cerambycid species in the subfamily Cerambycinae, and that identification of phero

107 The GH16 subfamily classification is publicly available in the CA

108 amilies (i.e. GH5, GH13, and GH43), this new subfamily classification provides a roadmap for function

109 sis; this category was more prevalent in the subfamily Colubrinae and less prevalent in Natricinae.

110 The existing structures do not include CXC subfamily complexes and lack information about the recep

111 with other monocot plants, the Poaceae TPS-a subfamily consists of five well-defined clades I-V, the

112 ted, actin-dependent regulator of chromatin, subfamily D, member 2) has recently been shown to have a

113 tion networks demonstrated eoxPL belonged to subfamilies defined by oxylipin composition.

114 The ovarian tumor (OTU) subfamily deubiquitinases have been implicated in the re

115 otion that ZgAgaC homologs define a new GH16 subfamily distinct from beta-porphyranases and classical

116 rouped the Capsicum ANK gene family into ten subfamilies distributed across all 12 pepper chromosomes

117 cation of the SEP/AGL6 and AP1/SQUA MADS-box subfamilies during angiosperm evolution.plantcell;31/12/

118 ory protein, potassium voltage-gated channel subfamily E (KCNE) subunit 4, acts as a dominant negativ

119 sified 390 CAZyme families into thousands of subfamilies each with distinguishing k-mer peptides.

120 The four other subfamilies (EFA6/PSD, IQSEC7/BRAG, FBX8, and TBS) are o

121 , a very deep phylogenetic split between the subfamilies Elasmotheriinae and Rhinocerotinae that incl

122 nhancer-enriched TE copies compared to their subfamily equivalents located in gene deserts.

123 ete genomes organized into gene families and subfamilies; evolutionary relationships between genes ar

124 sites (alpha, beta), and also a unique PMT2-subfamily exposed FKR motif.

125 sms, we recapitulated previously reported TE subfamily expression levels and revealed locus-specific

126 Mammalian ATP-binding cassette (ABC) subfamily F member 3 (ABCF3) is a class 2 ABC protein th

127 oductive PHAS loci in the genomes of Poaceae subfamilies from Panicoideae to Oryzoideae and to Poidea

128 We identified two ABCG1 (ABC subfamily G member 1) variants, which regulate cellular

129 efflux genes, including ATP binding cassette subfamily G member 5/8 (Abcg5/8) and cluster of differen

130 onsequence of increased ATP-binding cassette subfamily G member 5/8 activity given that NTCP inhibiti

131 r receptor class B member 1 (Scarb1) and ABC subfamily G member 8 (Abcg5/8), decreased hepatic and pl

132 (in adenosine triphosphate binding cassette subfamily G member 8 [ABCG8], sulfotransferase family 2A

133 3 x 10(-9)) of ATP-binding cassette protein, subfamily G, member 2 (ABCG2).

134 Heterotrimetic G proteins consist of four subfamilies (G(s), G(i/o), G(q/11), and G(12/13)) that m

135 re also required for the induction of SAUR63 subfamily genes by gibberellins (GAs).

136 In addition, the SAUR26 subfamily genes exhibit a high variation frequency and t

137 The SAUR26 subfamily genes play an important role in conferring var

138 nt elongation by direct activation of SAUR63 subfamily genes through conserved target sites in their

139 ssion of several SMALL AUXIN UP RNA (SAUR)63 subfamily genes, which contain TCP target motifs in thei

140 exes have been shown to act as GEFs for Rab7 subfamily GTPases [9-12].

141 ting proteins (GAPs), and in the Rho and Rab subfamilies, guanine nucleotide dissociation inhibitors

142 s of parvoviruses (PVs, family Parvoviridae; subfamily Hamaparvovirinae) infect penaeid shrimp.

143 ructure determination of all major aminergic subfamilies has enabled structure-based ligand design fo

144 The CAD7 subfamily has expanded in plant genomes but lost the lig

145 , most studies on plant receptor-like kinase subfamilies have focused on their kinase domains.

146 perfamily, but no eukaryotic members of this subfamily have been functionally characterized.

147 stant E3 ligase 1 (AREL1) belongs to "other" subfamily HECT that inhibits apoptosis by ubiquitinating

148 ase activity is specific to eukaryotic RecQ4 subfamily helicases, and genetic and biochemical data su

149 We show that TreeGrafter outperforms subfamily HMM scoring for correctly assigning subfamily

150 l genera of the Cactoideae and Pereskioideae subfamilies (Hylocereus, Cereus, Pilosocereus, Stenocere

151 evolutionarily conserved recruitment of bHLH subfamily II and III(a + c)1 in the regulation of tapetu

152 EAN1 belongs to the subfamily II and specifically forms heterodimers with th

153 or GPCRs to individual G-proteins instead of subfamilies; (ii) visually inspect the protein sequence

154 and specifically forms heterodimers with the subfamily III(a + c)1 members, which suggests a heterodi

155 nes were identified and clustered into eight subfamilies in Saccharum spontaneum.

156 alyses revealing the presence of numerous DP subfamilies in the plant kingdom.

157 08 also showed high selectivity for the GRK2 subfamily in a kinome panel of 104 kinases.

158 and functional diversification of the TPS-a subfamily in the Poaceae (the grass family), a plant fam

159 velopmental and functional roles of this Tmc subfamily in the zebrafish inner ear, we tested the effe

160 ed the role of OsHOX24, a member of HD-ZIP I subfamily, in abiotic stress responses.

161 f different species (and accessions) of both subfamilies, including their complete chemical profile r

162 Four terpene synthases (TPS) from the TPS-a subfamily, including two localised to the plastid, were

163 ggested that the pathway of two tapetal-bHLH subfamilies is conserved in all land plants, and likely

164 This study reveals that the SAUR26 subfamily is a key variation for thermo-responsive archi

165 The UGT2B subfamily is a major family of UGT enzymes expressed in

166 relaxation associated with potassium channel subfamily K member 3 (KCNK3) dysfunction.

167 nction mutations in KCNK3 (potassium channel subfamily K member 3) gene, which encodes an outward rec

168 tion assays using recombinant, purified SNF1-subfamily kinases confirmed postulated target specificit

169 members of the voltage-gated potassium (Kv) subfamilies Kv5, Kv6, Kv8, and Kv9 selectively modulate

170 G proteins make up two major subfamilies: "large" G proteins comprising three subunit

171 specific TE insertions rather than at the TE subfamily level.

172 nformational changes are unique for each RTK subfamily, limiting cross-activation between unrelated R

173 e Transient Receptor Potential (TRP) channel subfamily M (Trpm) as a critical channel that mediates t

174 transient receptor potential cation channel subfamily M member 4 (TRPM4), and perhaps TRPM5, Na(+) c

175 transient receptor potential cation channel subfamily M member 8 (TRPM8) channels to prolong calcium

176 channel transient receptor potential channel subfamily M member 8 (TRPM8) is the principal detector o

177 (transient receptor potential cation channel subfamily M member 8).

178 transient receptor potential cation channel, subfamily M, member 2) is a nonselective cation channel

179 yme (ACE2) and transmembrane protease/serine subfamily member 2 (TMPRSS2), their expression should de

180 nsient receptor potential melastatin channel subfamily member 2 (TRPM2) has an essential role in prot

181 of two promising candidates, MPP7 (MAGUK p55 subfamily member 7, a scaffolding protein involved in ce

182 subfamily members of the forkhead box (Foxp) subfamily member Foxp1 in Treg cells led to increased nu

183 structures of this carboxypeptidase, an S9C subfamily member from Deinococcus radiodurans, in its ac

184 CYP2C and CYP2J subfamily members actively metabolize fatty acids to bio

185 common promoter element; however, only three subfamily members are conserved in other fungi.

186 re, we report that the deletion of another P subfamily members of the forkhead box (Foxp) subfamily m

187 Neurotropic Alphaherpesvirinae subfamily members such as bovine herpesvirus 1 (BoHV-1)

188 idence of reactivation of Alphaherpesvirinae subfamily members.

189 y other agonists is not conserved among TRPV subfamily members.

190 P34.5 is widely encoded by alpha-herpesvirus subfamily members.

191 ubfamily HMM scoring for correctly assigning subfamily membership, and that it produces highly specif

192 The HECT E3 ligase family comprises three subfamilies: NEDD4 E3 ubiquitin protein ligase (NEDD4),

193 We find 45 distinct subfamilies of ABCFs that are widespread across bacteria

194 cterized actPTP domains from three different subfamilies of both receptor and non-receptor PTPs.

195 nd pU14, but also those conserved across all subfamilies of Herpesviridae.

196 e-based bioinformatic analysis identified 10 subfamilies of HeRs, suggesting their diverse biological

197 t of 16 representative GPCRs that cover most subfamilies of human GPCRs, where each has 300-5000 liga

198 The discovery of interactions between two subfamilies of IgSF cell surface proteins, the Dprs and

199 we report a critical role for B2, B3 and B4 subfamilies of Raf-like kinases (RAFs) in early osmotic

200 igate the deep-branching relationships among subfamilies of the Leguminosae (or Fabaceae), the third

201 ICD2, CRACR2a, and HOOK3, representing three subfamilies of unrelated adaptors, interact with the sam

202 e production of cadasides A (1) and B (2), a subfamily of acidic lipopeptides that is distinct from p

203 FigC belongs to a new subfamily of alanine racemase-fold PLP-dependent decarbo

204 The aquaglyceroporins are a subfamily of aquaporins that conduct both water and glyc

205 tivates one or more members of the AMPK/SNF1-subfamily of basophilic protein kinases.

206 odification or up-regulation of the BH3-only subfamily of BCL2 proteins.

207 receptors (AGPCRs) are a thirty-three-member subfamily of Class B GPCRs that control a wide array of

208 equence relatedness with F3'Hs in the CYP75B subfamily of cytochromes P450 than with those with known

209 and 2) are representative members of the OTU subfamily of deubiquitinylases.

210 esent work shows that expression of the PDE4 subfamily of enzymes is significantly up-regulated and c

211 ve on blood type A-antigen, along with a new subfamily of glycoside hydrolase 31 (GH31) that specific

212 the GIV2-GIV6 cluster is part of a 22-member subfamily of GPCRs, with many of them having in planta-s

213 nucleolar GTPase belonging to the HSR1_MMR1 subfamily of GTPases.

214 Alphaherpesviruses are a subfamily of herpesviruses that include the significant

215 ioC) transfers signals from the Galpha(q/11) subfamily of heterotrimeric G proteins to the small guan

216 upled receptor that couples to the Galpha(i) subfamily of heterotrimeric G-proteins and beta-arrestin

217 HD-ZIP I subfamily of homeobox transcription factors (TFs) are in

218 ken together, F. graminearum has an expanded subfamily of infection-related GPCRs for regulating vari

219 ses (KDMs), resulting in pan inhibition of a subfamily of KDMs.

220 GLI-similar 1-3 (GLIS1-3), a subfamily of Kruppel-like zinc finger transcription fact

221 nd elucidated as a representative of a novel subfamily of lanthipeptides, which we designate class V.

222 MAP kinase 6 (MKK6), which activates the p38 subfamily of MAPKs, we found that decaging active MKK6 i

223 icking and transmission via disc-large (DLG) subfamily of membrane-associated guanylate kinases (MAGU

224 of MRK-740 as a chemical probe for the PRDM subfamily of methyltransferases highlights the potential

225 CG3530 is homologous to the human MTMR6 subfamily of myotubularin-related 3-phosphatases, and th

226 , the ancestral Wirin evolved into the IgLON subfamily of neuronal receptors.

227 Hmx proteins are a subfamily of NK homeodomain-containing proteins that hav

228 anscription factor Nur77 belongs to the NR4A subfamily of nuclear hormone receptors.

229 that describes an emerging role for the PDE4 subfamily of phosphodiesterases in malignancy.

230 PP7L, PP7, and PP7-long constitute a subfamily of phosphoprotein phosphatases.

231 thway activating Rab23, a member of the Rab7 subfamily of Rabs, remains unclear.

232 erize a novel reaction catalyzed by one such subfamily of RaS enzymes during RiPP biosynthesis: insta

233 epidermal growth factor receptor (EGFR)/ERBB subfamily of receptor tyrosine kinases that regulates ce

234 RGS2 is a member of the R4 subfamily of RGS proteins and is unique in that it is se

235 The SAUR26 subfamily, a new subfamily of SAUR genes, was identified as a major locus

236 Here, we have identified a unique subfamily of silanols as the major determinant of silica

237 exacyclic calyciphylline B-type alkaloids, a subfamily of the Daphniphyllum natural products.

238 6B (HHV-6B) belongs to the beta-herpesvirus subfamily of the Herpesviridae.

239 s (Arabidopsis thaliana), which belongs to a subfamily of the monosaccharide transporter-like family.

240 A large subfamily of the type IV secretion systems (T4SSs), term

241 he ABC-B/multidrug resistance/P-glycoprotein subfamily of transporters in land plants, affected rhizo

242 One subfamily of transporters with proven clinical relevance

243 m channel TRPV6 is a member of the vanilloid subfamily of TRP channels that is permeable to cations a

244 layers and then become a large and important subfamily of two-dimensional (2D) materials.

245 observe increased expression of over 400 TE subfamilies, of which 262 appear to result from a proxim

246 All six subfamilies originated nearly simultaneously, suggesting

247 s from the delta-1 subclass of the p24 delta subfamily (p24delta3delta4delta5delta6 mutant).

248 hylininae and its sister relationship to the subfamily Paederinae have been broadly accepted accordin

249 QUAMOSA (SQUA) MADS-box transcription factor subfamilies play key roles in floral organ identity dete

250 nts contributed to ST gene expansions of two subfamilies, PLT and STP, in S. spontaneum, indicating a

251 lution of life-cycle strategies in the grass subfamily Pooideae and test if transitions between them

252 The grass subfamily Pooideae dominates the grass floras in cold te

253 e definitions are available via SPARCLE, the Subfamily Protein Architecture Labeling Engine.

254 Our results reveal CAD7 subfamily proteins as negative regulators of plant immun

255 C3A and LC3B, whereas binding to the GABARAP subfamily proteins was facilitated by residues either N-

256 e overlapping and distinct functions of ATG8 subfamily proteins.

257 rn, the four members of the petunia AP1/SQUA subfamily redundantly are required for inflorescence mer

258 This first demonstration that the Galpha(s) subfamily regulates activity of Rho GTPases extends our

259 ization of ErfA regulon across P. aeruginosa subfamilies revealed a second conserved target, the ergA

260 with others throughout GH5_4 and neighboring subfamilies reveals at least two residues (H149 and W203

261 Here, we review the known cross-subfamily RTK heterointeractions and their possible biol

262 We have synthesized a new GRK2 subfamily-selective inhibitor, CCG258747, which has nano

263 7 and 10 other inhibitors with different GRK subfamily selectivities and with either the paroxetine o

264 For one member of the ATCOPIA52 subfamily (SISYPHUS), cPPT intermediates were not observ

265 y by orienting the chemokine N terminus in a subfamily-specific direction.

266 iously unknown accessory subunit CydH, the L-subfamily-specific Q-loop domain, a structural ubiquinon

267 d adjacent C-terminal region as well as ATG8 subfamily-specific residues in the LIR docking site are

268 oth the novel predatory structure and of the subfamily Steninae (Coleoptera: Staphylinidae).

269 ther luminescent members of the Keroplatinae subfamily still remain to be fully elucidated.

270 other RGS proteins, little is known about RZ subfamily structure and regulation.

271 We also identified a cytohesin-derived subfamily, termed ankyrin repeat-containing cytohesin, t

272 mes within patrilines (i.e., father-daughter subfamilies) than between patrilines in each colony.

273 nd DIPs in protostomes, along with two other subfamilies that diversified independently across protos

274 se belonging to a previously uncharacterized subfamily that features two extra pairs of cysteine resi

275 CHE domains (especially those belonging to a subfamily that includes the AI-2 receptors identified in

276 d, short-tailed member of the myosin class I subfamily that supports a variety of actin-based functio

277 of sesquiterpene synthases within the TPS-b subfamily that typically contains mostly monoterpene syn

278 f direct and indirect recognition within NLR subfamilies, the regulation of NLRs by small RNAs, and t

279 te the T-type, or the low-voltage-activated, subfamily, the abnormal activities of which are associat

280 dding three extra families and an additional subfamily, thus greatly improving taxonomic coverage.

281 XP builds mappability signatures from LINE-1 subfamilies to deconvolve the effect of pervasive transc

282 om land plants can be divided into different subfamilies, TPS-a to TPS-h.

283 lming support for the monophyletic status of subfamily Trichomycterinae including Ituglanis and Scler

284 T5virus and a putative new genus within the subfamily Tunavirinae.

285 nases; however, the recently discovered P450 subfamily TxtE utilizes O(2) and NO to nitrate aromatic

286 that differential binding affinities of ARF subfamilies underlie diversity in cis-element function.

287 interaction is conserved, the three adaptor subfamilies use different folds (coiled-coil, EF-hand, H

288 transient receptor potential cation channel subfamily V member 1 (TRPV1) on sensory neurons to alter

289 (transient receptor potential cation channel subfamily V member 1) immunoreactivity (polymodal nocice

290 transient receptor potential cation channel subfamily V member 2 channels.

291 transient receptor potential cation channel subfamily V member 3 (TRPV3) channel plays a critical ro

292 transient receptor potential cation channel, subfamily V, member 4) channels.

293 inase B1 (LKB1), a master kinase of the AMPK subfamily, via CpG island methylation.

294 mammalian ancestor of the cytochrome P450 1B subfamily was herein characterized structurally and func

295 Placing GH5_4 in context with other related subfamilies, we highlight several possibilities for the

296 e and mechanism of the IMB3 karyopherin-beta subfamily whilst also highlighting differences with the

297 We also identified a subfamily-wide positive correlation between lichenase an

298 ome for the papilionoid legumes (the largest subfamily within the third largest family in flowering p

299 binantly produced 564 proteins selected from subfamilies without any biochemically characterized repr

300 mber of the receptor-like cytoplasmic kinase subfamily XII, in PRR-initiated immunity.