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1 nd the N-terminal half of Hen1 (Hen1-N) from Clostridium thermocellum.
2 lS, and CbhA) and the scaffoldin (CipA) from Clostridium thermocellum.
3 of a TTM protein (CthTTM) from the bacterium Clostridium thermocellum.
4 e domain of a bacterial homolog of Hen1 from Clostridium thermocellum and Anabaena variabilis, which
6 r (2.7- to 4.7-fold) for growing cultures of Clostridium thermocellum as compared with purified cellu
8 cohesin domain of the scaffoldin protein of Clostridium thermocellum ATCC 27405 were used to develop
9 he sactionine bond-forming enzyme CteB, from Clostridium thermocellum ATCC 27405, with both SAM and a
10 hydrogenase and heterologous expression of a Clostridium thermocellum bifunctional acetaldehyde/alcoh
12 The family IV cellulose-binding domain of Clostridium thermocellum CelK (CBD(CelK)) was expressed
16 racterize a ternary protein complex from the Clostridium thermocellum cellulosome that comprises a C-
18 the contribution of distinct residues at the Clostridium thermocellum cohesin-dockerin interface to b
19 of a multimodular heterodimeric complex from Clostridium thermocellum composed of the type-II cohesin
22 ucture reveals that the N-terminal domain of Clostridium thermocellum (Cth) Hen1, shaped like a left
23 olynucleotide kinase-phosphatase enzyme from Clostridium thermocellum (CthPnkp) can catalyze both of
24 identified a TTM protein from the bacterium Clostridium thermocellum (CthTTM) with the opposite subs
26 t under native conditions wild-type Doc from Clostridium thermocellum exocellulase Cel48S populates b
27 copy with a green fluorescent protein-tagged Clostridium thermocellum family 3 carbohydrate-binding m
28 from the cellulosomal scaffoldin subunit of Clostridium thermocellum has been determined at 1.75 A r
29 we present crystal structures of PCAT1 from Clostridium thermocellum in two different conformations.
37 tem of the anaerobic, cellulolytic bacterium Clostridium thermocellum is strongly inhibited by the ma
39 e crystal structures of the ligase domain of Clostridium thermocellum Pnkp in three functional states
41 ystal structure of the phosphatase domain of Clostridium thermocellum Pnkp with Mn(2+) and citrate in
49 crystal structure of FAE_XynZ, the domain of Clostridium thermocellum's cellulosomal xylanase Z that
50 hieved by the method on Escherichia coli and Clostridium thermocellum, substantial work is needed to
51 s in BiFae1B with the feruloyl esterase from Clostridium thermocellum suggest that both domains lack
52 cellulolytic and hemicellulolytic complex of Clostridium thermocellum, termed cellulosome, consists o
53 losome protein complex used by the bacterium Clostridium thermocellum to better understand how this p
54 e report the crystal structures of two novel Clostridium thermocellum type I cohesin-dockerin complex
55 ons to derive the genomic TU organization of Clostridium thermocellum using a machine-learning approa
57 omal cellulase cellobiohydrolase A (CbhA) of Clostridium thermocellum was solved in complex with cell
58 recombinant bacterial minicellulosomes from Clostridium thermocellum, we demonstrate the ability to
60 acid-pretreated transgenic switchgrass using Clostridium thermocellum with no added enzymes showed be
61 ily 3 carbohydrate binding module (CBM) from Clostridium thermocellum, with high affinity to cellulos
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