(Q41060398)

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WW domains

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Europe PubMed Central

PubMed publication ID

26 September 2017

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Europe PubMed Central

WW domains (English)

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Europe PubMed Central

PubMed publication ID

26 September 2017

author name string

Staub O

1

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Rotin D

2

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Europe PubMed Central

PubMed publication ID

26 September 2017

publication date

1 May 1996

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

495-499

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

WWP, a new amino acid motif present in single or multiple copies in various proteins including dystrophin and the SH3-binding Yes-associated protein YAP65

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The WW domain: a signalling site in dystrophin?

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The rsp5-domain is shared by proteins of diverse functions

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Protein modules and signalling networks

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A phosphotyrosine interaction domain

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of a novel protein-binding module--the WW domain

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The WW domain of Yes-associated protein binds a proline-rich ligand that differs from the consensus established for Src homology 3-binding modules

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Two binding orientations for peptides to the Src SH3 domain: development of a general model for SH3-ligand interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

An SH3 binding region in the epithelial Na+ channel (alpha rENaC) mediates its localization at the apical membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Formin binding proteins bear WWP/WW domains that bind proline-rich peptides and functionally resemble SH3 domains

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a set of genes with developmentally down-regulated expression in the mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

NPl1, an essential yeast gene involved in induced degradation of Gap1 and Fur4 permeases, encodes the Rsp5 ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

SPT3 interacts with TFIID to allow normal transcription in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Synaptotagmin I is a high affinity receptor for clathrin AP-2: implications for membrane recycling

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Primary structure of the uracil transport protein of Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

GAP1, the general amino acid permease gene of Saccharomyces cerevisiae. Nucleotide sequence, protein similarity with the other bakers yeast amino acid permeases, and nitrogen catabolite repression

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A rat brain mRNA encoding a transcriptional activator homologous to the DNA binding domain of retroviral integrases

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The regions of the Fe65 protein homologous to the phosphotyrosine interaction/phosphotyrosine binding domain of Shc bind the intracellular domain of the Alzheimer's amyloid precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

CD45 protein-tyrosine phosphatase associates with the WW domain-containing protein, CD45AP, through the transmembrane region

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the sites of interaction between lymphocyte phosphatase-associated phosphoprotein (LPAP) and CD45

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0969-2126(96)00054-8

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

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