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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.
5 e domain of a bacterial homolog of Hen1 from Clostridium thermocellum and Anabaena variabilis, which
7 r (2.7- to 4.7-fold) for growing cultures of Clostridium thermocellum as compared with purified cellu
9 cohesin domain of the scaffoldin protein of Clostridium thermocellum ATCC 27405 were used to develop
10 he sactionine bond-forming enzyme CteB, from Clostridium thermocellum ATCC 27405, with both SAM and a
11 hydrogenase and heterologous expression of a Clostridium thermocellum bifunctional acetaldehyde/alcoh
14 The family IV cellulose-binding domain of Clostridium thermocellum CelK (CBD(CelK)) was expressed
16 acoustic force spectroscopy (AFS) to probe a Clostridium thermocellum cellulosomal scaffoldin protein
19 racterize a ternary protein complex from the Clostridium thermocellum cellulosome that comprises a C-
21 the contribution of distinct residues at the Clostridium thermocellum cohesin-dockerin interface to b
22 of a multimodular heterodimeric complex from Clostridium thermocellum composed of the type-II cohesin
25 ucture reveals that the N-terminal domain of Clostridium thermocellum (Cth) Hen1, shaped like a left
26 olynucleotide kinase-phosphatase enzyme from Clostridium thermocellum (CthPnkp) can catalyze both of
27 identified a TTM protein from the bacterium Clostridium thermocellum (CthTTM) with the opposite subs
29 t under native conditions wild-type Doc from Clostridium thermocellum exocellulase Cel48S populates b
30 copy with a green fluorescent protein-tagged Clostridium thermocellum family 3 carbohydrate-binding m
31 from the cellulosomal scaffoldin subunit of Clostridium thermocellum has been determined at 1.75 A r
32 we present crystal structures of PCAT1 from Clostridium thermocellum in two different conformations.
33 )-PFKs of Clostridium thermosuccinogenes and Clostridium thermocellum indeed can convert S7P to SBP,
42 tem of the anaerobic, cellulolytic bacterium Clostridium thermocellum is strongly inhibited by the ma
44 iously the crystal structures of a PCAT from Clostridium thermocellum (PCAT1) were determined in the
45 e crystal structures of the ligase domain of Clostridium thermocellum Pnkp in three functional states
47 ystal structure of the phosphatase domain of Clostridium thermocellum Pnkp with Mn(2+) and citrate in
55 crystal structure of FAE_XynZ, the domain of Clostridium thermocellum's cellulosomal xylanase Z that
56 Certain thermophilic anaerobes, including Clostridium thermocellum, show promise for renewable eth
57 hieved by the method on Escherichia coli and Clostridium thermocellum, substantial work is needed to
58 s in BiFae1B with the feruloyl esterase from Clostridium thermocellum suggest that both domains lack
59 us on cellulose degradation of the canonical Clostridium thermocellum system to comprehend how microb
60 cellulolytic and hemicellulolytic complex of Clostridium thermocellum, termed cellulosome, consists o
61 losome protein complex used by the bacterium Clostridium thermocellum to better understand how this p
62 e report the crystal structures of two novel Clostridium thermocellum type I cohesin-dockerin complex
63 ons to derive the genomic TU organization of Clostridium thermocellum using a machine-learning approa
65 omal cellulase cellobiohydrolase A (CbhA) of Clostridium thermocellum was solved in complex with cell
66 recombinant bacterial minicellulosomes from Clostridium thermocellum, we demonstrate the ability to
69 acid-pretreated transgenic switchgrass using Clostridium thermocellum with no added enzymes showed be
70 ily 3 carbohydrate binding module (CBM) from Clostridium thermocellum, with high affinity to cellulos