5kht: Difference between revisions

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-'''Unreleased structure'''
-The entry 5kht is ON HOLD  until Jun 15 2018
+==Crystal structure of the N-terminal fragment of tropomyosin isoform Tpm1.1 at 1.5 A resolution==
+<StructureSection load='5kht' size='340' side='right'caption='[[5kht]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
-Authors: Kostyukova, A.S., Krieger, I., Yoon, Y.-H., Tolkatchev, D., Samatey, F.A.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5kht]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Saccharomyces_cerevisiae_S288C Saccharomyces cerevisiae S288C]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5KHT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5KHT FirstGlance]. <br>
-Description: Crystal structure of the N-terminal fragment of tropomyosin isoform Tpm1.1 at 1.5 A resolution
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.4964&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr>
-[[Category: Tolkatchev, D]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5kht FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5kht OCA], [https://pdbe.org/5kht PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5kht RCSB], [https://www.ebi.ac.uk/pdbsum/5kht PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5kht ProSAT]</span></td></tr>
-[[Category: Kostyukova, A.S]]
+</table>
-[[Category: Yoon, Y.-H]]
+== Disease ==
-[[Category: Krieger, I]]
+[https://www.uniprot.org/uniprot/TPM1_HUMAN TPM1_HUMAN] Left ventricular noncompaction;Familial isolated hypertrophic cardiomyopathy;Familial isolated dilated cardiomyopathy. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.
-[[Category: Samatey, F.A]]
+== Function ==
+[https://www.uniprot.org/uniprot/TPM1_HUMAN TPM1_HUMAN] Binds to actin filaments in muscle and non-muscle cells. Plays a central role, in association with the troponin complex, in the calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with caldesmon. In non-muscle cells is implicated in stabilizing cytoskeleton actin filaments.[https://www.uniprot.org/uniprot/GCN4_YEAST GCN4_YEAST] Is a transcription factor that is responsible for the activation of more than 30 genes required for amino acid or for purine biosynthesis in response to amino acid or purine starvation. Binds and recognize the DNA sequence: 5'-TGA[CG]TCA-3'.
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Saccharomyces cerevisiae S288C]]
+[[Category: Kostyukova AS]]
+[[Category: Krieger I]]
+[[Category: Samatey FA]]
+[[Category: Tolkatchev D]]
+[[Category: Yoon Y-H]]