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1 lysates, Man-6-P inhibited hexokinase (70%), phosphoglucose isomerase (65%), and glucose-6-phosphate
7 re we report the crystal structure of rabbit phosphoglucose isomerase complexed with 5PAH at 1.9 A re
8 three-dimensional structure of rabbit muscle phosphoglucose isomerase complexed with the competitive
10 tification of a protein model of AMF, namely phosphoglucose isomerase from rabbit muscle (RmPGI).
14 ococcus furiosus and Thermococcus litoralis, phosphoglucose isomerase (PGI) activity is catalyzed by
16 ources that are maintained through action of phosphoglucose isomerase (PGI) and phosphoglucose mutase
17 determine if alleles of the highly conserved phosphoglucose isomerase (pgi) gene correspond to the se
19 and with IS1016; a subset was examined with phosphoglucose isomerase (pgi) genotyping and pulsed-fie
28 e-6-phosphate (F6P --> G6P) by baker's yeast phosphoglucose isomerase (PGI) with regard to k(cat) and
29 enotype is complemented by the gene encoding phosphoglucose isomerase (pgi), and direct measurement o
30 ctrophoretic mobility classes for the enzyme phosphoglucose isomerase (PGI), despite evidence from ot
33 The crystal structure of a dual specificity phosphoglucose isomerase (PGI)/phosphomannose isomerase
35 d divergence was conducted for the cytosolic phosphoglucose isomerase (PGI:E.C.5.3.1.9) gene of five
43 ions, we sequenced portions of the cytosolic phosphoglucose isomerase (PgiC) gene in the plant genus
44 lphabetaalpha sandwich fold commonly seen in phosphoglucose isomerases (PGIs) that are found in bacte
45 zymes of the glycolysis cascade: hexokinase, phosphoglucose isomerase, phosphofructokinase and aldola
46 RNA levels of the glucose transporter GLUT1, phosphoglucose isomerase, phosphofructokinase, glycerald
47 zymes catalyzing near-equilibrium reactions, phosphoglucose isomerase, phosphoglucomutase, and triose
48 aliana) plants not exposed to VCs, plastidic phosphoglucose isomerase (pPGI) acts as an important det