Intermolecular interaction between R domains of cystic fibrosis transmembrane conductance regulator.

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Insight in eukaryotic ABC transporter function by mutation analysis.Oligomerization of human ATP-binding cassette transporters and its potential significance in human disease.Computational studies reveal phosphorylation-dependent changes in the unstructured R domain of CFTR.

P2860

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P2860

Intermolecular interaction between R domains of cystic fibrosis transmembrane conductance regulator.

Item

http://www.wikidata.org/entity/Q42606732

description

2003 nî lūn-bûn

@nan

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

2003年论文

@zh

2003年论文

@zh-cn

name

Intermolecular interaction bet ...... embrane conductance regulator.

@en

Intermolecular interaction bet ...... embrane conductance regulator.

@nl

type

Item

label

Intermolecular interaction bet ...... embrane conductance regulator.

@en

Intermolecular interaction bet ...... embrane conductance regulator.

@nl

prefLabel

Intermolecular interaction bet ...... embrane conductance regulator.

@en

Intermolecular interaction bet ...... embrane conductance regulator.

@nl

P1476

Intermolecular interaction bet ...... embrane conductance regulator.

@en

P2093

Jianjie Ma

http://www.w3.org/2001/XMLSchema#string

Junxia Xie

http://www.w3.org/2001/XMLSchema#string

Pamela B Davis

http://www.w3.org/2001/XMLSchema#string

Sanhita Gupta

http://www.w3.org/2001/XMLSchema#string

P2860

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity

A monomer is the minimum functional unit required for channel and ATPase activity of the cystic fibrosis transmembrane conductance regulator

Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain.

Conformation, independent of charge, in the R domain affects cystic fibrosis transmembrane conductance regulator channel openings

A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution

A short segment of the R domain of cystic fibrosis transmembrane conductance regulator contains channel stimulatory and inhibitory activities that are separable by sequence modification.

A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules.

Single chain Fv: a ligand in receptor-mediated gene delivery.

P304

242-248

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1165/RCMB.2002-0108OC

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2003-08-21T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

12933354

http://www.w3.org/2001/XMLSchema#string

P921

cystic fibrosis

transmembrane protein

Intermolecular interaction between R domains of cystic fibrosis transmembrane conductance regulator.

about

P2860

P2860

Intermolecular interaction between R domains of cystic fibrosis transmembrane conductance regulator.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921