4.1.1.18	1,5-pentanediamine	-	42870	
4.1.1.18	2-ethylhexyl diphenyl phosphate	-	225946	
4.1.1.18	6-aminohexanoate	-	2718	
4.1.1.18	Acridine orange	-	4219	
4.1.1.18	alpha-difluoromethyl-lysine	LCD suicide inhibitor, 74% inhibition at 1 mM	147308	
4.1.1.18	alpha-Difluoromethylcadaverine	-	96117	
4.1.1.18	alpha-Monofluoromethylcadaverine	-	96137	
4.1.1.18	alpha-Trifluoromethylcadaverine	-	96147	
4.1.1.18	alpha-Vinyllysine	-	96148	
4.1.1.18	Br-	-	332	
4.1.1.18	Ca2+	-	15	
4.1.1.18	CaCl2	-	218	
4.1.1.18	cadaverine	-	533	
4.1.1.18	cadaverine	competitive inhibition mechanism, 90% inhibition at 10 mM	533	
4.1.1.18	Cl-	-	141	
4.1.1.18	cucurbit[7]uril	CB7	225958	
4.1.1.18	diethyldithiocarbamic acid	-	12507	
4.1.1.18	DL-alpha-Difluoromethyllysine	-	20715	
4.1.1.18	DL-alpha-Difluoromethyllysine	competitive	20715	
4.1.1.18	DL-alpha-difluoromethylornithine	competitive and irreversible	13680	
4.1.1.18	F-	-	174	
4.1.1.18	Fe2+	-	25	
4.1.1.18	Fe3+	-	70	
4.1.1.18	FeCl2	-	1235	
4.1.1.18	GDP	-	53	
4.1.1.18	GTP	-	37	
4.1.1.18	guanosine 3'-diphosphate	-	120827	
4.1.1.18	guanosine 5'-diphosphate	-	44201	
4.1.1.18	H2PO4-	-	30061	
4.1.1.18	HgCl2	-	110	
4.1.1.18	HPO42-	-	2843	
4.1.1.18	hydroxylamine	-	85	
4.1.1.18	I-	-	507	
4.1.1.18	iodoacetamide	-	67	
4.1.1.18	KCl	-	79	
4.1.1.18	L-Arg	-	178	
4.1.1.18	L-lysine	substrate inhibition at high concentrations	134	
4.1.1.18	L-lysine	substrate inhibition is observed from 1.25 M	134	
4.1.1.18	LiCl	-	815	
4.1.1.18	MnCl2	-	307	
4.1.1.18	additional information	at pH values lower than 5.0, there is no effect of ppGpp, pppGpp, GDP and GTP on LdcI activity	2	
4.1.1.18	additional information	at 30°C the presence of L-Arg has little effect on the activity of the enzyme	2	
4.1.1.18	additional information	enzyme LdcC shows no or poor substrate inhibition by L-lysine	2	
4.1.1.18	additional information	inhibitory effect of organophosphate esters (OPEs) with aromatic, alkyl or chlorinated alkyl substituents on the activity of lysine decarboxylase (LDC) is assessed quantitatively with an economic and label-free fluorescence sensor and cell assay. Molecular docking analysis of the LDC/OPE complexes reveals that different binding modes contribute to the difference in their inhibitory effect. No inhibition by tris(2-ethylhexyl) phosphate, tributoxyethyl phosphate, tri-n-butyl phosphate, tri-n-propyl phosphate, triethyl phosphate, and trimethyl phosphate. In vivo cytotoxic effect of the compounds in Rattus norvegicus PC-12 cells, overview	2	
4.1.1.18	NaBH4	-	616	
4.1.1.18	NaCl	1 M, 45% inhibition	42	
4.1.1.18	NaCl	-	42	
4.1.1.18	NaCl	about 65% residual activity at 1 M	42	
4.1.1.18	PCMB	inhibition is eliminated by addition of 2-mercaptoethanol or glutathione, and pyridoxal 5'-phosphate	78	
4.1.1.18	ppGpp	addition of ppGpp at low salt concentrations (25-135 mM NaCl depending on the buffer) results in a dramatic inhibition of LdcI activity of about 10fold at pH values higher than 5.0	3703	
4.1.1.18	ppGpp	LdcI activity is strongly inhibited by the binding of ppGpp. The RavA-LdcI interaction reduces the inhibition of LdcI activity by ppGpp in vitro as well as in vivo	3703	
4.1.1.18	pppGpp	inhibits LdcI only at pH values higher than 6.5	33572	
4.1.1.18	Semicarbazide	-	382	
4.1.1.18	SO42-	-	245	
4.1.1.18	tri(2-chloro-1-(chloromethyl)ethyl) phosphate	-	225944	
4.1.1.18	tri(2-chloroethyl) phosphate	-	225948	
4.1.1.18	tri-m-cresyl phosphate	-	225943	
4.1.1.18	triphenyl phosphate	-	103700	
4.1.1.18	tris(2-chloroisopropyl)phosphate	-	225949	
4.1.1.18	Urea	-	116	
4.1.1.18	Zn2+	-	14