PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25531415-0	2015	Influence of the metal precursor on the catalytic behavior of Pt/ceria catalysts in the preferential oxidation of CO in the presence of H2 (PROX).	Metals	17-22	pyruvate dehydrogenase complex component X	Homo sapiens	140-144	
31990195-4	2020	In particular, Ru(II)-Prox catalyst 2c, in which there was no geminal substituent on the metal, was shown to have the highest enantioselectivities.	Metals	89-94	pyruvate dehydrogenase complex component X	Homo sapiens	22-26	
32064146-7	2019	When using a metal oxide as the active CO-PrOx catalyst, it is important for it to have significant reduction resistance to avoid the formation of undesired products, e.g., CH4.	Metals	13-24	pyruvate dehydrogenase complex component X	Homo sapiens	42-46	
17279653-3	2007	The lattice constant of PdHx is larger than that of the original metal, and the hydride formation generates high stress within the film.	Metals	65-70	pyruvate dehydrogenase complex component X	Homo sapiens	24-28	
25924357-3	2014	The promising PROX performance over the IrFe/MC can be attributed to the intrinsic surface properties of MC and its specific interaction with metal species.	Metals	142-147	pyruvate dehydrogenase complex component X	Homo sapiens	14-18	
20459102-3	2010	Subsequent studies of these NPs" catalytic properties for preferential CO oxidation in hydrogen-rich environments (PROX), combined with Density Functional Theory (DFT)-based mechanistic studies, elucidate important trends and provide fundamental understanding of the reactivity of Pt shells as a function of the core metal.	Metals	317-322	pyruvate dehydrogenase complex component X	Homo sapiens	115-119	
35388844-1	2022	The combination of a reducible transition metal oxide and a noble metal such as Pt often leads to active low-temperature catalysts for the preferential oxidation of CO in excess H2 gas (PROX reaction).	Metals	66-71	pyruvate dehydrogenase complex component X	Homo sapiens	186-190