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1 ide hydrolase from Crithidia fasciculata (IU-nucleoside hydrolase).
2 the inosine-uridine nucleoside hydrolase (IU-nucleoside hydrolase).
3 novani nucleoside hydrolase as a nonspecific nucleoside hydrolase.
4 tate analogue inhibitors for purine-specific nucleoside hydrolase.
5  conserved among the characterized protozoan nucleoside hydrolases.
6 o nonspecific and uridine-inosine-preferring nucleoside hydrolases.
7 minoribitol inhibitors yet described for the nucleoside hydrolases.
8 olysis of the N-ribosidic bond using several nucleoside hydrolases.
9                                              Nucleoside hydrolase 1 (NSH1) is known to be essential f
10 CYTIDINE DEAMINASE, GUANOSINE DEAMINASE, and NUCLEOSIDE HYDROLASE 1, demonstrating that the deoxyribo
11 njunction with a mass selective detector for nucleoside hydrolase, a purine-metabolizing enzyme.
12 ico studies suggest that HopQ1 might possess nucleoside hydrolase activity based on the presence of a
13             Although the conservation of the nucleoside hydrolases among protozoan parasites offers p
14 ng enzymes of therapeutic importance such as nucleoside hydrolases and purine nucleoside phosphorylas
15 tructure is similar to the C. fasciculata IU-nucleoside hydrolase apoenzyme.
16                                              Nucleoside hydrolases are involved in nucleoside salvage
17 e specificity data identify this L. donovani nucleoside hydrolase as a nonspecific nucleoside hydrola
18 states reveals novel intermediates along the nucleoside hydrolase-catalyzed hydrolytic reaction, incl
19 rovide nanomolar inhibition constants for IU-nucleoside hydrolase exhibit micromolar inhibition const
20                                           IU-nucleoside hydrolase from C. fasciculata and the protein
21 structure of the nonspecific inosine-uridine nucleoside hydrolase from Crithidia fasciculata (IU-nucl
22                                           IU-nucleoside hydrolase from Crithidia fasciculata and the
23                              The nonspecific nucleoside hydrolase from Crithidia fasciculata cocrysta
24 s 78% sequence identity with the nonspecific nucleoside hydrolase from Crithidia fasciculata.
25 itors are also described for the nonspecific nucleoside hydrolase from Crithidia fasciculata.
26                     The full-length cDNA for nucleoside hydrolase from Leishmania major was cloned an
27 -nanomolar inhibitor for the purine-specific nucleoside hydrolase from Trypanosoma brucei brucei.
28  a purine-specific nucleoside hydrolase (IAG-nucleoside hydrolase) from Trypanosoma brucei brucei.
29 ts of urate oxidase, xanthine dehydrogenase, nucleoside hydrolases, guanosine deaminase, and hypoxant
30   The mechanism of action of inosine-uridine nucleoside hydrolase has been investigated by long-term
31               The amino acid sequence for IU-nucleoside hydrolase has no close relatives among the kn
32 olysis of the N-ribosidic bond of inosine by nucleoside hydrolase has oxocarbenium character and a pr
33 e-specific and purine/pyrimidine-nonspecific nucleoside hydrolases have been reported.
34 , BxpC, CotY, and inosine-uridine-preferring nucleoside hydrolase; however, these spores retained hal
35 ism of action of inosine-adenosine-guanosine nucleoside hydrolase (IAG-NH) has been investigated by l
36 ed for this enzyme and for a purine-specific nucleoside hydrolase (IAG-nucleoside hydrolase) from Try
37 rugs, the existence of multiple and distinct nucleoside hydrolases in a single species demands specia
38                                              Nucleoside hydrolase is a central enzyme in the purine s
39                                           IU-nucleoside hydrolase is composed of a mixed eight-strand
40                            The most abundant nucleoside hydrolase is relatively nonspecific but prefe
41 rotein homologous to bacterial and protozoan nucleoside hydrolases is active as a pyrimidine nucleosi
42                            Several protozoan nucleoside hydrolase isozymes with distinct substrate sp
43                              Inosine-uridine nucleoside hydrolase (IU-NH) catalyzes the hydrolysis of
44 dimensional structure of the inosine-uridine nucleoside hydrolase (IU-NH) from C. fasciculata determi
45 Crithidia fasciculata is the inosine-uridine nucleoside hydrolase (IU-nucleoside hydrolase).
46 ibitors are isozyme-specific, with (Km/Ki IU-nucleoside hydrolase)/(Km/Ki IAG-nucleoside hydrolase) v
47 We also identified a SUSS cluster adopting a nucleoside hydrolase-like fold conserved among various g
48                                              Nucleoside hydrolases may play a crucial role in that sa
49 t the in vivo function of a second cytosolic nucleoside hydrolase, NSH2, is unclear.
50                                     Like the nucleoside hydrolases NUCLEOSIDE HYDROLASE1 (NSH1) and N
51   Binding of these inhibitors to nonspecific nucleoside hydrolase occurs primarily via interaction wi
52  leaving group on a glycoside, mimicking the nucleoside hydrolase of the parasite Trypanosoma vivax.
53        The crystal structure of the L. major nucleoside hydrolase revealed a bound Ca(2+) ion in the
54 sequence analysis revealed that the L. major nucleoside hydrolase shares 78% sequence identity with t
55 de hydrolase was identified as a nonspecific nucleoside hydrolase since it demonstrates the character
56 h (Km/Ki IU-nucleoside hydrolase)/(Km/Ki IAG-nucleoside hydrolase) values up to 39,000.
57                                 The L. major nucleoside hydrolase was identified as a nonspecific nuc
58                                 Further, the nucleoside hydrolase was localized to specific foci in L