7dkl: Difference between revisions

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== Structural highlights ==

<table><tr><td colspan='2'>[[7dkl]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7DKL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DKL FirstGlance]. <br>

<table><tr><td colspan='2'>[[7dkl]] 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=7DKL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DKL FirstGlance]. <br>

</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=7dkl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dkl OCA], [https://pdbe.org/7dkl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dkl RCSB], [https://www.ebi.ac.uk/pdbsum/7dkl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dkl ProSAT]</span></td></tr>

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.5Å</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=7dkl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dkl OCA], [https://pdbe.org/7dkl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dkl RCSB], [https://www.ebi.ac.uk/pdbsum/7dkl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dkl ProSAT]</span></td></tr>

</table>

== Function ==

[[https://www.uniprot.org/uniprot/DPTOR_HUMAN DPTOR_HUMAN]] Negative regulator of the mTORC1 and mTORC2 signaling pathways. Inhibits the kinase activity of both complexes.<ref>PMID:19446321</ref>

[https://www.uniprot.org/uniprot/DPTOR_HUMAN DPTOR_HUMAN] Negative regulator of the mTORC1 and mTORC2 signaling pathways. Inhibits the kinase activity of both complexes.<ref>PMID:19446321</ref>

== Publication Abstract from PubMed ==

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__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Liu~~, Y F~~]]

[[Category: Liu YF]]

[[Category: Shen~~, X X~~]]

[[Category: Shen XX]]

[[Category: Weng~~, Z F]]~~

[[Category: Weng ZF]]

~~[[Category: Anionic lipid binding protein]]~~

~~[[Category: Dep domain]]~~

~~[[Category: Lipid binding protein]]~~

~~[[Category: Mtor inhibitor]]~~

~~[[Category: Pa binding protein~~]]

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@@ Line 3: / Line 3: @@
 <StructureSection load='7dkl' size='340' side='right'caption='[[7dkl]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[7dkl]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7DKL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DKL FirstGlance]. <br>
+<table><tr><td colspan='2'>[[7dkl]] 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=7DKL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DKL FirstGlance]. <br>
-</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=7dkl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dkl OCA], [https://pdbe.org/7dkl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dkl RCSB], [https://www.ebi.ac.uk/pdbsum/7dkl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dkl ProSAT]</span></td></tr>
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.5&#8491;</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=7dkl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dkl OCA], [https://pdbe.org/7dkl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dkl RCSB], [https://www.ebi.ac.uk/pdbsum/7dkl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dkl ProSAT]</span></td></tr>
 </table>
 == Function ==
-[[https://www.uniprot.org/uniprot/DPTOR_HUMAN DPTOR_HUMAN]] Negative regulator of the mTORC1 and mTORC2 signaling pathways. Inhibits the kinase activity of both complexes.<ref>PMID:19446321</ref>
+[https://www.uniprot.org/uniprot/DPTOR_HUMAN DPTOR_HUMAN] Negative regulator of the mTORC1 and mTORC2 signaling pathways. Inhibits the kinase activity of both complexes.<ref>PMID:19446321</ref>
 <div style="background-color:#fffaf0;">
 == Publication Abstract from PubMed ==
@@ Line 21: / Line 22: @@
 __TOC__
 </StructureSection>
+[[Category: Homo sapiens]]
 [[Category: Large Structures]]
-[[Category: Liu, Y F]]
+[[Category: Liu YF]]
-[[Category: Shen, X X]]
+[[Category: Shen XX]]
-[[Category: Weng, Z F]]
+[[Category: Weng ZF]]
-[[Category: Anionic lipid binding protein]]
-[[Category: Dep domain]]
-[[Category: Lipid binding protein]]
-[[Category: Mtor inhibitor]]
-[[Category: Pa binding protein]]