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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 13-T (unidentified reading frame encoding 13-kD cms-T protein) gene in the cms-T cytoplasms.

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

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

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

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

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

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

36 dergoing endurance exercise training, the 14-kD actin fragment decreased to values similar to levels

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

38 who were undergoing hip arthroplasty, the 14-kD actin fragment level was correlated (r = 0.787, P < 0

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

40 t of approximately 66- and approximately 140-kD PrxII complexes into large filamentous oligomers.

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

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

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

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

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

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

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

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

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

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

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

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

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 ion kinase family interacting protein of 200 kD (FIP200) has been shown to regulate diverse cellular

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

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

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

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

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

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

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

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

86 lines in the accumulation of both 19- and 22-kD alpha-zeins, which resulted in higher lysine and tryp

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

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

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

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

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

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

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

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

95 iable Ig domains within an approximately 220 kD ectodomain.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

138 of 5.872, 11.311, 11.929, 12.727, and 13.349 kD were significantly higher in patients with BKVAN.

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 fied HS-1 associated protein-1 (HAX-1), a 35-kD BH-domain containing protein localized to the mitocho

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

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

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

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

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

148 owed that UNC-97 interacts with UNC-98, a 37-kD protein, containing four C2H2 Zn fingers, that locali

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

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

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

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

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

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

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

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

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

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

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

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

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

162 ing electrophoresis indicated that intact 42 kD FasL and an unidentified 24-kDa protein were associat

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

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

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

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

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

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

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

170 2, was used in combination with a small (1.5 kD) peptide, IMP288, labeled with (111)In and (177)Lu.

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

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

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

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

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

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

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

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

179 ody that appears to be targeted against a 50-kD nuclear envelope protein.

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

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

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

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

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

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

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

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

188 with a molecular weight of approximately 52 kD.

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

190 % of the subjects, mostly the anti-Ro/SSA-52-kD subtype detected by immuno-Western blotting only.

191 concerted action of three G proteins, the 54-kD subunit of SRP and the alpha- and beta-subunits of SR

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

224 17-kD PSII subunit P-like proteins and a 70-kD ATP-dependent zinc metalloprotease, FtsH.

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

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

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

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

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

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

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

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

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 ed differences in the profiles of 75- and 80-kD tyrosine-phosphorylated proteins in the zyxin-null ce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

271 6H4OH with an electron-withdrawing group (kH/kD = 0.6-0.7; X = Cl, CF3).

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

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

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

275 1red) and solvent-kinetic isotope (KIE = kH/kD) data (all three ions) indicate that protonated super

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

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

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

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

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

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

282 of the temperature dependence, a value of kH/kD of 16.6 (standard error between 6.5 and 43) is calcul

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