Analysis of human lecithin-cholesterol acyltransferase activity by carboxyl-terminal truncation (Q73129821)

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1 November 2019

title

Analysis of human lecithin-cholesterol acyltransferase activity by carboxyl-terminal truncation (English)

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1 November 2019

5

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author name string

Y P Lee

1

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1 November 2019

S Adimoolam

2

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1 November 2019

M Liu

3

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1 November 2019

P V Subbaiah

4

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1 November 2019

A Jonas

6

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language of work or name

English

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publication date

1 February 1997

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Biochimica et Biophysica Acta

1 November 2019

published in

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1 November 2019

volume

1344

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1 November 2019

issue

3

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1 November 2019

page(s)

250-261

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Lecithin-cholesterol acyltransferase in the metabolism of high-density lipoproteins

1 November 2019

cites work

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Cloning and expression of human lecithin-cholesterol acyltransferase cDNA

7 January 2021

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Structure-function relationships in human lecithin:cholesterol acyltransferase. Site-directed mutagenesis at serine residues 181 and 216.

7 January 2021

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Effects of site-directed mutagenesis on the serine residues of human lecithin:cholesterol acyltransferase

7 January 2021

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Effects of site-directed mutagenesis at residues cysteine-31 and cysteine-184 on lecithin-cholesterol acyltransferase activity

7 January 2021

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Roles of cysteines in human lecithin:cholesterol acyltransferase

7 January 2021

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Lecithin-cholesterol acyltransferase: effects of mutagenesis at N-linked oligosaccharide attachment sites on acyl acceptor specificity

7 January 2021

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Effects of site-directed mutagenesis on the N-glycosylation sites of human lecithin:cholesterol acyltransferase

7 January 2021

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Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele

7 January 2021

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A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

7 January 2021

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Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis

7 January 2021

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Lecithin-cholesterol acyltransferase (LCAT) deficiency with a missense mutation in exon 6 of the LCAT gene

7 January 2021

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Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease

7 January 2021

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In vitro expression of structural defects in the lecithin-cholesterol acyltransferase gene.

7 January 2021

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Substrate and positional specificities of human and mouse lecithin-cholesterol acyltransferases. Studies with wild type recombinant and chimeric enzymes expressed in vitro

7 January 2021

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The structure and function of proline-rich regions in proteins

7 January 2021

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Site-specific detection and structural characterization of the glycosylation of human plasma proteins lecithin:cholesterol acyltransferase and apolipoprotein D using HPLC/electrospray mass spectrometry and sequential glycosidase digestion

7 January 2021

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Expression of the mouse serum albumin gene introduced into differentiated and dedifferentiated rat hepatoma cells

7 January 2021

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Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

7 January 2021

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Bifunctional messenger RNAs in eukaryotes

7 January 2021

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Activation of plasma lysolecithin acyltransferase reaction by apolipoproteins A-I, C-I and E

7 January 2021

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Hydrolysis and transesterification of platelet-activating factor by lecithin-cholesterol acyltransferase

7 January 2021

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Influence of proline residues on protein conformation

7 January 2021

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Proline-rich domain and glycosylation are not essential for the enzymic activity of bile salt-activated lipase. Kinetic studies of T-BAL, a truncated form of the enzyme, expressed in Escherichia coli

7 January 2021

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Exon 11 of the rat cholesterol esterase gene encodes domains important for intracellular processing and bile salt-modulated activity of the protein

7 January 2021

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10.1016/S0005-2760(96)00149-X

7 January 2021

Identifiers

DOI

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1 November 2019

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