Identification of holocarboxylase synthetase (HCS) proteins in human placenta (Q24336638)

biotin-protein ligase activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

M Hiratsuka

1

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O Sakamoto

2

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X Li

3

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Y Suzuki

4

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Y Aoki

5

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K Narisawa

Biochimica et Biophysica Acta

6

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language of work or name

English

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publication date

11 June 1998

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published in

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volume

1385

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issue

1

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page(s)

165-71

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cites work

In Vitro Synthesis of Propionyl-CoA Holocarboxylase by a Partially Purified Mitochondrial Preparation from Biotin-Deficient Chicken Liver

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Regulation and intracellular localization of the biotin holocarboxylase synthetase of 3T3-L1 cells

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Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA

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Enzymatic diagnosis of holocarboxylase synthetase deficiency using apo-carboxyl carrier protein as a substrate.

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Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients

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Efficient selection for high-expression transfectants with a novel eukaryotic vector

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Intracellular Localization of Hepatic Propionyl-CoA Carboxylase and Methylmalonyl-CoA Mutase in Humans and Normal and Vitamin B12Deficient Rats

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A new method for simultaneous purification of cytochrome b5 and NADPH-cytochrome c reductase from rat liver microsomes

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Purification and properties of bovine liver holocarboxylase synthetase

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Clustering of mutations in the biotin-binding region of holocarboxylase synthetase in biotin-responsive multiple carboxylase deficiency

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Characterization of mutant holocarboxylase synthetase (HCS): a Km for biotin was not elevated in a patient with HCS deficiency

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Isolation of a cDNA encoding human holocarboxylase synthetase by functional complementation of a biotin auxotroph of Escherichia coli

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Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21

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