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8j7d

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(New page: '''Unreleased structure''' The entry 8j7d is ON HOLD Authors: Liu, D.S., Su, J.Y. Description: Human 3-methylcrotonyl-CoA carboxylase in BCCP-H1 state [[Category: Unreleased Structures...)
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'''Unreleased structure'''
 
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The entry 8j7d is ON HOLD
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==Human 3-methylcrotonyl-CoA carboxylase in BCCP-H1 state==
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<StructureSection load='8j7d' size='340' side='right'caption='[[8j7d]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
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Authors: Liu, D.S., Su, J.Y.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8j7d]] is a 12 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=8J7D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8J7D FirstGlance]. <br>
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Description: Human 3-methylcrotonyl-CoA carboxylase in BCCP-H1 state
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.7&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BTI:5-(HEXAHYDRO-2-OXO-1H-THIENO[3,4-D]IMIDAZOL-6-YL)PENTANAL'>BTI</scene></td></tr>
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[[Category: Liu, D.S]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8j7d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8j7d OCA], [https://pdbe.org/8j7d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8j7d RCSB], [https://www.ebi.ac.uk/pdbsum/8j7d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8j7d ProSAT]</span></td></tr>
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[[Category: Su, J.Y]]
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/MCCA_HUMAN MCCA_HUMAN] Defects in MCCC1 are the cause of methylcrotonoyl-CoA carboxylase 1 deficiency (MCC1D) [MIM:[https://omim.org/entry/210200 210200]. An autosomal recessive disorder of leucine catabolism. The phenotype is variable, ranging from neonatal onset with severe neurological involvement to asymptomatic adults. There is a characteristic organic aciduria with massive excretion of 3-hydroxyisovaleric acid and 3-methylcrotonylglycine, usually in combination with a severe secondary carnitine deficiency.<ref>PMID:11170888</ref> <ref>PMID:11406611</ref> <ref>PMID:11181649</ref> <ref>PMID:22150417</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/MCCA_HUMAN MCCA_HUMAN]
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== References ==
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<references/>
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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: Liu DS]]
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[[Category: Su JY]]

Current revision

Human 3-methylcrotonyl-CoA carboxylase in BCCP-H1 state

PDB ID 8j7d

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