Chelatable trace zinc causes low, irreproducible KDAC8 activity.

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Chelatable trace zinc causes low, irreproducible KDAC8 activity.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Chelatable trace zinc causes low, irreproducible KDAC8 activity.

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Chelatable trace zinc causes low, irreproducible KDAC8 activity.

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Chelatable trace zinc causes low, irreproducible KDAC8 activity.

@en

Chelatable trace zinc causes low, irreproducible KDAC8 activity.

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Chelatable trace zinc causes low, irreproducible KDAC8 activity.

@en

Chelatable trace zinc causes low, irreproducible KDAC8 activity.

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P1476

Chelatable trace zinc causes low, irreproducible KDAC8 activity.

@en

P2093

Brandon J Hylton

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Samantha A Edenfield

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Tasha B Toro

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Terry J Watt

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P2860

Regulation of cellular metabolism by protein lysine acetylation

The many roles of histone deacetylases in development and physiology: implications for disease and therapy

Histone deacetylases as targets for treatment of multiple diseases

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

Structural Studies of Human Histone Deacetylase 8 and Its Site-Specific Variants Complexed with Substrate and Inhibitors † , ‡

Lysine acetylation targets protein complexes and co-regulates major cellular functions

Substrate and functional diversity of lysine acetylation revealed by a proteomics survey

Residue-level interrogation of macromolecular crowding effects on protein stability.

Proteome-wide prediction of acetylation substrates.

Peptide arrays identify isoform-selective substrates for profiling endogenous lysine deacetylase activity

P304

9-14

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P31

scholarly article

P356

10.1016/J.AB.2017.10.024

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P407

English

P478

540-541

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P577

2017-10-31T00:00:00Z

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P698

29100752

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P921

reproducibility

P932

5712482

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