PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28949917-3	2017	HBV and its satellite hepatitis D virus (HDV) infect hepatocytes via binding of the preS1 domain of its large envelope protein to sodium taurocholate cotransporting polypeptide (NTCP).	Taurocholic Acid	130-149	large envelope protein;middle envelope protein;small envelope protein	Hepatitis B virus	84-89	
35580630-2	2022	Almost ten years ago the HBV receptor was identified as NTCP (sodium taurocholate co-transporting polypeptide), which interacts directly with the first 48 amino acid residues of the N-myristoylated N-terminal preS1 domain of the viral large (L) protein3.	Taurocholic Acid	62-81	large envelope protein;middle envelope protein;small envelope protein	Hepatitis B virus	209-214	
32446278-5	2021	APPROACH & RESULTS: We found that an 11 amino acid deletion (d11) in the preS1 region enhances the infectivity of cell culture-generated HBV (HBVcc) to sodium taurocholate co-transporting polypeptide-transduced HepG2 (HepG2/NTCP) cells.	Taurocholic Acid	152-171	large envelope protein;middle envelope protein;small envelope protein	Hepatitis B virus	73-78	
32911838-3	2020	The large HBV surface protein (LHBs) contains the integral pre-S1 domain, which binds to the HBV receptor sodium taurocholate co transporting polypeptide on the hepatocyte to facilitate viral entry.	Taurocholic Acid	106-125	large envelope protein;middle envelope protein;small envelope protein	Hepatitis B virus	31-35