4er3

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(New page: '''Unreleased structure''' The entry 4er3 is ON HOLD Authors: Wernimont, A.K., Tempel, W., Yu, W., Scopton, A., Li, Y., Nguyen, K.T., Federation, A., Marineau, J., Qi, J., Vedadi, M., B...)
Current revision (11:05, 1 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 4er3 is ON HOLD
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==Crystal Structure of Human DOT1L in complex with inhibitor EPZ004777==
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<StructureSection load='4er3' size='340' side='right'caption='[[4er3]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4er3]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ER3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4ER3 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.4&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0QK:7-{5-[(3-{[(4-TERT-BUTYLPHENYL)CARBAMOYL]AMINO}PROPYL)(PROPAN-2-YL)AMINO]-5-DEOXY-BETA-D-RIBOFURANOSYL}-7H-PYRROLO[2,3-D]PYRIMIDIN-4-AMINE'>0QK</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4er3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4er3 OCA], [https://pdbe.org/4er3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4er3 RCSB], [https://www.ebi.ac.uk/pdbsum/4er3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4er3 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/DOT1L_HUMAN DOT1L_HUMAN] Histone methyltransferase. Methylates 'Lys-79' of histone H3. Nucleosomes are preferred as substrate compared to free histones. Binds to DNA.
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Authors: Wernimont, A.K., Tempel, W., Yu, W., Scopton, A., Li, Y., Nguyen, K.T., Federation, A., Marineau, J., Qi, J., Vedadi, M., Bradner, J.E., Schapira, M., Arrowsmith, C.H., Edwards, A.M., Bountra, C., Brown, P.J., Structural Genomics Consortium (SGC)
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==See Also==
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*[[Histone methyltransferase 3D structures|Histone methyltransferase 3D structures]]
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Description: Crystal Structure of Human DOT1L in complex with inhibitor EPZ004777
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Arrowsmith CH]]
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[[Category: Bountra C]]
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[[Category: Bradner JE]]
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[[Category: Brown PJ]]
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[[Category: Edwards AM]]
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[[Category: Federation A]]
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[[Category: Li Y]]
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[[Category: Marineau J]]
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[[Category: Nguyen KT]]
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[[Category: Qi J]]
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[[Category: Schapira M]]
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[[Category: Scopton A]]
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[[Category: Tempel W]]
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[[Category: Vedadi M]]
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[[Category: Wernimont AK]]
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[[Category: Yu W]]

Current revision

Crystal Structure of Human DOT1L in complex with inhibitor EPZ004777

PDB ID 4er3

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