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1 nalling, driving the conformational cycle of group II chaperonins.
2 the substrate during the nucleotide cycle of group II chaperonins.
10 completely distinct closing mechanism in the group II chaperonins as compared with the group I chaper
12 a, there are one, two or three genes for the group II chaperonins, but whether they are essential for
13 nal reconstruction and modeling of Mm-cpn, a group II chaperonin, determined to 4.3 A resolution.
14 Lys-161, which is extremely conserved among group II chaperonins, forms interactions with the gamma-
16 engineering of a cysteine-less mutant of the group II chaperonin from methanogenic archaeon Methanoco
18 mic structure of the thermosome, an archaeal group II chaperonin, has been determined in a fully clos
19 conformations of the thermosome, an archaeal group II chaperonin, have been determined by cryo-electr
21 (cryo-EM) structures of Mm-cpn, an archaeal group II chaperonin, in the nucleotide-free (open) and n
22 uction, we describe three conformations of a group II chaperonin, including an asymmetric, bullet-sha
24 philic archaeon Sulfolobus shibatae contains group II chaperonins, known as rosettasomes, which are t
27 ort here that human erythrocytes contain the group II chaperonin T-complex polypeptide 1 (TCP-1) and
28 Some of these peptides were bound to the group II chaperonin TRiC and were protected from degrada
30 how that an adenosine-5'-triphosphate-driven group II chaperonin, which resembles a barrel with a bui