6eyz - Revision history

OCA at 08:28, 17 January 2018

OCA — Wed, 17 Jan 2018 08:28:54 GMT

←Older revision		Revision as of 08:28, 17 January 2018
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	<StructureSection load='6eyz' size='340' side='right' caption='[[6eyz]], [[Resolution\|resolution]] 2.20Å' scene=''>		<StructureSection load='6eyz' size='340' side='right' caption='[[6eyz]], [[Resolution\|resolution]] 2.20Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[6eyz]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EYZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EYZ FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[6eyz]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EYZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EYZ FirstGlance]. <br>
	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=C5W:2-methoxy-5-[4-[5-[(4-propan-2-ylpiperazin-1-yl)methyl]-1,3-oxazol-2-yl]-2~{H}-indazol-6-yl]pyridine-3-carboxylic+acid'>C5W</scene></td></tr>		</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=C5W:2-methoxy-5-[4-[5-[(4-propan-2-ylpiperazin-1-yl)methyl]-1,3-oxazol-2-yl]-2~{H}-indazol-6-yl]pyridine-3-carboxylic+acid'>C5W</scene></td></tr>
		+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">Pik3cd ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 LK3 transgenic mice])</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=6eyz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6eyz OCA], [http://pdbe.org/6eyz PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6eyz RCSB], [http://www.ebi.ac.uk/pdbsum/6eyz PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6eyz ProSAT]</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=6eyz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6eyz OCA], [http://pdbe.org/6eyz PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6eyz RCSB], [http://www.ebi.ac.uk/pdbsum/6eyz PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6eyz ProSAT]</span></td></tr>
	</table>		</table>
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	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Lk3 transgenic mice]]
	[[Category: Campos, S]]		[[Category: Campos, S]]
	[[Category: Convery, M A]]		[[Category: Convery, M A]]

OCA at 06:28, 20 December 2017

OCA — Wed, 20 Dec 2017 06:28:29 GMT

←Older revision		Revision as of 06:28, 20 December 2017
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-	'''Unreleased structure'''

-	~~The entry~~ 6eyz is ~~ON HOLD until Paper~~ Publication	+	==PI3 kinase delta in complex with 4-Fluorophenyl 5-(4-(5-((4-isopropylpiperazin-1-yl)methyl)oxazol-2-yl)-1H-indazol-6-yl)-2-methoxynicotinate==
		+	<StructureSection load='6eyz' size='340' side='right' caption='[[6eyz]], [[Resolution\|resolution]] 2.20Å' scene=''>
		+	== Structural highlights ==
		+	<table><tr><td colspan='2'>[[6eyz]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EYZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EYZ FirstGlance]. <br>
		+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=C5W:2-methoxy-5-[4-[5-[(4-propan-2-ylpiperazin-1-yl)methyl]-1,3-oxazol-2-yl]-2~{H}-indazol-6-yl]pyridine-3-carboxylic+acid'>C5W</scene></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=6eyz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6eyz OCA], [http://pdbe.org/6eyz PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6eyz RCSB], [http://www.ebi.ac.uk/pdbsum/6eyz PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6eyz ProSAT]</span></td></tr>
		+	</table>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Selective covalent inhibition of kinases by targeting poorly conserved cysteines has proven highly fruitful to date in the development of chemical probes and approved drugs. However, this approach is limited to ~200 kinases possessing such a cysteine near the ATP-binding pocket. Herein, we report a novel approach to achieve selective, irreversible kinase inhibition, by targeting the conserved catalytic lysine residue. We have illustrated our approach by developing selective, covalent PI3Kdelta inhibitors that exhibit nanomolar potency in cellular assays, and a duration of action >48 h in CD4+ T cells. Despite conservation of the lysine residue throughout the kinome, the lead compound shows high levels of selectivity over a selection of lipid and protein kinases in biochemical assays, as well as covalent binding to very few off-target proteins in live-cell proteomic studies. We anticipate this approach could offer an alternative general strategy, to targeting non-conserved cysteines, for the development of selective covalent kinase inhibitors.

-	~~Authors~~:	+	Selectively targeting the kinome-conserved lysine of PI3Kdelta as a general approach to covalent kinase inhibition.,Dalton SE, Dittus L, Thomas DA, Convery MA, Nunes J, Bush JT, Evans JP, Werner T, Bantscheff M, Murphy JA, Campos S J Am Chem Soc. 2017 Dec 12. doi: 10.1021/jacs.7b08979. PMID:29232121<ref>PMID:29232121</ref>

-	~~Description~~:	+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
-	[[Category: ~~Unreleased Structures~~]]	+	</div>
		+	<div class="pdbe-citations 6eyz" style="background-color:#fffaf0;"></div>
		+	== References ==
		+	<references/>
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Campos, S]]
		+	[[Category: Convery, M A]]
		+	[[Category: Dalton, S E]]
		+	[[Category: Complex]]
		+	[[Category: Covalent inhibitor]]
		+	[[Category: Drug discovery]]
		+	[[Category: Kinase]]
		+	[[Category: Transferase]]

OCA at 05:12, 29 November 2017

OCA — Wed, 29 Nov 2017 05:12:02 GMT

←Older revision		Revision as of 05:12, 29 November 2017
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	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 6eyz is ON HOLD	+	The entry 6eyz is ON HOLD until Paper Publication

	Authors:		Authors:

OCA: Protected "6eyz" [edit=sysop:move=sysop]

OCA — Wed, 22 Nov 2017 06:43:33 GMT

Protected "6eyz" [edit=sysop:move=sysop]

←Older revision

Revision as of 06:43, 22 November 2017

OCA: New page: '''Unreleased structure''' The entry 6eyz is ON HOLD Authors: Description: Category: Unreleased Structures

OCA — Wed, 22 Nov 2017 06:43:32 GMT

New page: '''Unreleased structure''' The entry 6eyz is ON HOLD Authors: Description: Category: Unreleased Structures

New page

'''Unreleased structure'''

The entry 6eyz is ON HOLD

Authors:

Description:
[[Category: Unreleased Structures]]