2.7.1.19	3-phosphoglycerate	74% inhibition at 6 mM and pH 7.2	194	
2.7.1.19	5,5'-dithiobis(2-nitrobenzoic acid)	DTNB, Ellman’s reagent, almost complete inhibition at 0.0045 mM	221	
2.7.1.19	6-phospho-D-gluconate	-	830	
2.7.1.19	6-phospho-D-gluconate	competitive with respect to D-ribulose 5-phosphate	830	
2.7.1.19	6-phosphogluconate	competitive inhibitor, 78% residual activity at 1 mM	391	
2.7.1.19	ADP	competitive, 1 mM	13	
2.7.1.19	ADP	-	13	
2.7.1.19	AMP	competitive, 1 mM	30	
2.7.1.19	AMP	50% inhibition at 0.08 mM	30	
2.7.1.19	AMP	-	30	
2.7.1.19	Ca2+	200 mM	15	
2.7.1.19	chloroplast protein 12	-	4747	
2.7.1.19	Co2+	200 mM	23	
2.7.1.19	Cu2+	-	19	
2.7.1.19	cystine	oxidized form, inhibition almost completely reversible by addition of reduced dithiothreitol	1967	
2.7.1.19	D-Ribulose 1,5-diphosphate	-	6044	
2.7.1.19	daphnetin	i.e. 7,8-dihydroxycoumarin	8088	
2.7.1.19	diethyl dicarbonate	27% residual activity at 0.04 mM	463	
2.7.1.19	dithiobis-(2-nitrobenzoic acid)	complete inactivation, 3 mM ATP protects	16464	
2.7.1.19	dithiothreitol	oxidized form	45	
2.7.1.19	dithiothreitol	light- and dark-adapted extract prepared and assayed without reducing agent, is not significantly affected by incubation with reduced dithiothreitol, however, subsequent incubation with oxidized dithiothreitol results in a significant reduction of enzyme activity under both light and dark conditions	45	
2.7.1.19	DL-glyceraldehyde	non competitive, 10 mM	487	
2.7.1.19	glutathione	oxidized form, inhibition almost completely reversible by addition of reduced dithiothreitol	44	
2.7.1.19	glutathione	oxidized form	44	
2.7.1.19	H2O2	complete inactivation, 3 mM ATP protects	22	
2.7.1.19	Hg2+	-	33	
2.7.1.19	iodoacetate	-	93	
2.7.1.19	L-aspartate	competitive, 1 mM	97	
2.7.1.19	L-malate	competitive, 1 mM	247	
2.7.1.19	Mn2+	200 mM	11	
2.7.1.19	additional information	inhibited by addition of strong oxidants, reversible by addition of reducing agents	2	
2.7.1.19	additional information	oxidizing agents inhibit enzyme activity	2	
2.7.1.19	additional information	not inhibited by 7-methyl-8-hydroxycoumarin	2	
2.7.1.19	p-chloromercuribenzoate	-	43	
2.7.1.19	phosphoenolpyruvate	50% inhibition at 0.32 mM	51	
2.7.1.19	phosphoenolpyruvate	competitive, 1 mM	51	
2.7.1.19	phosphoenolpyruvate	-	51	
2.7.1.19	pyridoxal 5'-phosphate	-	32	
2.7.1.19	pyridoxal 5'-phosphate	inactivation is protected by ATP in combination with NADH	32	
2.7.1.19	regulatory protein CP12	forming under oxidizing conditions a supramolecular complex (2 phosphoribulokinase dimers + 2 glyceraldehyde-3-phosphate dehydrogenase tetramers + 4 CP12 monomers)	155464