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6H4Z

Crystal structure of human KDM5B in complex with compound 16a

Summary for 6H4Z
Entry DOI10.2210/pdb6h4z/pdb
DescriptorLysine-specific demethylase 5B,Lysine-specific demethylase 5B, ZINC ION, MANGANESE (II) ION, ... (7 entities in total)
Functional Keywordshistone demethylase, inhibitor, transcription, oxidoreductase
Biological sourceHomo sapiens (Human)
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Total number of polymer chains1
Total formula weight57698.66
Authors
Le Bihan, Y.V.,Velupillai, S.,van Montfort, R.L.M. (deposition date: 2018-07-23, release date: 2019-06-12, Last modification date: 2024-01-17)
Primary citationLe Bihan, Y.V.,Lanigan, R.M.,Atrash, B.,McLaughlin, M.G.,Velupillai, S.,Malcolm, A.G.,England, K.S.,Ruda, G.F.,Mok, N.Y.,Tumber, A.,Tomlin, K.,Saville, H.,Shehu, E.,McAndrew, C.,Carmichael, L.,Bennett, J.M.,Jeganathan, F.,Eve, P.,Donovan, A.,Hayes, A.,Wood, F.,Raynaud, F.I.,Fedorov, O.,Brennan, P.E.,Burke, R.,van Montfort, R.L.M.,Rossanese, O.W.,Blagg, J.,Bavetsias, V.
C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-ones: Studies towards the identification of potent, cell penetrant Jumonji C domain containing histone lysine demethylase 4 subfamily (KDM4) inhibitors, compound profiling in cell-based target engagement assays.
Eur.J.Med.Chem., 177:316-337, 2019
Cited by
PubMed: 31158747
DOI: 10.1016/j.ejmech.2019.05.041
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

218500

数据于2024-04-17公开中

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