1x2p
From Proteopedia
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| - | [[Image:1x2p.jpg|left|200px]] | + | [[Image:1x2p.jpg|left|200px]] |
| - | + | ||
| - | '''Solution structure of the SH3 domain of the Protein arginine N-methyltransferase 2''' | + | {{Structure |
| + | |PDB= 1x2p |SIZE=350|CAPTION= <scene name='initialview01'>1x2p</scene> | ||
| + | |SITE= | ||
| + | |LIGAND= | ||
| + | |ACTIVITY= | ||
| + | |GENE= HRMT1L1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
| + | }} | ||
| + | |||
| + | '''Solution structure of the SH3 domain of the Protein arginine N-methyltransferase 2''' | ||
| + | |||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1X2P is a [ | + | 1X2P is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1X2P OCA]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: Saito, K.]] | [[Category: Saito, K.]] | ||
[[Category: Yokoyama, S.]] | [[Category: Yokoyama, S.]] | ||
| - | [[Category: national project on protein structural and functional | + | [[Category: national project on protein structural and functional analyse]] |
[[Category: nppsfa]] | [[Category: nppsfa]] | ||
[[Category: protein arginine n-methyltransferase]] | [[Category: protein arginine n-methyltransferase]] | ||
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[[Category: rsgi]] | [[Category: rsgi]] | ||
[[Category: sh3 domain]] | [[Category: sh3 domain]] | ||
| - | [[Category: structural | + | [[Category: structural genomic]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:04:25 2008'' |
Revision as of 13:04, 20 March 2008
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| Gene: | HRMT1L1 (Homo sapiens) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
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 Mar 20 15:04:25 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 analyse | Nppsfa | Protein arginine n-methyltransferase | Riken structural genomics/proteomics initiative | Rsgi | Sh3 domain | Structural genomic
