3c2i
From Proteopedia
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==About this Structure== | ==About this Structure== | ||
- | 3C2I is a | + | 3C2I 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=3C2I OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:18313390</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Protein complex]] | ||
[[Category: Bird, A P.]] | [[Category: Bird, A P.]] | ||
[[Category: Ho, K L.]] | [[Category: Ho, K L.]] | ||
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[[Category: Water mediated recognition]] | [[Category: Water mediated recognition]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 11:31:25 2009'' |
Revision as of 09:31, 17 February 2009
Contents |
The Crystal Structure of Methyl-CpG Binding Domain of Human MeCP2 in Complex with a Methylated DNA Sequence from BDNF
Template:ABSTRACT PUBMED 18313390
Disease
Known disease associated with this structure: Angelman syndrome OMIM:[300005], Encephalopathy, neonatal severe OMIM:[300005], Mental retardation, X-linked, Lubs type OMIM:[300005], Mental retardation, X-linked, syndromic 13 OMIM:[300005], Rett syndrome OMIM:[300005], Rett syndrome, preserved speech variant OMIM:[300005], Autism, susceptibility to, X-linked-3 OMIM:[300005]
About this Structure
3C2I is a 3 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Ho KL, McNae IW, Schmiedeberg L, Klose RJ, Bird AP, Walkinshaw MD. MeCP2 binding to DNA depends upon hydration at methyl-CpG. Mol Cell. 2008 Feb 29;29(4):525-31. PMID:18313390 doi:10.1016/j.molcel.2007.12.028
Page seeded by OCA on Tue Feb 17 11:31:25 2009
Categories: Homo sapiens | Bird, A P. | Ho, K L. | Klose, R J. | McNae, I W. | Schmiedeberg, L. | Walkinshaw, M D. | Alternative splicing | Asx-st-motif | Chromosomal rearrangement | Disease mutation | Dna-binding | Nucleus | Phosphoprotein | Polymorphism | Protein-methylated dna complex | Repressor | Transcription regulator | Water mediated recognition