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1 ermostable enzyme isolated from the archaeon Sulfolobus solfataricus.
2 ns-lesion (Y-class) DNA polymerase Dpo4 from Sulfolobus solfataricus.
3 imeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.
4 is by a model Y family polymerase, Dpo4 from Sulfolobus solfataricus.
5 protein from the thermoacidophilic archaeon Sulfolobus solfataricus.
6 neralized transcription in the crenarchaeote Sulfolobus solfataricus.
7 xidant from the hyperthermophilic acidophile Sulfolobus solfataricus.
8 -resolving enzyme; the Hje endonuclease from Sulfolobus solfataricus.
9 ion structure and properties of Sso10b2 from Sulfolobus solfataricus.
10 igh-resolution crystal structure of Hje from Sulfolobus solfataricus.
11 ed PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.
12 regulation in the hyperthermophilic archaeon Sulfolobus solfataricus.
13 e single-stranded DNA-binding protein SSB in Sulfolobus solfataricus.
14 e primase was identified in the crenarchaeon Sulfolobus solfataricus.
15 etergent extract of the membrane fraction of Sulfolobus solfataricus.
16 ed on the use of halocin A4 preparations and Sulfolobus solfataricus.
17 ases human Pol eta and P2 Pol IV (Dpo4) from Sulfolobus solfataricus.
18 erved in the hyperthermophilic crenarchaeote Sulfolobus solfataricus.
19 ation of SHMT from the thermophilic organism Sulfolobus solfataricus.
20 ubacteria, eukaryotes, and the crenarchaeote Sulfolobus solfataricus.
21 main Archaea, Methanosarcina thermophila and Sulfolobus solfataricus.
22 purified CRISPR-associated CMR complex from Sulfolobus solfataricus.
23 ding virus in the hyperthermophilic archaeon Sulfolobus solfataricus.
24 ymerase (YB site) bound to PCNA and DNA from Sulfolobus solfataricus.
25 dic hot springs where it infects the archeon Sulfolobus solfataricus.
26 og proteins, SsoRal3, from the crenarchaeaon Sulfolobus solfataricus.
27 it named PriX was identified in the archaeon Sulfolobus solfataricus.
28 tro using proteins derived from the archaeon Sulfolobus solfataricus.
29 se 3, SsTop3, from the thermophilic archaeon Sulfolobus solfataricus.
30 s required for pyramid formation in its host Sulfolobus solfataricus.
31 protein from the hyperthermophilic archaeon Sulfolobus solfataricus.
32 ation of an archaeal CASCADE (aCASCADE) from Sulfolobus solfataricus.
33 ics of a model Y-family polymerase Dpo4 from Sulfolobus solfataricus.
34 onally related archaeal exosome complex from Sulfolobus solfataricus.
35 h a model Y-family DNA polymerase, Dpo4 from Sulfolobus solfataricus.
36 omologous XPB proteins from the crenarchaeon Sulfolobus solfataricus.
37 ipaludis, Methanocaldococcus jannaschii, and Sulfolobus solfataricus.
39 se was purified from culture supernatants of Sulfolobus solfataricus 98/2 during growth on starch as
40 icative and lesion bypass DNA polymerases of Sulfolobus solfataricus, a hyperthermophilic crenarchaeo
41 efficient heterologous expression system for Sulfolobus solfataricus ADH-10 (Alcohol Dehydrogenase is
42 -3-phosphate dehydrogenase from the archaeon Sulfolobus solfataricus allows modeling of the B subunit
43 on consists of 15 genes; in the Crenarchaea, Sulfolobus solfataricus and Aeropyrum pernix, one and tw
45 re stability of the thermophilic CYP119 from Sulfolobus solfataricus and its active-site Thr213 and T
47 nt of the DinB homolog (Dbh) polymerase from Sulfolobus solfataricus and show that it is nonprocessiv
48 rk, we describe the generation of strains of Sulfolobus solfataricus and Sulfolobus acidocaldarius th
49 from the hyperthermophilic archaeabacterium Sulfolobus solfataricus and Sulfolobus acidocaldarius, r
51 Rad51/RecA protein homolog from the archaeon Sulfolobus solfataricus, and show that this protein, Rad
52 Orc1-1 and Orc1-3 paralogs from the archaeon Sulfolobus solfataricus, and tested their effect on orig
53 lserine (thiol)-lyase-B] in Pyrococcus spp., Sulfolobus solfataricus, and Thermoplasma acidophilum.
55 e present the crystal structure of Alba from Sulfolobus solfataricus at 2.6 A resolution (PDB code 1h
57 crystal structure of the archaeal RNAP from Sulfolobus solfataricus at 3.4 A resolution, completing
58 nding of RuvC of Escherichia coli and Hjc of Sulfolobus solfataricus can be followed by an increase i
59 rates, whereas the Cas4 protein SSO1391 from Sulfolobus solfataricus can cleave ssDNA in both the 5'
60 IV (Dpo4), a prototype Y-family enzyme from Sulfolobus solfataricus, can bypass 8-oxoG both efficien
61 Y-family DNA polymerases, such as Dpo4 from Sulfolobus solfataricus, can traverse a wide variety of
64 dentified splicing endonuclease homolog from Sulfolobus solfataricus, despite possessing all of the p
68 AP site bypass by two Y family TLS enzymes, Sulfolobus solfataricus DNA polymerase 4 (Dpo4) and huma
70 the kinetics and conformational dynamics of Sulfolobus solfataricus DNA polymerase B1 (PolB1) during
75 specifically placed dGAP lesion catalyzed by Sulfolobus solfataricus DNA polymerase IV (Dpo4), a mode
76 dducts derived from 1-NP, can be bypassed by Sulfolobus solfataricus DNA polymerase IV (Dpo4), althou
77 sequences were determined, with the Y-family Sulfolobus solfataricus DNA polymerase IV (Dpo4), at res
78 ction pathways of a Y-family DNA polymerase, Sulfolobus solfataricus DNA polymerase IV (Dpo4), for th
80 ased model to explore functional dynamics in Sulfolobus solfataricus DNA Y-family polymerase IV (DPO4
81 lication, we have detected an interaction of Sulfolobus solfataricus DnaG (SsoDnaG) with the replicat
83 the structures of the model DNA polymerases Sulfolobus solfataricus Dpo4 and Bacillus stearothermoph
84 revious work with the translesion polymerase Sulfolobus solfataricus Dpo4 showed a decrease in cataly
85 In contrast to replicative DNA polymerases, Sulfolobus solfataricus Dpo4 showed a limited decrease i
87 ing situations in structures of complexes of Sulfolobus solfataricus Dpo4, a bypass pol that favors C
91 ted that Lys-110 (numbering according to the Sulfolobus solfataricus enzyme) behaves as a general aci
92 we reveal that the highly studied PolB1 from Sulfolobus solfataricus exists as a heterotrimeric compl
94 and have applied it to Escherichia coli and Sulfolobus solfataricus for genome-wide prediction of nc
96 that the three RadA paralogs encoded by the Sulfolobus solfataricus genome are expressed under norma
97 rd of the open reading frames encoded in the Sulfolobus solfataricus genome were differentially expre
99 erent from those of the archaeal thermophile Sulfolobus solfataricus growing in the same temperature
104 The crystal structure of the apo GAPDH from Sulfolobus solfataricus has been determined by multiple
105 t the Cas4 protein SSO0001 from the archaeon Sulfolobus solfataricus has metal-dependent endonuclease
106 6 homologous proteins (MCM2-7), the archaeon Sulfolobus solfataricus has only 1 MCM protein (ssoMCM),
108 irst P450 identified in Archaea, CYP119 from Sulfolobus solfataricus, has been solved in two differen
109 deltaH, M. thermoautotrophicum Marburg, and Sulfolobus solfataricus, however, has been demonstrated
110 aX proteins) from Methanosarcina barkeri and Sulfolobus solfataricus hydrolyze Ser-tRNAAla and Gly-tR
111 proteins from Sulfolobus acidocaldarius and Sulfolobus solfataricus in N-terminal amino acid sequenc
112 spindle-shaped virus 1 (SSV1), which infects Sulfolobus solfataricus in volcanic hot springs at 80 de
113 undant proteins present in the crenarchaeote Sulfolobus solfataricus, including subunits of the therm
117 protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an attractive binding scaffol
118 by the DinB homolog (Dbh) DNA polymerase of Sulfolobus solfataricus is as stringent as in other poly
121 polymerase Dpo4, from the archaeon bacterium Sulfolobus solfataricus, is a member of the DinB family,
122 virus that infects the hyperthermoacidophile Sulfolobus solfataricus, is one of the most well-studied
123 se (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is shown here to possess a rema
127 of a thermophilic and barophilic CYP119 from Sulfolobus solfataricus offers a new opportunity to iden
129 rate synthase from the thermophilic Archaeon Sulfolobus solfataricus (optimum growth temperature = 85
130 ide was identified from tryptic digests from Sulfolobus solfataricus P1 by liquid chromatography-tand
131 investigated the ultrastructural changes of Sulfolobus solfataricus P2 associated with infection by
132 t the Y-family DNA polymerase IV (Dpo4) from Sulfolobus solfataricus P2 can preferentially insert C o
133 alyzed by an exonuclease-deficient mutant of Sulfolobus solfataricus P2 DNA polymerase B1 (PolB1 exo-
135 lysis of the products of primer extension by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) indi
138 mechanism of DNA polymerization catalyzed by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) is r
139 mational dynamics of the Y-family polymerase Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) usin
140 of translesion bypass of 1,N(2)-epsilondG by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4), lea
143 s of the complete genome of the crenarchaeon Sulfolobus solfataricus P2 reveal that it possesses a Di
144 (EC 1.1.1.34) from the thermophilic archaeon Sulfolobus solfataricus P2 was cloned and sequenced.
145 S2), an acidophilic and aerobic thermophile (Sulfolobus solfataricus P2), and an anaerobic hypertherm
146 ase Dpo4, from the thermophilic crenarchaeon Sulfolobus solfataricus P2, offers a valuable opportunit
147 etermined the X-ray crystal structure of the Sulfolobus solfataricus PCNA1-PCNA2 heterodimer, bound t
148 onuclease and the translesion DNA polymerase Sulfolobus solfataricus pol IV were used as models to di
149 PP1/2A/2B superfamily such as PP1-arch1 from Sulfolobus solfataricus, PP1alpha from rats, PP2A from S
151 mparable with that reported for the archaeal Sulfolobus solfataricus Pth2 and higher than that of the
155 , using in vitro selection, we show that the Sulfolobus solfataricus RadA protein displays the same p
156 ite of the homologous alpha-glucosidase from Sulfolobus solfataricus resulted in a shift from hydroly
157 itional microorganisms (Escherichia coli and Sulfolobus solfataricus) revealed species-specific assim
158 junction-resolving enzyme from the archaeon Sulfolobus solfataricus, reveals extensive structural ho
160 The archaeal homohexameric MCM helicase from Sulfolobus solfataricus serves as a model for understand
162 erol phosphate synthase from the thermophile Sulfolobus solfataricus (sIGPS) and the alpha subunit of
163 he indole-3-glycerol phosphate synthase from Sulfolobus solfataricus (sIGPS), was assessed by hydroge
165 re we have produced a fusion protein between Sulfolobus solfataricus SRP54 (Ffh) and a signal peptide
167 report a role for the thermophilic archaeal Sulfolobus solfataricus SSB (SsoSSB) in the presynaptic
169 acids, as for Methanococcus jannaschii, the Sulfolobus solfataricus SSB protein (SsoSSB) has a singl
170 xy-5'-methylthioadenosine phosphorylase from Sulfolobus solfataricus (SsMTAP) has been determined alo
174 ed within the hyperthermophilic crenarchaeon Sulfolobus solfataricus (Sso) and compared in vitro prim
175 major chromatin proteins, Alba and Sul7d, of Sulfolobus solfataricus (Sso) on the ability of the MCM
176 e replication DNA polymerase holoenzyme from Sulfolobus solfataricus (Sso) was investigated using pre
177 re of Csa3, a CRISPR-associated protein from Sulfolobus solfataricus (Sso1445), which reveals a dimer
178 protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7d-hFc was isolated from a c
179 The primary DNA replication polymerase from Sulfolobus solfataricus (SsoDpo1) has been shown previou
181 ichromosomal maintenance (MCM) helicase from Sulfolobus solfataricus (SsoMCM) is a model for understa
183 open reading frame sso2387 from the archaeon Sulfolobus solfataricus, SsoPK2, displayed several of th
185 tinct for each strain, indicating that these Sulfolobus solfataricus strains have differential respon
186 scribed here focuses on the response of four Sulfolobus solfataricus strains to ionizing radiation (I
187 we have characterized the responses of three Sulfolobus solfataricus strains to UV-C irradiation, whi
188 nly been examined in three archaeal species: Sulfolobus solfataricus, Sulfolobus islandicus, and Pyro
189 yses also predicted that the ancestor to the Sulfolobus solfataricus-Sulfolobus islandicus clade was
190 rmined structure of a MazG-like protein from Sulfolobus solfataricus supported the unification of the
192 se (Hje) from the thermophilic crenarchaeote Sulfolobus solfataricus that exhibits a high degree of s
193 A-binding proteins from the hyperthermophile Sulfolobus solfataricus that has been associated with DN
195 h the AS structure from the hyperthermophile Sulfolobus solfataricus, the S. marcescens structure sho
196 olases, including the beta-glycosidases from Sulfolobus solfataricus, Thermotoga maritima, and Caldoc
200 Methanococcus maripaludis tRNA2(Ile) and in Sulfolobus solfataricus total tRNA, indicating its proba
204 differences, we have characterized Dpo4 from Sulfolobus solfataricus using the same biochemical and c
205 ructure of the CSM complex from the archaeon Sulfolobus solfataricus, using a combination of electron
206 ctive wild-type Saccharomyces cerevisiae and Sulfolobus solfataricus Vps4 enzymes can form hexamers i
207 ative LipA from the hypothermophilic archaea Sulfolobus solfataricus was expressed in Escherichia col
208 aea, the splicing endonuclease from archaeum Sulfolobus solfataricus was found to contain two differe
210 etypal Y-family member from the thermophilic Sulfolobus solfataricus, was used to extend our kinetic
211 the third replication origin in the archaeon Sulfolobus solfataricus, we identify and characterise si
212 sidase (maltase) and flanking sequences from Sulfolobus solfataricus were cloned and characterized.
213 ) from the thermoacidophilic archaebacterium Sulfolobus solfataricus were compared to the well-charac
214 ts of the extreme acidothermophilic archaeon Sulfolobus solfataricus were incubated with [gamma-(32)P
215 d two origins of replication in the archaeon Sulfolobus solfataricus, whereas a second study used a d
216 e demonstrate that the XPF endonuclease from Sulfolobus solfataricus, which is dependent on the slidi
217 G-CoA reductase of the thermophilic archaeon Sulfolobus solfataricus, whose stability recommends it f
218 lesion-bypass DNA polymerase IV (Dpo4) from Sulfolobus solfataricus, with template guanine and Watso
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