2da7
From Proteopedia
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|ACTIVITY= | |ACTIVITY= | ||
|GENE= ZFHX1B ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= ZFHX1B ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
| + | |DOMAIN= | ||
| + | |RELATEDENTRY= | ||
| + | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2da7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2da7 OCA], [http://www.ebi.ac.uk/pdbsum/2da7 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2da7 RCSB]</span> | ||
}} | }} | ||
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[[Category: three helices with the dna binding helix-turn-helix motif]] | [[Category: three helices with the dna binding helix-turn-helix motif]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:32:00 2008'' |
Revision as of 23:32, 30 March 2008
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| Gene: | ZFHX1B (Homo sapiens) | ||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Solution structure of the homeobox domain of Zinc finger homeobox protein 1b (Smad interacting protein 1)
Disease
Known disease associated with this structure: Mowat-Wilson syndrome OMIM:[605802]
About this Structure
2DA7 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 02:32:00 2008
Categories: Homo sapiens | Single protein | Inoue, M. | Kigawa, T. | Koshiba, S. | Ohnishi, S. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Sato, M. | Yokoyama, S. | Homeobox domain | National project on protein structural and functional analyse | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic | Three helices with the dna binding helix-turn-helix motif
