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4pwy
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 4pwy is ON HOLD Authors: Tempel, W., Hong, B.S., Walker, J.R., Li, Y., Bountra, C., Arrowsmith, C.H., Edwards, A.M., Brown, P.J., Structural Genomic...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of a Calmodulin-lysine N-methyltransferase fragment== | |
| - | + | <StructureSection load='4pwy' size='340' side='right'caption='[[4pwy]], [[Resolution|resolution]] 1.90Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[4pwy]] 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=4PWY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4PWY 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]] 1.9Å</td></tr> | |
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MLI:MALONATE+ION'>MLI</scene>, <scene name='pdbligand=SAH:S-ADENOSYL-L-HOMOCYSTEINE'>SAH</scene>, <scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</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=4pwy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4pwy OCA], [https://pdbe.org/4pwy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4pwy RCSB], [https://www.ebi.ac.uk/pdbsum/4pwy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4pwy ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN] Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN] Catalyzes the trimethylation of 'Lys-116' in calmodulin.<ref>PMID:20975703</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Arrowsmith CH]] | ||
| + | [[Category: Bountra C]] | ||
| + | [[Category: Brown PJ]] | ||
| + | [[Category: Edwards AM]] | ||
| + | [[Category: Hong BS]] | ||
| + | [[Category: Li Y]] | ||
| + | [[Category: Tempel W]] | ||
| + | [[Category: Walker JR]] | ||
Current revision
Crystal structure of a Calmodulin-lysine N-methyltransferase fragment
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Categories: Homo sapiens | Large Structures | Arrowsmith CH | Bountra C | Brown PJ | Edwards AM | Hong BS | Li Y | Tempel W | Walker JR
