3ktf: Difference between revisions

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'''Unreleased structure'''
{{Seed}}
[[Image:3ktf.jpg|left|200px]]


The entry 3ktf is ON HOLD
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{{STRUCTURE_3ktf|  PDB=3ktf |  SCENE=  }}


Authors: Singh, N., Heroux, A., Thompson, J.R., Mer, G.
===Structure of the N-terminal BRCT domain of human microcephalin (MCPH1).===


Description: Structure of N-terminal BRCT domain of human MCPH1


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 9 14:44:28 2009''
==Disease==
Known disease associated with this structure: Microcephaly, autosomal recessive 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=607117 607117]], Premature chromosome condensation with microcephaly and mental retardation OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=607117 607117]]
 
==About this Structure==
3KTF is a 3 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3KTF OCA].
[[Category: Homo sapiens]]
[[Category: Heroux, A.]]
[[Category: Mer, G.]]
[[Category: Singh, N.]]
[[Category: Thompson, J R.]]
[[Category: Brct domain]]
[[Category: Cytoplasm]]
[[Category: Cytoskeleton]]
[[Category: Dwarfism]]
[[Category: Mcph1]]
[[Category: Mental retardation]]
[[Category: Microcephalin]]
[[Category: Phosphoprotein]]
[[Category: Polymorphism]]
[[Category: Primary microcephaly]]
 
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