Amino acid residues forming the active site of arylsulfatase A. Role in catalytic activity and substrate binding.
about
Cloning and characterization of two extracellular heparin-degrading endosulfatases in mice and humansArylsulfatase G, a novel lysosomal sulfataseA multiparametric computational algorithm for comprehensive assessment of genetic mutations in mucopolysaccharidosis type IIIA (Sanfilippo syndrome)Cloning of a mucin-desulfating sulfatase gene from Prevotella strain RS2 and its expression using a Bacteroides recombinant system.Escherichia coli K1 aslA contributes to invasion of brain microvascular endothelial cells in vitro and in vivoIdentification of MST1/STK4 and SULF1 proteins as autoantibody targets for the diagnosis of colorectal cancer by using phage microarrays.Deep Genotyping of the IDS Gene in Colombian Patients with Hunter Syndrome.Sulf-2: an extracellular modulator of cell signaling and a cancer target candidate.Post-Synthetic Regulation of HS Structure: The Yin and Yang of the Sulfs in Cancer.The heparin/heparan sulfate 2-O-sulfatase from Flavobacterium heparinum. A structural and biochemical study of the enzyme active site and saccharide substrate specificity.Heterologous expression in Pichia pastoris and biochemical characterization of the unmodified sulfatase from Fusarium proliferatum LE1.Low-scale expression and purification of an active putative iduronate 2-sulfate sulfatase-Like enzyme from Escherichia coli K12.Recognition of arylsulfatase A and B by the UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-phosphotransferase.Arylsulfatase K, a novel lysosomal sulfatase.Characterization of posttranslational formylglycine formation by luminal components of the endoplasmic reticulum.Effects of glycosylation and pH conditions in the dynamics of human arylsulfatase A.An Italian cohort study identifies four new pathologic mutations in the ARSA gene.Specialization of a polyphenism switch gene following serial duplications in Pristionchus nematodes.A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans.Enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA mice.The iron sulfur protein AtsB is required for posttranslational formation of formylglycine in the Klebsiella sulfatase.Catalytic mechanism of the arylsulfatase promiscuous enzyme from Pseudomonas aeruginosa.
P2860
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P2860
Amino acid residues forming the active site of arylsulfatase A. Role in catalytic activity and substrate binding.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Amino acid residues forming th ...... ctivity and substrate binding.
@ast
Amino acid residues forming th ...... ctivity and substrate binding.
@en
type
label
Amino acid residues forming th ...... ctivity and substrate binding.
@ast
Amino acid residues forming th ...... ctivity and substrate binding.
@en
prefLabel
Amino acid residues forming th ...... ctivity and substrate binding.
@ast
Amino acid residues forming th ...... ctivity and substrate binding.
@en
P2093
P2860
P356
P1476
Amino acid residues forming th ...... ctivity and substrate binding.
@en
P2093
P2860
P304
12284-12288
P356
10.1074/JBC.274.18.12284
P407
P577
1999-04-01T00:00:00Z