2dgz | pdb_00002dgz
From Proteopedia
Solution structure of the Helicase and RNase D C-terminal domain in Werner syndrome ATP-dependent helicase
| |||||||||||||
| 2dgz | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Gene: | WRN (Homo sapiens) | ||||||||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||||||||
Disease
Known disease associated with this structure: Werner syndrome OMIM:[604611]
About this Structure
2DGZ 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 02:34:31 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Abe, C.
- Inoue, M.
- Kigawa, T.
- Muto, Y.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Shirouzu, M.
- Terada, T.
- Yokoyama, S.
- Hrdc domain
- National project on protein structural and functional analyse
- Nppsfa
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomic