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4fmw
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 4fmw is ON HOLD Authors: DONG,A., ZENG,H., LOPPNAU,P., TEMPEL,W., Bountra,C., WEIGELT,J., Arrowsmith,C.H., EDWARDS,A.M., WU,H., Structural Genomics ...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of methyltransferase domain of human RNA (guanine-9-) methyltransferase domain containing protein 2== | |
| - | + | <StructureSection load='4fmw' size='340' side='right'caption='[[4fmw]], [[Resolution|resolution]] 2.00Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[4fmw]] is a 2 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=4FMW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4FMW FirstGlance]. <br> | |
| - | + | </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=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</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=4fmw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fmw OCA], [https://pdbe.org/4fmw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4fmw RCSB], [https://www.ebi.ac.uk/pdbsum/4fmw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4fmw ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/TM10A_HUMAN TM10A_HUMAN] Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/TM10A_HUMAN TM10A_HUMAN] RNA methyltransferase.<ref>PMID:25053765</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Arrowsmith CH]] | ||
| + | [[Category: Bountra C]] | ||
| + | [[Category: Dong A]] | ||
| + | [[Category: Edwards AM]] | ||
| + | [[Category: Loppnau P]] | ||
| + | [[Category: Tempel W]] | ||
| + | [[Category: Weigelt J]] | ||
| + | [[Category: Wu H]] | ||
| + | [[Category: Zeng H]] | ||
Current revision
Crystal structure of methyltransferase domain of human RNA (guanine-9-) methyltransferase domain containing protein 2
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Categories: Homo sapiens | Large Structures | Arrowsmith CH | Bountra C | Dong A | Edwards AM | Loppnau P | Tempel W | Weigelt J | Wu H | Zeng H
