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1 ikuyae (SyADH), or a variant of the ADH from Thermoanaerobacter ethanolicus (TeSADH W110A)) in a redo
2 h W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus (W110A TESADH) in Tris bu
3 sidase (xarB) from the thermophilic anaerobe Thermoanaerobacter ethanolicus JW200 was cloned, sequenc
4 kinase (xylB) from the thermophilic anaerobe Thermoanaerobacter ethanolicus were found to constitute
9 Heme-Nitric oxide/OXygen binding domain from Thermoanaerobacter tengcongensis (Tt H-NOX WT) and three
10 or OXygen binding domain (H-NOX domain) from Thermoanaerobacter tengcongensis (Tt H-NOX), has been in
11 signaling protein from the obligate anaerobe Thermoanaerobacter tengcongensis at 1.77-angstroms resol
12 of nucleotide divergence were detected, and Thermoanaerobacter tengcongensis exhibited the highest l
13 al structures of the preQ(1) riboswitch from Thermoanaerobacter tengcongensis in the preQ(1)-bound an
14 iptional Bacillus subtilis and translational Thermoanaerobacter tengcongensis preQ1 riboswitch aptame
15 several ribose-sensing proteins derived from Thermoanaerobacter tengcongensis ribose binding protein.
16 ctural feature of the H-NOX protein TtTar4H (Thermoanaerobacter tengcongensis Tar4 protein heme domai
17 present structures of the glmS ribozyme from Thermoanaerobacter tengcongensis that are bound with the
18 in named "helimerase", by physically linking Thermoanaerobacter tengcongensis UvrD helicase (TteUvrD)
19 uperimposable with the previously determined Thermoanaerobacter tengcongensis yitJ riboswitch structu
20 nd binds late (Bacillus subtilis) and early (Thermoanaerobacter tengcongensis) relative to pseudoknot
21 ion of H-NOX domain-containing proteins from Thermoanaerobacter tengcongensis, Vibrio cholerae, and C
22 NOX) protein from the thermophilic bacterium Thermoanaerobacter tengcongensis, we have shown that hem
23 solated from the hyperthermophilic bacterium Thermoanaerobacter tengcongensis, with retention of cata
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