2ct2 | pdb_00002ct2
From Proteopedia
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 Sat May 3 22:59:31 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
