5etb: Difference between revisions
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5RO:1-(7-METHYL-1~{H}-INDOL-3-YL)ETHANONE'>5RO</scene>, <scene name='pdbligand=NO3:NITRATE+ION'>NO3</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5RO:1-(7-METHYL-1~{H}-INDOL-3-YL)ETHANONE'>5RO</scene>, <scene name='pdbligand=NO3:NITRATE+ION'>NO3</scene></td></tr> | ||
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5eq1|5eq1]]</td></tr> | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5eq1|5eq1]]</td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5etb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5etb OCA], [http://pdbe.org/5etb PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5etb RCSB], [http://www.ebi.ac.uk/pdbsum/5etb PDBsum]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5etb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5etb OCA], [http://pdbe.org/5etb PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5etb RCSB], [http://www.ebi.ac.uk/pdbsum/5etb PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5etb ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | == Function == |
Revision as of 05:35, 13 July 2016
Crystal structure of the human BRPF1 bromodomain in complex with SEED13Crystal structure of the human BRPF1 bromodomain in complex with SEED13
Structural highlights
Function[BRPF1_HUMAN] Component of the MOZ/MORF complex which has a histone H3 acetyltransferase activity. Positively regulates the transcription of RUNX1 and RUNX2.[1] [2] Publication Abstract from PubMedBRPF1 plays a scaffolding role in transcription. We report on fragment screening by high-throughput docking to the BRPF1 bromodomain which resulted in six chemotypes with very favorable ligand efficiency (0.45-0.50 kcal/mol per non-hydrogen atom). Twenty crystal structures of BRPF1/ligand complexes show structural conservation in the acetyllysine binding site, common binding motifs, and unusual interactions (e.g., the replacement of a conserved water molecule). The structural information is useful for the design of chemical probes. Twenty Crystal Structures of Bromodomain and PHD Finger Containing Protein 1 (BRPF1)/Ligand Complexes Reveal Conserved Binding Motifs and Rare Interactions.,Zhu J, Caflisch A J Med Chem. 2016 May 24. PMID:27167503[3] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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