6qe4: Difference between revisions

Line 1:

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

The entry ~~6qe4~~ is ~~ON HOLD~~ ~~until Feb 01 2020~~

==Re-refinement of 5OLI human IBA57-I3C==

== Structural highlights ==

<table><tr><td colspan='2'>[[6qe4]] is a 1 chain structure. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=5oli 5oli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6QE4 OCA]. For a guided tour on the structure components use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6QE4 FirstGlance].

</td></tr><tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat"><scene name='pdbligand=I3C:5-AMINO-2,4,6-TRIIODOBENZENE-1,3-DICARBOXYLIC+ACID'>I3C</scene></td></tr>

<tr id='related'><td class="sblockLbl">[[Related_structure|Related:]]</td><td class="sblockDat">[[6esr|6esr]]</td></tr>

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6qe4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6qe4 OCA], [http://pdbe.org/6qe4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6qe4 RCSB], [http://www.ebi.ac.uk/pdbsum/6qe4 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6qe4 ProSAT]</td></tr>

</table>

== Disease ==

[[http://www.uniprot.org/uniprot/CAF17_HUMAN CAF17_HUMAN]] Hypotonia-cerebral atrophy-hyperglycinemia syndrome. 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 ==

[[http://www.uniprot.org/uniprot/CAF17_HUMAN CAF17_HUMAN]] Involved in the maturation of mitochondrial 4Fe-4S proteins functioning late in the iron-sulfur cluster assembly pathway.<ref>PMID:23462291</ref>

~~Authors~~: ~~Calderone, V., Ciofi-Baffoni, S., Gourdoupis, S., Banci, L., Nasta, V.~~

==See Also==

*[[Journal:Acta Cryst D:S2059798319000214|Journal:Acta Cryst D:S2059798319000214]]

~~Description~~: ~~Re-refinement of 5OLI human IBA57-I3C~~

== References ==

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

__TOC__

</StructureSection>

[[Category: Large Structures]]

[[Category: Banci, L]]

[[Category: Calderone, V]]

[[Category: ~~Banci~~, L]]

[[Category: Ciofi-Baffoni, S]]

[[Category: Gourdoupis, S]]

~~[[Category: Ciofi-Baffoni, S]]~~

[[Category: Nasta, V]]

[[Category: Fe-s protein biogenesis]]

[[Category: I3c phasing]]

[[Category: Infantile leukodystrophy]]

[[Category: Mitochondrial protein]]

[[Category: Protein binding]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 6qe4 is ON HOLD  until Feb 01 2020
+==Re-refinement of 5OLI human IBA57-I3C==
+<StructureSection load='6qe4' size='340' side='right'caption='[[6qe4]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6qe4]] is a 1 chain structure. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=5oli 5oli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6QE4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6QE4 FirstGlance]. <br>
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=I3C:5-AMINO-2,4,6-TRIIODOBENZENE-1,3-DICARBOXYLIC+ACID'>I3C</scene></td></tr>
+<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6esr|6esr]]</td></tr>
+<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=6qe4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6qe4 OCA], [http://pdbe.org/6qe4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6qe4 RCSB], [http://www.ebi.ac.uk/pdbsum/6qe4 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6qe4 ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[http://www.uniprot.org/uniprot/CAF17_HUMAN CAF17_HUMAN]] Hypotonia-cerebral atrophy-hyperglycinemia syndrome. 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 ==
+[[http://www.uniprot.org/uniprot/CAF17_HUMAN CAF17_HUMAN]] Involved in the maturation of mitochondrial 4Fe-4S proteins functioning late in the iron-sulfur cluster assembly pathway.<ref>PMID:23462291</ref>
-Authors: Calderone, V., Ciofi-Baffoni, S., Gourdoupis, S., Banci, L., Nasta, V.
+==See Also==
+*[[Journal:Acta Cryst D:S2059798319000214|Journal:Acta Cryst D:S2059798319000214]]
-Description: Re-refinement of 5OLI human IBA57-I3C
+== References ==
-[[Category: Unreleased Structures]]
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Large Structures]]
+[[Category: Banci, L]]
 [[Category: Calderone, V]]
-[[Category: Banci, L]]
+[[Category: Ciofi-Baffoni, S]]
 [[Category: Gourdoupis, S]]
-[[Category: Ciofi-Baffoni, S]]
 [[Category: Nasta, V]]
+[[Category: Fe-s protein biogenesis]]
+[[Category: I3c phasing]]
+[[Category: Infantile leukodystrophy]]
+[[Category: Mitochondrial protein]]
+[[Category: Protein binding]]