PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33724114-4	2022	The reactivity of monosaccharides, disaccharides and their transportation with GLUT1 and GLUT3 as prognostic indicators for cancer were investigated.	Monosaccharides	18-33	solute carrier family 2 member 1	Homo sapiens	79-84	
16785788-1	2006	The facilitative transport of monosaccharides in human cells is accomplished by a family of transmembrane proteins, GLUT-1 to GLUT-7, that differ in their tissue distribution, affinities for specific monosaccharides, and physiologic regulation.	Monosaccharides	30-45	solute carrier family 2 member 1	Homo sapiens	116-122	
16785788-1	2006	The facilitative transport of monosaccharides in human cells is accomplished by a family of transmembrane proteins, GLUT-1 to GLUT-7, that differ in their tissue distribution, affinities for specific monosaccharides, and physiologic regulation.	Monosaccharides	200-215	solute carrier family 2 member 1	Homo sapiens	116-122	
15132717-2	2004	Diseases such as glucose-galactose malabsorption, Fanconi-Bickel syndrome and De Vivo disease (GLUT1 deficiency syndrome (GLUT1DS)) arise from heritable mutations in transporter-encoding genes that impair monosaccharide uptake, which becomes rate-limiting in tissues where the transporters serve as the main glucose carrier systems.	Monosaccharides	205-219	solute carrier family 2 member 1	Homo sapiens	122-129	
11078819-2	2000	Since GLUT1, rather than GLUT2, represents the major carrier system for the transport of monosaccharides across the islet B-cell plasma membrane in human subjects, the uptake of D-mannoheptulose and its metabolic and secretory effects were investigated in human islets.	Monosaccharides	89-104	solute carrier family 2 member 1	Homo sapiens	6-11	
11681785-2	2001	Despite the lack of a crystal structure for any of the facilitative monosaccharide transport proteins, detailed information regarding primary and secondary structure, membrane topology, transport kinetics, and functionally important residues has allowed the construction of a sophisticated working model for GLUT1 tertiary structure.	Monosaccharides	68-82	solute carrier family 2 member 1	Homo sapiens	308-313	
33886296-6	2021	Through a deeper mechanistic description of glucose (GLUT) transporters and multidrug resistance (MDR) antiporters, we outline novel refinements to the rocker-switch alternating-access model, such as a latch mechanism for proton-coupled monosaccharide transport.	Monosaccharides	237-251	solute carrier family 2 member 1	Homo sapiens	53-57	
22943001-7	2012	Although great strides have been made in characterizing GLUT-catalyzed monosaccharide transport and mapping GLUT membrane topography and determinants of substrate specificity, a unifying model for GLUT structure and function remains elusive.	Monosaccharides	71-85	solute carrier family 2 member 1	Homo sapiens	56-60	
22943001-9	2012	This is accomplished through a multiplicity of GLUT-dependent glucose sensing and effector mechanisms that regulate monosaccharide ingestion, absorption,distribution, cellular transport and metabolism, and recovery/retention.	Monosaccharides	116-130	solute carrier family 2 member 1	Homo sapiens	47-51