ATP-dependent substrate occlusion by the human erythrocyte sugar transporter.
about
Ligand-modulation of the stability of the glucose transporter GLUT 1Molecular dynamics simulation studies of GLUT4: substrate-free and substrate-induced dynamics and ATP-mediated glucose transport inhibitionWZB117 (2-Fluoro-6-(m-hydroxybenzoyloxy) Phenyl m-Hydroxybenzoate) Inhibits GLUT1-mediated Sugar Transport by Binding Reversibly at the Exofacial Sugar Binding Site.Determinants of ligand binding affinity and cooperativity at the GLUT1 endofacial sitePredicting the three-dimensional structure of the human facilitative glucose transporter glut1 by a novel evolutionary homology strategy: insights on the molecular mechanism of substrate migration, and binding sites for glucose and inhibitory molecuDocking studies show that D-glucose and quercetin slide through the transporter GLUT1.Homology modeling of GLUT4, an insulin regulated facilitated glucose transporter and docking studies with ATP and its inhibitors.Characterization of bovine glucose transporter 1 kinetics and substrate specificities in Xenopus oocytes.Caffeine inhibits glucose transport by binding at the GLUT1 nucleotide-binding site.Structural basis of GLUT1 inhibition by cytoplasmic ATP.Role of monosaccharide transport proteins in carbohydrate assimilation, distribution, metabolism, and homeostasis.Evidence for interindividual heterogeneity in the glucose gradient across the human red blood cell membrane and its relationship to hemoglobin glycationalpha- and beta-monosaccharide transport in human erythrocytes.Caffeine inhibition of GLUT1 is dependent on the activation state of the transporter.Regulation of glucose transporters by insulin and extracellular glucose in C2C12 myotubes.Osmotic water transport with glucose in GLUT2 and SGLT.Endofacial competitive inhibition of the glucose transporter 1 activity by gossypol.Definitively, my cup of tea. Focus on "Caffeine inhibits glucose transport by binding at the GLUT1 nucleotide-binding site".ATP-dependent sugar transport complexity in human erythrocytes.Interactions of ATP, oestradiol, genistein and the anti-oestrogens, faslodex (ICI 182780) and tamoxifen, with the human erythrocyte glucose transporter, GLUT1.Glucose transporter in bovine mammary epithelial cells is an asymmetric carrier that exhibits cooperativity and trans-stimulation.Description of glucose transport in isolated bovine mammary epithelial cells by a three-compartment model.Kinetics of glucose transport and sequestration in lactating bovine mammary glands measured in vivo with a paired indicator/nutrient dilution technique.Modulation of monocarboxylic acid transporter-1 kinetic function by the cAMP signaling pathway in rat brain endothelial cells.Kinetic Basis of Cis- and Trans-Allostery in GLUT1-Mediated Sugar Transport.
P2860
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P2860
ATP-dependent substrate occlusion by the human erythrocyte sugar transporter.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
ATP-dependent substrate occlusion by the human erythrocyte sugar transporter.
@en
type
label
ATP-dependent substrate occlusion by the human erythrocyte sugar transporter.
@en
prefLabel
ATP-dependent substrate occlusion by the human erythrocyte sugar transporter.
@en
P2093
P356
P1433
P1476
ATP-dependent substrate occlusion by the human erythrocyte sugar transporter.
@en
P2093
P304
P356
10.1021/BI991931U
P407
P577
2000-03-01T00:00:00Z