2ct2: Difference between revisions
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|PDB= 2ct2 |SIZE=350|CAPTION= <scene name='initialview01'>2ct2</scene> | |PDB= 2ct2 |SIZE=350|CAPTION= <scene name='initialview01'>2ct2</scene> | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=ZN:ZINC ION'>ZN</scene> | |LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene> | ||
|ACTIVITY= | |ACTIVITY= | ||
|GENE= TRIM32 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= TRIM32 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
|DOMAIN= | |||
|RELATEDENTRY= | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ct2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ct2 OCA], [http://www.ebi.ac.uk/pdbsum/2ct2 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ct2 RCSB]</span> | |||
}} | }} | ||
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==Disease== | ==Disease== | ||
Known | Known disease associated with this structure: Bardet-Biedl syndrome 11 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602290 602290]], Muscular dystrophy, limb-girdle, type 2H OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602290 602290]] | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Tochio, N.]] | [[Category: Tochio, N.]] | ||
[[Category: Yokoyama, S.]] | [[Category: Yokoyama, S.]] | ||
[[Category: national project on protein structural and functional analyse]] | [[Category: national project on protein structural and functional analyse]] | ||
[[Category: nppsfa]] | [[Category: nppsfa]] | ||
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[[Category: zinc-finger protein ht2a]] | [[Category: zinc-finger protein ht2a]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:26:03 2008'' | ||
Revision as of 23:26, 30 March 2008
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| 2ct2 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ligands: | ZN | ||||||||||||
| Gene: | TRIM32 (Homo sapiens) | ||||||||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||||||||
Solution Structure of the RING domain of the Tripartite motif protein 32
Disease
Known disease associated with this structure: Bardet-Biedl syndrome 11 OMIM:[602290], Muscular dystrophy, limb-girdle, type 2H OMIM:[602290]
About this Structure
2CT2 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Mar 31 02:26:03 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Inoue, M.
- Kigawa, T.
- Koshiba, S.
- Miyamoto, K.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Sato, M.
- Tochio, N.
- Yokoyama, S.
- National project on protein structural and functional analyse
- Nppsfa
- Riken structural genomics/proteomics initiative
- Ring domain
- Rsgi
- Structural genomic
- Tat-interacting protein
- Tripartite motif protein 32
- Zinc-finger protein ht2a
