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1  protein that is monomeric, well-folded, and hyperthermophilic.
2 study demonstrates coenzyme engineering of a hyperthermophilic 6PGDH and its application to high-temp
3 s islandicus rod-shaped virus 2) infects the hyperthermophilic acidophile Sulfolobus islandicus, whic
4 aracterized an archaeal antioxidant from the hyperthermophilic acidophile Sulfolobus solfataricus.
5 s it is in the filamentous viruses infecting hyperthermophilic acidophiles.
6 l mobilities differ between a mesophilic and hyperthermophilic adenylate kinase, but are strikingly s
7 nal regulator SurR of Pyrococcus furiosus, a hyperthermophilic anaerobe.
8                           The cpn10 from the hyperthermophilic, ancient bacterium Aquifex aeolicus (A
9                                          The hyperthermophilic and anaerobic bacterium Thermotoga mar
10  family involved in heat shock regulation in hyperthermophilic and mesophilic Archaea organisms.
11                                         This hyperthermophilic and strictly anaerobic crenarchaeon pr
12 ogue (TP0823) for neelaredoxin, an enzyme of hyperthermophilic and sulfate-reducing anaerobes shown t
13 nt comparison of ECAK dynamics with those of hyperthermophilic Aquifex aeolicus AK (AAAK), our result
14 ) accumulates as a compatible solute in many hyperthermophilic archaea (e.g., Archaeoglobus fulgidus)
15 riginated in an extreme environment, such as hyperthermophilic archaea (Pyrococcus furiosus), are sig
16 RNA-encoding DNA analysis places many of the hyperthermophilic Archaea (species with an optimum growt
17 f structures and complete genomes of several hyperthermophilic archaea and bacteria revealed that org
18 bilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and is required for growth at
19 interaction with uracil is not restricted to hyperthermophilic archaea and that the polymerase from m
20  from common yeasts to extremophiles such as hyperthermophilic archaea can also generate high current
21            So far, little is known about how hyperthermophilic Archaea cope with such pyrimidine dama
22       Here we describe a consortium of three hyperthermophilic archaea enriched from a continental ge
23                                              Hyperthermophilic archaea grow at temperatures that dest
24    In particular, the approaches employed by hyperthermophilic archaea have been a general source of
25 f the DNA replication-associated proteins of hyperthermophilic archaea have yielded considerable insi
26    Inositol monophosphatase (EC 3.1.3.25) in hyperthermophilic archaea is thought to play a role in t
27                   Hsp16.5, isolated from the hyperthermophilic Archaea Methanococcus jannaschii, is a
28 o establish the key cell-cycle parameters of hyperthermophilic archaea of the genus Sulfolobus.
29 rs contained in a microbiome-associated with hyperthermophilic archaea of the order Sulfolobales reco
30                            Viruses infecting hyperthermophilic archaea of the phylum Crenarchaeota di
31 ficity and binding mechanism of MCM from the hyperthermophilic Archaea Sulfolobus solfataricus on var
32                                  However, in hyperthermophilic archaea that live optimally at tempera
33                            Viruses infecting hyperthermophilic archaea typically do not encode DNA po
34 quences (ISs) are abundant and widespread in hyperthermophilic archaea, but few experimental studies
35 e that the intracellular proteins of certain hyperthermophilic archaea, especially the crenarchaea Py
36                                           In hyperthermophilic archaea, however, TIM exists as a tetr
37 d over a contiguous 16 kb region between two hyperthermophilic Archaea, Pyrococcus furiosus and Therm
38 esponses have been of particular interest in hyperthermophilic archaea, since these microbes live und
39 s of recombination involving short ssDNAs in hyperthermophilic archaea, we evaluated oligonucleotide-
40 spanning all domains of life, from humans to hyperthermophilic archaea.
41 d response mechanism that is present even in hyperthermophilic archaea.
42 ting experiments for bacteria and 90-99% for hyperthermophilic archaea.
43 like CPSase such as those present in several hyperthermophilic archaea.
44  in rRNA, tRNA, non-coding RNA and mRNA from hyperthermophilic archaea.
45 enzymes in sugar and peptide fermentation of hyperthermophilic archaea.
46  communities dominated by several species of hyperthermophilic Archaea.
47 ed to study its impact on DNA replication in hyperthermophilic Archaea.
48 7d are two small chromatin proteins from the hyperthermophilic archaeabacterium Sulfolobus solfataric
49                          The two recombinant hyperthermophilic archaeal [2Fe-2S] cluster-binding prot
50     Moreover, this latest example of a split hyperthermophilic archaeal DNA polymerase further illust
51 els for dNTP, ddNTP, and acyNTP selection by hyperthermophilic archaeal DNA polymerases to rationaliz
52 the parameters for dNTP incorporation by the hyperthermophilic archaeal Family B Vent DNA polymerase
53 trand RNA viruses that probably replicate in hyperthermophilic archaeal hosts and are highly divergen
54                  Pyrococcus woesei (Pw) is a hyperthermophilic archaeal organism that exists under co
55 Analysis of the genome sequence of the small hyperthermophilic archaeal parasite Nanoarchaeum equitan
56                                          The hyperthermophilic archaeal parasite, Nanoarcheaum equita
57 first structure of a catalytic domain from a hyperthermophilic archaeal viral integrase reveals a min
58 gle-stranded (ss) DNA genome among the known hyperthermophilic archaeal viruses.
59                    Archaeoglobus fulgidus, a hyperthermophilic, archaeal sulfate reducer, is one of t
60                      Here, we found that the hyperthermophilic archaeaon, Pyrococcus furiosus, active
61 a voltage-dependent K+ (K(V)) channel from a hyperthermophilic archaebacterium from an oceanic therma
62 structure of adenylosuccinate lyase from the hyperthermophilic archaebacterium Pyrobaculum aerophilum
63 is work, we characterize the enzyme from the hyperthermophilic archaebacterium Pyrococcus furiosus.
64                                          The hyperthermophilic archaeon Acidianus ambivalens expresse
65                                          The hyperthermophilic archaeon Aeropyrum pernix (A. pernix)
66 m chain alcohol dehydrogenase (ADH) from the hyperthermophilic archaeon Aeropyrum pernix has been sol
67 he Aeropyrum coil-shaped virus (ACV), of the hyperthermophilic archaeon Aeropyrum pernix, with a viri
68                                          The hyperthermophilic archaeon Archaeoglobus fulgidus contai
69   A new carboxyl esterase, AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has be
70               The heat shock response of the hyperthermophilic archaeon Archaeoglobus fulgidus strain
71  structure of the 104 residue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, desig
72 homogeneity from the soluble fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.
73 ed, expressed and purified components of the hyperthermophilic archaeon Archaeoglobus fulgidus.
74 ctures, to our knowledge, of an ACD from the hyperthermophilic archaeon Candidatus Korachaeum cryptof
75 Sulfolobus acidocaldarius is so far the only hyperthermophilic archaeon in which genetic recombinatio
76                                          The hyperthermophilic archaeon Methanocaldococcus jannaschii
77                                 MAT from the hyperthermophilic archaeon Methanococcus jannaschii (MjM
78                                          The hyperthermophilic archaeon Methanococcus jannaschii enco
79                                          The hyperthermophilic archaeon Methanococcus jannaschii enco
80                                          The hyperthermophilic archaeon Methanococcus jannaschii has
81                                 However, the hyperthermophilic archaeon Methanopyrus kandleri harbors
82               This 12.7-kDa protein from the hyperthermophilic archaeon Pyrobaculum aerophilum adopts
83 lectron transfer flavoprotein (ETF) from the hyperthermophilic archaeon Pyrobaculum aerophilum The Et
84                                          The hyperthermophilic archaeon Pyrobaculum aerophilum used 2
85                 The nitrate reductase of the hyperthermophilic archaeon Pyrobaculum aerophilum was pu
86 an endonuclease III homolog, PaNth, from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose
87 ation of a putative DNA glycosylase from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose
88 is of intracellular disulfide bonding in the hyperthermophilic archaeon Pyrobaculum aerophilum.
89 ORFs of the recently sequenced genome of the hyperthermophilic archaeon Pyrobaculum aerophilum.
90                                          The hyperthermophilic archaeon Pyrobaculum islandicum uses t
91 odABC transport system, was predicted in the hyperthermophilic archaeon Pyrobaculum.
92 transcarbamoylase (OTCase) from the deep sea hyperthermophilic archaeon Pyrococcus abyssi demonstrate
93 ned the solution structure of RPP21 from the hyperthermophilic archaeon Pyrococcus furiosus ( Pfu) us
94 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) have
95 echanism of the H(+)-dependent MATE from the hyperthermophilic archaeon Pyrococcus furiosus (PfMATE).
96 es from Escherichia coli (EcMetAP-I) and the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-
97 ng for the methionyl aminopeptidase from the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-
98 tic studies were conducted on the POP of the hyperthermophilic archaeon Pyrococcus furiosus (Pfu) 85
99 protons of perdeuterated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus and the m
100                    The LrpA protein from the hyperthermophilic archaeon Pyrococcus furiosus belongs t
101 ylase was identified in cell extracts of the hyperthermophilic archaeon Pyrococcus furiosus by its ab
102            Cell extracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus contain h
103 shed membrane preparations from cells of the hyperthermophilic archaeon Pyrococcus furiosus contain h
104        The original genome annotation of the hyperthermophilic archaeon Pyrococcus furiosus contained
105                                          The hyperthermophilic archaeon Pyrococcus furiosus genome en
106                                          The hyperthermophilic archaeon Pyrococcus furiosus grows opt
107           Crystal structures of SOR from the hyperthermophilic archaeon Pyrococcus furiosus have been
108     The cytoplasmic hydrogenase (SHI) of the hyperthermophilic archaeon Pyrococcus furiosus is an NAD
109 ss of PfMATE, a proton-coupled MATE from the hyperthermophilic archaeon Pyrococcus furiosus Pairs of
110             Identification of operons in the hyperthermophilic archaeon Pyrococcus furiosus represent
111                                          The hyperthermophilic archaeon Pyrococcus furiosus uses carb
112         Iron is an essential element for the hyperthermophilic archaeon Pyrococcus furiosus, and many
113 nder anaerobic, reducing conditions from the hyperthermophilic archaeon Pyrococcus furiosus.
114 e rare biological form of RNA circles in the hyperthermophilic archaeon Pyrococcus furiosus.
115 vate synthetase (PpsA) was purified from the hyperthermophilic archaeon Pyrococcus furiosus.
116 nsferase at resolutions up to 1.2 A from the hyperthermophilic archaeon Pyrococcus furiosus.
117 e report random insertion mutagenesis in the hyperthermophilic archaeon Pyrococcus furiosus.
118 A intein located in the ATPase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is stro
119  domain of life, with the discovery that the hyperthermophilic archaeon Sulfolobus has three replicat
120  II chaperonins known as rosettasomes in the hyperthermophilic archaeon Sulfolobus shibatae, are not
121                                          The hyperthermophilic archaeon Sulfolobus solfataricus emplo
122                                          The hyperthermophilic archaeon Sulfolobus solfataricus grows
123                   The Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an
124 ce of a global gene regulatory system in the hyperthermophilic archaeon Sulfolobus solfataricus is de
125 ral modules of the homomultimeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.
126 in chromatin structure and regulation in the hyperthermophilic archaeon Sulfolobus solfataricus.
127 noncatalytic subunit, denoted PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.
128 eavage of mRNA from an invading virus in the hyperthermophilic archaeon Sulfolobus solfataricus.
129 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus.
130 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7
131                     Pyrococcus furiosus is a hyperthermophilic archaeon that grows optimally at 100 d
132 structure of TIM from Thermoproteus tenax, a hyperthermophilic archaeon that has an optimum growth te
133 cture of the ribosomal protein L30e from the hyperthermophilic archaeon Thermococcus celer determined
134 that ribonucleotides are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis bot
135                                          The hyperthermophilic archaeon Thermococcus litoralis strain
136                     Pyrococcus furiosus is a hyperthermophilic archaeon which grows optimally near 10
137 ncovered a putative MIG protein from another hyperthermophilic archaeon, Aeropyrum pernix.
138 ted Box C/D RNAs from Pyrococcus furiosus, a hyperthermophilic archaeon, into the nuclei of oocytes f
139                                          The hyperthermophilic archaeon, Pyrococcus furiosus, was gro
140 leaves the 5' side of deoxyinosine, from the hyperthermophilic archaeon, Pyrococcus furiosus.
141 ily DNA replication polymerase (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is
142  evolution, have not been determined for any hyperthermophilic archaeon.
143 st description of a nitrate reductase from a hyperthermophilic archaeon.
144 ution assay of homologous recombination in a hyperthermophilic archaeon.
145 ifies a putative primordial Orai sequence in hyperthermophilic archaeons.
146         The open reading frame ST0928 from a hyperthermophilic archaeron Sulfolobus tokodaii was clon
147 aracterized an unusual type IA enzyme from a hyperthermophilic archaeum, Nanoarchaeum equitans, which
148                                          The hyperthermophilic archeon Pyrococcus furiosus produces a
149        CopA from Archaeoglobus fulgidus is a hyperthermophilic ATPase responsible for the cellular ex
150  methanarchaeon, Methanococcus jannaschii, a hyperthermophilic, autotrophic, and strictly hydrogenotr
151 e gyrase is a DNA topoisomerase specific for hyperthermophilic bacteria and archaea.
152 merases and positive plasmid supercoiling in hyperthermophilic bacteria and archea.
153 existence of peptide-based quorum sensing in hyperthermophilic bacteria and indicate that cellular co
154 .4 A resolution, of the class I BPL from the hyperthermophilic bacteria Aquifex aeolicus (AaBPL) in i
155 ins taken from mesophilic, thermophilic, and hyperthermophilic bacteria are studied using these metho
156       In contrast, archaeal rRNA and that of hyperthermophilic bacteria differ from the rRNA of mesop
157     Our results explain the root location of hyperthermophilic bacteria in the phylogenetic tree for
158 th is more similar to that of A. aeolicus, a hyperthermophilic bacteria.
159 vated C:G content of the rRNA of archaea and hyperthermophilic bacteria.
160               Cpn10 from the deep-branching, hyperthermophilic bacterium Aquifex aeolicus (Aacpn10) s
161 onate-8-phosphate synthase (KDO8PS) from the hyperthermophilic bacterium Aquifex aeolicus differs fro
162                                          The hyperthermophilic bacterium Aquifex aeolicus has a MutL
163 tural features of the NtrC1 protein from the hyperthermophilic bacterium Aquifex aeolicus suggested t
164      An NAD(+)-dependent DNA ligase from the hyperthermophilic bacterium Aquifex aeolicus was cloned,
165 rt the crystal structures of GatCAB from the hyperthermophilic bacterium Aquifex aeolicus, complexed
166 he crystal structure of a homologue from the hyperthermophilic bacterium Aquifex aeolicus, that share
167 -6-phosphate dehydrogenase (tG6PDH) from the hyperthermophilic bacterium Aquifex aeolicus.
168 usA is also present in the chromosome of the hyperthermophilic bacterium Aquifex aeolicus.
169 shift assays with rRNA and proteins from the hyperthermophilic bacterium Aquifex aeolicus.
170 focus on the energy substrate traffic in the hyperthermophilic bacterium Aquifex aeolicus.
171 eport the crystal structure of TatC from the hyperthermophilic bacterium Aquifex aeolicus.
172  unknown type of protein-only RNase P in the hyperthermophilic bacterium Aquifex aeolicus: Without an
173 is of the crystal structure of MurI from the hyperthermophilic bacterium Aquifex pyrophilus, we perfo
174 us ribose-binding protein, isolated from the hyperthermophilic bacterium Thermoanaerobacter tengconge
175 RAP-PBP (open reading frame tm0322) from the hyperthermophilic bacterium Thermotoga maritima (TM0322)
176  define how the type III-B effector from the hyperthermophilic bacterium Thermotoga maritima discrimi
177 hosphogluconate dehydrogenase (6PGDH) from a hyperthermophilic bacterium Thermotoga maritima from its
178       A thermostable endonuclease V from the hyperthermophilic bacterium Thermotoga maritima has been
179                   The genome sequence of the hyperthermophilic bacterium Thermotoga maritima MSB8 pre
180                                          The hyperthermophilic bacterium Thermotoga maritima MSB8 was
181 ide expression patterns during growth of the hyperthermophilic bacterium Thermotoga maritima on 14 mo
182 eterodimeric ABC exporter TM287/288 from the hyperthermophilic bacterium Thermotoga maritima using al
183 The biochemical behavior of RNase III of the hyperthermophilic bacterium Thermotoga maritima was anal
184    The structure of RNase P protein from the hyperthermophilic bacterium Thermotoga maritima was dete
185  of proteins from one specific organism, the hyperthermophilic bacterium Thermotoga maritima, and tho
186                         In the genome of the hyperthermophilic bacterium Thermotoga maritima, TM0504
187 es is apparent in the genome sequence of the hyperthermophilic bacterium Thermotoga maritima.
188 nt of the MI catabolic pathway in the marine hyperthermophilic bacterium Thermotoga maritima.
189 rsion dynamics in real time in ThyX from the hyperthermophilic bacterium Thermotoga maritima.
190 stallographic studies of the enzyme from the hyperthermophilic bacterium, Aquifex aeolicus.
191 tandemly repeated GTP-binding domains from a hyperthermophilic bacterium, Thermotoga maritima, was cl
192 ermatoga maritima, an evolutionarily ancient hyperthermophilic bacterium.
193 otes, was cloned from Thermotoga maritima, a hyperthermophilic bacterium.
194                            CbpA is the first hyperthermophilic cellobiose phosphorylase to be charact
195                     Archaea and particularly hyperthermophilic crenarchaea are hosts to many unusual
196                                              Hyperthermophilic crenarchaea in the genus Pyrobaculum a
197 nstrate that the Thermoproteales, a clade of hyperthermophilic Crenarchaea, lack a canonical SSB.
198                               Members of the hyperthermophilic crenarchaea, that lack tubulin-like pr
199 A4 were found to be toxic for members of the hyperthermophilic crenarchaeal genus Sulfolobus.
200 es or genes that are first in operons in the hyperthermophilic crenarchaeon P. aerophilum proceeds mo
201 tion crystal structure of SurEalpha from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum (P
202 and a PCNA homolog (Pa-PCNA1), both from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum (T
203 ionine beta-synthase domain protein from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum.
204 h10b, a member of the Sac10b family from the hyperthermophilic crenarchaeon Sulfolobus shibatae, bind
205 erial-like DnaG primase contained within the hyperthermophilic crenarchaeon Sulfolobus solfataricus (
206                                          The hyperthermophilic crenarchaeon Sulfolobus solfataricus P
207 erase-Like Lactonases (PLLs) family from the hyperthermophilic crenarchaeon Vulcanisaeta moutnovskia
208 NA polymerases of Sulfolobus solfataricus, a hyperthermophilic crenarchaeon.
209 ea, and an activity has been observed in the hyperthermophilic crenarchaeote Sulfolobus solfataricus.
210             Moreover, the robustness of this hyperthermophilic DH, in terms of both catalytic activit
211 architecture of this protein is uncommon for hyperthermophilic endoglucanases, and two of the four do
212                                    Thus, the hyperthermophilic enzyme has evolved to have optimum act
213 or directly assaying the activity of another hyperthermophilic enzyme, 1,4-beta-D-glucan glucohydrola
214  AK (ECAK) at 30 degrees C, TNAK is a unique hyperthermophilic enzyme.
215 ut the substrate specificity of two specific hyperthermophilic enzymes and the first test of some nat
216                   Herein, the utilization of hyperthermophilic enzymes in a microwave reactor is repo
217 as a general explanation for the activity of hyperthermophilic enzymes.
218 neralizable approach to enzyme recycling for hyperthermophilic enzymes.
219 s been purified from native membranes of the hyperthermophilic eubacterium Aquifex aeolicus.
220        DNA-binding properties of HU from the hyperthermophilic eubacterium Thermotoga maritima are sh
221                We show here that HU from the hyperthermophilic eubacterium Thermotoga maritima HU ben
222                                          The hyperthermophilic eubacterium Thermotoga maritima posses
223                                          The hyperthermophilic euryarchaeon Methanococcus jannaschii
224                                          The hyperthermophilic euryarchaeon Methanococcus jannaschii
225 p in CoM biosynthesis, was identified in the hyperthermophilic euryarchaeon Methanococcus jannaschii.
226                                         Some hyperthermophilic heterotrophs in the genus Thermococcus
227                                        Seven hyperthermophilic heterotrophs isolated from low-tempera
228 nd molecular screens, although abundances of hyperthermophilic heterotrophs were relatively high.
229 be partly ameliorated by H(2) syntrophy with hyperthermophilic heterotrophs.
230 discovered IgnaviCas9, a Cas9 protein from a hyperthermophilic Ignavibacterium identified through min
231 essure, which is significantly different for hyperthermophilic (IPPase) and mesophilic (HEWL) protein
232                      This is the case of the hyperthermophilic laccase HB27 from Thermus thermophilus
233 sitions -40 to +1 of the gdh promoter of the hyperthermophilic marine archaea, Pyrococcus furiosus (P
234 s of this family have been identified in the hyperthermophilic marine archaeon Methanococcus jannasch
235 ha family (family B) DNA polymerase from the hyperthermophilic marine archaeon Thermococcus sp. 9 deg
236  of Thermofilum pendens, a deeply branching, hyperthermophilic member of the order Thermoproteales in
237        CopA from Archaeoglobus fulgidus is a hyperthermophilic member of this ATPase subfamily and is
238                         However, a number of hyperthermophilic members of the Kingdom Crenarchaea, in
239     I focus primarily on viruses that infect hyperthermophilic members of the phylum Crenarchaeota.
240 To our knowledge, Amt proteins are the first hyperthermophilic membrane transport proteins shown to b
241 d stability from the hot-start toward modern hyperthermophilic, mesophilic, and psychrophilic organis
242 thanocaldococcus jannaschii--a deeply rooted hyperthermophilic methanogen growing only on H2 plus CO2
243  first structures of archaeal G1PDH from the hyperthermophilic methanogen Methanocaldococcus jannasch
244                   The genome sequence of the hyperthermophilic methanogen Methanococcus jannaschii co
245  have been detected in a non-nitrogen-fixing hyperthermophilic methanogen, Methanocaldococcus jannasc
246 ata support our estimated H(2) threshold for hyperthermophilic methanogenesis at vents and highlight
247 pure culture H(2) threshold measurements for hyperthermophilic methanogenesis in low-temperature hydr
248          Here we show that ORF MJ1117 of the hyperthermophilic, methanogenic archaeon Methanocaldococ
249  of genome sequence data from mesophilic and hyperthermophilic micro-organisms has revealed a strong
250              Thermotoga maritima is a marine hyperthermophilic microorganism that degrades a wide ran
251 is a large oligomeric protein derived from a hyperthermophilic microorganism that is found near hydro
252 aled that, on a global scale, populations of hyperthermophilic microorganisms are isolated from one a
253 redicted to be particularly energy-rich, and hyperthermophilic microorganisms that broadly reflect su
254            The 16S ribosomal RNA gene of the hyperthermophilic nitrogen fixer, designated FS406-22, w
255 The family 4 uracil-DNA glycosylase from the hyperthermophilic organism Archaeoglobus fulgidus (AFUDG
256          The enzyme from Aquifex aeolicus, a hyperthermophilic organism of ancient lineage, was clone
257 minating unpaired regions in the genome of a hyperthermophilic organism.
258               Proteins from thermophilic and hyperthermophilic organisms are stable and function at h
259                                      Several hyperthermophilic organisms contain an unusual phosphata
260                                              Hyperthermophilic organisms must protect their constitue
261       Because POP is found in mesophilic and hyperthermophilic organisms, and is distributed among al
262 roteins have been characterized in extremely hyperthermophilic organisms, and most function as repres
263 ungsten, which substitutes for molybdenum in hyperthermophilic organisms, could also be ligated to mo
264  other Archaea or Bacteria, particularly the hyperthermophilic organisms.
265  used frequently in regulatory proteins from hyperthermophilic organisms.
266 ion, biosynthesis and role of fatty acids in hyperthermophilic organisms.
267 sing DNA composition bias in genomes of some hyperthermophilic organisms: simply screening for GC-ric
268 ndidates for a specific association with the hyperthermophilic phenotype.
269 used thioredoxin (Trx) folds, belongs to the hyperthermophilic protein disulfide oxidoreductase famil
270 n enzymatically active, soluble variant of a hyperthermophilic protein that is normally insoluble whe
271 utions to the folding free energy of several hyperthermophilic proteins and their mesophilic homologs
272 aken together, our results suggest that many hyperthermophilic proteins enhance electrostatic interac
273 o 100 degrees C emphasizes the importance in hyperthermophilic proteins of the specific location of i
274 tabilizing forces required for extracellular hyperthermophilic proteins to tolerate high-temperature
275 of improving the low-temperature activity of hyperthermophilic proteins, likely by facilitating the i
276  in 1998, the method has been used to create hyperthermophilic proteins, to evolve novel folded domai
277 ties similar to the natural thermophilic and hyperthermophilic proteins.
278 labile amino-acid residues (i.e. N and Q) in hyperthermophilic proteins.
279                      Here, we describe three hyperthermophilic PrxQ crystal structures originally det
280 ys+1, in an intein precursor composed of the hyperthermophilic Pyrococcus abyssi PolII intein and ext
281 We report the solution NMR structures of the hyperthermophilic Pyrococcus abyssi PolII intein, which
282 idium pasteurianum (Topt = 37 degrees C) and hyperthermophilic Pyrococcus furiosus (Topt = 95 degrees
283 n to activate transcription by its conjugate hyperthermophilic RNA polymerase.
284       Here we present the NMR structure of a hyperthermophilic rubredoxin variant (PFRD-XC4) and the
285 g agent, dextran 20, on the folded states of hyperthermophilic (S16Thermo) and mesophilic (S16Meso) h
286 coli and WrbA from Archaeoglobus fulgidus, a hyperthermophilic species from the Archaea domain, shows
287 jor osmoprotecting metabolite in a number of hyperthermophilic species of archaea and bacteria.
288 d refined the structure of the mIPS from the hyperthermophilic sulfate reducer Archaeoglobus fulgidus
289  (diaphorase) activity was isolated from the hyperthermophilic sulfate-reducing anaerobe Archaeoglobu
290 inantly expressed components of SRP from the hyperthermophilic, sulfate-reducing archaeon Archaeoglob
291 onlytic temperate viruses were isolated from hyperthermophilic Sulfolobus hosts, and both viruses sha
292 loned and purified the RadA protein from the hyperthermophilic, sulphate-reducing archaeon Archaeoglo
293 ior previously observed for thermophilic and hyperthermophilic superoxide dismutases but over a lower
294 um, a facultatively aerobic nitrate-reducing hyperthermophilic (T(opt) = 100 degrees C) crenarchaeon.
295       In solution, however, and unlike other hyperthermophilic TIMs, the T.tenax enzyme exhibits an e
296 , it has been suggested that thermophilic or hyperthermophilic (Tm) enzymes have lower catalytic powe
297                    Mutants created using the hyperthermophilic TnAK were found to support growth with
298 scuous natural human IgG-binding domain, the hyperthermophilic variant of protein G (HTB1), into a hi
299 , single-point core mutants of a 57-residue, hyperthermophilic variant of the B1 domain of protein G
300            We report here the structure of a hyperthermophilic virus isolated from an archaeal host f

 
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