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2cp9

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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2cp9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cp9 OCA], [http://www.ebi.ac.uk/pdbsum/2cp9 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2cp9 RCSB]</span>
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'''Solution structure of RSGI RUH-042, a UBA domain from human mitochondrial elongation factor Ts'''
'''Solution structure of RSGI RUH-042, a UBA domain from human mitochondrial elongation factor Ts'''
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==Disease==
 
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Known disease associated with this structure: Combined oxidative phosphorylation deficiency 3 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604723 604723]]
 
==About this Structure==
==About this Structure==
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[[Category: uba]]
[[Category: uba]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:18:16 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:24:41 2008''

Revision as of 23:24, 30 March 2008


PDB ID 2cp9

Drag the structure with the mouse to rotate
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Solution structure of RSGI RUH-042, a UBA domain from human mitochondrial elongation factor Ts


About this Structure

2CP9 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Mar 31 02:24:41 2008

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