4bxu

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m (Protected "4bxu" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 4bxu is ON HOLD
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==Structure of Pex14 in complex with Pex5 LVxEF motif==
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<StructureSection load='4bxu' size='340' side='right'caption='[[4bxu]]' scene=''>
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Authors: Kooshapur, H., Meyer, H., Madl, T., Sattler, M.
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== Structural highlights ==
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<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>
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Description: Structure of Pex14 in complex with Pex5 LVxEF motif
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</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>
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</table>
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== Disease ==
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[[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.
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== Function ==
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[[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.
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Kooshapur H]]
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[[Category: Madl T]]
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[[Category: Meyer HN]]
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[[Category: Sattler M]]

Current revision

Structure of Pex14 in complex with Pex5 LVxEF motif

PDB ID 4bxu

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