(Q47630698)

English

A structural model of the copper ATPase ATP7B to facilitate analysis of Wilson disease-causing mutations and studies of the transport mechanism.

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

A structural model of the copper ATPase ATP7B to facilitate analysis of Wilson disease-causing mutations and studies of the transport mechanism (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

author name string

Maya Schushan

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

Ashima Bhattacharjee

2

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4 February 2020

Svetlana Lutsenko

4

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4 February 2020

publication date

13 June 2012

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4 February 2020

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

7

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PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

669-678

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

describes a project that uses

1 reference

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC6365107/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Function and regulation of human copper-transporting ATPases

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Supplying copper to the cuproenzyme peptidylglycine alpha-amidating monooxygenase

1 reference

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21 January 2018

Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes

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21 January 2018

Unexpected role of the copper transporter ATP7A in PDGF-induced vascular smooth muscle cell migration

1 reference

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21 January 2018

Wilson's disease: an update.

1 reference

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21 January 2018

Neonatal diagnosis and treatment of Menkes disease

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system

1 reference

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21 January 2018

Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin

1 reference

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21 January 2018

Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

The distinct functional properties of the nucleotide-binding domain of ATP7B, the human copper-transporting ATPase: analysis of the Wilson disease mutations E1064A, H1069Q, R1151H, and C1104F

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Solution structure of the N-domain of Wilson disease protein: distinct nucleotide-binding environment and effects of disease mutations

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Difference in stability of the N-domain underlies distinct intracellular properties of the E1064A and H1069Q mutants of copper-transporting ATPase ATP7B.

1 reference

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21 January 2018

The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B.

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?

1 reference

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21 January 2018

Structural organization of human Cu-transporting ATPases: learning from building blocks

1 reference

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The transport mechanism of bacterial Cu+-ATPases: distinct efflux rates adapted to different function

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Intermediate phosphorylation reactions in the mechanism of ATP utilization by the copper ATPase (CopA) of Thermotoga maritima

1 reference

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21 January 2018

Functional properties of the copper-transporting ATPase ATP7B (the Wilson's disease protein) expressed in insect cells

1 reference

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Bacterial transition metal P(1B)-ATPases: transport mechanism and roles in virulence.

1 reference

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Structure of the two transmembrane Cu+ transport sites of the Cu+ -ATPases

1 reference

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Reaction cycle of Thermotoga maritima copper ATPase and conformational characterization of catalytically deficient mutants

1 reference

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The different intermolecular interactions of the soluble copper-binding domains of the menkes protein, ATP7A.

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Metal Binding Domains 3 and 4 of the Wilson Disease Protein: Solution Structure and Interaction with the Copper(I) Chaperone HAH1 † ‡

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Structure of human Wilson protein domains 5 and 6 and their interplay with domain 4 and the copper chaperone HAH1 in copper uptake

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Solution structures of the actuator domain of ATP7A and ATP7B, the Menkes and Wilson disease proteins

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Crystal structure of a copper-transporting PIB-type ATPase

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

FFAS03: a server for profile--profile sequence alignments

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

The HHpred interactive server for protein homology detection and structure prediction

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

PUDGE: a flexible, interactive server for protein structure prediction

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

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UniRef: comprehensive and non-redundant UniProt reference clusters

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

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MAFFT version 5: improvement in accuracy of multiple sequence alignment

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

ConSurf 2010: calculating evolutionary conservation in sequence and structure of proteins and nucleic acids

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Quality assessment of protein model-structures using evolutionary conservation

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Detection of functionally important regions in "hypothetical proteins" of known structure

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

The Binding Mode of ATP Revealed by the Solution Structure of the N-domain of Human ATP7A

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Identification of novel mutations and the three most common mutations in the human ATP7B gene of Korean patients with Wilson disease

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Novel mutations of the ATP7B gene in Japanese patients with Wilson disease.

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Haplotype and mutation analysis in Japanese patients with Wilson disease

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

The toxic milk mouse is a murine model of Wilson disease

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Functional studies on the Wilson copper P-type ATPase and toxic milk mouse mutant

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Identification of the transmembrane metal binding site in Cu+-transporting PIB-type ATPases

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Diverse functional properties of Wilson disease ATP7B variants

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

The lumenal loop Met672-Pro707 of copper-transporting ATPase ATP7A binds metals and facilitates copper release from the intramembrane sites

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

On the accuracy of homology modeling and sequence alignment methods applied to membrane proteins

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Crystal structures of the CusA efflux pump suggest methionine-mediated metal transport

1 reference

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Transport of cisplatin by the copper efflux transporter ATP7B.

1 reference

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Mutation analysis of Wilson disease in the Spanish population - identification of a prevalent substitution and eight novel mutations in the ATP7B gene

1 reference

https://api.crossref.org/works/10.1039%2FC2MT20025B

21 January 2018

Functional analysis of the N-terminal CXXC metal-binding motifs in the human Menkes copper-transporting P-type ATPase expressed in cultured mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

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based on heuristic

inferred from PubMed ID database lookup

Molecular analysis and diagnosis in Japanese patients with Wilson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective cellular localization of mutant ATP7B in Wilson's disease patients and hepatoma cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cu(I) binding and transfer by the N terminus of the Wilson disease protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence variation database for the Wilson disease copper transporter, ATP7B

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OPM database and PPM web server: resources for positioning of proteins in membranes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22692182

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1039/C2MT20025B

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22692182%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

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