PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24858300-1	2014	Etimicin intermediate 3,2"",6""-N,N,N-triacetyl gentamicin C1a (P1), is a key intermediate of etimicin, which is a semi-synthetic aminoglycoside antibiotic effective to both gram-positive and gram-negative bacteria infections.	Aminoglycosides	130-144	endogenous retrovirus group K member 1	Homo sapiens	59-62	
6994206-1	1980	Sisomicin is a new broad-spectrum aminoglycoside most closely related structurally to gentamicin C1a.	Aminoglycosides	34-48	endogenous retrovirus group K member 1	Homo sapiens	97-100	
11401545-14	2001	Furthermore, comparison of enzyme-bound conformations of isepamicin to the RNA-bound conformation of gentamycin C1a also showed remarkable similarities between the enzyme-bound and RNA-bound aminoglycoside antibiotic conformations.	Aminoglycosides	191-205	endogenous retrovirus group K member 1	Homo sapiens	112-115	
12517339-2	2003	Structures of an A site RNA oligonucleotide free in solution and bound to the aminoglycosides paromomycin or gentamicin C1a have been determined by NMR.	Aminoglycosides	78-93	endogenous retrovirus group K member 1	Homo sapiens	120-123	
21444173-1	2011	Etimicin sulfate is a semi-synthetic aminoglycoside which is modified from gentamicin C1a, used as an antibiotic effective both to Gram-positive and Gram-negative bacteria infections.	Aminoglycosides	37-51	endogenous retrovirus group K member 1	Homo sapiens	86-89	
11237616-2	2001	The structures of a prokaryotic decoding region A-site oligonucleotide free in solution and bound to the aminoglycosides paromomycin and gentamicin C1A have been determined.	Aminoglycosides	105-120	endogenous retrovirus group K member 1	Homo sapiens	148-151	
1449515-5	1992	Using a series of different aminoglycosides, we showed that molecules with a lower inhibitory potential (gentamicin B, amikacin and isepamicin) are surrounded by both hydrophobic and hydrophilic envelopes whereas aminoglycosides which are more inhibitory are enveloped primarily by either hydrophilic (kanamycin A or B) or hydrophobic (gentamicin C1a) envelopes.	Aminoglycosides	28-43	endogenous retrovirus group K member 1	Homo sapiens	347-350	
1449515-5	1992	Using a series of different aminoglycosides, we showed that molecules with a lower inhibitory potential (gentamicin B, amikacin and isepamicin) are surrounded by both hydrophobic and hydrophilic envelopes whereas aminoglycosides which are more inhibitory are enveloped primarily by either hydrophilic (kanamycin A or B) or hydrophobic (gentamicin C1a) envelopes.	Aminoglycosides	213-228	endogenous retrovirus group K member 1	Homo sapiens	347-350