8qsw: Difference between revisions

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~~'''Unreleased structure'''~~

~~The entry 8qsw is ON HOLD~~

==Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease==

~~Authors: Jeyaprakash, A.A., Abad, M.A.~~

== Structural highlights ==

<table><tr><td colspan='2'>[[8qsw]] 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=8QSW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8QSW FirstGlance]. <br>

~~Description:~~ Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.5Å</td></tr>

[[Category: ~~Unreleased~~ Structures]]

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8qsw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8qsw OCA], [https://pdbe.org/8qsw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8qsw RCSB], [https://www.ebi.ac.uk/pdbsum/8qsw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8qsw ProSAT]</span></td></tr>

[[Category: ~~Jeyaprakash, A.A~~]]

</table>

[[Category: ~~Abad, M.A~~]]

== Function ==

[https://www.uniprot.org/uniprot/CI114_HUMAN CI114_HUMAN]

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Abad MA]]

[[Category: Jeyaprakash AA]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 8qsw is ON HOLD
+==Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease==
+<StructureSection load='8qsw' size='340' side='right'caption='[[8qsw]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
-Authors: Jeyaprakash, A.A., Abad, M.A.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8qsw]] 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=8QSW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8QSW FirstGlance]. <br>
-Description: Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8qsw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8qsw OCA], [https://pdbe.org/8qsw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8qsw RCSB], [https://www.ebi.ac.uk/pdbsum/8qsw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8qsw ProSAT]</span></td></tr>
-[[Category: Jeyaprakash, A.A]]
+</table>
-[[Category: Abad, M.A]]
+== Function ==
+[https://www.uniprot.org/uniprot/CI114_HUMAN CI114_HUMAN]
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Abad MA]]
+[[Category: Jeyaprakash AA]]