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New page: '''Unreleased structure''' The entry 6zxe is ON HOLD Authors: Description: Category: Unreleased Structures
 
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'''Unreleased structure'''


The entry 6zxe is ON HOLD
==Cryo-EM structure of a late human pre-40S ribosomal subunit - State F2==
<StructureSection load='6zxe' size='340' side='right'caption='[[6zxe]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6zxe]] is a 10 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=6ZXE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6ZXE FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</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=6zxe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6zxe OCA], [https://pdbe.org/6zxe PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6zxe RCSB], [https://www.ebi.ac.uk/pdbsum/6zxe PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6zxe ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/RS17_HUMAN RS17_HUMAN] Blackfan-Diamond disease. Diamond-Blackfan anemia 4 (DBA4) [MIM:[https://omim.org/entry/612527 612527]: A form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of developing leukemia. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:17647292</ref> <ref>PMID:19061985</ref>
== Function ==
[https://www.uniprot.org/uniprot/RS17_HUMAN RS17_HUMAN]


Authors:  
==See Also==
 
*[[Ribosome 3D structures|Ribosome 3D structures]]
Description:  
*[[3D sructureseceptor for activated protein kinase C 1|3D sructureseceptor for activated protein kinase C 1]]
[[Category: Unreleased Structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ameismeier M]]
[[Category: Beckmann R]]
[[Category: Berninghausen O]]
[[Category: Kutay U]]
[[Category: Thoms M]]
[[Category: Zemp I]]
[[Category: Van den Heuvel J]]
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