PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28363510-0	2017	X-Linked Cobalamin Disorder (HCFC1) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic Acid.	Glycine	113-120	host cell factor C1	Homo sapiens	29-34	
8650173-5	1996	This activity is as much as 3 to 5 times stronger than VP16 at activating transcription and requires a large stretch of amino acids that contain glutamine-glycine rich and serine-threonine-basic amino acid rich regions.	Glycine	155-162	host cell factor C1	Homo sapiens	55-59	
28363510-11	2017	CONCLUSIONS: This boy had X-linked cobalamin deficiency (HCFC1) with increased cerebrospinal fluid glycine and methylmalonic acid and increased cerebrospinal fluid to plasma glycine ratio suggesting a brain hyperglycinemia.	Glycine	99-106	host cell factor C1	Homo sapiens	57-62	
28363510-11	2017	CONCLUSIONS: This boy had X-linked cobalamin deficiency (HCFC1) with increased cerebrospinal fluid glycine and methylmalonic acid and increased cerebrospinal fluid to plasma glycine ratio suggesting a brain hyperglycinemia.	Glycine	174-181	host cell factor C1	Homo sapiens	57-62	
28363510-12	2017	Putative binding sites for HCFC1 and its binding partner THAP11 were identified near genes of the glycine cleavage enzyme, providing a potential mechanistic link between HCFC1 mutations and increased glycine.	Glycine	98-105	host cell factor C1	Homo sapiens	27-32	
28363510-12	2017	Putative binding sites for HCFC1 and its binding partner THAP11 were identified near genes of the glycine cleavage enzyme, providing a potential mechanistic link between HCFC1 mutations and increased glycine.	Glycine	98-105	host cell factor C1	Homo sapiens	170-175	
28363510-12	2017	Putative binding sites for HCFC1 and its binding partner THAP11 were identified near genes of the glycine cleavage enzyme, providing a potential mechanistic link between HCFC1 mutations and increased glycine.	Glycine	200-207	host cell factor C1	Homo sapiens	27-32	
28363510-12	2017	Putative binding sites for HCFC1 and its binding partner THAP11 were identified near genes of the glycine cleavage enzyme, providing a potential mechanistic link between HCFC1 mutations and increased glycine.	Glycine	200-207	host cell factor C1	Homo sapiens	170-175	
20805357-5	2010	Moreover, HCF-1 interacts with the middle region of YY1 encompassing the glycine-lysine-rich domain and is essential for the formation of a ternary complex with YY1 and BAP1 in vivo.	Glycine	73-80	host cell factor C1	Homo sapiens	10-15	
10464271-2	1999	Its C-terminal 202 amino acids form a potent glycine/glutamine rich activation domain (GQ domain) that can transactivate reporter genes to levels 5-fold higher than VP16 in several mammalian cell lines.	Glycine	45-52	host cell factor C1	Homo sapiens	165-169