4uvb
From Proteopedia
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| == Structural highlights == | == Structural highlights == | ||
| <table><tr><td colspan='2'>[[4uvb]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UVB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4UVB FirstGlance]. <br> | <table><tr><td colspan='2'>[[4uvb]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UVB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4UVB FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=D51:[(2R,3S,4R,5R)-5-(6-AMINO-9H-PURIN-9-YL)-3,4-DIHYDROXYTETRAHYDROFURAN-2-YL]METHYL+(2R,3S,4S)-5-[(1R,3S,3AS,7AS)-1-AMINO-1,10,11-TRIMETHYL-4,6-DIOXO-3-PHENYL-2,3,5,6,7,7A-HEXAHYDRO-1H-BENZO[G]PYRROLO[2,1-E]PTERIDIN-8(4H)-YL]-2,3,4-TRIHYDROXYPENTYL+DIHYDROGEN+DIPHOSPHATE'>D51</scene>< | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=D51:[(2R,3S,4R,5R)-5-(6-AMINO-9H-PURIN-9-YL)-3,4-DIHYDROXYTETRAHYDROFURAN-2-YL]METHYL+(2R,3S,4S)-5-[(1R,3S,3AS,7AS)-1-AMINO-1,10,11-TRIMETHYL-4,6-DIOXO-3-PHENYL-2,3,5,6,7,7A-HEXAHYDRO-1H-BENZO[G]PYRROLO[2,1-E]PTERIDIN-8(4H)-YL]-2,3,4-TRIHYDROXYPENTYL+DIHYDROGEN+DIPHOSPHATE'>D51</scene></td></tr> | 
| - | <tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4uv8|4uv8]], [[4uv9|4uv9]], [[4uva|4uva]], [[4uvc|4uvc]]</td></tr> | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4uv8|4uv8]], [[4uv9|4uv9]], [[4uva|4uva]], [[4uvc|4uvc]]</td></tr> | 
| - | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4uvb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4uvb OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4uvb RCSB], [http://www.ebi.ac.uk/pdbsum/4uvb 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=4uvb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4uvb OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4uvb RCSB], [http://www.ebi.ac.uk/pdbsum/4uvb PDBsum]</span></td></tr> | 
| - | <table> | + | </table> | 
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/KDM1A_HUMAN KDM1A_HUMAN]] Histone demethylase that demethylates both 'Lys-4' (H3K4me) and 'Lys-9' (H3K9me) of histone H3, thereby acting as a coactivator or a corepressor, depending on the context. Acts by oxidizing the substrate by FAD to generate the corresponding imine that is subsequently hydrolyzed. Acts as a corepressor by mediating demethylation of H3K4me, a specific tag for epigenetic transcriptional activation. Demethylates both mono- (H3K4me1) and di-methylated (H3K4me2) H3K4me. May play a role in the repression of neuronal genes. Alone, it is unable to demethylate H3K4me on nucleosomes and requires the presence of RCOR1/CoREST to achieve such activity. Also acts as a coactivator of androgen receptor (ANDR)-dependent transcription, by being recruited to ANDR target genes and mediating demethylation of H3K9me, a specific tag for epigenetic transcriptional repression. The presence of PRKCB in ANDR-containing complexes, which mediates phosphorylation of 'Thr-6' of histone H3 (H3T6ph), a specific tag that prevents demethylation H3K4me, prevents H3K4me demethylase activity of KDM1A. Demethylates di-methylated 'Lys-370' of p53/TP53 which prevents interaction of p53/TP53 with TP53BP1 and represses p53/TP53-mediated transcriptional activation. Demethylates and stabilizes the DNA methylase DNMT1. Required for gastrulation during embryogenesis. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development.<ref>PMID:12032298</ref> <ref>PMID:15620353</ref> <ref>PMID:16079795</ref> <ref>PMID:17805299</ref> <ref>PMID:20228790</ref>  [[http://www.uniprot.org/uniprot/RCOR1_HUMAN RCOR1_HUMAN]] Essential component of the BHC complex, a corepressor complex that represses transcription of neuron-specific genes in non-neuronal cells. The BHC complex is recruited at RE1/NRSE sites by REST and acts by deacetylating and demethylating specific sites on histones, thereby acting as a chromatin modifier. In the BHC complex, it serves as a molecular beacon for the recruitment of molecular machinery, including MeCP2 and SUV39H1, that imposes silencing across a chromosomal interval. Plays a central role in demethylation of Lys-4 of histone H3 by promoting demethylase activity of KDM1A on core histones and nucleosomal substrates. It also protects KDM1A from the proteasome. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development and controls hematopoietic differentiation.<ref>PMID:11516394</ref> <ref>PMID:11171972</ref> <ref>PMID:12032298</ref> <ref>PMID:12399542</ref> <ref>PMID:12493763</ref> <ref>PMID:16140033</ref> <ref>PMID:16079794</ref>   | ||
| <div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
| == Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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| __TOC__ | __TOC__ | ||
| </StructureSection> | </StructureSection> | ||
| - | [[Category: Botrugno, O | + | [[Category: Botrugno, O]] | 
| - | [[Category: Cappa, A | + | [[Category: Cappa, A]] | 
| - | [[Category: Ciossani, G | + | [[Category: Ciossani, G]] | 
| - | [[Category: Dessanti, P | + | [[Category: Dessanti, P]] | 
| - | [[Category: Mai, A | + | [[Category: Mai, A]] | 
| - | [[Category: Mattevi, A | + | [[Category: Mattevi, A]] | 
| - | [[Category: Mercurio, C | + | [[Category: Mercurio, C]] | 
| - | [[Category: Meroni, G | + | [[Category: Meroni, G]] | 
| - | [[Category: Minucci, S | + | [[Category: Minucci, S]] | 
| - | [[Category: Thaler, F | + | [[Category: Thaler, F]] | 
| - | [[Category: Tortorici, M | + | [[Category: Tortorici, M]] | 
| - | [[Category: Trifiro, P | + | [[Category: Trifiro, P]] | 
| - | [[Category: Valente, S | + | [[Category: Valente, S]] | 
| - | [[Category: Varasi, M | + | [[Category: Varasi, M]] | 
| - | [[Category: Vianello, P | + | [[Category: Vianello, P]] | 
| - | [[Category: Villa, M | + | [[Category: Villa, M]] | 
| [[Category: Covalent inhibitor]] | [[Category: Covalent inhibitor]] | ||
| [[Category: Transcription]] | [[Category: Transcription]] | ||
Revision as of 16:30, 25 December 2014
LSD1(KDM1A)-CoREST in complex with 1-Methyl-Tranylcypromine (1S,2R)
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Categories: Botrugno, O | Cappa, A | Ciossani, G | Dessanti, P | Mai, A | Mattevi, A | Mercurio, C | Meroni, G | Minucci, S | Thaler, F | Tortorici, M | Trifiro, P | Valente, S | Varasi, M | Vianello, P | Villa, M | Covalent inhibitor | Transcription
