PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23201271-5	2013	Distinct preferences of UBC12 and UBE2F peptides for inhibiting different DCNLs, including the oncogenic DCNL1 protein, suggest it may be possible to develop small molecules blocking specific N-acetyl-methionine-dependent protein interactions.	N-acetylmethionine	192-211	ubiquitin conjugating enzyme E2 F (putative)	Homo sapiens	34-39	
23201271-4	2013	Structures of DCNL2 and DCNL3 complexes with N-terminally acetylated peptides from UBC12 and UBE2F illuminate a common mechanism by which DCNL proteins recognize N-terminally acetylated E2s and how selectivity for interactions dependent on N-acetyl-methionine are established through side chains recognizing distal residues.	N-acetylmethionine	240-259	ubiquitin conjugating enzyme E2 F (putative)	Homo sapiens	93-98