3.1.2.1	1,2-dimyristoylphosphatidylglycerol	activates mutant form lacking START domain	732297	
3.1.2.1	1-oleoyl-2-lysophosphatidylglycerol	activates mutant form lacking START domain	732297	
3.1.2.1	3-thiadicarboxylic acid	activity increases	94490	
3.1.2.1	acetate	-	94486	
3.1.2.1	acetate	hydrolase increased 3fold by 100-250 mM acetate	94468	
3.1.2.1	acetyl-CoA	at time of rewarming 0.5 mM acetyl-CoA restores the activity about 50%	94477	
3.1.2.1	adenosine 5'-[beta,gamma-imido]triphosphate	with adoPP[CH2]P a 2.5fold activation of the cold-labile cytosolic enzyme at 2 mM, with adoPP[NH]P a 3.7fold activation respectively	94479	
3.1.2.1	ADP	0.0001 mM activates	94469	
3.1.2.1	albumin	albumin enhances the reactivation of the monomeric form	94477	
3.1.2.1	alpha-(p-chlorophenoxy)isobutyric acid	high activity of the enzyme for over 72h	94481	
3.1.2.1	ATP	-	94476, 94480, 94481, 94482, 94484, 94492, 94493	
3.1.2.1	ATP	14fold activation of the cold-labile enzyme at 2 mM	94479	
3.1.2.1	ATP	2 mM increases the hydrolytic rate	94472, 94475	
3.1.2.1	ATP	at time of rewarming ATP greatly enhances the restoration of the activity, 2 mM ATP restores the enzyme activity about 70%	94477	
3.1.2.1	ATP	cytosolic enzyme is stimulated, the mitochondrial enzyme seems unaffected	94490	
3.1.2.1	bis(carboxymethylthio)-l,10 decane	rats fed a high-carbohydrate diet	94490	
3.1.2.1	CTP	counteracts the inhibition of the cold-labile cytosolic enzyme by ADP	94479	
3.1.2.1	cystamine	-	94474	
3.1.2.1	cystamine	10 mM activates by a mechanism of disulfide exchange	94473	
3.1.2.1	diacetylcystamine	activation	94473	
3.1.2.1	diphosphate	450 mM pyrophosphate restores the activity about 80% at time of rewarming	94477	
3.1.2.1	disulfide peptides	activation	94474	
3.1.2.1	dithiothreitol	oxidized, activation	94473	
3.1.2.1	DL-beta-hydroxy-butyrate	hydrolase increases 50-70% by 100 mM DL-beta-hydroxy-butyrate	94468	
3.1.2.1	Dopa	activates mutant form lacking START domain	732297	
3.1.2.1	ethyl chlorophenoxyisobutyrate	in rats on diet containing 0.5% clofibrate the activity increases 2-3fold	94492	
3.1.2.1	ethyl chlorophenoxyisobutyrate	no markable increase on clofibrate treatment	94493	
3.1.2.1	Ferredoxin	dependent on	94491	
3.1.2.1	fluoroacetate	hydrolase increases 50-70% by 100 mM fluoroacetate	94468	
3.1.2.1	galactose	higher activity	94486	
3.1.2.1	GDP	at 0.5 mM nucleoside phosphate 100% stimulation in Trypanosoma brucei brucei MIAG 103 and 75% in Trypanosoma brucei brucei 427	94467	
3.1.2.1	glycerol	-	94486, 94494	
3.1.2.1	GSH	activation	94473	
3.1.2.1	GSSG	activation	94473	
3.1.2.1	GTP	-	94482	
3.1.2.1	GTP	4.6fold activation of the cold-labile cytosolic enzyme at 2 mM	94479	
3.1.2.1	L(-)-carnitine	stimulation at 3mM	94467	
3.1.2.1	additional information	the enzyme is induced in mitochondria by di(2-ethylhexyl)phthalate	664215	
3.1.2.1	NADH	stimulation	94490	
3.1.2.1	Oxytocin	activation	94474	
3.1.2.1	penicillamine disulfide	activation	94473	
3.1.2.1	phosphate	920 mM phosphate restores the activity about 80% at time of rewarming	94477	
3.1.2.1	phosphatidic acid	activates mutant form lacking START domain	732297	
3.1.2.1	pressinoic acid	activation	94474	
3.1.2.1	propionate	hydrolase increases 50-70% by 250 mM propionate	94468	
3.1.2.1	Somatostatin	like[tyr1]somatostatin and tyr-somatostatin the most potent activator	94474	
3.1.2.1	tetradecylthioacetic acid	activity increases	94490	
3.1.2.1	triiodothyronine	activity increases	94481	
3.1.2.1	Tyr-somatostatin	activation	94474	
3.1.2.1	Vasopressin	activation	94474	
3.1.2.1	[arg8]vasotocin	activation	94474	
3.1.2.1	[tyr1]somatostatin	activation	94474