(Q24300742)

protein homodimerization activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Svante Pääbo

6

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James C. Stroud

1

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author name string

Yongqing Wu

2

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Darren L Bates

3

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Aidong Han

4

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Katja Nowick

5

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Harry Tong

7

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Lin Chen

Solution structure of the DNA-binding domain of interleukin enhancer binding factor 1 (FOXK1a)

8

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language of work or name

English

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publication date

January 2006

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published in

Structure

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volume

14

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page(s)

159-66

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issue

1

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Structural analysis of disease-causing mutations in the P-subfamily of forkhead transcription factors.

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Forkhead transcription factors: key players in development and metabolism

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Dynamic DNA contacts observed in the NMR structure of winged helix protein-DNA complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Solution structure and dynamics of the DNA-binding domain of the adipocyte-transcription factor FREAC-11

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

A helix propensity scale based on experimental studies of peptides and proteins

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Processing of X-ray diffraction data collected in oscillation mode

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Fox's in development and disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Phylogenetic relationships of the Fox (Forkhead) gene family in the Bilateria

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Solution structure of the DNA binding domain of the human forkhead transcription factor AFX (FOXO4)

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Exposing the human nude phenotype.

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Structure of the DNA-binding domains from NFAT, Fos and Jun bound specifically to DNA

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

A forkhead-domain gene is mutated in a severe speech and language disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Structural basis of cell-cell adhesion by cadherins

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome.

1 reference

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7 January 2021

Foxp3 interacts with nuclear factor of activated T cells and NF-kappa B to repress cytokine gene expression and effector functions of T helper cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Specificity of cell-cell adhesion by classical cadherins: Critical role for low-affinity dimerization through beta-strand swapping

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

DNA-binding properties and secondary structural model of the hepatocyte nuclear factor 3/fork head domain

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Constitutive binding of the transcription factor interleukin-2 (IL-2) enhancer binding factor to the IL-2 promoter

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Truncating mutations in FOXC2 cause multiple lymphedema syndromes

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Improved methods for building protein models in electron density maps and the location of errors in these models

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

Multiple hepatocyte-enriched nuclear factors function in the regulation of transthyretin and alpha 1-antitrypsin genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.STR.2005.10.005

7 January 2021

10.1016/J.STR.2005.10.005

Identifiers

DOI

0 references

Fatcat ID

release_mf2w3ljzuncy7kn32msym7ao6q

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/mf2w3ljzuncy7kn32msym7ao6q

24 November 2022