6raa: Difference between revisions

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~~'''Unreleased structure'''~~

~~The entry~~ 6raa is ~~ON HOLD~~

==CLK1 Kinase domain with bound imidazopyridin inhibitor TP003==

== Structural highlights ==

<table><tr><td colspan='2'>[[6raa]] 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=6RAA OCA]. For a guided tour on the structure components use [https://proteopedia.org/fgij/fg.htm?mol=6RAA FirstGlance].

</td></tr><tr id='method'><td class="sblockLbl">[[Empirical_models|Method:]]</td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr>

<tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=JWN:4-[2-methyl-1-(4-methylpiperazin-1-yl)-1-oxidanylidene-propan-2-yl]-~{N}-(6-pyridin-4-ylimidazo[1,2-a]pyridin-2-yl)benzamide'>JWN</scene></td></tr>

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[https://proteopedia.org/fgij/fg.htm?mol=6raa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6raa OCA], [https://pdbe.org/6raa PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6raa RCSB], [https://www.ebi.ac.uk/pdbsum/6raa PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6raa ProSAT]</td></tr>

</table>

== Function ==

[https://www.uniprot.org/uniprot/CLK1_HUMAN CLK1_HUMAN] Dual specificity kinase acting on both serine/threonine and tyrosine-containing substrates. Phosphorylates serine- and arginine-rich (SR) proteins of the spliceosomal complex and may be a constituent of a network of regulatory mechanisms that enable SR proteins to control RNA splicing. Phosphorylates: SRSF1, SRSF3 and PTPN1. Regulates the alternative splicing of tissue factor (F3) pre-mRNA in endothelial cells and adenovirus E1A pre-mRNA.<ref>PMID:10480872</ref> <ref>PMID:19168442</ref>

~~Authors: Schroeder, M., Arrowsmith, C., Knapp, S., Bountra, C., Edwards, A., Structural Genomics Consortium (SGC)~~

==See Also==

*[[Dual specificity protein kinase 3D structures|Dual specificity protein kinase 3D structures]]

~~Description: CLK1 Kinase domain with bound imidazopyridin inhibitor TP003~~

== References ==

[[Category: ~~Unreleased Structures~~]]

[[Category: ~~Arrowsmith, C~~]]

__TOC__

[[Category: ~~Schroeder, M~~]]

</StructureSection>

[[Category: ~~Knapp, S~~]]

[[Category: Homo sapiens]]

[[Category: ~~Structural Genomics Consortium (Sgc)~~]]

[[Category: Large Structures]]

[[Category: ~~Edwards, A~~]]

[[Category: Arrowsmith C]]

[[Category: ~~Bountra, C~~]]

[[Category: Bountra C]]

[[Category: Edwards A]]

[[Category: Knapp S]]

[[Category: Schroeder M]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 6raa is ON HOLD
+==CLK1 Kinase domain with bound imidazopyridin inhibitor TP003==
+<StructureSection load='6raa' size='340' side='right'caption='[[6raa]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6raa]] 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=6RAA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6RAA FirstGlance]. <br>
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
+<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=JWN:4-[2-methyl-1-(4-methylpiperazin-1-yl)-1-oxidanylidene-propan-2-yl]-~{N}-(6-pyridin-4-ylimidazo[1,2-a]pyridin-2-yl)benzamide'>JWN</scene></td></tr>
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6raa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6raa OCA], [https://pdbe.org/6raa PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6raa RCSB], [https://www.ebi.ac.uk/pdbsum/6raa PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6raa ProSAT]</span></td></tr>
+</table>
+== Function ==
+[https://www.uniprot.org/uniprot/CLK1_HUMAN CLK1_HUMAN] Dual specificity kinase acting on both serine/threonine and tyrosine-containing substrates. Phosphorylates serine- and arginine-rich (SR) proteins of the spliceosomal complex and may be a constituent of a network of regulatory mechanisms that enable SR proteins to control RNA splicing. Phosphorylates: SRSF1, SRSF3 and PTPN1. Regulates the alternative splicing of tissue factor (F3) pre-mRNA in endothelial cells and adenovirus E1A pre-mRNA.<ref>PMID:10480872</ref> <ref>PMID:19168442</ref>
-Authors: Schroeder, M., Arrowsmith, C., Knapp, S., Bountra, C., Edwards, A., Structural Genomics Consortium (SGC)
+==See Also==
+*[[Dual specificity protein kinase 3D structures|Dual specificity protein kinase 3D structures]]
-Description: CLK1 Kinase domain with bound imidazopyridin inhibitor TP003
+== References ==
-[[Category: Unreleased Structures]]
+<references/>
-[[Category: Arrowsmith, C]]
+__TOC__
-[[Category: Schroeder, M]]
+</StructureSection>
-[[Category: Knapp, S]]
+[[Category: Homo sapiens]]
-[[Category: Structural Genomics Consortium (Sgc)]]
+[[Category: Large Structures]]
-[[Category: Edwards, A]]
+[[Category: Arrowsmith C]]
-[[Category: Bountra, C]]
+[[Category: Bountra C]]
+[[Category: Edwards A]]
+[[Category: Knapp S]]
+[[Category: Schroeder M]]