1qmz: Difference between revisions
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|PDB= 1qmz |SIZE=350|CAPTION= <scene name='initialview01'>1qmz</scene>, resolution 2.2Å | |PDB= 1qmz |SIZE=350|CAPTION= <scene name='initialview01'>1qmz</scene>, resolution 2.2Å | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene> | |LIGAND= <scene name='pdbligand=ATP:ADENOSINE-5'-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene> | ||
|ACTIVITY= | |ACTIVITY= | ||
|GENE= | |GENE= | ||
|DOMAIN= | |||
|RELATEDENTRY= | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1qmz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1qmz OCA], [http://www.ebi.ac.uk/pdbsum/1qmz PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1qmz RCSB]</span> | |||
}} | }} | ||
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[[Category: Johnson, L N.]] | [[Category: Johnson, L N.]] | ||
[[Category: Noble, M E.M.]] | [[Category: Noble, M E.M.]] | ||
[[Category: cdk]] | [[Category: cdk]] | ||
[[Category: complex (protein kinase/cyclin)]] | [[Category: complex (protein kinase/cyclin)]] | ||
| Line 34: | Line 35: | ||
[[Category: substrate complex]] | [[Category: substrate complex]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 23 | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:16:04 2008'' | ||
Revision as of 23:16, 30 March 2008
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| , resolution 2.2Å | |||||||
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| Ligands: | , , | ||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX
OverviewOverview
Progression through the eukaryotic cell cycle is driven by the orderly activation of cyclin-dependent kinases (CDKs). For activity, CDKs require association with a cyclin and phosphorylation by a separate protein kinase at a conserved threonine residue (T160 in CDK2). Here we present the structure of a complex consisting of phosphorylated CDK2 and cyclin A together with an optimal peptide substrate, HHASPRK. This structure provides an explanation for the specificity of CDK2 towards the proline that follows the phosphorylatable serine of the substrate peptide, and the requirement for the basic residue in the P+3 position of the substrate. We also present the structure of phosphorylated CDK2 plus cyclin A3 in complex with residues 658-668 from the CDK2 substrate p107. These residues include the RXL motif required to target p107 to cyclins. This structure explains the specificity of the RXL motif for cyclins.
About this StructureAbout this Structure
1QMZ is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
The structural basis for specificity of substrate and recruitment peptides for cyclin-dependent kinases., Brown NR, Noble ME, Endicott JA, Johnson LN, Nat Cell Biol. 1999 Nov;1(7):438-43. PMID:10559988
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