PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18801477-5	2008	Therefore, we conclude that activation of thioglycoside donors by MeOTf to glycosylate at O-4 of a glucosamine acceptor is best accomplished following the temporary protection of the N-acetyl group as a methyl imidate, especially when the donors are highly reactive and prone to degradation.	Glucosamine	99-110	immunoglobulin kappa variable 1D-37 (non-functional)	Homo sapiens	90-93	
18801477-6	2008	In contrast, if donor and acceptor can withstand multiple equivalents of BF(3) x OEt(2), glycosylations at O-4 of a glucosamine acceptor with a trichloroacetimidate donor does not benefit from the temporary protection of the N-acetyl group as a methyl imidate.	Glucosamine	116-127	immunoglobulin kappa variable 1D-37 (non-functional)	Homo sapiens	107-110	
17880931-0	2007	Differential O-3/O-4 regioselectivity in the glycosylation of alpha and beta anomers of 6-O-substituted N-dimethylmaleoyl-protected D-glucosamine acceptors.	Glucosamine	132-145	immunoglobulin kappa variable 1D-37 (non-functional)	Homo sapiens	17-20