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1 ns from Gram-positive bacteria (B. subtilis, Thermoanaerobacter brockii) and Gram-negative pathogens
2 ikuyae (SyADH), or a variant of the ADH from Thermoanaerobacter ethanolicus (TeSADH W110A)) in a redo
3 h W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus (W110A TESADH) in Tris bu
4 sidase (xarB) from the thermophilic anaerobe Thermoanaerobacter ethanolicus JW200 was cloned, sequenc
5 kinase (xylB) from the thermophilic anaerobe Thermoanaerobacter ethanolicus were found to constitute
7 Here, we report the crystal structure of the Thermoanaerobacter italicus TagA enzyme bound to UDP-N-a
8 cetogenic bacteria Acetobacterium woodii and Thermoanaerobacter kivui employ a single flavin mononucl
9 lex of the thermophilic acetogenic bacterium Thermoanaerobacter kivui is indeed a respiratory enzyme.
11 s-level studies of the thermophilic acetogen Thermoanaerobacter kivui when growth rate is varied over
13 ilibrium, whereas the homologous enzyme from Thermoanaerobacter mathranii (Tam HydS) shows activity o
14 putatively sensory Group D hydrogenase from Thermoanaerobacter mathranii (TamHydS) has a thousand-fo
15 metry of a particular FeFe hydrogenase, from Thermoanaerobacter mathranii, which is very unusual in t
19 Heme-Nitric oxide/OXygen binding domain from Thermoanaerobacter tengcongensis (Tt H-NOX WT) and three
20 or OXygen binding domain (H-NOX domain) from Thermoanaerobacter tengcongensis (Tt H-NOX), has been in
21 tal structures of synthetic ligands with the Thermoanaerobacter tengcongensis (Tte)-PreQ(1) riboswitc
22 signaling protein from the obligate anaerobe Thermoanaerobacter tengcongensis at 1.77-angstroms resol
23 of nucleotide divergence were detected, and Thermoanaerobacter tengcongensis exhibited the highest l
24 al structures of the preQ(1) riboswitch from Thermoanaerobacter tengcongensis in the preQ(1)-bound an
25 iptional Bacillus subtilis and translational Thermoanaerobacter tengcongensis preQ1 riboswitch aptame
26 several ribose-sensing proteins derived from Thermoanaerobacter tengcongensis ribose binding protein.
27 ctural feature of the H-NOX protein TtTar4H (Thermoanaerobacter tengcongensis Tar4 protein heme domai
28 present structures of the glmS ribozyme from Thermoanaerobacter tengcongensis that are bound with the
29 in named "helimerase", by physically linking Thermoanaerobacter tengcongensis UvrD helicase (TteUvrD)
30 uperimposable with the previously determined Thermoanaerobacter tengcongensis yitJ riboswitch structu
31 nd binds late (Bacillus subtilis) and early (Thermoanaerobacter tengcongensis) relative to pseudoknot
32 ion of H-NOX domain-containing proteins from Thermoanaerobacter tengcongensis, Vibrio cholerae, and C
33 NOX) protein from the thermophilic bacterium Thermoanaerobacter tengcongensis, we have shown that hem
34 solated from the hyperthermophilic bacterium Thermoanaerobacter tengcongensis, with retention of cata