1x2p | pdb_00001x2p
From Proteopedia
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Solution structure of the SH3 domain of the Protein arginine N-methyltransferase 2
Disease
Known disease associated with this structure: Congenital disorder of glycosylation, type Ik OMIM:[605907]
About this Structure
1X2P is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Fri Feb 15 17:08:12 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Chikayama, E.
- Inoue, M.
- Kigawa, T.
- Koshiba, S.
- RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.
- Saito, K.
- Yokoyama, S.
- National project on protein structural and functional analyses
- Nppsfa
- Protein arginine n-methyltransferase
- Riken structural genomics/proteomics initiative
- Rsgi
- Sh3 domain
- Structural genomics
