1x2p
From Proteopedia
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[[Category: Kigawa, T.]] | [[Category: Kigawa, T.]] | ||
[[Category: Koshiba, S.]] | [[Category: Koshiba, S.]] | ||
| - | [[Category: RSGI, RIKEN | + | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] |
[[Category: Saito, K.]] | [[Category: Saito, K.]] | ||
[[Category: Yokoyama, S.]] | [[Category: Yokoyama, S.]] | ||
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[[Category: structural genomics]] | [[Category: structural genomics]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:50:26 2008'' |
Revision as of 13:50, 21 February 2008
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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 Thu Feb 21 15:50:26 2008
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
