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1 yruvate dehydrogenase multienzyme complex of Bacillus stearothermophilus.
2 te in the structure of alanine racemase from Bacillus stearothermophilus.
3 A, the master regulator of sporulation, from Bacillus stearothermophilus.
4 t of VanT with the Air alanine racemase from Bacillus stearothermophilus.
5 ystal structure of ribosomal protein S4 from Bacillus stearothermophilus.
6 ere detected in Methanococcus jannaschii and Bacillus stearothermophilus.
7 O6MeG in a high-fidelity DNA polymerase from Bacillus stearothermophilus.
8 phile, Bacillus subtilis, and a thermophile, Bacillus stearothermophilus.
9 2)) 153-kDa pyruvate decarboxylase (E1) from Bacillus stearothermophilus.
10 and compared with that from the thermophile Bacillus stearothermophilus.
11 yruvate dehydrogenase multienzyme complex of Bacillus stearothermophilus.
12 ain hexameric replicative helicase DnaB from Bacillus stearothermophilus.
13 Bacillus halodurans, Bacillus anthracis and Bacillus stearothermophilus.
15 of the isolated N-domain (residues 1-174) of Bacillus stearothermophilus 3-phosphoglycerate kinase (P
16 are conserved in the Mn-dependent iPGAM from Bacillus stearothermophilus (33% overall sequence identi
17 es at A2451 were generated by reconstituting Bacillus stearothermophilus 50S subunits from in vitro t
18 the catalytic base in the l-isomer case) of Bacillus stearothermophilus alanine racemase on cycloser
19 ry of each domain is very similar to that of Bacillus stearothermophilus alanine racemase, but the ro
20 ycloserine inactivated crystal structures of Bacillus stearothermophilus alanine racemase, which corr
21 The catalytic chemistry of the thermophilic Bacillus stearothermophilus alcohol dehydrogenase (HtADH
22 ent of the pyruvate dehydrogenase complex of Bacillus stearothermophilus allowed a molecular comparis
23 e of a monomeric form of a DNA helicase from Bacillus stearothermophilus, alone and in a complex with
24 arity to the crystal structure of ErmC' from Bacillus stearothermophilus and a lesser similarity to s
25 meric dihydrolipoyl acyltransferase cores of Bacillus stearothermophilus and Enterococcus faecalis py
26 Although the active site residues in the Bacillus stearothermophilus and human tyrosyl-tRNA synth
27 ependent phosphoglycerate mutase (iPGM) from Bacillus stearothermophilus and its 3-phosphoglycerate s
28 tal structures of the CCA-adding enzyme from Bacillus stearothermophilus and its complexes with ATP o
29 ligase could be identified in the genomes of Bacillus stearothermophilus and other gram-positive bact
30 lify the corresponding region of spoIIA from Bacillus stearothermophilus and Paenibacillus polymyxa (
31 on structures of GDP-bound and apo-IF2-G2 of Bacillus stearothermophilus and provide evidence that th
32 4-5' domain rRNA complex from a thermophile, Bacillus stearothermophilus, and points out unexpected d
35 cilitated by investigating the homologs from Bacillus stearothermophilus as well as co-expression of
36 yruvate dehydrogenase multienzyme complex of Bacillus stearothermophilus assemble to form a pentagona
37 report the crystal structure of N-Spo0A from Bacillus stearothermophilus at 1.6 A spacing, revealing
38 ity polymerase from a thermostable strain of Bacillus stearothermophilus (Bacillus fragment) bound to
39 ogues to determine how DNA polymerase I from Bacillus stearothermophilus (BF), a prototypical A famil
40 , a B family enzyme, and DNA polymerase from Bacillus stearothermophilus (BF), an A family enzyme, ge
43 espite the similarity between these ligands, Bacillus stearothermophilus (Bs)TrpRS preferentially bin
46 obilization of maltogenic alpha-amylase from Bacillus stearothermophilus (BsMa) onto novel porous pol
47 teric site on phosphofructokinase (EC ) from Bacillus stearothermophilus (BsPFK) diminishes the abili
48 n-shifted mutant of phosphofructokinase from Bacillus stearothermophilus (BsPFK) have been examined.
50 hosphofructokinases from E. coli (EcPFK) and Bacillus stearothermophilus (BsPFK) reveals a structure
52 ion structure has been obtained for L18 from Bacillus stearothermophilus (BstL18), a ribosomal protei
56 domain of phosphoglycerate kinase (PGK) from Bacillus stearothermophilus combined equilibrium amide e
57 a(2)beta(2)) component of the PDH complex of Bacillus stearothermophilus, considered possible proton
59 L- and D-alanine-d3 by alanine racemase from Bacillus stearothermophilus directly observed by (2)H NM
60 er tengcongensis UvrD helicase (TteUvrD) and Bacillus stearothermophilus DNA polymerase I Large Fragm
62 stal structures of a thermostable bacterial (Bacillus stearothermophilus) DNA polymerase I large frag
63 tion and assignment of two resonances in the Bacillus stearothermophilus DnaB hexamer (320 kDa), demo
64 structures of p16 from Escherichia coli and Bacillus stearothermophilus DnaG proteins revealed a uni
65 ndle, peripheral subunit binding domain from Bacillus stearothermophilus (E3BD) were determined by te
67 ds, and a well folded deletion mutant of the Bacillus stearothermophilus enzyme served as starting po
69 oned in Escherichia coli by amplification of Bacillus stearothermophilus genomic DNA using PCR and in
70 on endonuclease was purified from the native Bacillus stearothermophilus H3 cells and its N-terminal
72 n to quantitate these interactions, L11 from Bacillus stearothermophilus has been overexpressed and i
73 e dehydrogenase (PDH) multienzyme complex of Bacillus stearothermophilus has indicated the importance
74 DHFR) from a moderate thermophilic organism, Bacillus stearothermophilus, has been cloned and express
75 ee energy profiles for alanine racemase from Bacillus stearothermophilus have been determined at pH 6
76 properties of phosphofructokinase (PFK) from Bacillus stearothermophilus have been studied from 5 to
77 the Bacillus subtilis loader protein and the Bacillus stearothermophilus helicase, as well as the hel
78 eric thermophilic alcohol dehydrogenase from Bacillus stearothermophilus (ht-ADH) has been mutated at
79 carried out on the homodimeric HU protein of Bacillus stearothermophilus (HUBst) and a 222-bp DNA fra
83 h TRAP proteins from Bacillus halodurans and Bacillus stearothermophilus, implying that the structura
84 homologous tryptophanyl-tRNA synthetase from Bacillus stearothermophilus in a complex with the cognat
85 te transporters from Bacillus caldotenax and Bacillus stearothermophilus in a monodisperse, detergent
87 D1 polypeptide, we overexpressed Mn-SOD from Bacillus stearothermophilus in the cytoplasm of sod1Delt
89 se) of the pyruvate dehydrogenase complex of Bacillus stearothermophilus is a heterotetramer (alpha2b
91 residue catalytic domain of RNase P RNA from Bacillus stearothermophilus is immobilized in a microflu
93 stallographic structure of Fpg obtained from Bacillus stearothermophilus is stabilized through intera
94 uvate dehydrogenase multienzyme complex from Bacillus stearothermophilus is stably folded, despite it
95 together with an amber suppressor tRNA from Bacillus stearothermophilus is then used to site-specifi
96 oBI is a type II restriction enzyme found in Bacillus stearothermophilus JN209 that recognizes the sy
97 osed surface return loop (alpha E-beta D) of Bacillus stearothermophilus L-lactate dehydrogenase (bsL
98 er trypsin digestion conditions that degrade Bacillus stearothermophilus L11 to small fragments, the
100 tylate (SSL) and monoacylglycerols (MAG) and Bacillus stearothermophilus maltogenic alpha-amylase (BS
102 A recognition by an adenine DNA glycosylase, Bacillus stearothermophilus MutY, have previously been r
103 ied the energetics of the charge transfer in Bacillus stearothermophilus MutY-DNA complex using multi
104 OSY NMR spectra of TRAP from the thermophile Bacillus stearothermophilus over an extended range of te
106 ral in the present structure and that of the Bacillus stearothermophilus ParC-CTD structure suggests
107 C221 stimulates the helicase activity of the Bacillus stearothermophilus PcrA DNA helicase in vitro.
108 ivity; however, recent structural studies of Bacillus stearothermophilus PcrA have led to suggestions
109 stimulates the in vitro helicase activity of Bacillus stearothermophilus PcrA helicase upon a variety
112 two such helicases, Escherichia coli Rep and Bacillus stearothermophilus PcrA, show that the 2B sub-d
113 is on a prototypical superfamily 1 helicase, Bacillus stearothermophilus PcrA, we discovered that Pcr
117 cture of the N and C-terminal domains of the Bacillus stearothermophilus protein have been solved by
118 of the thermophilic, Gram-positive organism Bacillus stearothermophilus PV72/p2 forms a crystalline,
119 lipoamide acetyltransferase component of the Bacillus stearothermophilus pyruvate dehydrogenase multi
121 the hexameric replicative helicase DnaB from Bacillus stearothermophilus revealed specific functions
122 report the crystal structure of C-Spo0A from Bacillus stearothermophilus revealing a single alpha-hel
127 uctures of PGK isolated from horse, pig, and Bacillus stearothermophilus (rms deviations between equi
128 d structural determinants for the RNA in the Bacillus stearothermophilus S15-rRNA interaction have be
129 structure of the C-terminal 158 residues of Bacillus stearothermophilus S4 has been solved by both X
133 NAD(+)-dependent alcohol dehydrogenase from Bacillus stearothermophilus strain LLD-R (htADH) was det
134 r PEP inhibition in phosphofructokinase from Bacillus stearothermophilus, suggesting that these two h
135 e of the pyruvate dehydrogenase complex from Bacillus stearothermophilus taken by low-dose electron c
137 yruvate dehydrogenase multienzyme complex of Bacillus stearothermophilus, the interaction between the
138 was expressed from the moderate thermophile Bacillus stearothermophilus to quantitatively compare st
139 e promoter and bgaB (beta-galactosidase from Bacillus stearothermophilus) to create a translational f
141 resemble those of human TrpRS than those of Bacillus stearothermophilus TrpRS (bsTrpRS) indicate dif
145 r tryptophan versus tyrosine by contemporary Bacillus stearothermophilus tryptophanyl-tRNA synthetase
146 entropic contributions play in catalysis by Bacillus stearothermophilus tyrosyl-tRNA synthetase (Tyr
148 vation of l-tyrosine by the K233A variant of Bacillus stearothermophilus tyrosyl-tRNA synthetase disp
149 to elucidate how the catalytic mechanism of Bacillus stearothermophilus tyrosyl-tRNA synthetase evol
151 ture sequence motifs, "HIGH" and "KMSKS." In Bacillus stearothermophilus tyrosyl-tRNA synthetase, the
152 phosphate moiety of the ATP substrate in the Bacillus stearothermophilus tyrosyl-tRNA synthetase.
154 ric trp RNA-binding Attenuation Protein from Bacillus stearothermophilus using nearest-neighbor stati
155 molecular structure of alanine racemase from Bacillus stearothermophilus was determined by X-ray crys
156 uvate dehydrogenase multienzyme complex from Bacillus stearothermophilus was reconstituted in vitro f
157 tructure of a 417-nt ribonuclease P RNA from Bacillus stearothermophilus was solved to 3.3-A resoluti
158 of the multidomain ribosomal protein L9 from Bacillus stearothermophilus was studied by a novel combi
159 advantage of the stable DnaB-DnaG complex in Bacillus stearothermophilus, we have reviewed conflictin
161 amic properties of ribosomal protein L9 from Bacillus stearothermophilus were investigated in solutio
162 ity of adenylate kinase from the thermophile Bacillus stearothermophilus were monitored during the si
164 olysis of the NAD+-dependent DNA ligase from Bacillus stearothermophilus with thermolysin results in
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