Naturally occurring mutants of human steroid 21-hydroxylase (P450c21) pinpoint residues important for enzyme activity and stability (Q74299290)

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10 November 2019

title

Naturally occurring mutants of human steroid 21-hydroxylase (P450c21) pinpoint residues important for enzyme activity and stability (English)

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10 November 2019

2

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10 November 2019

author name string

A Nikoshkov

1

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10 November 2019

A Vlamis-Gardikas

3

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10 November 2019

L Tranebjaerg

4

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10 November 2019

M Holst

5

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10 November 2019

A Wedell

6

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10 November 2019

H Luthman

7

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10 November 2019

language of work or name

English

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publication date

1 March 1998

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Journal of Biological Chemistry

10 November 2019

published in

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volume

273

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issue

11

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10 November 2019

page(s)

6163-6165

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The P450 superfamily: update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature

10 November 2019

cites work

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Molecular biology of steroid hormone synthesis

21 January 2018

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Molecular and clinical advances in congenital adrenal hyperplasia

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Congenital adrenal hyperplasia. (1).

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Structure of human steroid 21-hydroxylase genes

21 January 2018

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Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

21 January 2018

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Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

21 January 2018

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Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

21 January 2018

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Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations

21 January 2018

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Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene

21 January 2018

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Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations.

21 January 2018

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Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

21 January 2018

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Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiency.

21 January 2018

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Analysis of synthesis, processing, and secretion of proteins expressed in mammalian cells

21 January 2018

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 January 2018

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Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

21 January 2018

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High-resolution crystal structure of cytochrome P450cam

21 January 2018

1 reference

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Crystal structure of hemoprotein domain of P450BM-3, a prototype for microsomal P450's

21 January 2018

1 reference

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Crystal structure and refinement of cytochrome P450terp at 2.3 A resolution

21 January 2018

1 reference

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Structure of cytochrome P450eryF involved in erythromycin biosynthesis

21 January 2018

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A novel nonsense mutation in the HMG box of the SRY gene in a patient with XY sex reversal

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.273.11.6163

1 reference

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10 November 2019

1 reference