1e50
From Proteopedia
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| - | [[Image:1e50.gif|left|200px]] | + | [[Image:1e50.gif|left|200px]] |
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| - | '''AML1/CBF COMPLEX''' | + | {{Structure |
| + | |PDB= 1e50 |SIZE=350|CAPTION= <scene name='initialview01'>1e50</scene>, resolution 2.60Å | ||
| + | |SITE= | ||
| + | |LIGAND= | ||
| + | |ACTIVITY= | ||
| + | |GENE= AML1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
| + | }} | ||
| + | |||
| + | '''AML1/CBF COMPLEX''' | ||
| + | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1E50 is a [ | + | 1E50 is a [[Protein complex]] structure of sequences 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=1E50 OCA]. |
==Reference== | ==Reference== | ||
| - | Structural basis for the heterodimeric interaction between the acute leukaemia-associated transcription factors AML1 and CBFbeta., Warren AJ, Bravo J, Williams RL, Rabbitts TH, EMBO J. 2000 Jun 15;19(12):3004-15. PMID:[http:// | + | Structural basis for the heterodimeric interaction between the acute leukaemia-associated transcription factors AML1 and CBFbeta., Warren AJ, Bravo J, Williams RL, Rabbitts TH, EMBO J. 2000 Jun 15;19(12):3004-15. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10856244 10856244] |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
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[[Category: transcription factor]] | [[Category: transcription factor]] | ||
| - | ''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 10:49:48 2008'' |
Revision as of 08:49, 20 March 2008
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| , resolution 2.60Å | |||||||
|---|---|---|---|---|---|---|---|
| Gene: | AML1 (Homo sapiens) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
AML1/CBF COMPLEX
Contents |
Overview
Mutations in the genes encoding the interacting proteins AML1 and CBFbeta are the most common genetic abnormalities in acute leukaemia, and congenital mutations in the related AML3 gene are associated with disorders of osteogenesis. Furthermore, the interaction of AML1 with CBFbeta is essential for haematopoiesis. We report the 2.6 A resolution crystal structure of the complex between the AML1 Runt domain and CBFbeta, which represents a paradigm for the mode of interaction of this highly conserved family of transcription factors. The structure demonstrates that point mutations associated with cleidocranial dysplasia map to the conserved heterodimer interface, suggesting a role for CBFbeta in osteogenesis, and reveals a potential protein interaction platform composed of conserved negatively charged residues on the surface of CBFbeta.
Disease
Known diseases associated with this structure: Leukemia, acute myeloid OMIM:[151385], Myeloid leukemia, acute, M4Eo subtype OMIM:[121360], Platelet disorder, familial, with associated myeloid malignancy OMIM:[151385], Rheumatoid arthritis, susceptibility to OMIM:[151385]
About this Structure
1E50 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Structural basis for the heterodimeric interaction between the acute leukaemia-associated transcription factors AML1 and CBFbeta., Warren AJ, Bravo J, Williams RL, Rabbitts TH, EMBO J. 2000 Jun 15;19(12):3004-15. PMID:10856244
Page seeded by OCA on Thu Mar 20 10:49:48 2008
