4bxu: Difference between revisions

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

~~The entry~~ 4bxu is ~~ON HOLD~~

==Structure of Pex14 in complex with Pex5 LVxEF motif==

~~Authors~~: ~~Kooshapur~~, H., ~~Meyer~~, H., ~~Madl~~, T.~~, Sattler, M~~.

== Structural highlights ==

<table><tr><td colspan='2'>[[4bxu]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BXU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BXU FirstGlance]. <br>

~~Description~~: ~~Structure~~ of ~~Pex14 in complex~~ with ~~Pex5 LVxEF motif~~

</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=4bxu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bxu OCA], [https://pdbe.org/4bxu PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4bxu RCSB], [https://www.ebi.ac.uk/pdbsum/4bxu PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4bxu ProSAT]</span></td></tr>

</table>

== Disease ==

[[https://www.uniprot.org/uniprot/PEX14_HUMAN PEX14_HUMAN]] Zellweger syndrome;Neonatal adrenoleukodystrophy;Infantile Refsum disease. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.

== Function ==

[[https://www.uniprot.org/uniprot/PEX14_HUMAN PEX14_HUMAN]] Component of the peroxisomal translocation machinery with PEX13 and PEX17. Interacts with both the PTS1 and PTS2 receptors. Binds directly to PEX17.

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Kooshapur H]]

[[Category: Madl T]]

[[Category: Meyer HN]]

[[Category: Sattler M]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 4bxu is ON HOLD
+==Structure of Pex14 in complex with Pex5 LVxEF motif==
+<StructureSection load='4bxu' size='340' side='right'caption='[[4bxu]]' scene=''>
-Authors: Kooshapur, H., Meyer, H., Madl, T., Sattler, M.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[4bxu]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BXU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BXU FirstGlance]. <br>
-Description: Structure of Pex14 in complex with Pex5 LVxEF motif
+</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=4bxu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bxu OCA], [https://pdbe.org/4bxu PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4bxu RCSB], [https://www.ebi.ac.uk/pdbsum/4bxu PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4bxu ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[https://www.uniprot.org/uniprot/PEX14_HUMAN PEX14_HUMAN]] Zellweger syndrome;Neonatal adrenoleukodystrophy;Infantile Refsum disease. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.
+== Function ==
+[[https://www.uniprot.org/uniprot/PEX14_HUMAN PEX14_HUMAN]] Component of the peroxisomal translocation machinery with PEX13 and PEX17. Interacts with both the PTS1 and PTS2 receptors. Binds directly to PEX17.
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Kooshapur H]]
+[[Category: Madl T]]
+[[Category: Meyer HN]]
+[[Category: Sattler M]]