5fbe

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m (Protected "5fbe" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5fbe is ON HOLD until Paper Publication
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==COMPLEMENT FACTOR D IN COMPLEX WITH COMPOUND2==
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<StructureSection load='5fbe' size='340' side='right' caption='[[5fbe]], [[Resolution|resolution]] 1.43&Aring;' scene=''>
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Authors: Ostermann, N., Zink, F.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5fbe]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5FBE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5FBE FirstGlance]. <br>
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Description: COMPLEMENT FACTOR D IN COMPLEX WITH COMPOUND2
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5W5:METHYL+2-[[[(2~{S})-2-[[3-(TRIFLUOROMETHYLOXY)PHENYL]CARBAMOYL]PYRROLIDIN-1-YL]CARBONYLAMINO]METHYL]BENZOATE'>5W5</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Complement_factor_D Complement factor D], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.46 3.4.21.46] </span></td></tr>
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<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=5fbe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5fbe OCA], [http://pdbe.org/5fbe PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5fbe RCSB], [http://www.ebi.ac.uk/pdbsum/5fbe PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5fbe ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/CFAD_HUMAN CFAD_HUMAN]] Defects in CFD are the cause of complement factor D deficiency (CFDD) [MIM:[http://omim.org/entry/613912 613912]]. CFDD is an immunologic disorder characterized by increased susceptibility to bacterial infections, particularly Neisseria infections, due to a defect in the alternative complement pathway.
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== Function ==
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[[http://www.uniprot.org/uniprot/CFAD_HUMAN CFAD_HUMAN]] Factor D cleaves factor B when the latter is complexed with factor C3b, activating the C3bbb complex, which then becomes the C3 convertase of the alternate pathway. Its function is homologous to that of C1s in the classical pathway.
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__TOC__
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</StructureSection>
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[[Category: Complement factor D]]
[[Category: Ostermann, N]]
[[Category: Ostermann, N]]
[[Category: Zink, F]]
[[Category: Zink, F]]
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[[Category: Hydrolase]]

Revision as of 18:40, 26 October 2016

COMPLEMENT FACTOR D IN COMPLEX WITH COMPOUND2

5fbe, resolution 1.43Å

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