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2ct2
From Proteopedia
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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: ZN]] | ||
[[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
| |||||||
| Ligands: | |||||||
| 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
Categories: 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
