ライフサイエンスコーパス: kD

1 units (68.1 kD each), one beta-subunit (56.0 kD), one gamma-subunit (24.8 kD), and one delta-subunit

2 psbA gene product) from the massive (>1,000 kD) water-oxidizing and O2-evolving PSII holocomplex.

3 tides associated with an approximately 1,000-kD pigment-protein supercomplex that contains components

4 protein composed of two alpha-subunits (68.1 kD each), one beta-subunit (56.0 kD), one gamma-subunit

5 Incubation of Dex3(1 kD)-Cyt c with mercaptoethanol caused significant loss i

6 ght glycans (lactose and two dextrans with 1 kD and 10 kD) were chemically coupled to surface exposed

7 s (lactose and two dextrans with 1 kD and 10 kD) were chemically coupled to surface exposed Cyt c lys

8 Low-molecular mass (10 kD) cytosolic acyl-coenzyme A-binding protein (ACBP) has

9 mentation of PMC, producing approximately 10-kD domains with intact inhibitory capacity and faster di

10 f ligand 10 (CXCL-10)/IFN-gamma-inducible 10-kD protein (IP-10).

11 thaliana; AtCGL20), which is a Pro-rich, ~10-kD protein that is targeted to mitochondria and chloropl

12 embryos, ise2 mutants continue to traffic 10-kD fluorescent dextran in the mid-torpedo stage of devel

13 oteins >9 nm in diameter ( approximately 100 kD) are restricted from entering cilia, and we confirm t

14 ine and Voluven were similar despite the 100 kD difference in weight-average molecular weight.

15 observed for synaptic associated protein 102 kD (SAP102) and neuronal nitric oxide synthase (nNOS) mR

16 an U5 small ribonucleoprotein-associated 102-kD protein and to the yeast pre-mRNA splicing factors Pr

17 arises from a tight interaction between 107-kD plant-type PEPC and 118-kD bacterial-type (BTPC) subu

18 oubiquitinated 110-kD and phosphorylated 107-kD PEPC polypeptides (p110 and p107, respectively).

19 dlD cells, both with molecular masses of 110 kD.

20 educed the mass of neutrophil hLAMP-2 to 110 kD and enabled autoantibody binding.

21 ing of an 85-kD regulatory subunit and a 110-kD catalytic subunit.

22 an equivalent ratio of monoubiquitinated 110-kD and phosphorylated 107-kD PEPC polypeptides (p110 and

23 A1-FER messenger RNA and fusion protein (114 kD) in the hepatocellular carcinoma cell line HUH7, as w

24 ction between 107-kD plant-type PEPC and 118-kD bacterial-type (BTPC) subunits.

25 ex, multivesicular body sorting factor of 12 kD (Mvb12), and demonstrate that Mvb12 binds to the coil

26 nucleoid-associated candidate proteins a 12-kD SWIB (SWI/SNF complex B) domain-containing protein wa

27 D spectrin break down product (SBDP) and 120 kD SBDP, respectively.

28 is major surface glycoprotein (Msg) is a 120-kD surface protein complex on the organism with importan

29 For instance, the Nicotiana alata 120-kD glycoprotein (120K) is an abundant arabinogalactan pr

30 ncodes CSLD5 a plasma membrane localized 129 kD D-type cellulose synthase with eight transmembrane do

31 13-T (unidentified reading frame encoding 13-kD cms-T protein) gene in the cms-T cytoplasms.

32 fact involving an endogenous ER-localized 13-kD FK506 binding protein (FKBP13) competing with the FKB

33 either 6% HES with a molecular weight of 130 kD and a molar substitution ratio of 0.4 (130/0.4, Voluv

34 After cleavage, a 14-kD membrane-bound fragment of KIM-1, which contains two

35 easome system and leaves a characteristic 14-kD actin fragment in the insoluble fraction of a muscle

36 caspase-3 leaves behind a characteristic 14-kD actin fragment in the insoluble fraction of muscle, a

37 rate that SIM encodes a nuclear-localized 14-kD protein containing a cyclin binding motif and a motif

38 The experimental results suggest that the 14-kD actin fragment in muscle biopsies is increased in cat

39 try of 1:1:1 and had a molecular mass of 140 kD.

40 bonds in the termini of a 1314-residue (144-kD) protein, specify previously unidentified disulfide b

41 in the degradation of alpha-spectrin to 145 kD spectrin break down product (SBDP) and 120 kD SBDP, r

42 in several chromatographic steps, and a 145-kD protein was identified as the enzyme most likely to p

43 ting in a mature peptide of approximately 15 kD that is attached to the sieve element plasma membrane

44 to their unique properties of small size (15 kD), intrinsic stability, high affinity and specificity,

45 ent molecular mass of approximately 10 to 15 kD; however, mature GAXs from wheat cell walls had large

46 protein in fruit, roots, and leaves and a 15-kD species in mature ripe fruit.

47 erythrin-labeled monoclonal antibody to a 15-kD surface-membrane protein, and quantitative polymerase

48 T of 27-kD AcCYS1 in vitro to produce the 15-kD species.

49 of soluble carbohydrates, expression of a 16-kD dehydrin absent under long photoperiod, and increased

50 ng from approximately 8 to approximately 160 kD could be mapped with coverage of 100% for six protein

51 ed by direct binding to Akt substrate of 160 kD (AS160), a Rab GTPase-activating protein that regulat

52 e particle cryo-EM reconstruction of an ~160-kD N-terminal fragment of the lipid transport protein VP

53 The 165-kD crystal structure of the central domain of Sec16 in c

54 OE17 (oxygen-evolving complex subunit of 17 kD) precursor protein.

55 ith this PSI-Cyt b(6)/f supercomplex, two 17-kD PSII subunit P-like proteins and a 70-kD ATP-dependen

56 particular, ribonuclease HI (RNase H), an 18 kD globular protein that hydrolyzes the RNA strand of RN

57 )F-GE180 for imaging activated microglia (18-kD translocator protein ligand [TSPO]) and static 30- to

58 PET radioligand binding to the 18-kD translocator protein (TSPO) in the brains of patients

59 us nephropathy specifically identified a 185-kD glycoprotein in nonreduced glomerular extract.

60 d recombinant PLA(2)R and bound the same 185-kD glomerular protein as did the monospecific anti-PLA(2

61 the hypoxia-inducible death protein Bcl-2 19-kD interacting protein 3 (Bnip3) to the unique glycolyti

62 nd found that Bnip3 (Bcl-2/adenovirus E1B 19-kD interacting protein), a BH3-only proapoptotic protein

63 The 19-kD alpha-zein is uniformly distributed throughout the co

64 glycosylated native neutrophil hLAMP-2 (190 kD).

65 e insulator proteins Centrosomal Protein 190 kD (CP190) and Modifier of mdg4 67.2 kD (Mod67.2).

66 ein 190 kD (CP190) and Modifier of mdg4 67.2 kD (Mod67.2).

67 used to assess the activity of Ara h 2/6 (20 kD) and CPE without the 20 kD fraction (CPE w/o 20 kD) f

68 el was also used to administer Ara h 2/6 (20 kD) in an immunotherapy protocol, in which peanut-allerg

69 gether in a 13-25 kD fraction (Ara h 2/6; 20 kD fraction) on gel filtration chromatography, account f

70 control CPE, mice challenged with CPE w/o 20 kD experienced reduced symptoms (P < 0.05) and a smaller

71 ve as treatment with CPE, whereas CPE w/o 20 kD was significantly less effective for higher dose pean

72 d CPE without the 20 kD fraction (CPE w/o 20 kD) for allergic provocation challenge and immunotherapy

73 of Ara h 2/6 (20 kD) and CPE without the 20 kD fraction (CPE w/o 20 kD) for allergic provocation cha

74 ich peanut-allergic mice treated with the 20 kD fraction experienced significantly reduced symptoms,

75 Importantly, immunotherapy with the 20 kD fraction was just as effective as treatment with CPE,

76 lecular weight of the complex was around 200 kD, which is consistent with the association of DRAG wit

77 A group of morphologically distinct, 200-kD neurofilament-immunopositive myelinated afferent fibe

78 een 8 of 27 cysteines in a 1714-residue (200-kD) protein, and correct sequence predictions in two pro

79 for the first time in human lung tissue, 200-kD neurofilament subunit.

80 P21 (neuron-enriched endosomal protein of 21 kD) as a regulator of L1/NgCAM sorting in somatodendriti

81 aller forms are cleavage products of the 210-kD protein and were the predominant forms in flagella.

82 molecular weight, while showing increased 22 kD HBeAg proprotein accumulation in Huh7 cells.

83 ant protein bodies ectopically accumulate 22-kD alpha-zeins in the gamma-zein-rich periphery and cent

84 Reduction in both 19- and 22-kD alpha-zein subfamilies severely restricted protein bo

85 o form approximately 9- and approximately 22-kD fragments, then increasing quantities of smaller pept

86 pha-kafirins, the homologues of the maize 22-kD alpha-zeins in sorghum (Sorghum bicolor), in the beta

87 ation by facilitating the localization of 22-kD alpha-zein and that this is essential for the formati

88 , which result from reduction of only the 22-kD alpha-zein class.

89 uble null mutant for the delta-zeins, the 22-kD alpha-zein, the beta-zein, and the gamma-zein RNA int

90 showed that FL1 DUF593 interacts with the 22-kD alpha-zein.

91 Substantial loss of the 22-kD alpha-zeins by z1CRNAi resulted in protein body buddi

92 ndicating that a sufficient amount of the 22-kD zeins is necessary for maintenance of a normal protei

93 iable Ig domains within an approximately 220 kD ectodomain.

94 rotein kinase D-interacting substrate of 220 kD (Kidins220)/ankyrin repeat-rich membrane-spanning pro

95 ysis for Rac2 interactors identified the 226 kD protein Myh9.

96 in two proteins, one with 2153 residues (229 kD).

97 Mig-7 protein of ~23 kD is produced from Mig-7 cDNA that contains multiple st

98 hat CIAF1 specifically interacts with the 23-kD TYKY-1 matrix domain subunit of Complex I and likely

99 ana NUCLEAR PORE ANCHOR (NUA) encoding a 237-kD protein with similarity to Tpr.

100 VUP1) gene encodes a predicted protein of 24 kD with no annotated functional domains but containing d

101 t, which lacks exon 1 of PRTN3, encodes a 24-kD protein (p24(PR3/MBN)) with a sequence similar to tha

102 encodes a 28-kD nuclear autoantigen and a 24-kD small GTP-ase, termed HRES-1/Rab4.

103 VE KERNEL1 (DEK1) calpain is a conserved 240-kD key regulator of three-dimensional body patterning in

104 and Ara h 6, co-purified together in a 13-25 kD fraction (Ara h 2/6; 20 kD fraction) on gel filtratio

105 have 10(3)-fold lower cytotoxicities than 25 kD bPEI, while maintaining gene-silencing efficiencies t

106 raded peptides and proteins smaller than ~25 kD.

107 Brr2 is a large protein ( approximately 250 kD) that consists of an N-terminal domain ( approximatel

108 -->3),(1-->4)-beta-D-Glucans of at least 250 kD were isolated from cell walls, but much larger aggreg

109 -glucans of an average molecular mass of 250 kD and higher were detected in isolated Golgi membranes.

110 recognized a glomerular protein that was 250 kD in size.

111 cyclin-dependent kinase substrate 1) is a 27 kD chromosomal, vertebrate-specific protein, for which l

112 Immunoblot analysis identified a 27-kD protein in fruit, roots, and leaves and a 15-kD speci

113 by microsomal membranes giving rise to a 27-kD species.

114 This work identifies 27-kD gamma-zein as an opaque2 modifier gene within the lar

115 tracts proteolytically removed the NTT of 27-kD AcCYS1 in vitro to produce the 15-kD species.

116 omplex one, encoding small (approximately 28 kD) and large (approximately 68 kD) polypeptides.

117 The HRES-1 human ERV encodes a 28-kD nuclear autoantigen and a 24-kD small GTP-ase, termed

118 Immunoblot analyses identified a 29 kD (mature Ee-BAM1 after cleavage of the transit peptide

119 ana cpRNPs CP31A and CP29A (for 31 kD and 29 kD chloroplast protein, respectively), associate with la

120 Both 35 and 29 kD proteins were constitutively expressed in growth-indu

121 A approximately 29 kD fH-binding protein expressed in the meningococcal out

122 us necrosis-inducing toxin between 10 and 30 kD in size.

123 the bulky CA II protein (MW approximately 30 kD) to the ion channel-forming peptides (MW approximatel

124 tride nanopores allow the analysis of sub-30 kD protein molecules with unprecedented time resolution

125 The Arabidopsis thaliana ortholog of the 30-kD subunit of the mammalian Cleavage and Polyadenylation

126 that encodes the probable ortholog of the 30-kD subunit of the mammalian cleavage and polyadenylation

127 assembly into a complex of approximately 300 kD.

128 ar form, lacking SSIII, of approximately 300 kD.

129 1 encodes an ortholog of BPTF, a large (>300 kD) multidomain subunit of the NURF chromatin remodeling

130 The 600- and 300-kD complexes were stable at high salt concentration, sug

131 both ISA1 and ISA2, and an approximately 300-kD complex contained ISA1 but not ISA2.

132 s required for assembly/stability of the 300-kD TIM22 complex.

133 en [collagen alpha3(IV)NC1; approximately 31 kD] that was incubated with B cell lysosomes was cleaved

134 psis thaliana cpRNPs CP31A and CP29A (for 31 kD and 29 kD chloroplast protein, respectively), associa

135 fermenting1-related protein kinases and a 32-kD 14-3-3 protein are candidate central regulators of st

136 ing and replacing the photoinactivated D1/32-kD reaction center protein (the chloroplast-encoded psbA

137 In vitro, 32-kD sCD44 was isolated from human sera, biotinylated, and

138 Toc34 receptor (34-kD subunit of the translocon of the outer envelope) reco

139 er cleavage of the transit peptide) and a 35 kD (unprocessed EeBAM1) protein.

140 to a high molecular mass contrast agent (35 kD Gadomer) by dynamic contrast-enhanced magnetic resona

141 small, specific-sized hyaluronic acid of 35 kD (HA35) on ethanol-induced sensitization of Kupffer ce

142 F) is a heterodimer consisting of 65- and 35-kD proteins that bind the polypyrimidine tract (PPT) and

143 e chose annexin A5 (AnxA5), a recombinant 35-kD protein extensively used for the in vitro and in vivo

144 The gene for the 35-kD subunit of U2AF gives rise to two protein isoforms (t

145 polyglutamine expansion in huntingtin, a 350 kD protein that is ubiquitously expressed and widely dis

146 ively stained Vps13p indicates that this 358-kD protein is folded into a compact rod-shaped density (

147 estern blotting detected ASPA as a single 38 kD band.

148 y secreted antigen target-6), Acr1, Acr2, 38-kD antigen, or heat-killed H37Rv M. tuberculosis.

149 ctional polyethylene glycol moiety (PEG, 3.4 kD) and a 2,2',2'',2'''-(1,4,7,10-tetraazacyclododecane-

150 ted interferon alpha-2a (Peg-IFNalpha-2a; 40 kD)/ribavirin (RBV) at standard doses for 24 or 48 weeks

151 lytic conversion of the highly insoluble ~40 kD Wnt-5a protein to a soluble 36 mer amino acid peptide

152 davalintide (AC2307), with an intervening 40 kD PEG moiety.

153 ith Raf-1 and proline-rich AKT substrate, 40 kD(a) and neutralized the ability of 14-3-3 to activate

154 iator of Rap80 Interactions and Targeting 40 kD)/(C19orf62) as a Rap80-associated protein that is ess

155 that OMA1 is normally cleaved from 60 to 40 kD by another as of yet unidentified protease.

156 anslocase of outer mitochondrial membrane 40-kD subunit (TOM40), the TOM20s, and the Rieske FeS prote

157 Two complexes of approximately 400 kD contained both ISA1 and ISA2, and an approximately 30

158 (Arabidopsis thaliana) gene BT2 encodes a 41-kD protein that possesses an amino-terminal BTB domain,

159 Furthermore, distance measurement in a 42 kD DNA was demonstrated.

160 that found in E. coli XL-1 Blue and had a 42 kD fusion protein immunoreactive to polyclonal antibodie

161 e mutant had a greatly reduced level of a 42-kD kinase activity capable of phosphorylating peptides f

162 d interleukin 10 (IL-10) responses to the 42-kD C-terminal fragment of Plasmodium falciparum merozoit

163 ansactive response DNA-binding protein of 43 kD (TDP-43)-positive inclusions and neuronal ceroid lipo

164 Transactive response DNA-binding protein 43 kD (TDP-43) is an aggregation-prone prion-like domain-co

165 ted that p110 and p107 are subunits of a 430-kD heterotetramer and that they both originate from the

166 ntified Ldo45 (LD organization protein of 45 kD) as a crucial targeting determinant.

167 pophilin, and tail-interacting protein of 47 kD) family.

168 ich is called tail-interacting protein of 47 kD, moved a fraction of the proteins from their parental

169 2, was used in combination with a small (1.5 kD) peptide, IMP288, labeled with (111)In and (177)Lu.

170 annel-forming peptides (MW approximately 2.5 kD) either reduced the tendency of these peptides to sel

171 nits (68.8 kD each), one gamma-subunit (22.5 kD), and one delta-subunit (11.9 kD).

172 no- and carboxy-terminal domains of the 21.5-kD sieve element-specific ENOD are posttranslationally c

173 HIPM, a 6.5-kD protein, interacted with HrpN in yeast and in vitro.

174 n the largest cluster, 10 ( approximately 50 kD), could be observed as the intact cluster demonstrati

175 tein EBP50 (ERM-binding phosphoprotein of 50 kD), consisting of two PDZ domains and an ezrin-binding

176 P50/NHERF1 (ERM-binding phosphoprotein of 50 kD/Na(+)-H(+) exchanger regulatory factor), a microvilla

177 Here, we characterize p50(Nesp1), a 50-kD isoform that localizes to processing bodies (PBs), wh

178 Here, we identified and characterized a 50-kD pumpkin (Cucurbita maxima cv Big Max) phloem RNA bind

179 se pair deletion encompassing the 27- and 50-kD gamma-zein genes on chromosome 7 and a deletion of at

180 ma-zein deletion had intermediate 27- and 50-kD gamma-zein levels and were semivitreous, indicating h

181 deletion mutant was null for the 27- and 50-kD gamma-zeins and abolished vitreous endosperm formatio

182 ntitative trait locus and may suggest the 50-kD gamma-zein also contributes to this quantitative trai

183 ree to 7 days after stroke, levels of the 50-kD heparanase, basic fibroblast growth factor (FGF-2), a

184 es and most bacteria, and functions as a 500 kD homo-tetramer.

185 stern analysis resolved fibrocystin as a 500 kD product without other forms in the 15-550 kD range.

186 pproximately 75-kDa KSRP, a approximately 52-kD KSRP, t-KSRP, is present in the cytoplasm of a subpop

187 % of the subjects, mostly the anti-Ro/SSA-52-kD subtype detected by immuno-Western blotting only.

188 hydin was specific for an approximately 540-kD flagellar protein that is missing from axonemes of st

189 t Src kinase-associated phosphoprotein of 55 kD (SKAP55) is required for microcluster persistence and

190 kD product without other forms in the 15-550 kD range.

191 terminally fused to a small (approximately 6 kD) membrane protein (AtRCI2A) and stably expressed in A

192 granulomas: The bacterial secreted protein 6-kD early secreted antigenic target (ESAT-6), which has l

193 mbrane sialoglycoprotein of approximately 60 kD, which contains an extracellular Ig-like domain homol

194 ught to decrease dramatically beyond a 30-60-kD size threshold.

195 tion of PINK1 is inhibited, stabilizing a 60-kD form inside mitochondria.

196 Loss of membrane potential causes 60-kD protein to accumulate, suggesting that OMA1 is attenu

197 ontact site and cristae organizing system 60-kD subunit, the translocase of outer mitochondrial membr

198 usage of the a, b, and c variants of the 60-kD structural subunit BAF60 (BRG1/BRM-associated factor

199 igh molecular mass form of approximately 600 kD, and SSIIa, BEIIa, and BEIIb also migrated in a secon

200 sential component of the yeast NPC, the ~600-kD heptameric Nup84 complex, to a precision of ~1.5 nm.

201 ial is dissipated, PINK1 accumulates as a 63-kD full-length form on the outer mitochondrial membrane,

202 ssue sections were triple-labeled for the 65 kD isoform of glutamic acid decarboxylase (GAD65), PV an

203 We have now identified a 65-kD adaptor protein that links P0 with the receptor for a

204 Thus, specific 65-kD Gbps coordinate a potent oxidative and vesicular traf

205 The 65-kD isoform of glutamic acid decarboxylase (GAD65) is a m

206 irus antigens glycoprotein B (gB) and the 65-kD phosphoprotein (pp65), respectively, is in developmen

207 lacked complex I but had low levels of a 650-kD assembly intermediate, similar to mutations in the ho

208 ls had larger apparent molecular masses (>66 kD).

209 e high molecular weight pattern (approx. 670 kD) on size-exclusion HPLC.

210 igh molecular mass form of approximately 670 kD, so that SSIII, SSIIa, SBEIIa, and SBEIIb most likely

211 yl starch solution (Hextend, Hospira, MW 670 kD) occurred.

212 PHP resides in an approximately 670-kD protein complex in nuclear extracts, and physically i

213 SBEIIa, and SBEIIb for assembly into the 670-kD complex.

214 oximately 28 kD) and large (approximately 68 kD) polypeptides.

215 assessed using both albumin-Alexa568 and 69-kD FITC-dextran; however, diabetic animals demonstrated

216 transcription factor (220 amino acids; 25.7 kD) that activates a series of biosynthetic genes leadin

217 nearly neutral fluorescent dextran (3 and 70 kD) solute penetration distance in the hydrogels and OHS

218 nase (Syk) and zeta-associated protein of 70 kD (ZAP-70) tyrosine kinases are both expressed during e

219 ssion of zeta-chain-associated protein of 70 kD.

220 Expression of the 70 kD N-terminal fragment of FN blocks FN fibril assembly a

221 We identify lysine 31 in the 70 kD subunit (Ku70 K31) as the primary candidate nucleophi

222 70-kD FITC-dextran added apically to Myo5b KO intestinal ex

223 17-kD PSII subunit P-like proteins and a 70-kD ATP-dependent zinc metalloprotease, FtsH.

224 of talin that results in the release of a 70-kD C-terminal fragment, which serves as a substrate of p

225 This antibody recognized a 70-kD protein in the A. thaliana chloroplast membrane fract

226 lear ribonucleoprotein (snRNP)-associated 70-kD protein (U1 70K) and with the small subunit of the U2

227 The sieving coefficient of 70-kD dextran was found to be around 0.001.

228 The 70-kD family of heat shock proteins (Hsp70s) is involved in

229 d by LC-MS/MS analysis confirmed that the 70-kD protein was encoded by the OEP80 cDNA.

230 pression of OEP80 and accumulation of the 70-kD protein.

231 for two unique missense mutations in the 70-kD T cell receptor zeta-chain associated protein (ZAP-70

232 hondrial calcium uniporter (mtCU) is an ~700-kD multisubunit channel residing in the inner mitochondr

233 AtCPSF73-II) that share homology with the 73 kD subunit of the mammalian CPSF complex.

234 Thus, two 73 kD subunits of the AtCPSF complex appear to have special

235 ic complex with molecular weight of about 75 kD was formed only in the presence of EDC/NHS in the cro

236 H2 domain-containing leukocyte protein of 76 kD (SLP-76) is recruited to microclusters at the plasma

237 in-containing leukocyte phosphoprotein of 76 kD (SLP76), an adaptor that plays a critical role in pla

238 in-containing leukocyte phosphoprotein of 76 kD) and ADAP (adhesion and degranulation promoting adapt

239 ides (encoding a protein of approximately 78 kD), thereby providing an invaluable tool to accelerate

240 This study is to explore the role of 78 kD glucose-regulated protein (GRP78) in the development

241 a-subunit (56.0 kD), one gamma-subunit (24.8 kD), and one delta-subunit (13.9 kD).

242 rotein comprised of two alpha-subunits (68.8 kD each), one gamma-subunit (22.5 kD), and one delta-sub

243 The LC8 family of small ~8 kD proteins are highly conserved and interact with multi

244 The evolutionarily conserved 8-kD protein NEDD8 (NEURAL PRECURSOR CELL EXPRESSED, DEVEL

245 D PROTEIN8) is an evolutionarily conserved 8-kD protein that is closely related to ubiquitin and that

246 that the molecular weight of OEP80 is ca. 80 kD.

247 paralog of Toc75, outer envelope protein 80 kD (OEP80), also uses a transit peptide but has a distin

248 embly of Complex I is stalled at 650 and 800 kD intermediates in mitochondria isolated from ciaf1 mut

249 The metazoan-specific approximately 800-kD ROD-Zwilch-ZW10 (RZZ) complex builds a fibrous corona

250 e heterodimeric proteins consisting of an 85-kD regulatory subunit and a 110-kD catalytic subunit.

251 bunit (22.5 kD), and one delta-subunit (11.9 kD).

252 bunit (24.8 kD), and one delta-subunit (13.9 kD).

253 hree forms of this protein (210, 120, and 90 kD) were detected in whole cells; the two smaller forms

254 of AID with eEF1A and heat-shock protein 90 kD (HSP90) are inversely correlated.

255 is) a novel, allosterically desensitized 910-kD Class-2 PEPC hetero-octameric complex, arises from a

256 Chloroplast 93-kD heat shock protein (Hsp93/ClpC), an Hsp100 family mem

257 in E. chaffeensis (75-kDa) and E. canis (95-kD) whole-cell lysates and supernatants were identified

258 FliI GLD 2-6 showed lower binding affinity (kD = 0.8584 muM).

259 n-salt-water system on protein diffusion and kD in the context of Nernst-Planck theory.

260 The values of kH and kD vary appreciably with the substituents on the double

261 n to the observed exchange rate gives kH and kD, the rate constants for H* (D*) transfer from (etha(5

262 ecommend comparing experimentally determined kD values to theoretically predicted excluded-volume con

263 hronic pain conditions, we observe disrupted kD, in proportion to individuals' pain intensity, and as

264 the extent of degree rank order disruption, kD, identifies the chronic pain state.

265 both [6((i)Pr)] and [HOPh] and exhibits a kH/kD of 1.9 when DOPh is employed.

266 nt of (2.3 0.2) x 10(4) M(-1) s(-1) and a kH/kD of 7.7 1.2.

267 [Rh] was in the half-order regime, and a kH/kD value of 6.7(6) when [Rh] was in the first-order regi

268 A large kinetic isotope effect (kH/kD = 20) suggests proton coupled electron transfer in th

269 The kinetic isotope effect (kH/kD) increased from 28 at 23 degrees C to 360 at -30 degr

270 riments yield a deuterium isotope effect, kH/kD approximately 3 for ABLM decay, indicating the involv

271 Kinetic isotope effects (kH/kD) for oxidations of benzyl alcohol and ethylbenzene we

272 6H4OH with an electron-withdrawing group (kH/kD = 0.6-0.7; X = Cl, CF3).

273 -C6H4OH with an electron-releasing group (kH/kD = 1.7-2.5; X = OMe, Et), whereas an inverse isotope e

274 ent of the temperature dependence of just kH/kD can be used to establish more unequivocally whether t

275 a large kinetic isotope effect at 298 K, kH/kD approximately 150, associated with an intramolecular

276 1red) and solvent-kinetic isotope (KIE = kH/kD) data (all three ions) indicate that protonated super

277 he observed kinetic isotope effect (KIE = kH/kD) ranged from 1.2 to 1.4, where the KIE was observed t

278 action site, as indicated by the measured kH/kD ratios and by theory.

279 inetic isotope effect (KIE) measurements (kH/kD = 3.0 +/- 0.2), the isolation of the catalytically ac

280 ction leading to complex 6 is negligible; kH/kD = 0.98 +/- 0.02.

281 cant kinetic isotope effect was observed, kH/kD = 1.3.

282 elatively small kinetic isotope effect of kH/kD = 7 for the iron(IV)-tosylimido complex.

283 (*) to BnO(*) and with the observation of kH/kD ratios close to unity in the reactions of BnO(*).

284 The values of kH/kD, 4.58-5.15, in the range 185.8-153.8 degrees C, on ex

285 lar C-H amination of toluene [PhCH3/PhCD3 kH/kD: 15.5(3); PhCH2D kH/kD: 11(1)].

286 luene [PhCH3/PhCD3 kH/kD: 15.5(3); PhCH2D kH/kD: 11(1)].

287 The kinetic isotope study (kH/kD = 2.9) suggests that the cleavage of the C-H bond tak

288 ith precatalysts 2 and 2-Cl indicate that kH/kD = 3.3(5) and 2.6(4), respectively.

289 n line with the computed C-H BDEs and the kH/kD ratios.

290 s(-1), and the kinetic isotope effect was kH/kD = 4.4.

291 We showed that the 27-kilodalton (kD) gamma-zein controls protein body initiation but is n

292 ly 500-residue, approximately 50-kilodalton (kD) dissociation limitation of this top-down methodology

293 we examined a complete mouse 65-kilodalton (kD) guanylate-binding protein (Gbp) gene family as part

294 e Swain-Schaad exponents, SSE = ln(kH/kT)/ln(kD/kT), for this reaction have been computed over the te

295 predicted for a random single-hit model (lnS=kD).

296 ein (GLD 1-6) with the rod domain of NMMIIA (kD = 0.146 muM), whereas FliI GLD 2-6 showed lower bindi

297 nt onset of back pain exhibited emergence of kD only when the pain became chronic.

298 ressed in terms of the interaction parameter kD) is often used to infer whether protein-protein inter

299 Similarly, in neuropathic rats kD emerged weeks after injury, in proportion to pain-lik

300 The kD 2/ kH 2 ratio for the slow component was 1.62 +/- 0.0