Diminished FAD binding in the Y459H and V492E Antley-Bixler syndrome mutants of human cytochrome P450 reductase. (Q50475576)

14 March 2018

title

Diminished FAD binding in the Y459H and V492E Antley-Bixler syndrome mutants of human cytochrome P450 reductase. (English)

1 reference

14 March 2018

main subject

Antley-Bixler syndrome

1 reference

3

1 reference

14 March 2018

author name string

Christopher C Marohnic

series ordinal

1

1 reference

14 March 2018

Satya P Panda

series ordinal

2

1 reference

14 March 2018

Bettie Sue Masters

series ordinal

4

1 reference

14 March 2018

language of work or name

English

0 references

publication date

24 September 2006

1 reference

14 March 2018

Journal of Biological Chemistry

published in

1 reference

14 March 2018

volume

281

1 reference

14 March 2018

issue

47

1 reference

14 March 2018

page(s)

35975-35982

1 reference

14 March 2018

FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome.

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPH-cytochrome P450 oxidoreductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Identification of novel roles of the cytochrome p450 system in early embryogenesis: effects on vasculogenesis and retinoic Acid homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Three-dimensional structure of NADPH-cytochrome P450 reductase: prototype for FMN- and FAD-containing enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Atomic structure of ferredoxin-NADP+ reductase: prototype for a structurally novel flavoenzyme family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

NADPH-cytochrome P450 oxidoreductase. Structural basis for hydride and electron transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Chemical and biological evolution of nucleotide-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Redox properties of microsomal reduced nicotinamide adenine dinucleotide-cytochrome b5reductase and cytochrome b5

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Determination of the redox properties of human NADPH-cytochrome P450 reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Role of a hydrophobic polypeptide in the N-terminal region of NADPH-cytochrome P-450 reductase in complex formation with P-450lm

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Engineering of proteolytically stable NADPH-cytochrome P450 reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Role of acidic residues in the interaction of NADPH-cytochrome P450 oxidoreductase with cytochrome P450 and cytochrome c.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Structure and function of cytochromes P450: a comparative analysis of three crystal structures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

The genetic and functional basis of isolated 17,20-lyase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Molecular modeling of human P450c17 (17alpha-hydroxylase/17,20-lyase): insights into reaction mechanisms and effects of mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Association of cytochromes P450 with their reductases: opposite sign of the electrostatic interactions in P450BM-3 as compared with the microsomal 2B4 system

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Expressed CYP4A4 metabolism of prostaglandin E(1) and arachidonic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

The Structure of the S127P Mutant of Cytochrome b5 Reductase that Causes Methemoglobinemia Shows the AMP Moiety of the Flavin Occupying the Substrate Binding Site

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Catalytic and immunochemical properties of NADPH-cytochrome P450 reductase from fungus Rhizopus nigricans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Preparation and characterization of a 5'-deazaFAD T491V NADPH-cytochrome P450 reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Vitamin B 6 -Responsive and -Unresponsive Cystathioninuria: Two Variant Molecular Forms

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Abnormality of a thiamine-requiring enzyme in patients with Wernicke-Korsakoff syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

LIGPLOT: a program to generate schematic diagrams of protein-ligand interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

Riboflavin-responsive epilepsy in a patient with SER209 variant form of short-chain acyl-CoA dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607095200

21 January 2018

Identifiers

DOI

10.1074/JBC.M607095200

1 reference

14 March 2018

PubMed ID

16998238

1 reference

14 March 2018