PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16494447-3	2006	In contrast, (S)-proline-catalyzed reactions give mainly syn-products with high enantioselectivities.	Proline	13-24	synemin	Homo sapiens	57-60	
16494447-4	2006	Computational studies reveal that the energetic preference between the transition structures involving the s-cis-enamine and the s-trans-enamine is smaller for the pipecolic acid as compared to proline, yielding the (2S,3R)-anti and the (2S,3S)-syn Mannich product in nearly equal amounts.	Proline	194-201	synemin	Homo sapiens	245-248