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5LY1

JMJD2A/ KDM4A COMPLEXED WITH NI(II) AND Macrocyclic PEPTIDE Inhibitor CP2 (13-mer)

Summary for 5LY1
Entry DOI10.2210/pdb5ly1/pdb
Related2OX0 2YBP 4AI9 4BIS 4V2V 5LY2
DescriptorLysine-specific demethylase 4A, CP2, NICKEL (II) ION, ... (8 entities in total)
Functional Keywordsjmjd2a, kdm4a, oxidoreductase, non-heme, iron, 2-oxoglutarate, dioxygenase, oxygenase, double-stranded beta helix, dsbh, facial triad, demethylase, histone, jmjc domain, metal binding protein, epigenetic and transcription regulation, chromatin regulator, hydroxylation
Biological sourceHomo sapiens (Human)
More
Cellular locationNucleus : O75164
Total number of polymer chains5
Total formula weight180504.67
Authors
King, O.N.F.,Chowdhury, R.,Kawamura, A.,Schofield, C.J. (deposition date: 2016-09-23, release date: 2017-04-12, Last modification date: 2024-01-17)
Primary citationKawamura, A.,Munzel, M.,Kojima, T.,Yapp, C.,Bhushan, B.,Goto, Y.,Tumber, A.,Katoh, T.,King, O.N.,Passioura, T.,Walport, L.J.,Hatch, S.B.,Madden, S.,Muller, S.,Brennan, P.E.,Chowdhury, R.,Hopkinson, R.J.,Suga, H.,Schofield, C.J.
Highly selective inhibition of histone demethylases by de novo macrocyclic peptides.
Nat Commun, 8:14773-14773, 2017
Cited by
PubMed: 28382930
DOI: 10.1038/ncomms14773
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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