2ct2 | pdb_00002ct2
From Proteopedia
Solution Structure of the RING domain of the Tripartite motif protein 32
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Disease
Known diseases 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 with ZN as ligand. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 21:22:50 2007
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.
- ZN
- National project on protein structural and functional analyses
- Nppsfa
- Riken structural genomics/proteomics initiative
- Ring domain
- Rsgi
- Structural genomics
- Tat-interacting protein
- Tripartite motif protein 32
- Zinc-finger protein ht2a
