PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31823361-2	2020	Pyruvate kinase (PK) catalyzes the last step of glycolysis and exists as four isoenzymes: PKL, PKR, PKM1 and PKM2.	Pyruvates	0-8	pyruvate kinase L/R	Homo sapiens	90-93	
32043619-1	2020	Pyruvate kinase (PK) deficiency is a rare recessive congenital hemolytic anemia caused by mutations in the PKLR gene.	Pyruvates	0-8	pyruvate kinase L/R	Homo sapiens	107-111	
31823361-2	2020	Pyruvate kinase (PK) catalyzes the last step of glycolysis and exists as four isoenzymes: PKL, PKR, PKM1 and PKM2.	Pyruvates	0-8	pyruvate kinase L/R	Homo sapiens	95-98	
32072180-7	2020	We also analyzed the L-type pyruvate kinase (PKLR) promoter sequence to identify the regulatory effect of HNF-1a on PKLR transcription and confirmed the HNF-1a binding site in the PKLR promoter via a chromatin immunoprecipitation assay.	Pyruvates	28-36	pyruvate kinase L/R	Homo sapiens	45-49	
31618280-1	2019	Pyruvate Kinase Deficiency (PKD) is a rare erythroid metabolic disease caused by mutations in the PKLR gene, which encodes the erythroid specific Pyruvate Kinase enzyme.	Pyruvates	0-8	pyruvate kinase L/R	Homo sapiens	98-102