5.1.1.15	2-Methyl-3-benzothiazolonehydrazone hydrochloride	-	97575	
5.1.1.15	5,5'-dithiobis(2-nitrobenzoic acid)	complete inhibition at 1 mM	221	
5.1.1.15	8-hydroxyquinoline	59% inhibition at 1 mM	321	
5.1.1.15	Ag+	88% inhibition at 1 mM	75	
5.1.1.15	Al3+	57% inhibition at 1 mM	264	
5.1.1.15	Ala	weak	369	
5.1.1.15	Ca2+	44% inhibition at 5 mM	15	
5.1.1.15	Cd2+	57% inhibition at 1 mM	52	
5.1.1.15	Co2+	32% inhibition at 1 mM	23	
5.1.1.15	Co2+	59% inhibition at 5 mM	23	
5.1.1.15	Cr3+	23% inhibition at 1 mM	895	
5.1.1.15	Cu2+	complete inhibition at 1 mM	19	
5.1.1.15	Cu2+	92% inhibition at 5 mM	19	
5.1.1.15	CuSO4	-	263	
5.1.1.15	D-alpha-Amino-delta-valerolactam	-	43969	
5.1.1.15	D-alpha-aminobutyrate	-	43970	
5.1.1.15	D-cycloserine	-	874	
5.1.1.15	D-cycloserine	21% inhibition at 1 mM	874	
5.1.1.15	D-Lys	-	2732	
5.1.1.15	D-Orn	-	5960	
5.1.1.15	D-penicillamine	88% inhibition at 1 mM	2733	
5.1.1.15	epsilon-Caprolactam	-	96474	
5.1.1.15	Fe2+	97% inhibition at 5 mM	25	
5.1.1.15	Glu	weak	343	
5.1.1.15	Gly	-	163	
5.1.1.15	Hg2+	complete inhibition at 1 mM	33	
5.1.1.15	HgCl2	-	110	
5.1.1.15	hydroxylamine	5 mM	85	
5.1.1.15	hydroxylamine	-	85	
5.1.1.15	hydroxylamine	complete inhibition at 1 mM	85	
5.1.1.15	iodoacetic acid	12% inhibition at 1 mM	213	
5.1.1.15	L-alpha-Amino-delta-valerolactam	inactivation is due to conversion of the enzyme-bound pyridoxal 5'-phosphate into pyridoxamine 5'-phosphate by transamination with L-alpha-amino-delta-valerolactam	30774	
5.1.1.15	L-alpha-aminobutyrate	-	1873	
5.1.1.15	L-Arg	-	178	
5.1.1.15	L-His	-	834	
5.1.1.15	L-Lys	-	502	
5.1.1.15	L-Met	-	468	
5.1.1.15	L-Orn	-	885	
5.1.1.15	L-Phe	weak	203	
5.1.1.15	L-Trp	weak	420	
5.1.1.15	Leu	weak	421	
5.1.1.15	Mg2+	45% inhibition at 5 mM	6	
5.1.1.15	Mn2+	62% inhibition at 1 mM	11	
5.1.1.15	Mn2+	49% inhibition at 5 mM	11	
5.1.1.15	additional information	racemization activity can partially be recovered by the subsequent addition of 1.0 mM pyridoxal 5'-phosphate	2	
5.1.1.15	additional information	poor inhibition by EDTA at 2-10 mM	2	
5.1.1.15	N-ethylmaleimide	50% inhibition at 1 mM	49	
5.1.1.15	NEM	-	89	
5.1.1.15	Ni2+	58% inhibition at 1 mM	38	
5.1.1.15	Ni2+	55% inhibition at 5 mM	38	
5.1.1.15	PCMB	-	78	
5.1.1.15	phenylhydrazine	-	398	
5.1.1.15	phenylmethane sulfonyl fluoride	59% inhibition at 1 mM	44690	
5.1.1.15	Pro	weak	816	
5.1.1.15	Sodium borohydride	-	2356	
5.1.1.15	taurine	-	595	
5.1.1.15	Zn2+	43% inhibition at 1 mM	14