8xl8: Difference between revisions

Line 1:

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

The ~~entry 8xl8~~ is ~~ON HOLD until Paper Publication~~

==Structure of human 3-methylcrotonyl-CoA carboxylase in complex with propionyl-CoA (MCC-PCO)==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[8xl8]] 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=8XL8 OCA]. For a guided tour on the structure components use [https://proteopedia.org/fgij/fg.htm?mol=8XL8 FirstGlance].

~~Description~~:

</td></tr><tr id='method'><td class="sblockLbl">[[Empirical_models|Method:]]</td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.36Å</td></tr>

[[Category: ~~Unreleased~~ Structures]]

<tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=1VU:PROPIONYL+COENZYME+A'>1VU</scene>, <scene name='pdbligand=BTN:BIOTIN'>BTN</scene></td></tr>

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[https://proteopedia.org/fgij/fg.htm?mol=8xl8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xl8 OCA], [https://pdbe.org/8xl8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xl8 RCSB], [https://www.ebi.ac.uk/pdbsum/8xl8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xl8 ProSAT]</td></tr>

</table>

== Disease ==

[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>

== Function ==

[https://www.uniprot.org/uniprot/MCCA_HUMAN MCCA_HUMAN]

== References ==

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Hu Q]]

[[Category: Zhang YY]]

[[Category: Zhou FY]]

[[Category: Zhou Q]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 8xl8 is ON HOLD  until Paper Publication
+==Structure of human 3-methylcrotonyl-CoA carboxylase in complex with propionyl-CoA (MCC-PCO)==
+<StructureSection load='8xl8' size='340' side='right'caption='[[8xl8]], [[Resolution|resolution]] 2.36&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8xl8]] 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=8XL8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8XL8 FirstGlance]. <br>
-Description:
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.36&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=1VU:PROPIONYL+COENZYME+A'>1VU</scene>, <scene name='pdbligand=BTN:BIOTIN'>BTN</scene></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=8xl8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xl8 OCA], [https://pdbe.org/8xl8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xl8 RCSB], [https://www.ebi.ac.uk/pdbsum/8xl8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xl8 ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[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>
+== Function ==
+[https://www.uniprot.org/uniprot/MCCA_HUMAN MCCA_HUMAN]
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Hu Q]]
+[[Category: Zhang YY]]
+[[Category: Zhou FY]]
+[[Category: Zhou Q]]