4jlg
From Proteopedia
(Difference between revisions)
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- | + | ==SETD7 in complex with inhibitor (R)-PFI-2 and S-adenosyl-methionine== | |
- | + | <StructureSection load='4jlg' size='340' side='right' caption='[[4jlg]], [[Resolution|resolution]] 1.90Å' scene=''> | |
- | + | == Structural highlights == | |
- | ==Function== | + | <table><tr><td colspan='2'>[[4jlg]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4JLG OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4JLG FirstGlance]. <br> |
+ | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=1L8:8-FLUORO-N-{(2R)-1-OXO-1-(PYRROLIDIN-1-YL)-3-[3-(TRIFLUOROMETHYL)PHENYL]PROPAN-2-YL}-1,2,3,4-TETRAHYDROISOQUINOLINE-6-SULFONAMIDE'>1L8</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene>, <scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</scene></td></tr> | ||
+ | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">SETD7, KIAA1717, KMT7, SET7, SET9 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> | ||
+ | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Histone-lysine_N-methyltransferase Histone-lysine N-methyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.1.1.43 2.1.1.43] </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=4jlg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4jlg OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4jlg RCSB], [http://www.ebi.ac.uk/pdbsum/4jlg PDBsum]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
[[http://www.uniprot.org/uniprot/SETD7_HUMAN SETD7_HUMAN]] Histone methyltransferase that specifically monomethylates 'Lys-4' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. Plays a central role in the transcriptional activation of genes such as collagenase or insulin. Recruited by IPF1/PDX-1 to the insulin promoter, leading to activate transcription. Has also methyltransferase activity toward non-histone proteins such as p53/TP53, TAF10, and possibly TAF7 by recognizing and binding the [KR]-[STA]-K in substrate proteins. Monomethylates 'Lys-189' of TAF10, leading to increase the affinity of TAF10 for RNA polymerase II. Monomethylates 'Lys-372' of p53/TP53, stabilizing p53/TP53 and increasing p53/TP53-mediated transcriptional activation.<ref>PMID:12588998</ref> <ref>PMID:15099517</ref> <ref>PMID:16141209</ref> <ref>PMID:17108971</ref> <ref>PMID:12540855</ref> <ref>PMID:15525938</ref> | [[http://www.uniprot.org/uniprot/SETD7_HUMAN SETD7_HUMAN]] Histone methyltransferase that specifically monomethylates 'Lys-4' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. Plays a central role in the transcriptional activation of genes such as collagenase or insulin. Recruited by IPF1/PDX-1 to the insulin promoter, leading to activate transcription. Has also methyltransferase activity toward non-histone proteins such as p53/TP53, TAF10, and possibly TAF7 by recognizing and binding the [KR]-[STA]-K in substrate proteins. Monomethylates 'Lys-189' of TAF10, leading to increase the affinity of TAF10 for RNA polymerase II. Monomethylates 'Lys-372' of p53/TP53, stabilizing p53/TP53 and increasing p53/TP53-mediated transcriptional activation.<ref>PMID:12588998</ref> <ref>PMID:15099517</ref> <ref>PMID:16141209</ref> <ref>PMID:17108971</ref> <ref>PMID:12540855</ref> <ref>PMID:15525938</ref> | ||
- | |||
- | ==About this Structure== | ||
- | [[4jlg]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4JLG OCA]. | ||
==See Also== | ==See Also== | ||
*[[Histone methyltransferase|Histone methyltransferase]] | *[[Histone methyltransferase|Histone methyltransferase]] | ||
- | + | == References == | |
- | == | + | <references/> |
- | <references | + | __TOC__ |
+ | </StructureSection> | ||
[[Category: Histone-lysine N-methyltransferase]] | [[Category: Histone-lysine N-methyltransferase]] | ||
[[Category: Human]] | [[Category: Human]] | ||
- | [[Category: Arrowsmith, C H | + | [[Category: Arrowsmith, C H]] |
- | [[Category: Bakkouri, M El | + | [[Category: Bakkouri, M El]] |
- | [[Category: Barsyte, D | + | [[Category: Barsyte, D]] |
- | [[Category: Bountra, C | + | [[Category: Bountra, C]] |
- | [[Category: Brown, P J | + | [[Category: Brown, P J]] |
- | [[Category: Bunnage, M | + | [[Category: Bunnage, M]] |
- | [[Category: Dong, A | + | [[Category: Dong, A]] |
- | [[Category: Edwards, A M | + | [[Category: Edwards, A M]] |
- | [[Category: Owen, D | + | [[Category: Owen, D]] |
- | [[Category: | + | [[Category: Structural genomic]] |
- | [[Category: Tatlock, J | + | [[Category: Tatlock, J]] |
- | [[Category: Vedadi, M | + | [[Category: Vedadi, M]] |
- | [[Category: Wu, H | + | [[Category: Wu, H]] |
- | [[Category: Zeng, H | + | [[Category: Zeng, H]] |
[[Category: Histone lysine methyltransferase]] | [[Category: Histone lysine methyltransferase]] | ||
[[Category: Histone modification]] | [[Category: Histone modification]] | ||
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[[Category: Set domain]] | [[Category: Set domain]] | ||
[[Category: Sgc]] | [[Category: Sgc]] | ||
- | [[Category: Structural genomic]] | ||
- | [[Category: Structural genomics consortium]] | ||
[[Category: Transcription regulation]] | [[Category: Transcription regulation]] | ||
[[Category: Transferase-transferase inhibitor complex]] | [[Category: Transferase-transferase inhibitor complex]] |
Revision as of 13:49, 24 December 2014
SETD7 in complex with inhibitor (R)-PFI-2 and S-adenosyl-methionine
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Categories: Histone-lysine N-methyltransferase | Human | Arrowsmith, C H | Bakkouri, M El | Barsyte, D | Bountra, C | Brown, P J | Bunnage, M | Dong, A | Edwards, A M | Owen, D | Structural genomic | Tatlock, J | Vedadi, M | Wu, H | Zeng, H | Histone lysine methyltransferase | Histone modification | Inhibitor | Methyltransferase | S-adenosyl-l-methionine | Set domain | Sgc | Transcription regulation | Transferase-transferase inhibitor complex