8f6d: Difference between revisions

Line 1:

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

The entry ~~8f6d is ON HOLD until Paper Publication~~

==Crystal structure of the CNNM2 CBS-pair domain in complex with ARL15==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[8f6d]] is a 8 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=8F6D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8F6D FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.2Å</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=8f6d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8f6d OCA], [https://pdbe.org/8f6d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8f6d RCSB], [https://www.ebi.ac.uk/pdbsum/8f6d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8f6d ProSAT]</span></td></tr>

</table>

== Disease ==

[https://www.uniprot.org/uniprot/CNNM2_HUMAN CNNM2_HUMAN] Familial primary hypomagnesemia with normocalcuria and normocalcemia. The disease is caused by mutations affecting the gene represented in this entry.

== Function ==

[https://www.uniprot.org/uniprot/CNNM2_HUMAN CNNM2_HUMAN] Divalent metal cation transporter. Mediates transport of divalent metal cations in an order of Mg(2+) > Co(2+) > Mn(2+) > Sr(2+) > Ba(2+) > Cu(2+) > Fe(2+) (By similarity).

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Gehring K]]

[[Category: Kozlov G]]

[[Category: Mahbub L]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 8f6d is ON HOLD  until Paper Publication
+==Crystal structure of the CNNM2 CBS-pair domain in complex with ARL15==
+<StructureSection load='8f6d' size='340' side='right'caption='[[8f6d]], [[Resolution|resolution]] 3.20&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8f6d]] is a 8 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=8F6D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8F6D FirstGlance]. <br>
-Description:
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.2&#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=8f6d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8f6d OCA], [https://pdbe.org/8f6d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8f6d RCSB], [https://www.ebi.ac.uk/pdbsum/8f6d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8f6d ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[https://www.uniprot.org/uniprot/CNNM2_HUMAN CNNM2_HUMAN] Familial primary hypomagnesemia with normocalcuria and normocalcemia. The disease is caused by mutations affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/CNNM2_HUMAN CNNM2_HUMAN] Divalent metal cation transporter. Mediates transport of divalent metal cations in an order of Mg(2+) > Co(2+) > Mn(2+) > Sr(2+) > Ba(2+) > Cu(2+) > Fe(2+) (By similarity).
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Gehring K]]
+[[Category: Kozlov G]]
+[[Category: Mahbub L]]