3ktf

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3ktf.jpg|left|200px]]
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The entry 3ktf is ON HOLD
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{{STRUCTURE_3ktf| PDB=3ktf | SCENE= }}
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Authors: Singh, N., Heroux, A., Thompson, J.R., Mer, G.
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===Structure of the N-terminal BRCT domain of human microcephalin (MCPH1).===
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Description: Structure of N-terminal BRCT domain of human MCPH1
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 9 14:44:28 2009''
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==Disease==
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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]]
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==About this Structure==
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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].
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[[Category: Homo sapiens]]
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[[Category: Heroux, A.]]
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[[Category: Mer, G.]]
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[[Category: Singh, N.]]
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[[Category: Thompson, J R.]]
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[[Category: Brct domain]]
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[[Category: Cytoplasm]]
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[[Category: Cytoskeleton]]
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[[Category: Dwarfism]]
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[[Category: Mcph1]]
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[[Category: Mental retardation]]
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[[Category: Microcephalin]]
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[[Category: Phosphoprotein]]
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[[Category: Polymorphism]]
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[[Category: Primary microcephaly]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 16 14:34:29 2009''

Revision as of 12:34, 16 December 2009

Image:3ktf.jpg

Template:STRUCTURE 3ktf

Structure of the N-terminal BRCT domain of human microcephalin (MCPH1).

Disease

Known disease associated with this structure: Microcephaly, autosomal recessive 1 OMIM:[607117], Premature chromosome condensation with microcephaly and mental retardation OMIM:[607117]

About this Structure

3KTF is a 3 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Wed Dec 16 14:34:29 2009

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OCA

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