(Q43730398)

English

Mapping the unique activation function 3 in the progesterone B-receptor upstream segment. Two LXXLL motifs and a tryptophan residue are required for activity

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scholarly article

1 reference

Europe PubMed Central

26 November 2017

Mapping the unique activation function 3 in the progesterone B-receptor upstream segment. Two LXXLL motifs and a tryptophan residue are required for activity (English)

1 reference

Europe PubMed Central

26 November 2017

author name string

Tung L

1

1 reference

Europe PubMed Central

26 November 2017

Shen T

2

1 reference

Europe PubMed Central

26 November 2017

Abel MG

3

1 reference

Europe PubMed Central

26 November 2017

Powell RL

4

1 reference

Europe PubMed Central

26 November 2017

Takimoto GS

5

1 reference

Europe PubMed Central

26 November 2017

Sartorius CA

6

1 reference

Europe PubMed Central

26 November 2017

Horwitz KB

7

1 reference

Europe PubMed Central

26 November 2017

language of work or name

0 references

publication date

23 August 2001

1 reference

Europe PubMed Central

26 November 2017

number of pages

9

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based on heuristic

inferred from page(s)

Journal of Biological Chemistry

1 reference

Europe PubMed Central

26 November 2017

276

1 reference

Europe PubMed Central

26 November 2017

39843-39851

1 reference

Europe PubMed Central

26 November 2017

43

1 reference

Europe PubMed Central

26 November 2017

Nuclear receptor coregulators: cellular and molecular biology

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Nuclear receptor coactivators: multiple enzymes, multiple complexes, multiple functions.

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Progesterone receptor coactivators

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A signature motif in transcriptional co-activators mediates binding to nuclear receptors

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A third transactivation function (AF3) of human progesterone receptors located in the unique N-terminal segment of the B-isoform

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The progesterone antagonist RU486 acquires agonist activity upon stimulation of cAMP signaling pathways

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The leucine zippers of c-fos and c-jun for progesterone receptor dimerization: A-dominance in the A/B heterodimer

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An N-terminal inhibitory function, IF, suppresses transcription by the A-isoform but not the B-isoform of human progesterone receptors

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Mice lacking progesterone receptor exhibit pleiotropic reproductive abnormalities

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Reproductive phenotpes of the progesterone receptor null mutant mouse

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Transgenic mice carrying an imbalance in the native ratio of A to B forms of progesterone receptor exhibit developmental abnormalities in mammary glands

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Impact of progesterone receptor on cell-fate decisions during mammary gland development

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The N-terminal region of human progesterone B-receptors: biophysical and biochemical comparison to A-receptors

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Core LXXLL motif sequences in CREB-binding protein, SRC1, and RIP140 define affinity and selectivity for steroid and retinoid receptors

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Role of phosphorylation on DNA binding and transcriptional functions of human progesterone receptors

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Three amino acid substitutions selectively disrupt the activation but not the repression function of the glucocorticoid receptor N terminus.

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The unique tryptophan residue of the vitamin D receptor is critical for ligand binding and transcriptional activation

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Dissection of the LXXLL nuclear receptor-coactivator interaction motif using combinatorial peptide libraries: discovery of peptide antagonists of estrogen receptors alpha and beta

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Allosteric effects of DNA on transcriptional regulators

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Ligand-dependent, transcriptionally productive association of the amino- and carboxyl-terminal regions of a steroid hormone nuclear receptor

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Interaction between the amino- and carboxyl-terminal regions of the rat androgen receptor modulates transcriptional activity and is influenced by nuclear receptor coactivators.

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Hormone-dependent interaction between the amino- and carboxyl-terminal domains of progesterone receptor in vitro and in vivo.

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Role of important hydrophobic amino acids in the interaction between the glucocorticoid receptor tau 1-core activation domain and target factors

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The AF1 and AF2 domains of the androgen receptor interact with distinct regions of SRC1

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Differential regulation of glucocorticoid receptor transcriptional activation via AF-1-associated proteins

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The human homologue of the yeast DNA repair and TFIIH regulator MMS19 is an AF-1-specific coactivator of estrogen receptor

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FXXLF and WXXLF sequences mediate the NH2-terminal interaction with the ligand binding domain of the androgen receptor

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Influence of a steroid receptor DNA-binding domain on transcriptional regulatory functions

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Delineation of a small region within the major transactivation domain of the human glucocorticoid receptor that mediates transactivation of gene expression

1 reference

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Identification of a phosphorylation site in the hinge region of the human progesterone receptor and additional amino-terminal phosphorylation sites

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Activation function 1 of retinoic acid receptor beta 2 is an acidic activator resembling VP16.

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Solution Structure of the KIX Domain of CBP Bound to the Transactivation Domain of CREB: A Model for Activator:Coactivator Interactions

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Structural characterization of a minimal functional transactivation domain from the human glucocorticoid receptor

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Transcriptional activation domain of the herpesvirus protein VP16 becomes conformationally constrained upon interaction with basal transcription factors.

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The transcriptional activator GCN4 contains multiple activation domains that are critically dependent on hydrophobic amino acids

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Analysis of an activator:coactivator complex reveals an essential role for secondary structure in transcriptional activation

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Identification of seven hydrophobic clusters in GCN4 making redundant contributions to transcriptional activation

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Role of hydrophobic amino acid clusters in the transactivation activity of the human glucocorticoid receptor

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Local Structural Elements in the Mostly Unstructured Transcriptional Activation Domain of Human p53

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Mutations in the glucocorticoid receptor DNA-binding domain mimic an allosteric effect of DNA 1 1Edited by P. E. Wright

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Transcription in yeast activated by a putative amphipathic α helix linked to a DNA binding unit

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The human progesterone receptor A-form functions as a transcriptional modulator of mineralocorticoid receptor transcriptional activity

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Differential expression of uterine progesterone receptor forms A and B during the menstrual cycle

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Progesterone receptor isoforms, PR-B and PR-A, in breast cancer: correlations with clinicopathologic tumor parameters and expression of AP-1 factors

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The N-terminal region of the human progesterone A-receptor. Structural analysis and the influence of the DNA binding domain

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The production of antibodies against the conserved cysteine region of steroid receptors and their use in characterizing the avian progesterone receptor

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Immunologic analysis of human breast cancer progesterone receptors. 1. Immunoaffinity purification of transformed receptors and production of monoclonal antibodies

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Mapping and characterization of the functional domains responsible for the differential activity of the A and B isoforms of the human progesterone receptor

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Activation Function 2 in the Human Androgen Receptor Ligand Binding Domain Mediates Interdomain Communication with the NH2-terminal Domain

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The conformation of the glucocorticoid receptor af1/tau1 domain induced by osmolyte binds co-regulatory proteins

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Modulation of transcription factor Ets-1 DNA binding: DNA-induced unfolding of an alpha helix

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Role of acidic and phosphorylated residues in gene activation by the glucocorticoid receptor

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Identifiers

10.1074/JBC.M106843200

1 reference

Europe PubMed Central

26 November 2017

1 reference

Europe PubMed Central

26 November 2017

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