ライフサイエンスコーパス: ring

1 - and beta-polypeptides in an individual LH1 ring.

2 roups are on the same face of the cyclohexyl ring.

3 d envelope conformation of the five-membered ring.

4 ketone functionality within the macrocyclic ring.

5 tion proceeds via formation of the dioxetane ring.

6 sitional hourglass, as well as in the double ring.

7 (LMW-PAH) (liver > muscle) with 2-3 aromatic ring.

8 fluorophenyl ring and electron-rich naphthyl ring.

9 of two ring complexes, the MS-ring and the C-ring.

10 lic C=C double bond at the 2-position of the ring.

11 ll surface for the proper location for the Z-ring.

12 ReB(4)(-) is found to be a planar pentagonal ring.

13 an exo-cyclic double bond in the pyrrolidine ring.

14 ane having a phenyl substituent at C3 of the ring.

15 g and fragmentation of the parent butenolide ring.

16 the pyrimidine ring compared to the pyridine ring.

17 ogenic center on the C2 of the five-membered ring.

18 of domino reactions on the benzothiadiazole ring.

19 acts with the ortho position of the aromatic ring.

20 the dimerizing tail of the motor to the AAA+ ring.

21 ear topology via an unsaturated six-membered ring.

22 doping or the incorporation of non-benzenoid rings.

23 gen substitution in position 4 of the phenyl rings.

24 of ClpAP variants with completely active D2 rings.

25 zenoids, consisting of only fused 6-membered rings.

26 nly described to give five- and six-membered rings.

27 xygens within Mn-mu-S-CH(2) -C-O, 5-membered rings.

28 e transition involving Weyl points and nodal rings.

29 lices, and, supreme wonder, of the Borromean rings.

30 nium tethered to one of the cyclopentadienyl rings.

31 are confined within the smaller 12-membered ring (12-MR) micropores of Ti-Beta.

32 - 1 kg m(-2) ) received primed continuous l-[ring-(2) H(5) ]phenylalanine before consuming a mixed me

33 groups in the fifth position of the oxazole ring (29 examples; up to 88% yields).

34 60 polyps; P < .001), including with the fat ring (48% and 31%, P < .001).

35 le single nucleotide mutation within the PTC-ring, A-loop and P-loop, 180 total point mutations.

36 ion into the ortho positions of the aromatic rings allows for the rings to become coplanar; this mani

37 tes is dependent on a contractile actomyosin ring (AMR), composed of F-actin, myosin II, and other ac

38 12 ATPase active sites of ClpA, 6 in the D1 ring and 6 in the D2 ring, work together to fuel ATP-dep

39 s two cytokinetic structures-a septin double ring and an actomyosin ring-and also defines the essenti

40 C-labeled cholesterol show that C17 on the D ring and C9 at the intersection of B and C rings are ~7.

41 een the electron-deficient pentafluorophenyl ring and electron-rich naphthyl ring.

42 sfully treated using FLACS, capsular tension ring and intraocular lens (IOL) implantation.

43 ferent substitution patterns on the aromatic ring and the alkene.

44 rotor made up of two ring complexes, the MS-ring and the C-ring.

45 awing ability/power of the condensed furoxan ring and the low aromatic character of the benzofuroxan

46 contains a pair of distinct ClpP1 and ClpP2 rings and also requires the presence of activator peptid

47 o[8,7-b]indole architectures, with six fused rings and four contiguous chiral centers, is reported.

48 elaxation induced by acetylcholine in aortic rings and reduced NADPH oxidase activity in DOCA-salt an

49 be extended to the formation of six-membered rings and to N-homoallylindoles.

50 n and nonmuscle myosin II in the cytokinetic ring, and faster cytokinetic furrowing, following deplet

51 e flyby show that Arrokoth has no detectable rings, and no satellites (larger than 180 meters in diam

52 tures-a septin double ring and an actomyosin ring-and also defines the essential roles of a RhoGEF-an

53 -R substituent is key in directing the inter-ring angle and the extent of LUMO stabilization about th

54 asites and is associated to the apical polar ring (APR).

55 rawing or -donor substituents in the benzene ring are higher than that of the unsubstituted phthalimi

56 talyst ring size effect, as larger hydrazide rings are able to accommodate optimal transition-state g

57 etrazolium (TNBT) in which all four phenolic rings are nitrated, (6) cytoplasmic vesicles in vascular

58 Pyridine rings are prominent amongst these motifs.

59 rted to date, in which bryostatin's A- and B-rings are replaced by a glutarate linker.

60 D ring and C9 at the intersection of B and C rings are ~7.0 angstrom from the F673 side-chain 4-(19)F

61 ulfide bond network that creates an embedded ring around one of the strands.

62 d, and its orbit appears to cross the debris ring around the star without the expected gravitational

63 nd their analogues with modified A, B, and C rings, as well as hybrid compounds derived from colchici

64 copy imaging in air and liquids to visualize ring assembly, DNA binding, and unwinding activity of in

65 hese two phases involves opening of the P(3) ring at the base of the P(4)Se(3) molecules and subseque

66 a double ring that sandwiches the actomyosin ring at the onset of cytokinesis [10-13].

67 lease from chromatin involves opening of the ring at the Smc3-Scc1 interface in a reaction that is co

68 amics of theorized network structures called ring attractors elegantly account for these properties,

69 trans-dialkyl substituents in both pyrroline rings (B and D).

70 We examined tree-ring-based radial growth along with stable carbon (C) an

71 col) results in the formation of pyrrolidine rings bearing a new stereogenic center on the C2 of the

72 shows continuous red-shifts as the adjacent ring becomes more electron rich.

73 he N-tier ring in front and the C-tier motor ring behind.

74 il splayed into a side pocket and its corrin ring buried.

75 the deuterated positions on the cyclohexene ring can be controlled precisely.

76 at 7I with a stable linker and a quinoxaline ring can be used as a lead for further optimization of t

77 es that are linked between two five-membered rings can access planarized structures with reduced opti

78 idity of BAr(3) by modifications of the aryl rings can lead to improved reactivity.

79 e is isolated for the five- and six-membered ring cases.

80 al fibre was integrated into an active fibre ring cavity with optical gain and interrogated by the OF

81 Primary cutaneous signet-ring cell/histiocytoid carcinoma of the eyelid is an ext

82 ues <6 angstrom from the pigments' porphyrin ring centers.

83 Readily available pyridotriazoles undergo ring-chain isomerization to produce uniquely reactive al

84 to this problem for a critical floating tree-ring chronology from the East Mediterranean Bronze-Iron

85 lendar placement of a Middle Bronze Age tree-ring chronology.

86 ential hydroxylation of the ring followed by ring cleavage and mineralization of the resulting produc

87 e formation of products of reactions between ring cleavage products and the model nucleophile N-alpha

88 ing the formation mechanisms and identity of ring cleavage products, especially at higher chlorine do

89 dy focuses on the formation of electrophilic ring cleavage products-a class of compounds that poses p

90 raise concerns about the formation of toxic ring-cleavage products during the initial stage of oxida

91 mine, followed by a Grignard-mediated double ring-closure reaction.

92 e cross-ring fragmentation of the pyrimidine ring compared to the pyridine ring.

93 stically significant in most of the assessed rings compared to controls (p < 0.001).

94 While the MT nucleator, gamma-tubulin ring complex (gamma-TuRC) has been identified, precisely

95 The gamma-tubulin ring complex (gamma-TuRC) is an essential regulator of c

96 y localising the MT nucleator, gamma-Tubulin Ring Complex (gamma-TuRC), within the cell.

97 ructural basis for active single- and double-ring complexes coexisting in the mHsp60-mHsp10 chaperoni

98 s surrounding a central rotor made up of two ring complexes, the MS-ring and the C-ring.

99 We found that the ring component anillin contains a nuclear localization s

100 Here we report how two novel cytokinetic ring components, GCK-1 (germinal center kinase-1) and CC

101 addition to the ipso position of the phenyl ring concerted with C-O scission.

102 s amide rotamer propensities irrespective of ring conformation, while a novel residue, gamma-oxo-delt

103 amed open (O-) and closed (C-), based on the ring conformations in the vicinity of the N-O bond.

104 th either no substitutions on the TPE phenyl ring containing the antiestrogenic side chain of endoxif

105 , VSMC stiffness (-46.6%) and ex vivo aortic ring contraction force (-40.1%) were lowered and VSMC ac

106 We propose that ring currents in organic semiconductors, which commonly

107 cular interactions with the amplification of ring currents in stacked aggregates.

108 The largest ring currents occur when the porphyrin units have fracti

109 the enone (E, 70%; Z, 3%); subsequent double-ring cyclization of the E-enone (via Nazarov, electrophi

110 y to survive future droughts by using a tree-ring database of surviving and now-dead trees from 118 s

111 However, azo coupling resulted in a ring-degenerate rearrangement toward a 2-aryl-4-azotriaz

112 However the proposal that the RING dependent closed conformation of E2~Ub represents t

113 n into water - as demonstrated by a rotating ring disc experiment - and performed quasi-reversible he

114 RNF4 is a ssE3 ligase with a C-terminal RING domain and disordered N-terminal region containing

115 patient-associated missense mutations in the RING domain and N-terminal region compromise its activit

116 4 N-terminus promote compaction, juxtaposing RING domain and SIMs to facilitate substrate ubiquitinat

117 A construct combining the RING domain of ubiquitin E3 ligase RNF4 with a protein-s

118 nescent wave (EW) with high-sensitive cavity ring-down spectroscopy (CRDS) technique using a diode la

119 the setup in detail and achieved an optimum ring-down time of 159.4 ns and a minimum absorption coef

120 The Cullin 5 (CUL5) Ring E3 ligase uses adaptors Elongins B and C (ELOB/C) t

121 We previously identified a novel cullin-RING E3 ligase utilizing F-box only protein 44 (FBXO44)

122 RUL138 is a poorly characterized RNA-binding RING E3-ubiquitin ligase with functions in embryonic dev

123 D, but also offers a basis to understand how RING E3s may have properties that are tailored to pair w

124 nfine ions, a high DC field, and a wide exit ring electrode.

125 model system 1 to study the effects of aryl ring electronic density on the qualitative characteristi

126 The presence of Bronsted acid sites in the 8-ring enhances the diffusion process due to the formation

127 We suggest that the actomyosin ring evolved as one way to improve the efficiency of a c

128 attenuated ANP-mediated relaxation of aortic rings ex vivo.

129 th borane to furnish a heteroatomic group 13 ring exhibiting a sigma-aromatic nature concomitant with

130 arbolines undergo sodium periodate oxidative ring expansion in the presence of formaldehyde and other

131 ydro-4H-1,2-oxazines via a Cloke-Wilson-type ring expansion of the aryl-substituted cyclopropane carb

132 ytochrome P450 that catalyses the remarkable ring expansion reaction that is required to produce the

133 e, our new quasiperiodic Fibonacci multicore ring fibers provide a new class of quasiperiodic photoni

134 The new multicore ring fibers provide a new platform for experiments of qu

135 ophy, likely because of repression of muscle RING finger 1 (MuRF1), a proatrophic FOXO1 target gene.

136 RING-finger E3 ligases are instrumental in the regulatio

137 tion pathway-sequential hydroxylation of the ring followed by ring cleavage and mineralization of the

138 BCH070 preferentially kills early ring-form trophozoites, and, importantly, equally inhibi

139 explain the nucleotide dependence of mHsp60 ring formation, and reveal an inter-ring nucleotide symm

140 protein EB1/EBP-2 around the wound and actin ring formation, dependent on ARP2/3 branched actin polym

141 tes ECT-2 to promote cytokinetic contractile ring formation, we show that the ECT-2 regulator NOP-1,

142 involve powerful dearomatizations and medium ring formations.

143 e results obtained displayed many more cross-ring fragmentation of the pyrimidine ring compared to th

144 Thoracic aorta rings from Sprague Dawley rats were mounted in isolated

145 ddition of the formed six- or seven-membered ring-fused cyclopentadiene system, and a final protectio

146 ion precedes pyrrole annulation and bicyclic ring fusion.

147 he overall stereochemical disposition of its ring fusions is distinct from those of related natural p

148 anticorrelation between calendar-dated tree-ring growth responses to climatically effective volcanis

149 The Arabidopsis E3 ubiquitin ligases RING-H2 FINGER A3A (RHA3A) and RHA3B mediate the monoubi

150 depending on the steric effects of porphyrin rings) have different pathways to make H(2) .

151 nal structure as a function of the number of ring height levels.

152 tic compound oxidation that do not result in ring hydroxylation, we identified products formed after

153 eomycin analogues, we describe a cleavage of ring I from paromomycin that proceeds in the presence of

154 acceptor for the installation of a modified ring I.

155 s found in the H-transfer from the tetrazole ring in 5-(2-pyridyl)tetrazole to the pyridine ring with

156 an ring in oxabenzosapphyrin and the pyrrole ring in benzosapphyrin, which are present opposite to th

157 ontains a Mcm2-7 motor ring, with the N-tier ring in front and the C-tier motor ring behind.

158 revealed that in fused sapphyrins, the furan ring in oxabenzosapphyrin and the pyrrole ring in benzos

159 nverted sapphyrins), whereas the selenophene ring in selenabenzosapphyrin and the tellurophene ring i

160 in selenabenzosapphyrin and the tellurophene ring in tellurabenzosapphyrin did not show ring inversio

161 al sulfur bond and adaptation of cyclopropyl ring in the S2'-subsite.

162 te green possessing a central eight-membered ring in three steps.

163 1 C-C, 1 C-O and 2 C-N) and two heterocyclic rings in a single operation.

164 We discovered that contractile rings in cps1-191 cells constrict slowly and that an mto

165 alyze the substitution patterns of benzenoid rings in small molecule APIs approved by the FDA through

166 ofilaments form a ring-like structure, the Z-ring, in most bacterial species.

167 ne periodic skeleton (MPS) composed of actin rings interconnected by spectrin.

168 osite to the benzodipyrrole moiety, attained ring inversion (inverted sapphyrins), whereas the seleno

169 e ring in tellurabenzosapphyrin did not show ring inversion (normal sapphyrins).

170 th the 24-fold symmetric SctD inner membrane ring (IR) via an adaptor protein (SctK).

171 hat modulating the size of the central acene ring is a highly effective molecular design strategy to

172 the gap front at which a pluricellular actin ring is already assembled.

173 rocarbon triangulene, to which an additional ring is annulated in the zigzag region.

174 of the alkyne terminus not bearing a phenyl ring is because the cyclization is thermodynamically dis

175 indicate that addition of H to the aromatic ring is involved in the rate-limiting step.

176 evealed that the rotation of the imidazolium rings is restricted, with an activation energy as high a

177 hypothesize that one function of the P and L rings is to seal the outer membrane after motor disassem

178 g three isomers of fluoroamphetamine and two ring-isomers of both MDA and MDMA, we demonstrate the ab

179 first step towards connecting semiconductor ring lasers and microresonator frequency combs(13).

180 By contrast, in ring lasers instabilities are considered to occur only u

181 ng the aromaticity of the neighboring phenyl ring, leading to rapid cleavage.

182 ion studies indicated that the ZSWIM8 Cullin-RING ligase accelerates degradation of numerous miRNAs i

183 h full-length antibodies disclosed a stable, ring-like antigen-antibody structure in which the two Fa

184 The L protein is organized as a core ring-like domain containing the RNA-dependent RNA polyme

185 tomic force microscopy (AFM) showed that the ring-like structure of the human Mre11/Rad50 complex tra

186 s of cytokinesis, FtsZ protofilaments form a ring-like structure, the Z-ring, in most bacterial speci

187 olydimethylsiloxane (PDMS) and fixed bilayer rings made of silicone grease and steel.

188 rough-space probing of RNA folding using the RING-MaP correlated chemical probing framework.

189 ggest that banding a sleeve using a silicone ring may decrease weight regain and improve weight loss.

190 me system, a process we describe as antibody RING-mediated destruction (ARMeD).

191 In ring microresonator combs(5,6), an injected monochromati

192 pposite ends of the cell and preventing FtsZ-ring misassembly at the poles.

193 hird route involves the addition of the c(8)-ring module to the complete F(1)-PS complex.

194 asymmetry and frequency of irregular hyperAF ring morphologies according to mode of inheritance and d

195 Nevertheless, both asymmetry and irregular ring morphologies are also observed.

196 rowth factor receptor b (Fgfrb) signaling in ring muscles defines tentacle primordia in fed polyps.

197 h model, and the great potential to use tree-ring networks and results as a calibration target for ne

198 activity in the Csx1 domain and a potent cA4 ring nuclease activity in the C-terminal Crn2 domain.

199 F domain fold, and the mechanistic basis for ring nuclease activity is discussed.

200 ct effectors, and presence or absence of the ring nuclease activity.

201 Subsequently, we identified the cellular ring nuclease Crn1, which slowly degrades cA(4) to reset

202 PR immunity by means of a potent anti-CRISPR ring nuclease variant AcrIII-1.

203 zymes specialised for this task are known as ring nucleases, but are limited in their distribution.

204 f mHsp60 ring formation, and reveal an inter-ring nucleotide symmetry consistent with the absence of

205 reaction occurs at the central four-membered ring of biphenylene.

206 d the electron density for the isoalloxazine ring of FMN and induced a conformational change in resid

207 and within 20 angstrom of the isoalloxazine ring of FMN.

208 , consistent with BVM binding to an internal ring of hydrophobic side chains of L279 residues.

209 containing a characteristic horseshoe-shaped ring of nuclei that are present within granulomas of inf

210 through this pathway can retain the aromatic ring of parent aromatics, shedding light on the fact tha

211 the C(sp(3))-H bond adjacent to the pyridine ring of pharmacologically prevalent picolyl amides with

212 A ring of phenylalanine residues repositions to expose pre

213 components: a ~60-nucleotide U7 snRNA and a ring of seven proteins, with Lsm10 and Lsm11 replacing t

214 es a nucleophilic attack to form the pyrrole ring of the indole, followed by a decarboxylation that r

215 re induced by rotation of the central phenyl ring of the linker, from a coplanar arrangement to a twi

216 ompact structure comprising two intercalated rings of C-type lectin-like domains, where the N-termina

217 ication vesicle diameters, the resulting two rings of membrane interaction sites constrain the vesicl

218 ds and their similar groups and even benzene rings of spicy compounds were fund to be critical in the

219 tructures of the N-confused N-methyl pyrrole rings of the macrocycles.

220 Six rings of this system form the core of Clar's hydrocarbon

221 ling of Ti imidos with nitriles and alkynes, ring opening of 2-imino-2H-azirines, or direct metalatio

222 he results reveal that the rate constant for ring opening of radical cations derived from 1'-methyl-3

223 onding radical cation undergoes cyclopropane ring opening with a rate constant of only 4.1 x 10(4) s(

224 are suitable substrates for enantioselective ring opening with CsF and a chiral bis-urea catalyst.

225 r heterocycles and acyclic compounds through ring-opening and fragmentation of the parent butenolide

226 ieved via unprecedented Ph(3)P-I(2) mediated ring-opening of 1,3-dihydro-1H-benzimidazol-2-ones with

227 A nucleophilic retro-Claisen ring-opening of donor-acceptor cyclobutenes, formed with

228 ether, dioxolane (DOL), is known to undergo ring-opening polymerization inside electrochemical cells

229 Finally, the structure of the anticipated ring-opening product, dibenzosuberenone, bearing a beta-

230 ed electrolytes are in situ polymerized by a ring-opening reaction in the presence of aluminum fluori

231 a-keto radical chemistry, and acid-catalyzed ring-opening, as well as all other methods for the C-C b

232 n of cyclopropanols, including base-mediated ring-opening, metal-catalyzed C-C insertions and elimina

233 catalyzes different reactions (styrene oxide ring-opening, vesidryl synthesis, Friedel-Crafts alkylat

234 valency, and the inverse relationship to the rung-opening rate coefficient.

235 irst, the flavin-dependent RslO5 reductively ring-opens the epoxide moiety of an advanced polycyclic

236 eir targets, these cups are organized into a ring or ruffle of actin-driven protrusion encircling a n

237 s, failed surgical repairs with annuloplasty rings or severe mitral annular calcification who are poo

238 The method employs a small-ring organophosphorus-based catalyst (1,2,2,3,4,4-hexame

239 ed Cas12a (dCas12a) to construct dynamic RNA ring oscillators that cycle continuously between states

240 Three valve-in-ring patients required the implantation of a second valv

241 on the Wittig-Horner coupling of the known A-ring phosphine oxide with the corresponding Grundmann ke

242 reviously showed that active Ran coordinates ring positioning with chromatin.

243 While FlrA and the flagellar C-ring protein FliM have an overlapping binding site on Fl

244 to enable the subsequent functions of cullin-RING proteins.

245 hydrological modeling and new 1200-year tree-ring reconstructions of summer soil moisture to demonstr

246 nstructions of surface temperature from tree-ring records, we find little evidence to support signifi

247 ck the canonical FtsZ-membrane anchors and Z-ring regulators described for E. coli.

248 In this study, we endow a single ring resonator with two independent physical synthetic d

249 is (ASN) after long-term Intacs intracorneal ring segment (ICRS) implantation.

250 An actin-ring segment switching process then occurs by fusion of

251 A ring-shaped helicase unwinds DNA during chromosome repli

252 implements a drift-diffusion process over a ring-shaped manifold.

253 ese RNAs are bound and stabilized by Ro60, a ring-shaped protein that is a target of autoantibodies i

254 in patients presenting with either irregular ring shapes or asymmetric disease, emphasis should be pl

255 In this conformation, ring sigma(C-O)* orbitals oriented antiperiplanar to the

256 s and lanceolate endings at the level of the ring sinus revealed unique anatomical features that may

257 The computations also explain the catalyst ring size effect, as larger hydrazide rings are able to

258 hozoites, and, importantly, equally inhibits ring-stage survival of wild-type and artemisinin-resista

259 des COBE, two other substrates with aromatic ring structures were also used in this biphasic bioelect

260 stinct inter-subunit interactions around the ring, suggesting a coordinated and directional GTP-hydro

261 icrometric scale resembling diffused "coffee rings" surrounding the ocher particles imbedded in the r

262 ([1,2,3]triazolo)[5,1-a:4',5'-c]isoquinoline ring system is elaborated using a simple synthetic strat

263 ,4,6-positions or expansion of the condensed ring system.

264 ns provide an expeditious route to construct ring systems in a highly convergent and stereoselective

265 eans to achieve the construction of multiple ring systems in a single step.

266 construction of diverse sp(3) -rich skeletal ring systems is of importance to drug discovery programm

267 apid construction of complex polysubstituted ring systems starting from widely available heterocyclic

268 Appending conformationally restraining ring systems to the cyanine chromophore creates exceptio

269 commonly relies on an actomyosin contractile ring that drives equatorial furrowing and separation int

270 ly, the predominant view of cohesin was as a ring that encircled and cohered replicated chromosomes u

271 Our images show an eccentric ring that is misaligned with the orbital planes and the

272 The hourglass is remodeled into a double ring that sandwiches the actomyosin ring at the onset of

273 ive results is presented to address acoustic ringing that is often associated with high-sensitivity c

274 It is composed of four stacked heptameric rings that form a barrel-like structure, sequestering pr

275 formation, with ordered inner and peripheral rings, that prevents dimerization and activation of the

276 However, even in cells that have such rings, they are not always essential for furrow formatio

277 hers and subsequent cleavage of the covalent ring/thread ester linkages.

278 e III Dio (Dio3), which deiodinates TH inner rings through a selenocysteine (Sec) residue, revealed a

279 o requirement for adjacent modules in either ring to be active for efficient enzyme function.

280 he Min system restricts assembly of the FtsZ-ring to midcell, oscillating between the opposite ends o

281 dentify the orientation of the cyclopentenyl ring to the plane of the core quinoline to be a crucial

282 sitions of the aromatic rings allows for the rings to become coplanar; this manifests in a more ribbo

283 ches used to study legacy effects, from tree rings to whole forests.

284 nd ketones due to their strained four-member ring transition states.

285 his work, we present the results of a Metabo-ring trial involving 16 CE-MS platforms among 13 differe

286 surprisingly robust, something that we show rings true for invertebrate ears too.

287 RING-type E3 ligases catalyze both reactions in collabor

288 We identified a cullin-RING ubiquitin ligase (CRL), containing the substrate ad

289 t the molecular level, many MAGEs bind to E3 RING ubiquitin ligases and, thus, regulate their substra

290 es via direct lithiation of the 1,3-thiazole ring was developed.

291 Based on this varying P(ex) within an annual ring, we propose a targeted sampling strategy for differ

292 identify the unfurling of the second lectin ring which enables tetramer formation.

293 ]CPP selectively reduces the BN heterocyclic ring, which upon hydrolysis produces a rare example of a

294 iven approach based on a combination of tree ring width (TRW) records, growing season length and simu

295 ated subdaily soil hydrology to parameterize ring width increment simulations.

296 ng in 5-(2-pyridyl)tetrazole to the pyridine ring with a subsequent formation of 1H-2-(diazomethylene

297 ure of TerS(P76-26) revealed that it forms a ring with a wide central pore and radially arrayed helix

298 Aromatic rings with high electron density are believed to interac

299 m2-7, GINS) helicase contains a Mcm2-7 motor ring, with the N-tier ring in front and the C-tier motor

300 es of ClpA, 6 in the D1 ring and 6 in the D2 ring, work together to fuel ATP-dependent degradation is