1h9d
From Proteopedia
Line 1: | Line 1: | ||
[[Image:1h9d.gif|left|200px]] | [[Image:1h9d.gif|left|200px]] | ||
- | + | <!-- | |
- | + | The line below this paragraph, containing "STRUCTURE_1h9d", creates the "Structure Box" on the page. | |
- | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
- | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
- | + | or leave the SCENE parameter empty for the default display. | |
- | + | --> | |
- | + | {{STRUCTURE_1h9d| PDB=1h9d | SCENE= }} | |
- | | | + | |
- | | | + | |
- | }} | + | |
'''AML1/CBF-BETA/DNA COMPLEX''' | '''AML1/CBF-BETA/DNA COMPLEX''' | ||
Line 30: | Line 27: | ||
[[Category: Bravo, J.]] | [[Category: Bravo, J.]] | ||
[[Category: Warren, A J.]] | [[Category: Warren, A J.]] | ||
- | [[Category: | + | [[Category: Transcription factor]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 18:36:01 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 15:36, 2 May 2008
AML1/CBF-BETA/DNA COMPLEX
Contents |
Overview
We have determined the structure, at 2.6 A resolution, of the AML1 (Runx1) Runt domain--CBF beta--DNA ternary complex, the most common target for mutations in human leukemia. The structure reveals that the Runt domain DNA binding mechanism is unique within the p53 family of transcription factors. The extended C-terminal 'tail' and 'wing' elements adopt a specific DNA-bound conformation that clamps the phosphate backbone between the major and minor grooves of the distorted B-form DNA recognition site. Furthermore, the extended 'tail' mediates most of the NF-kappa B/Rel-like base-specific contacts in the major groove. The structure clearly explains the molecular basis for the loss of DNA binding function of the Runt domain--CBF beta complex as a consequence of the human disease-associated mutations in leukemogenesis and cleidocranial dysplasia.
Disease
Known disease associated with this structure: Leukemia, acute myeloid OMIM:[151385], Platelet disorder, familial, with associated myeloid malignancy OMIM:[151385], Rheumatoid arthritis, susceptibility to OMIM:[151385], Myeloid leukemia, acute, M4Eo subtype OMIM:[121360]
About this Structure
1H9D is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
The leukemia-associated AML1 (Runx1)--CBF beta complex functions as a DNA-induced molecular clamp., Bravo J, Li Z, Speck NA, Warren AJ, Nat Struct Biol. 2001 Apr;8(4):371-8. PMID:11276260 Page seeded by OCA on Fri May 2 18:36:01 2008