Molecular identification of hydroxylysine kinase and of ammoniophospholyases acting on 5-phosphohydroxy-L-lysine and phosphoethanolamine.
about
C7orf10 encodes succinate-hydroxymethylglutarate CoA-transferase, the enzyme that converts glutarate to glutaryl-CoAStructural Basis for Phospholyase Activity of a Class III Transaminase HomologueMetabolite proofreading in carnosine and homocarnosine synthesis: molecular identification of PM20D2 as β-alanyl-lysine dipeptidaseCHRNA3 polymorphism modifies lung adenocarcinoma risk in the Chinese Han populationSocial stress increases expression of hemoglobin genes in mouse prefrontal cortex.Eicosapentaenoic and docosahexaenoic acid-enriched high fat diet delays the development of fatty liver in miceGenome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality.The role of haplotype in 15q25.1 locus in lung cancer risk: results of scanning chromosome 15.Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida.Enzyme complexity in intermediary metabolism.Genetic and hormonal control of hepatic steatosis in female and male mice.AGXT2L1 is down-regulated in heptocellular carcinoma and associated with abnormal lipogenesis.Focus on O-phosphohydroxylysine, O-phosphohydroxyproline, N 1-phosphotryptophan and S-phosphocysteine.Endogenous sphingomyelin segregates into submicrometric domains in the living erythrocyte membrane.A Bayesian approach to identify genes and gene-level SNP aggregates in a genetic analysis of cancer data.Kinetic characterization of the human O-phosphoethanolamine phospho-lyase reveals unconventional features of this specialized pyridoxal phosphate-dependent lyase.Confronting the catalytic dark matter encoded by sequenced genomes.Plasma amino acid profiling in major depressive disorder treated with selective serotonin reuptake inhibitors.PHYKPL tetramer hydrolyses 5PHLETNPPL tetramer hydrolyses PETAHYKK phosphorylates 5HLYSPropagation of human corneal endothelial cells: a novel dual media approach.Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria.
P2860
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P2860
Molecular identification of hydroxylysine kinase and of ammoniophospholyases acting on 5-phosphohydroxy-L-lysine and phosphoethanolamine.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
name
Molecular identification of hy ...... ysine and phosphoethanolamine.
@ast
Molecular identification of hy ...... ysine and phosphoethanolamine.
@en
Molecular identification of hy ...... ysine and phosphoethanolamine.
@nl
type
label
Molecular identification of hy ...... ysine and phosphoethanolamine.
@ast
Molecular identification of hy ...... ysine and phosphoethanolamine.
@en
Molecular identification of hy ...... ysine and phosphoethanolamine.
@nl
prefLabel
Molecular identification of hy ...... ysine and phosphoethanolamine.
@ast
Molecular identification of hy ...... ysine and phosphoethanolamine.
@en
Molecular identification of hy ...... ysine and phosphoethanolamine.
@nl
P2093
P2860
P921
P356
P1476
Molecular identification of hy ...... ysine and phosphoethanolamine.
@en
P2093
Farah Hadi
Maria Veiga-da-Cunha
Thomas Balligand
Vincent Stroobant
P2860
P304
P356
10.1074/JBC.M111.323485
P407
P577
2012-01-12T00:00:00Z