1x2p
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 Mon Nov 12 19:57:59 2007
Categories: 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
