2ysq
From Proteopedia
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{{STRUCTURE_2ysq| PDB=2ysq | SCENE= }} | {{STRUCTURE_2ysq| PDB=2ysq | SCENE= }} | ||
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===Solution structure of the SH3 domain from Rho guanine nucleotide exchange factor 9=== | ===Solution structure of the SH3 domain from Rho guanine nucleotide exchange factor 9=== | ||
+ | ==Disease== | ||
+ | [[http://www.uniprot.org/uniprot/ARHG9_HUMAN ARHG9_HUMAN]] Defects in ARHGEF9 are the cause of pileptic encephalopathy, early infantile, type 8 (EIEE8) [MIM:[http://omim.org/entry/300607 300607]]. A disorder characterized by hyperekplexia and early infantile epileptic encephalopathy. Neurologic features include exaggerated startle response, seizures, impaired psychomotor development, and mental retardation. Seizures can be provoked by tactile stimulation or extreme emotion.<ref>PMID:15215304</ref> | ||
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+ | ==Function== | ||
+ | [[http://www.uniprot.org/uniprot/ARHG9_HUMAN ARHG9_HUMAN]] Acts as guanine nucleotide exchange factor (GEF) for CDC42. Promotes formation of GPHN clusters.<ref>PMID:10559246</ref> | ||
==About this Structure== | ==About this Structure== | ||
[[2ysq]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YSQ OCA]. | [[2ysq]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YSQ OCA]. | ||
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+ | ==Reference== | ||
+ | <references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Hayashi, F.]] | [[Category: Hayashi, F.]] |
Revision as of 00:07, 25 March 2013
Contents |
Solution structure of the SH3 domain from Rho guanine nucleotide exchange factor 9
Disease
[ARHG9_HUMAN] Defects in ARHGEF9 are the cause of pileptic encephalopathy, early infantile, type 8 (EIEE8) [MIM:300607]. A disorder characterized by hyperekplexia and early infantile epileptic encephalopathy. Neurologic features include exaggerated startle response, seizures, impaired psychomotor development, and mental retardation. Seizures can be provoked by tactile stimulation or extreme emotion.[1]
Function
[ARHG9_HUMAN] Acts as guanine nucleotide exchange factor (GEF) for CDC42. Promotes formation of GPHN clusters.[2]
About this Structure
2ysq is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
- ↑ Harvey K, Duguid IC, Alldred MJ, Beatty SE, Ward H, Keep NH, Lingenfelter SE, Pearce BR, Lundgren J, Owen MJ, Smart TG, Luscher B, Rees MI, Harvey RJ. The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. J Neurosci. 2004 Jun 23;24(25):5816-26. PMID:15215304 doi:10.1523/JNEUROSCI.1184-04.2004
- ↑ Reid T, Bathoorn A, Ahmadian MR, Collard JG. Identification and characterization of hPEM-2, a guanine nucleotide exchange factor specific for Cdc42. J Biol Chem. 1999 Nov 19;274(47):33587-93. PMID:10559246
Categories: Homo sapiens | Hayashi, F. | Qin, X R. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Yokoyama, S. | National project on protein structural and functional analyse | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Sh3 domain | Signaling protein | Structural genomic