4fmw: Difference between revisions

Line 1:

==Crystal structure of methyltransferase domain of human RNA (guanine-9-) methyltransferase domain containing protein 2==

== Structural highlights ==

<table><tr><td colspan='2'>[[4fmw]] is a 2 chain structure with sequence from [http://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 guided tour on the structure components use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4FMW FirstGlance].

<table><tr><td colspan='2'>[[4fmw]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4FMW OCA]. For a guided tour on the structure components use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4FMW FirstGlance].

</td></tr><tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</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='NonStdRes'><td class="sblockLbl">[[Non-Standard_Residue|NonStd Res:]]</td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>

<tr id='gene'><td class="sblockLbl">[[Gene|Gene:]]</td><td class="sblockDat">RG9MTD2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 ~~Homo sapiens~~])</td></tr>

<tr id='gene'><td class="sblockLbl">[[Gene|Gene:]]</td><td class="sblockDat">RG9MTD2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4fmw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fmw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4fmw RCSB], [http://www.ebi.ac.uk/pdbsum/4fmw PDBsum]</td></tr>

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4fmw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fmw OCA], [http://pdbe.org/4fmw PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4fmw RCSB], [http://www.ebi.ac.uk/pdbsum/4fmw PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4fmw ProSAT]</td></tr>

</table>

== Disease ==

[[http://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 ==

[[http://www.uniprot.org/uniprot/~~RG9D2_HUMAN RG9D2_HUMAN~~]] ~~Probable~~ RNA methyltransferase ~~(By similarity)~~.

[[http://www.uniprot.org/uniprot/TM10A_HUMAN TM10A_HUMAN]] RNA methyltransferase.<ref>PMID:25053765</ref>

== References ==

__TOC__

</StructureSection>

[[Category: ~~Homo sapiens~~]]

[[Category: Human]]

[[Category: Arrowsmith, C H]]

[[Category: Bountra, C]]

Navigation menu

Page actions

Page actions

Personal tools

Navigation

Search

Tools

@@ Line 1: / Line 1: @@
 ==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]] 2.00&Aring;' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[4fmw]] is a 2 chain structure with sequence from [http://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 [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4FMW FirstGlance]. <br>
+<table><tr><td colspan='2'>[[4fmw]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. 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 [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4FMW FirstGlance]. <br>
 </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</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='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>
-<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">RG9MTD2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr>
+<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">RG9MTD2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
-<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4fmw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fmw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4fmw RCSB], [http://www.ebi.ac.uk/pdbsum/4fmw PDBsum]</span></td></tr>
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4fmw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fmw OCA], [http://pdbe.org/4fmw PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4fmw RCSB], [http://www.ebi.ac.uk/pdbsum/4fmw PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4fmw ProSAT]</span></td></tr>
 </table>
+== Disease ==
+[[http://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 ==
-[[http://www.uniprot.org/uniprot/RG9D2_HUMAN RG9D2_HUMAN]] Probable RNA methyltransferase (By similarity).
+[[http://www.uniprot.org/uniprot/TM10A_HUMAN TM10A_HUMAN]] RNA methyltransferase.<ref>PMID:25053765</ref>
+== References ==
+<references/>
 __TOC__
 </StructureSection>
-[[Category: Homo sapiens]]
+[[Category: Human]]
 [[Category: Arrowsmith, C H]]
 [[Category: Bountra, C]]