Structure of PDB 1urc Chain B Binding Site BS01
Receptor Information
>1urc Chain B (length=258) Species:
9606
(Homo sapiens) [
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VPDYHEDIHTYLREMEVKCKPKVGYMKKQPDITNSMRAILVDWLVEVGEE
YKLQNETLHLAVNYIDRFLSSMSVLRGKLQLVGTAAMLLASKFEEIYPPE
VAEFVYITDDTYTKKQVLRMEHLVLKVLTFDLAAPTVNQFLTQYFLHQQP
ANCKVESLAMFLGELSLIDADPYLKYLPSVIAGAAFHLALYTVTGQSWPE
SLIRKTGYTLESLKPCLMDLHQTYLKAPQHAQQSIREKYKNSKYHGVSLL
NPPETLNL
Ligand information
>1urc Chain E (length=5) Species:
32630
(synthetic construct) [
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RKLFG
Receptor-Ligand Complex Structure
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PDB
1urc
Design, synthesis, biological activity and structural analysis of cyclic peptide inhibitors targeting the substrate recruitment site of cyclin-dependent kinase complexes.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
M210 I213 W217 Q254 I281 T282 D283
Binding residue
(residue number reindexed from 1)
M36 I39 W43 Q80 I107 T108 D109
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0016538
cyclin-dependent protein serine/threonine kinase regulator activity
Biological Process
GO:0044772
mitotic cell cycle phase transition
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Molecular Function
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Biological Process
External links
PDB
RCSB:1urc
,
PDBe:1urc
,
PDBj:1urc
PDBsum
1urc
PubMed
15455144
UniProt
P20248
|CCNA2_HUMAN Cyclin-A2 (Gene Name=CCNA2)
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