Create issue ticket

256 Possible Causes for AMINOPEPTIDASE, B NAPHTHYLAMIDE,, L LEUCYL, LEUCINE

Show results in: Română

  • Aminoaciduria

    […] amino resin amino-acid dating aminoacetic acid aminoaciduria aminobenzene aminobenzoic acid aminocarb aminocitric acid aminocyclohexane aminoglutethimide aminoglycoside aminopeptidase[wordreference.com] .), and Fluorometric methods (using ninhydran and L-leucyl-L-alanine with phenylalanine to produce fluorescence) What is the reference range for serum phenylalanine at an[quizlet.com] Values above normal were recorded for alanine, leucine, valine, phenylalanine and glutamic acid, correlating proportionally with their increased blood levels, and preceding[ncbi.nlm.nih.gov] […] excretion of amino acids seems to be of considerable significance as marked elevation of urine concentrations of alanine, asparagine, cystine, glycine, histidine, isoleucine and leucine[ncbi.nlm.nih.gov]

    Missing: B NAPHTHYLAMIDE
  • HIV-proteinase Inhibitor

    We showed previously that HIV PIs alter the hydrolytic activities of nonaspartyl proteases, such as proteasomes and aminopeptidases ( 8 ).[jimmunol.org] B.[google.com] Compounds [ edit ] Aprotinin Bestatin Calpain inhibitor I and II Chymostatin E-64 Leupeptin ( N -acetyl- L -leucyl- L -leucyl- L -argininal) alpha-2-Macroglobulin Pefabloc[en.wikipedia.org] […] known to cleave peptide bonds between larger hydrophobic amino acids, but preferred the P 1 and P’ 1 sites; Sap1, Sap2 and Sap6 preferred phenylalanine, while Sap3 preferred leucine[wjgnet.com]

  • HMG-CoA Lyase Deficiency

    B. 1. von Verdauungsenzymen (Aminopeptidasen, Carboxypeptidase, Amylase). 1 of digestive enzymes (aminopeptidase, carboxypeptidase, amylase). 2. des Enzyms Carboanhydrase,[google.com] HMG-CoA lyase deficiency is a rare genetic disorder characterized by the deficiency of an enzyme that is necessary for the synthesis of ketone bodies and metabolism of leucine[symptoma.com] Abstract 3-Hydroxy-3-Methylglutaryl coenzyme A lyase (HMG-CoA) deficiency is a rare inborn error of leucine catabolism.[ncbi.nlm.nih.gov] Abstract 3-Hydroxy-3-methylglutaryl-CoA lyase (HL) deficiency is a rare autosomal recessive genetic disorder that affects ketogenesis and l-leucine catabolism, which generally[ncbi.nlm.nih.gov]

    Missing: B NAPHTHYLAMIDE L LEUCYL
  • Nephronophthisis-Like Nephropathy

    aminopeptidase (aminopeptidase P) 3, putative , X-Pro aminopeptidase 3 , probable Xaa-Pro aminopeptidase 3 , aminopeptidase P3 Selected quality suppliers for anti-X-Prolyl[antibodies-online.com] The mtDNA contains 22 tRNAs, one for each amino acid, except leucine and serine, which have two mitochondrial tRNAs.[dovepress.com] Renal complications in a patient with A-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA. Intern Med 2002;41(2):113-8.[revistanefrologia.com] Publikationstyp Artikel: Journalartikel Dokumenttyp Wissenschaftlicher Artikel Schlagwörter Aminopeptidases/genetics; Aminopeptidases/metabolism*; Animals; Centrosome/enzymology[push-zb.helmholtz-muenchen.de]

    Missing: B NAPHTHYLAMIDE L LEUCYL
  • Porphyromonas Gingivalis

    Studies on the aminopeptidase activities of Porphyromonas gingivalis . Oral Microbiol. Immunol., in press. View Abstract[doi.org] - l -valyl- l -leucyl- l -lysine-4-methylcoumaryl-7-amide, respectively (Peptide Institute, Osaka, Japan), as described previously ( 37 ).[doi.org] The BspA protein ( 34 ) belongs to the leucine-rich repeat (LRR) protein family ( 17 ).[doi.org] AdpC is a Prevotella intermedia 17 leucine-rich repeat internalin-like protein. Infect. Immun . 78 , (6), 2385-2396 (2010). Usage Statistics[jove.com]

    Missing: B NAPHTHYLAMIDE
  • Glucomannan

    3.4.11.2 Membrane alanyl aminopeptidase 3.4.11.3 Cystinyl aminopeptidase 3.4.11.4 Tripeptide aminopeptidase 3.4.11.5 Prolyl aminopeptidase 3.4.11.6 Aminopeptidase B 3.4.11.7[enzyme.expasy.org] (Tyr) C01652 tRNA(Trp) C03512 L-Tryptophanyl-tRNA(Trp) C01651 tRNA(Thr) C02992 L-Threonyl-tRNA(Thr) C01645 tRNA(Leu) C02047 L-Leucyl-tRNA C01644 tRNA(Ile) C03127 L-Isoleucyl-tRNA[aber.ac.uk] Disodium inosinate E632 Dipotassium inosinate E633 Calcium inosinate E634 Calcium 5'-ribonucleotides E635 Disodium 5'-ribonucleotides E640 Glycine and its sodium salt E641 L-leucine[food.gov.uk] […] entries : 5-Phospho-alpha-D-ribose 1-diphosphate C00120 : 3 entries : Biotin C00121 : 5 entries : D-Ribose, D-ribose C00122 : 5 entries : Fumarate C00123 : 3 entries : L-Leucine[ezcatdb.cbrc.jp]

    Missing: B NAPHTHYLAMIDE
  • Chloroquine

    (aminopeptidase P [APP], M1-family alanyl aminopeptidase [AAP], M17-family leucyl aminopeptidase [LAP], and M18-family aspartyl aminopeptidase [DAP]).[doi.org] The chemicals, cycloheximide, actinomycin, carbobenzoxy- l -leucyl- l -leucyl- l -leucinal (MG-132), para-nitrophenyl phosphate (pNPP), and orthovanadate were from Sigma-Aldrich[doi.org] An aliquot of 10 5 cells of the transformed pool was subsequently plated on a solid synthetic complete medium that lacked leucine (SC-Leu) but contained 20 µM CQ to select[doi.org] (BP2), equivalent to the 2 P. falciparum DV falcipains FP-2 and FP-3; bergheilysin (BLN), the ortholog of P. falciparum falcilysin; dipetidyl peptidase 1 (DPAP1); and 4 aminopeptidases[doi.org]

    Missing: B NAPHTHYLAMIDE
  • Chronic Periodontitis

    Community metabolism (categories E, G, H, C, I, F, Q) was different in periodontitis and was characterised by the enrichment of COGs related to peptide catabolism (dipeptidyl aminopeptidases[nature.com] Three anaerobic bacteria, P. gingivalis , T. denticola , and B. forsythus , are among the BANA-positive species found in plaques ( 150 ).[cmr.asm.org] […] following 21 amino acids and related molecules were measured: Glycine (Gly), Alanine (Ala), Serine (Ser), Proline (Pro), Valine (Val), Threonine (Thr), Isoleucine (Ile), Leucine[dx.doi.org] COGs related to peptide catabolism (dipeptidyl aminopeptidases, dipeptidases and tripeptidases) and degradation of amino acids (category E, aspartate, glycine, glutamate, leucine[nature.com]

    Missing: L LEUCYL
  • Doxycycline

    The activity of a number of urinary enzymes, including alanine aminopeptidase, N- acetyl-ß-D-glucosaminidase, leucine aminopeptidase and ß-glucurinidase, has been shown to[inchem.org] )amino]-4- (dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro- 3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2- naphthacenecarboxamide; [4S-(4alpha,12aalpha)]-9-[(L-Leucyl)amino[brevets-patents.ic.gc.ca] N-(tert-butoxycarbonyl)-N-methyl-L-leucine is coupled with 9-amino-5-hydroxy-6-deoxytetracycline to give the protected intermediate which is then deprotected and purified[freepatentsonline.com] )amino]-4-(dimethylamino]-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacencarboxamid; [4S-(4alpha,12aalpha)]-9-[(L-Leucyl)amino]-[patents.google.com]

    Missing: B NAPHTHYLAMIDE
  • 2-Methylbutyryl-CoA Dehydrogenase Deficiency

    Deficiency of amine oxidase (copper-containing) • Deficiency of amine oxidase • Deficiency of aminoacyl-histidine dipeptidase • Deficiency of aminoacyltransferase • Deficiency of aminopeptidase[coding-pro.com] For these infants, elevated C5-acylcarnitines suggested a diagnosis of isovaleric acidemia (IVA), a metabolic defect of leucine metabolism.[ncbi.nlm.nih.gov] […] of amino acid metabolism ( E70–E72 , 270 ) K acetyl-CoA Lysine /straight chain Glutaric acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria Leucine[wiki30.com] […] and Isoleucine Degradation HMDB Pathways Name Valine, Leucine and Isoleucine Degradation Image Show KEGG Pathways Name Valine, Leucine and Isoleucine Degradation Image Show[cowmetdb.ca]

    Missing: B NAPHTHYLAMIDE L LEUCYL