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1 muscle and Deinococcus geothermalis glycogen branching enzyme.
2 red to avoid steric clashes with Trp(298) of branching enzyme.
3 ssed in the absence of the endogenous glucan-branching enzyme.
4 ialyltransferases, and at least one O-linked branching enzyme.
5 roup H expression together with up-regulated branching enzymes.
6 f a conserved Cys-containing domain in plant branching enzymes.
7 P-GlcNAc, the donor substrate shared by Mgat branching enzymes.
8 he glucan chains further or for branching by branching enzymes.
9 the significance of the conserved Asp/Glu in branching enzymes.
13 e asked if this motif could be essential for branching enzyme action.We used site-directed mutagenesi
14 ain magnetic resonance imaging, and glycogen branching enzyme activity and GBE1 molecular analysis.
16 synthase (GS), glycogenin (GN), and glycogen branching enzyme and forms particles that range in size
17 phorylation sites are conserved in all plant branching enzymes and are located at opposite openings o
19 synthetic enzyme (starch/glycogen synthases, branching enzymes, and debranching enzymes) are differen
20 es the notion that the catalytic centers for branching enzymes are exclusively located in the central
21 that some of the starch synthases and starch-branching enzymes are trapped inside the starch granule
22 nitiated from UDP-GlcNAc by the medial-Golgi branching enzymes as well as the trans-Golgi poly-LacNAc
23 , we investigated the functions of different branching enzyme (BE) types by expressing proteins from
25 em, including starch synthases (SSs), starch branching enzymes (BEs), and starch debranching enzymes;
26 er epithelial cancers that have up-regulated branching enzymes but diminished expression of H antigen
28 ve sequences for glycogen synthase, glycogen branching enzyme, chitin synthase, and for the first enz
30 heir different requirements for the O-glycan branching enzyme core 2 beta1,6-N-acetylglucosaminyltran
31 The neuromuscular presentation of glycogen branching enzyme deficiency includes a severe infantile
32 s (e.g. phosphorylase-b-kinase deficiency or branching enzyme deficiency), whereas they form long lis
37 cid sequence identity with those of glycogen-branching enzymes from such animals as mouse, horse, and
40 ka1) mRNAs, along with those of the glycogen branching enzyme (GBE) and the phosphorylase b kinase al
44 downregulated and the levels of the glycogen branching enzyme (Gbe1) and muscle-type PhKalpha subunit
45 well-known c.986A>C mutation in the glycogen branching enzyme gene (GBE1) but harbored no other known
48 icant levels of starch synthase I and starch branching enzyme II (BEII) remained granule associated.
50 e amylose-extender (Ae) gene encoding starch-branching enzyme IIb (SBEIIb) in maize is predominantly
52 s starch synthase IIa (SSIIa), SSIII, starch branching enzyme IIb (SBEIIb), and SBEIIa for assembly i
53 waxy protein, starch synthase I, and starch-branching enzyme IIb, remained refractory to proteolysis
55 enesis of the Glu-459 residue in the E. coli branching enzyme in order to determine the significance
56 t revealed that SBEIIa is the primary active branching enzyme in the leaf and that in its absence pla
58 ing glucosaminyl (N-acetyl) transferase 2, I-branching enzyme, is overexpressed in highly metastatic
59 (glycogen synthase) and DeltaglgB (glycogen-branching enzyme) mutants are glycogen-deficient and exh
61 Full length cDNAs encoding a second starch branching enzyme (SBE A) isoform have been isolated from
63 Expression of the maize (Zea mays L.) starch branching enzyme (SBE) genes Sbe1 and Sbe2 were characte
64 dies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu
66 fic activities of starch synthase and starch-branching enzyme (SBE), but not the cytosolic marker alc
70 like Kidney beans have an isoforms of Starch-Branching-Enzyme (SBE) helps in converting amylose to am
71 maize (Zea mays L.) three isoforms of starch-branching enzyme (SBEI, SBEIIa, and SBEIIb) are involved
74 hat of all the other amylase family enzymes, branching enzyme shares the structure of all three domai
75 of the oligosaccharides modeled well in the branching enzyme structure, an approximate 50 degrees ro
76 discovered by cloning cDNAs that the core 2 branching enzyme, termed core 2 beta-1,6-N-acetylglucosa
78 ltaneously inhibiting two isoforms of starch branching enzyme to below 1% of the wild-type activities
79 ice lacking both core 1 extension and core 2 branching enzymes to assess the functions of O-glycan-bo
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