1.14.11.4 2-oxoglutarate competitive substrate inhibition 34 1.14.11.4 Adrenochrome slight 15613 1.14.11.4 Ca2+ - 15 1.14.11.4 catechol - 156 1.14.11.4 Cd2+ - 52 1.14.11.4 CO2 - 28 1.14.11.4 Cu2+ - 19 1.14.11.4 dehydroascorbate - 434 1.14.11.4 dipyridyl a non-specific hydroxylase inhibitor; a non-specific hydroxylase inhibitor; a non-specific hydroxylase inhibitor 12878 1.14.11.4 DL-Serine 2-[(2,3,4-trihydroxyphenyl)methyl]hydrazide most potent 93286 1.14.11.4 dopamine - 242 1.14.11.4 ephedrine slight 20259 1.14.11.4 epinephrine - 1141 1.14.11.4 homogentisic acid - 30076 1.14.11.4 Hydroxylysine-rich peptides - 96619 1.14.11.4 iodoacetamide - 67 1.14.11.4 L-alpha-hydroxyglutarate the enzyme activity is inhibited by L-alpha-hydroxyglutarate but not its enantiomer D-alpha-hydroxyglutarate 224391 1.14.11.4 malaoxon mechanism of inhibition 6153 1.14.11.4 malathion mechanism of inhibition 1888 1.14.11.4 minoxidil 0.4 mM inhibits LH1 completely, 1 mM inhibits LH2b and LH3 incompletely 9671 1.14.11.4 minoxidil specific inhibition of lysyl hydroxylases; specific inhibition of lysyl hydroxylases; specific inhibition of lysyl hydroxylases 9671 1.14.11.4 additional information the endoplasmic reticulum complex including SC65 and prolyl 3-hydroxylase 3affects the activity of lysyl-hydroxylase 1 potentially through interactions with the enzyme and/or cyclophilin B. Loss of Sc65 in the mouse results in instability of this complex, altered collagen lysine hydroxylation and cross-linking leading to connective tissue defects that include low bone mass and skin fragility, while it has no effect on prolyl 3-hydroxylation. CRTAP, a non-enzymic member of the Leprecan family of proteins which includes Synaptonemal Complex 65 (SC65) and the prolyl 3-hydroxylases (P3H1, P3H2 and P3H3), is an essential third subunit of a complex with prolyl 3-hydroxylase 1 (aka LEPRECAN) and cyclophilin B (CYPB) in the endoplasmic reticulum, forming the so-called collagen prolyl 3-hydroxylation complex 2 1.14.11.4 N-ethylmaleimide - 49 1.14.11.4 NaCl reduces the activity of the isozymes LH1, LH2a, LH2b, and LH3 with most of the synthetic nonpeptide substrates tested, in some cases the isozyme is activated or completely inhibited, overview 42 1.14.11.4 nitroblue tetrazolium - 2573 1.14.11.4 norepinephrine - 975 1.14.11.4 p-chloromercuribenzoate - 43 1.14.11.4 p-mercuribenzoate - 686 1.14.11.4 phenylalanine slight 429 1.14.11.4 Phenylephedrine slight 98184 1.14.11.4 Pyridine 2,4-dicarboxylate - 1592 1.14.11.4 Pyridine 2,5-dicarboxylate - 3361 1.14.11.4 pyridine 2-carboxylate - 9252 1.14.11.4 pyrogallol most potent 658 1.14.11.4 SC65 directly interacts with lysyl-hydroxylase 1, LH1 224390 1.14.11.4 succinate - 58 1.14.11.4 tyrosine slight 709 1.14.11.4 Zn2+ - 14