PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11683413-9	2001	Ala substitutions for the Val residue in the VTT motif of the beta1 tail or for the conserved Asp and Glu residues in the membrane-proximal region of the beta3 tail greatly diminished the ability of tac-beta1 and tac-beta3 to inhibit cell spreading, but had minimal effects in other assays.	Glutamic Acid	102-105	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	203-208	
11851339-5	2002	Hence, the interaction between Lys beta D3 and +1 Glu is energetically coupled.	Glutamic Acid	50-53	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	35-49	
28054934-2	2017	In this study, the potential of chitosan/beta-1,3-glucan/hydroxyapatite (chit/glu/HA) material as a scaffold for bone regeneration applications was evaluated by behaviour comparison of adult stem cells derived from both origins-adipose derived mesenchymal stem cell (ADSC) tissue and bone marrow derived mesenchymal stem cells (BMDSCs).	Glutamic Acid	50-53	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	41-49	
28658312-10	2017	beta-1,3-glucanase protein structural model revealed that active sites Glutamate 628 and Aspartate 569 of the catalytic domain acted as proton donor and nucleophile having role in cleaving beta-1,3-glycosidic bonds and pathogen hyphal lysis.	Glutamic Acid	71-80	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	189-197	
28412362-3	2017	However, it remains unsettled whether the Glu residue in the gamma1 tail is involved in integrin binding by coordinating the metal ion in the metal ion-dependent adhesion site of beta1 integrin (beta1-MIDAS), or by stabilizing the conformation of alpha5/LG1-3.	Glutamic Acid	42-45	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	179-184	
28325314-3	2017	Obtained results demonstrated that unlike thermal method-prepared beta-1,3-glucan/hydroxyapatite material (glu/HAT), bone scaffold fabricated via dialysis method (glu/HA D) possessed rough surface resulting from the presence of CaCl2 precipitates as proven by SEM and EDS analysis.	Glutamic Acid	75-78	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	66-74	
28325314-5	2017	Since glu/HA D material exhibited better bioactivity and biocompatibility compared to the glu/HA T scaffold, it may be concluded that the dialysis method is more suitable for beta-1,3-glucan/hydroxyapatite biomaterial fabrication.	Glutamic Acid	6-9	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	175-183	
27239050-2	2016	The aim of this study was to establish new method for fabrication of beta-1,3-glucan/hydroxyapatite (glu/HA) scaffold using ion-exchanging dialysis for curdlan gelation that allows for the modifications of the glu/HA material with thermo-sensitive agents like growth factors or adhesive proteins.	Glutamic Acid	78-81	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	69-77	
27239050-2	2016	The aim of this study was to establish new method for fabrication of beta-1,3-glucan/hydroxyapatite (glu/HA) scaffold using ion-exchanging dialysis for curdlan gelation that allows for the modifications of the glu/HA material with thermo-sensitive agents like growth factors or adhesive proteins.	Glutamic Acid	101-104	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	69-77