2egq: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:2egq. | {{Seed}} | ||
[[Image:2egq.png|left|200px]] | |||
<!-- | <!-- | ||
| Line 9: | Line 10: | ||
{{STRUCTURE_2egq| PDB=2egq | SCENE= }} | {{STRUCTURE_2egq| PDB=2egq | SCENE= }} | ||
===Solution structure of the fourth LIM domain from human four and a half LIM domains 1=== | |||
==Disease== | ==Disease== | ||
Known disease associated with this structure: Hemophagocytic lymphohistiocytosis, familial OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=267700 267700]], Myopathy, X-linked, with postural muscle atrophy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]], Scapuloperoneal myopathy, X-linked dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]] | Known disease associated with this structure: Hemophagocytic lymphohistiocytosis, familial OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=267700 267700]], Myopathy, X-linked, with postural muscle atrophy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]], Myopathy, reducing body, X-linked, severe early-onset, 300717 (3), Myopathy, reducing body, X-linked, childhood-onset OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]], Scapuloperoneal myopathy, X-linked dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]] | ||
==About this Structure== | ==About this Structure== | ||
2EGQ is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full | 2EGQ is a [[Single protein]] structure of 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=2EGQ OCA]. | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
| Line 34: | Line 35: | ||
[[Category: Structural genomic]] | [[Category: Structural genomic]] | ||
[[Category: Structural protein]] | [[Category: Structural protein]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Sep 28 16:19:51 2008'' | |||
Revision as of 13:20, 28 September 2008
Solution structure of the fourth LIM domain from human four and a half LIM domains 1
Disease
Known disease associated with this structure: Hemophagocytic lymphohistiocytosis, familial OMIM:[267700], Myopathy, X-linked, with postural muscle atrophy OMIM:[300163], Myopathy, reducing body, X-linked, severe early-onset, 300717 (3), Myopathy, reducing body, X-linked, childhood-onset OMIM:[300163], Scapuloperoneal myopathy, X-linked dominant OMIM:[300163]
About this Structure
2EGQ is a Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Sun Sep 28 16:19:51 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Hayashi, F.
- Inoue, K.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Yokoyama, S.
- Fhl-1
- Four and a half lim domains protein 1
- Lim domain
- National project on protein structural and functional analyse
- Nppsfa
- Riken structural genomics/proteomics initiative
- Rsgi
- Skeletal muscle lim- protein 1
- Slim 1
- Structural genomic
- Structural protein