ライフサイエンスコーパス: bound form

1 R lacking metal, but are buried in the metal-bound form.

2 to the outward-facing state in a KCl- or HCl-bound form.

3 re similar to that of its fully active Na(+)-bound form.

4 s monomeric cytosolic or oligomeric membrane-bound form.

5 ibosylation factor (ARF5) in its active, GTP-bound form.

6 s the reaction product, Chlide, in an enzyme-bound form.

7 of p120RasGAP (RASA1) in its apo and peptide-bound form.

8 s and sometimes sampling the fully open, CD4-bound form.

9 +/- 3 muM and 2.7 +/- 0.1 muM in the calcium-bound form.

10 molecules only upon conversion to its Ca(2+)-bound form.

11 sociation constant of 2-5 muM in the calcium-bound form.

12 ecture of GluN2A LBD compared to the agonist-bound form.

13 rystal structure of human PI4KIIalpha in ADP-bound form.

14 om the inhibitor backbone in the cathepsin-G-bound form.

15 ulate conformations typical of the substrate-bound form.

16 y to exist that, in part, resemble the final bound form.

17 ly clips H3 in its free as well as chromatin-bound form.

18 , 2BC, and 2BC3AB polyproteins in a membrane-bound form.

19 ctivity and remains always in its active GTP-bound form.

20 but was autophagy-independent for a membrane-bound form.

21 zymatic release or restrict it to a membrane-bound form.

22 of cofactor D, specifically when in the GDP-bound form.

23 as accessible when TG2 was in a cell surface-bound form.

24 ate-free form to a pi helix in the substrate-bound form.

25 ormation similar to the gapped DNA-substrate-bound form.

26 cent penicillin, Bocillin-FL, in free or PBP-bound form.

27 t is more similar to the GDP than to the GTP-bound form.

28 rotein moiety, as compared to the nucleotide-bound form.

29 phenolic acids in cereals in either free or bound form.

30 mall molecules that target CDK8 in its MED12-bound form.

31 e inactive GDP-bound state to the active GTP-bound form.

32 endent conformations, alternative to the ATP-bound form.

33 se by converting Hyperkinetic to the NADP(+)-bound form.

34 jority of phenolic acids were present in the bound form.

35 llosteric site that remains in the substrate-bound form.

36 -Ras is not as signaling-competent as its PM-bound form.

37 signaling and helps maintain RAS in the GTP-bound form.

38 o the FANCD2:FANCI heterodimer in only a DNA-bound form.

39 from mouse right atrium was in the prodomain-bound form.

40 -products exist in the soluble and insoluble-bound forms.

41 res and dynamics of their free and inhibitor-bound forms.

42 dynamic than MN4 in the free and both ligand-bound forms.

43 spective (iii) calcium-free and (iv) calcium-bound forms.

44 tes RHEB shuttling between GDP-bound and GTP-bound forms.

45 ermined, both as free proteins and in glycan-bound forms.

46 rom Escherichia coli in apo, GDP-, and ppGpp-bound forms.

47 As, activate PKR in TRAP-free and TRAP/l-Trp-bound forms.

48 cherichia coli RppH (EcRppH) in apo- and RNA-bound forms.

49 ct RIalpha (91-379) in its apo, cAMP2, and C-bound forms.

50 of Roquin paralog RC3H2 in both apo- and RNA-bound forms.

51 splicing factor/splicing factor 2 (ASF/SF2)-bound forms.

52 stinguished by its glass adsorbed versus DNA-bound forms.

53 84 intestinal cells in both the apo and iron-bound forms.

54 in the apo and S-adenosyl-L-methionine (SAM)-bound forms.

55 ocator, in both membrane-associated and PcrH-bound forms.

56 BR2 in the apo, agonist-bound and antagonist-bound forms.

57 ary of ~2,000 binding surface types from the bound forms.

58 ained for the protein in the apo- and Ca(2+)-bound forms.

59 re known to occur in free and glycosidically bound forms.

60 pha-Syn exists in both solution and membrane-bound forms.

61 ated the total phenol pools in both free and bound forms.

62 d N-Ras, and can identify GEFs by use of GDP-bound forms.

63 es as well as between cytosolic and membrane bound forms.

64 ellular sensor domain in both apo and ligand-bound forms.

65 rved yeast protein Rtt107 in free and ligand-bound forms.

66 n NEK1 in its apo- and ATP-mimetic inhibitor bound forms.

67 rhodopsin, accelerating the decay of ligand-bound forms.

68 ng between inactive GDP-bound and active GTP-bound forms.

69 mations in succinyl-CoA-bound and acetyl-CoA-bound forms.

70 nt crystal structures of AgeI in apo and DNA-bound forms.

71 full-length hexameric Mtb Mpa in apo and ADP-bound forms.

72 argely as a result of dissolution of surface-bound forms.

73 ions of the tandem domains in different cAMP-bound forms.

74 herapeutics present in free-(49.3-75.4%) and bound-forms (24.6-50.7%) in tissues, even without a targ

75 effector of Rab26 and binds Rab26 in its GTP-bound form, albeit only with low affinity.

76 wer levels, we expressed CD40L in a membrane-bound form, along with SIV antigens, in a nucleic acid (

77 The phenolics liberated from their bound form also had greater antioxidant activities.

78 s, (i) as a Ca(2+)-binding protein in Zn(2+)-bound form and (ii) as a protease in Zn(2+)-free form, c

79 f differentiating between the neutral ligand bound form and adsorbed ion pairs is discussed.

80 urface molecule that is found in both a cell-bound form and cell-free form in the host during an infe

81 coupled in the unliganded and single agonist-bound form and only upon binding both agonists the trans

82 EF-G binds to the ribosome in a GTP-bound form and subsequently catalyzes GTP hydrolysis.

83 inactive apo state, two intermediate agonist-bound forms and an active form in which the heterodimer

84 tein alpha subunit in its apo and nucleotide-bound forms and characterized their dynamical features a

85 nd VanXYG in apo and transition state analog-bound forms and of VanXYC in complex with the D-Ala-D-Al

86 rystal structure of RovA in the free and DNA-bound forms and provide evidence that thermo-induced los

87 HAR) in the native, ascorbate-bound, and GSH-bound forms and refined their resolutions to 1.9, 1.7, a

88 occur in the free, esterified and insoluble-bound forms and serve as natural antioxidants by prevent

89 sured free anti-oxLDL (unbound and partially bound forms) and Assay B measured total anti-oxLDL.

90 levels of terpenes (indicating hydrolysis of bound forms) and fermentation-derived volatiles, compare

91 petitive antagonist-bound states, an agonist-bound form, and a state bound with agonists and the allo

92 that Rabs are soluble in their inactive GDP-bound form, and only upon activation and conversion to t

93 G11.2) that recognizes, in both free and HDL-bound forms, apoA-I harboring a 3-nitrotyrosine at posit

94 Rabs in their GDP-bound form are kept soluble in the cytoplasm by the GDP

95 he Galpha subdomain, whereas the apo and GDP-bound forms are considerably more open and dynamic.

96 rganic and iron-bound P species into calcium-bound forms, as a possible consequence of the partial mi

97 domain of CD23 in its Ca(2+)-free and Ca(2+)-bound forms, as well as the crystal structure of the Ca(

98 FAAH) from Arabidopsis in its apo and ligand-bound forms at 2.1- and 3.2- angstrom resolutions, respe

99 rions in ligand-free, antibody-bound and CD4-bound forms at subnanometer resolution.

100 Similar to partition ParA proteins this ATP-bound form binds nonspecific-DNA.

101 delta2 interacts with omega2 and, in the ATP-bound form, binds to nonspecific DNA (nsDNA), forming sm

102 in plants and plant foods not only in their bound form but also as free acids that can be extracted

103 sults not from faster association of the ATP-bound form but faster dissociation leading to less stabl

104 hich was primarily presented in its membrane-bound form by follicular dendritic cells.

105 Heme-free mPGES2 was converted to the heme-bound form by mixing it with pig liver extract, indicati

106 o it is possible to gain insight into ligand-bound forms by considering conformational variation in a

107 glycosylated HIV gp120 in unliganded and CD4-bound forms by using small-angle X-ray scattering to vis

108 remains unclear whether any of these ligand-bound forms can be observed by ESI-MS.

109 can be toxic when it occurs in a non-protein-bound form; cells maintain a fine balance between heme s

110 structures of TgAMA4 in the apo and TgRON2L1-bound forms complemented with alanine scanning mutagenes

111 phenolic acids increased (30%) and insoluble-bound forms decreased (17%), suggesting partial conversi

112 es of LarE in ligand-free and several ligand-bound forms, demonstrating that LarE is a member of the

113 was observed for hydroxytyrosol and tyrosol bound forms, determinant for the health claim, which wer

114 rmations for E108 residue in the ATP and ADP bound forms, E108Q adapts the same conformation irrespec

115 bound-forms hydrolysis, being both free and bound forms equally affected by temperature.

116 xo-1(2H)-pyri midinepropanoic acid (UBP-282)-bound form exhibiting the widest range of cleft closure

117 he orientation of the enzyme in its membrane-bound form experimentally.

118 tures of folding competent substrates in the bound form have not been well characterized.

119 x properties of both the Fe(III)- and Fe(II)-bound forms have been characterized using the UV-visible

120 mperature range tested had a minor effect on bound-forms hydrolysis, being both free and bound forms

121 ved for an activated transition-state analog-bound form II ribulose-1,5-bisphosphate carboxylase/oxyg

122 release of the free drug from the covalently bound form in a desired fashion.

123 pyrrole pigment usually found as the protein-bound form in cyanobacteria and red algae.

124 entified for the first time in the insoluble-bound form in lentils.

125 ween an inactive soluble and active membrane-bound form in response to changes in membrane lipid comp

126 propose that conversion of ARF6 into the GDP-bound form in the apical domain of hair cells is essenti

127 LC-DAD was the most abundant compound in its bound form in the OHF, but decreased by 57% in TNF.

128 s been investigated to assess the role of Fe-bound forms in NIF-specific Fe-S cluster biogenesis.

129 stacking structure of these molecules in the bounded form in water medium.

130 with the circulating form of BMP9 (prodomain-bound form) in solution leads to the release of the prod

131 fluorescence was also observed in its actin-bound form, indicating that the dystrophin N-ABD binds t

132 7 in the apo structure but not in the ligand-bound form, indicating that this region likely confers p

133 not PsV expressing a cytoplasmic or membrane-bound form, induced circulating and intravaginal-tissue-

134 within the ER both in secretory and membrane-bound forms, inducing their degradation following retrot

135 It is shown that the Cu(II)-tyrosinate bound form is directly active in biogenesis.

136 s suggest that conversion of ARF6 to its GDP-bound form is necessary for final stabilization of the h

137 ugh the function of its predominant membrane-bound form is well established, the source and biologica

138 mponent in both membrane-bound and chaperone-bound forms is a key step for the eventual development o

139 In its [4Fe-4S] cluster-bound form it represses iron uptake by binding to IRO Bo

140 gh it is known that the carboxyl-terminus of bound-form Lpp is located in the periplasm, the precise

141 RAS is persistently frozen in its active GTP-bound form may not be accurate.

142 d conformation, in contrast to the inositide-bound form obtained previously in a closed conformation.

143 of the protein from the unbound form to the bound form occurs before or after encountering the ligan

144 for an allosterically inhibited and agonist-bound form of a functional NMDA receptor; however, other

145 e the coordination of copper to the membrane-bound form of alpha-syn.

146 o70, and Sec5 bind preferentially to the GTP-bound form of Arl13b, consistent with the exocyst being

147 nd of ppGpp to BipA, indicate that the ppGpp-bound form of BipA adopts the structure of the GDP form.

148 g subunit-subunit interface in the substrate-bound form of BsPFK.

149 The Ca(2+)-bound form of CaBP7 NTD is monomeric and exhibits an ope

150 quired the specific interaction of the Cu(+)-bound form of CopA with apo-CusF for subsequent metal tr

151 The CDK-bound form of CR8 has a solvent-exposed pyridyl moiety t

152 n agreement with previous work, the membrane bound form of Cripto-1 potentiated signaling, revealing

153 gene regulatory region occupancy by the DNA-bound form of cyclin D1 and induction of CIN gene expres

154 -wide ChIP sequencing and found that the DNA-bound form of cyclin D1 occupied the regulatory region o

155 ridging sulfides in the [4Fe-4S](2+) cluster-bound form of FNR facilitated identification of resonant

156 rum of the O(2)-exposed [2Fe-2S](2+) cluster-bound form of FNR.

157 that VVC-resistant viruses use the inhibitor-bound form of Galphai-coupled CCR5 more efficiently than

158 nd this interaction is stronger with the GDP-bound form of Galphao.

159 A metabolically biotinylated, membrane-bound form of Gaussia luciferase was synthesized, termed

160 disordered switch II in the uncomplexed GTP-bound form of H-Ras.

161 Only the ATP-bound form of Hsp90 interacts with disordered CTA1, and

162 sticity of the dimeric state of the [2Fe-2S] bound form of human GRX5 (holo hGRX5) is the crucial fac

163 The GTP-bound form of IF2 accelerates subunit joining, whereas I

164 in the inactive guanosine diphosphate (GDP)-bound form of KRAS(G12C), sparing the wild-type protein.

165 tein-Barr virus (EBV) increases the membrane-bound form of LC3 (LC3-II) and LC3-containing punctate s

166 )C}(7)Li dipolar recoupling experiments, the bound form of lithium in the active site of wild-type E.

167 The Clp protease system destabilizes a zinc-bound form of Mpy recruitment factor (Mrf), which is sta

168 ollectively, these results show that the ATP-bound form of MRN is the critical conformation for ATM a

169 We now report that a membrane-bound form of murine CD80 similarly reduces PDL1-PD1-med

170 the central beta-sheet similarly to the ATP-bound form of Ncd.

171 The bound form of Neu5Gc is bioavailable, undergoing metabol

172 We also find that the serum protein-bound form of NY is photoacoustically well-behaved and s

173 ions to refine the structure of the membrane-bound form of Pf1 coat protein in explicit lipid bilayer

174 we report the crystal structure of the lipid-bound form of PgpB.

175 The bound form of phenolics was the component present in hig

176 EPI64B almost completely abolished the GTP-bound form of Rab27B, without affecting GTP-Rab3D.

177 -bound RAB7, but not a dominant-negative GDP-bound form of RAB7, promoting rapid transfer and lysosom

178 Rif2 discharges the ATP-bound form of Rad50, which is essential for all MRX-depe

179 ike molecules that bind to a site on the GDP-bound form of Ral.

180 Gef3p interacts physically with the GTP-bound form of Rho3p.

181 ognate eukaryotic effectors, as only the GTP-bound form of RhoA family members stimulates enzymatic a

182 y of Ssq1 and is most pronounced for the ADP-bound form of Ssq1, which interacts with Isu1 most tight

183 MD simulations of the Ca(2+)-bound form of Syt1 revealed that Syt1 conformational fle

184 es to generate a molecular model of a Ca(2+)-bound form of Syt1.

185 ciated with characterization of the membrane-bound form of talin have prevented us from understanding

186 The chlorowillardiine- and nitrowillardiine-bound form of the agonist-binding domain probes a narrow

187 sociated with the expression of the membrane-bound form of the CD40L by CD4(+) T cells in lymph nodes

188 as 1B6 that recognize the more abundant GAG-bound form of the chemokine may not be the optimal strat

189 ists in the characterization of the receptor-bound form of the chemokine.

190 ntify an unforeseen principle by which a GDP-bound form of the conserved small G protein Rho GTPase d

191 d conformation and propose that the membrane-bound form of the cytodomain represents its native confo

192 n (SH3) client protein interact with the ADP-bound form of the DnaK chaperone.

193 ction occurs whereby mutations shift the ADP-bound form of the enzyme towards an ATP-like state in a

194 otably, the methyl-thiazole prefers the NADH-bound form of the enzyme with a Kd of ~13.7 nM, as again

195 with a Kd of ~13.7 nM, as against the NAD(+)-bound form of the enzyme.

196 The ATP-bound form of the Escherichia coli DnaA protein binds 'D

197 The ATP-bound form of the Escherichia coli DnaA replication init

198 Using the membrane-bound form of the fd coat protein as a model membrane pr

199 fection of human tumor cells with a membrane-bound form of the human costimulatory molecule CD80 prev

200 iptional expression switch from the membrane-bound form of the immunoglobulin heavy chain to its secr

201 A crystal structure of the ADP-bound form of the KIF14 motor domain reveals a dramatica

202 The LPS-bound form of the protein was substantially more resista

203 osure states relative to the iodowillardiine bound form of the protein, with the antagonist (alphaS)-

204 he tetraphenylphosphonium (TPP(+)) substrate-bound form of the protein.

205 resistance describe an ability to use a drug-bound form of the receptor, leading to reduction in maxi

206 r modeling docking studies using the agonist-bound form of the X-ray crystal structure of the acetylc

207 nism involves signaling between the membrane-bound form of TNF-alpha on activated CD8(+) T cells and

208 he cleaved form of alphaKlotho, the membrane-bound form of which is an FGF23 coreceptor, serves as a

209 a are consistent with a model in which a DNA-bound form of Yap8 acts directly as an As(III) sensor.

210 ree Fe(II) from both the Fe(II)- and Fe(III)-bound forms of (Nif)IscA.

211 in-cell NMR signals from unbound and ligand-bound forms of a given DNA target.

212 rved under acidic conditions, whereas sulfur-bound forms of Ag dominated in neutral to alkaline soils

213 diine > chlorowillardiine > nitrowillardiine-bound forms of agonist-binding domain.

214 he crystal structures of apo- and ADP/Mg(2+)-bound forms of Aquifex aeolicus LpxK to a resolution of

215 free, esterified, glycosylated and insoluble-bound forms of araticum pulp, peel and seed were for the

216 ent in the free, soluble ester and insoluble-bound forms of blackberry, black raspberry and blueberry

217 MAP3K protein MRK directly binds to the GTP-bound forms of both RhoA and RhoC in vitro.

218 nalysis demonstrates that the apo and Mg(2+)-bound forms of CBD12 are highly flexible, whereas Ca(2+)

219 Crystal structures of the apo and PEP-bound forms of D12A BsPFK have been determined (Protein

220 h closely resemble the autoinhibited and DNA bound forms of Ets-1.

221 contrast to the prevailing view that the GDP-bound forms of G proteins are inactive, our study reveal

222 e dynamics and structure of the apo and heme-bound forms of HO1 and HO2.

223 We determined structures of ATP-free and -bound forms of human TRPV4-ARD and compared them with av

224 o detect conformational dynamics in free and bound forms of IDPs under conditions approaching physiol

225 h to spatially map NADH in both the free and bound forms of live undifferentiated and differentiated

226 The purified and membrane-bound forms of MBH both preferentially evolved H2 with t

227 lyzing purified preparations of apo- and ion-bound forms of NCX_Mj-WT and its mutant, NCX_Mj-5L6-8.

228 le, atomistic simulations of the unbound and bound forms of NorM in a phospholipid lipid bilayer allo

229 ort is likely a gradient of the GDP- and GTP-bound forms of Ran, a small GTPase.

230 striking exception to the rule that only GTP-bound forms of Ras-superfamily GTPases have active confo

231 y to characterize the ligand-free and ligand-bound forms of SAM-II riboswitch.

232 MD) simulations of Ca(2+)-unbound and Ca(2+)-bound forms of Syt1.

233 Although the structures of free and bound forms of TAR are well characterized, the conformat

234 00-ns trajectories of the free and substrate-bound forms of TEM-1 (with benzylpenicillin) and PSE-4 (

235 The biliverdin-bound forms of the BphPs have the additional property of

236 n microscopy reconstructions of free and DNA-bound forms of the Cascade/I-C surveillance complex reve

237 s in the unbound, cocaine-bound, and quinine-bound forms of the cocaine-binding DNA aptamer.

238 e report here structures of the free and DNA-bound forms of the DBD of NtrC4 (4DBD) from Aquifex aeol

239 the nucleotide binds to the free and singly bound forms of the enzyme with nearly equal affinity ove

240 In all of the bound forms of the enzyme, however, the proposed catalyt

241 arrangement in the apo form and GDP- and GTP-bound forms of the factor, raising the question of how S

242 and remarkably different for GDP- and GppNHp-bound forms of the G domain, indicating that the GTP-bin

243 uce mRNAs encoding the secreted and membrane-bound forms of the immunoglobulin (Ig) heavy chain.

244 vey common foods for free and glycosidically bound forms of the nonhuman sialic acid N-glycolylneuram

245 ive NMR analysis of the apo, cGMP-, and cAMP-bound forms of the PKG cyclic nucleotide-binding domain

246 the labeled sites between the apo and ligand-bound forms of the proteins, which are easily distinguis

247 The cycling between GDP- and GTP- bound forms of the Ras protein is partly regulated by th

248 ws signal rejection of diffusing relative to bound forms of the same PS-FP, rsFastLime.

249 ch FKBP51 binds to both the apo- and hormone-bound forms of the steroid receptor to modulate its affi

250 pond differently to the soluble and membrane-bound forms of their respective ligands.

251 esent crystal structures of the free and CMP-bound forms of WaaA from Aquifex aeolicus, an ancient Gr

252 r previously reported data for the glutamate-bound forms of wild type and T686S mutant proteins, show

253 Omicron-(gamma-thio)triphosphate (GTPgammaS)-bound) form of Tr*, we found that Tr* activated PDE at a

254 or both active (GTP-bound) and inactive (GDP-bound) forms of Galpha subunits.

255 ions of active (GTP-bound) and inactive (GDP-bound) forms of wild-type and mutant K-Ras, with an inte

256 by the interconversion between GTP- and GDP-bound forms partly regulated by the binding of the guani

257 ermination of protein-free and total (free + bound forms) positron emission tomography (PET) radiolig

258 5M-thrombin), were compared to the substrate-bound form (PPACK-thrombin).

259 uggest that the mobility of the full agonist-bound form primes the GPCR to couple to IBPs.

260 lexibility, when three Ca2+ or two Mg2+ were bound forming probably the structural basis for the modi

261 d form promoted by GEFs and its inactive GDP-bound form promoted by GAPs to affect the control of var

262 Ras GTPase cycles between its active GTP-bound form promoted by GEFs and its inactive GDP-bound f

263 In their active GTP-bound form, Rab proteins interact with proteins termed e

264 excited kynurenines in both free and protein-bound forms rapidly oxidized ASC, and such oxidation occ

265 e ligand "slips" between bidentate and arene-bound forms: rather than dissociation, the cobalt slides

266 The observed constant free to bound forms ratio showed that the temperature range test

267 RecA, in the ATP . Mg(2+)-bound form (RecA . ATP), can nucleate and form filament

268 as switchable landmarks with the active GTP-bound form recruiting to the membrane a specific set of

269 free or weakly bound molecule and a tightly bound form released by acid hydrolysis, at concentration

270 hin (44.56 mg/100 g) in free, esterified and bound form respectively.

271 in ligand-free, antagonist-bound, or calcium-bound forms, revealing how robust conformational changes

272 The full-length cAMP-bound form reveals the sensory N-terminus to be a domain

273 A comparison of the Hb-free and Hb-bound forms reveals that Hb binding alters the positioni

274 of ligand-free CouR and its p-coumaroyl-CoA-bound form showed no significant conformational differen

275 s of the IL-2 superkine in free and receptor-bound forms showed that the evolved mutations are princi

276 an open conformation, whereas the nucleotide-bound form shows a half-closed conformation, in contrast

277 of E. coli ACPS in unliganded and holo-ACPP-bound forms solved by X-ray crystallography to 2.05and 4

278 nsition of Cas9 from its apo form to the RNA-bound form, suggesting a mechanism for RNA recruitment i

279 concentrations of beta-damascenone, and some bound-form terpenoids.

280 pigmented rice, being three-fold greater in bound form than in soluble form.

281 ecular switch in a constitutively active GTP-bound form that drives, unchecked, oncogenic downstream

282 tively unfolded and monomeric and a membrane-bound form that is composed of an alpha-helical multimer

283 In the active, membrane-bound form, the AI helices are displaced and engage the

284 of transcription factor signaling via a DNA-bound form, the induction of chromosomal instability, en

285 nly binds MreB in the guanosine triphosphate-bound form, the motility complexes are assembled at the

286 lanine is not specially favored in the lipid-bound form; the chimeric construct with polyalanine prod

287 of this dual domain in both apo- and ligand-bound form: thermodynamic analysis of the ligand associa

288 e of 509+/-51 s(-1) , whereas in the glucose-bound form these exchange processes were quenched.

289 droxymethyl of Thr(772) rotates to stabilize bound Form(+) through water molecules, and 3) the rotame

290 amily that is highly expressed in a membrane-bound form throughout the respiratory tract.

291 o the [4Fe-4S] cluster, and exposure of this bound form to O2 results in cluster conversion to the [2

292 mploys quantification of PSA in its free and bound forms to enumerate the risk of prostate cancer and

293 We find that cryoreduction at 77 K of the O2-bound form, trapped in the conformation of the parent ox

294 creased fluctuations are seen in the camphor-bound form using all three techniques, dominated by chan

295 undetectable in its parent form, whereas the bound form was readily quantified, employing the modifie

296 atural peptides in their free and HLA-B*0801-bound forms, we characterized the mode of action of ERAP

297 t DDXs promote phase separation in their ATP-bound form, whereas ATP hydrolysis induces compartment t

298 ctional states, the DNA-bound and the ligand-bound form, which are allosterically regulated.

299 s of HiNmlR in both the DNA-free and two DNA-bound forms, which suggest that HiNmlR enhances target g

300 diate states characterized by a Tyr(75)-iron-bound form with open conformation of loop L1.