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1 dulated during infection by association with T7 lysozyme.
2 was relatively unaffected by the presence of T7 lysozyme.
3 iments in the absence and in the presence of T7 lysozyme.
7 is related to that of the cell wall amidase, T7 lysozyme, and contains a conserved zinc coordination
8 used the co-crystal structure of T7RNAP and T7 lysozyme as a model to define a potential Mtf1 intera
12 changes in the N-terminal domain of T7 RNAP, T7 lysozyme causes an increased production of abortive p
13 polymerase (T7RP) and the T7 RNA polymerase-T7 lysozyme complex (T7RPL) in forms suitable for struct
15 e X-ray structures of T7RNAP and of a T7RNAP:T7 lysozyme complex reveals that lysozyme causes the C t
18 quilibrium DNA binding studies indicate that T7 lysozyme does not inhibit the formation of the preini
19 r and the GTP Kd is about 2-fold higher, but T7 lysozyme does not inhibit the initial rate of RNA syn
20 The specific inhibitor of T7 transcription, T7 lysozyme, does not compete with T7 RNA polymerase for
22 le, might therefore be a consequence of: (1) T7 lysozyme generally reducing the affinity of the polym
26 transcription in the presence and absence of T7 lysozyme indicated that the inhibition of runoff prod
32 ng nucleotide concentration, indicating that T7 lysozyme represses transcription by interfering with
33 the formation of the ternary complex between T7 lysozyme, T7 RNA polymerase and the promoter DNA.
35 ent with the results that in the presence of T7 lysozyme the rate of G ladder RNA synthesis is about
36 hich cause resistance or hypersensitivity to T7 lysozyme, these observations suggest that the structu
38 scription repression of T7 RNA polymerase by T7 lysozyme was investigated using a combination of kine
40 on of class II versus class III promoters by T7 lysozyme, which appears to be important for the switc
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