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Class I HDACs Share a Common Mechanism of Regulation by Inositol Phosphates

Molecular cell, 2013-07, Vol.51 (1), p.57-67

2013

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Insights into the activation mechanism of class I HDAC complexes by inositol phosphates

Nature communications, 2016-04, Vol.7 (1), p.11262-11262, Article 11262

2016

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PROTAC-mediated degradation of class I histone deacetylase enzymes in corepressor complexes

Chemical communications (Cambridge, England), 2020-04, Vol.56 (32), p.4476-4479

2020

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Structural Basis of Receptor Sulfotyrosine Recognition by a CC Chemokine: The N-Terminal Region of CCR3 Bound to CCL11/Eotaxin-1

Structure (London), 2014-11, Vol.22 (11), p.1571-1581

2014

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The MiDAC histone deacetylase complex is essential for embryonic development and has a unique multivalent structure

Nature communications, 2020-06, Vol.11 (1), p.3252-3252, Article 3252

2020

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A variant NuRD complex containing PWWP2A/B excludes MBD2/3 to regulate transcription at active genes

Nature communications, 2018-09, Vol.9 (1), p.3798-14, Article 3798

2018

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Histone deacetylase (HDAC) 1 and 2 are essential for accurate cell division and the pluripotency of embryonic stem cells

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (27), p.9840-9845

2014

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The structure of the core NuRD repression complex provides insights into its interaction with chromatin

eLife, 2016-04, Vol.5, p.e13941-e13941

2016

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An evolving understanding of nuclear receptor coregulator proteins

Journal of molecular endocrinology, 2013-12, Vol.51 (3), p.T23-T36

2013

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Diverse nucleosome Site-Selectivity among histone deacetylase complexes

eLife, 2020-06, Vol.9

2020

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Structural and functional characterization of a cell cycle associated HDAC1/2 complex reveals the structural basis for complex assembly and nucleosome targeting

Nucleic acids research, 2015-02, Vol.43 (4), p.2033

2015

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The IDOL-UBE2D complex mediates sterol-dependent degradation of the LDL receptor

Genes & development, 2011-06, Vol.25 (12), p.1262-1274

2011

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Targeting Class I Histone Deacetylases in a “Complex” Environment

Trends in pharmacological sciences (Regular ed.), 2017-04, Vol.38 (4), p.363-377

2017

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Identification and structural analysis of type I collagen sites in complex with fibronectin fragments

Proceedings of the National Academy of Sciences - PNAS, 2009-03, Vol.106 (11), p.4195-4200

2009

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The topology of chromatin-binding domains in the NuRD deacetylase complex

Nucleic acids research, 2020-12, Vol.48 (22), p.12972

2020

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The Role of the Fibronectin IGD Motif in Stimulating Fibroblast Migration

The Journal of biological chemistry, 2007-12, Vol.282 (49), p.35530-35535

2007

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Synthesis of HDAC Substrate Peptidomimetic Inhibitors Using Fmoc Amino Acids Incorporating Zinc-Binding Groups

Organic letters, 2019-05, Vol.21 (9), p.3178-3182

2019

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Towards an understanding of the structure and function of MTA1

Cancer and metastasis reviews, 2014-12, Vol.33 (4), p.857-867

2014

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A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis

Human molecular genetics, 2019-08, Vol.28 (15), p.2501-2513

2019

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Hydroxamic Acid-Modified Peptide Library Provides Insights into the Molecular Basis for the Substrate Selectivity of HDAC Corepressor Complexes

ACS chemical biology, 2022-09, Vol.17 (9), p.2572-2582

2022

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Recombinant protein expression for structural biology in HEK 293F suspension cells: a novel and accessible approach

Journal of visualized experiments, 2014-10 (92), p.e51897-e51897

2014

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Tyrosine Sulfation Influences the Chemokine Binding Selectivity of Peptides Derived from Chemokine Receptor CCR3

Biochemistry (Easton), 2011-03, Vol.50 (9), p.1524-1534

2011

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The Streptococcal Binding Site in the Gelatin-binding Domain of Fibronectin Is Consistent with a Non-linear Arrangement of Modules

The Journal of biological chemistry, 2010-11, Vol.285 (47), p.36977-36983

2010

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Preparation of recombinant fibronectin fragments for functional and structural studies

Methods in molecular biology (Clifton, N.J.), 2009, Vol.522, p.73

2009

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Gelatin binding to the 8F19F1 module pair of human fibronectin requires site-specific N-glycosylation

FEBS letters, 2005-08, Vol.579 (20), p.4529-4534

2005

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Class I HDACs Share a Common Mechanism of Regulation by Inositol Phosphates

Insights into the activation mechanism of class I HDAC complexes by inositol phosphates

PROTAC-mediated degradation of class I histone deacetylase enzymes in corepressor complexes

Structural Basis of Receptor Sulfotyrosine Recognition by a CC Chemokine: The N-Terminal Region of CCR3 Bound to CCL11/Eotaxin-1

The MiDAC histone deacetylase complex is essential for embryonic development and has a unique multivalent structure

A variant NuRD complex containing PWWP2A/B excludes MBD2/3 to regulate transcription at active genes

Histone deacetylase (HDAC) 1 and 2 are essential for accurate cell division and the pluripotency of embryonic stem cells

The structure of the core NuRD repression complex provides insights into its interaction with chromatin

An evolving understanding of nuclear receptor coregulator proteins

Diverse nucleosome Site-Selectivity among histone deacetylase complexes

Structural and functional characterization of a cell cycle associated HDAC1/2 complex reveals the structural basis for complex assembly and nucleosome targeting

The IDOL-UBE2D complex mediates sterol-dependent degradation of the LDL receptor

Targeting Class I Histone Deacetylases in a “Complex” Environment

Identification and structural analysis of type I collagen sites in complex with fibronectin fragments

The topology of chromatin-binding domains in the NuRD deacetylase complex

The Role of the Fibronectin IGD Motif in Stimulating Fibroblast Migration

Synthesis of HDAC Substrate Peptidomimetic Inhibitors Using Fmoc Amino Acids Incorporating Zinc-Binding Groups

Towards an understanding of the structure and function of MTA1

A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis

Hydroxamic Acid-Modified Peptide Library Provides Insights into the Molecular Basis for the Substrate Selectivity of HDAC Corepressor Complexes

Recombinant protein expression for structural biology in HEK 293F suspension cells: a novel and accessible approach

Tyrosine Sulfation Influences the Chemokine Binding Selectivity of Peptides Derived from Chemokine Receptor CCR3

The Streptococcal Binding Site in the Gelatin-binding Domain of Fibronectin Is Consistent with a Non-linear Arrangement of Modules

Preparation of recombinant fibronectin fragments for functional and structural studies

Gelatin binding to the 8F19F1 module pair of human fibronectin requires site-specific N-glycosylation

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