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PDBsum entry 3qhr
Go to PDB code:
Transferase/protein binding
PDB id
3qhr
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Contents
Protein chains
298 a.a.
261 a.a.
Ligands
PRO-LYS-THR-PRO-
LYS-LYS-ALA-LYS-
LYS-LEU
×4
ADP
×2
MGF
×2
GOL
×17
Metals
_MG
×4
_CL
×2
Waters
×601
PDB id:
3qhr
Links
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CATH
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PDBSWS
PDBePISA
ProSAT
Name:
Transferase/protein binding
Title:
Structure of a pcdk2/cyclina transition-state mimic
Structure:
Cell division protein kinase 2. Chain: a, c. Synonym: p33 protein kinase. Engineered: yes. Cyclin-a2. Chain: b, d. Fragment: unp residues 163-422. Synonym: cyclin-a. Engineered: yes.
Source:
Homo sapiens. Human. Organism_taxid: 9606. Gene: cdk2. Expressed in: escherichia coli. Expression_system_taxid: 562. Mus musculus. Mouse. Organism_taxid: 10090.
Resolution:
2.17Å
R-factor:
0.181
R-free:
0.210
Authors:
M.A.Young,D.M.Jacobsen,Z.Q.Bao
Key ref:
Z.Q.Bao et al. (2011). Briefly bound to activate: transient binding of a second catalytic magnesium activates the structure and dynamics of CDK2 kinase for catalysis.
Structure
,
19
, 675-690.
PubMed id:
21565702
Date:
26-Jan-11
Release date:
25-May-11
PROCHECK
Headers
References
Protein chains
?
P24941
(CDK2_HUMAN) - Cyclin-dependent kinase 2 from Homo sapiens
Seq:
Struc:
298 a.a.
298 a.a.
*
Protein chains
?
P51943
(CCNA2_MOUSE) - Cyclin-A2 from Mus musculus
Seq:
Struc:
422 a.a.
261 a.a.
*
Key:
PfamA domain
Secondary structure
CATH domain
*
PDB and UniProt seqs differ at 2 residue positions (black crosses)
Enzyme reactions
Enzyme class:
Chains A, C:
E.C.2.7.11.22
- cyclin-dependent kinase.
[IntEnz]
[ExPASy]
[KEGG]
[BRENDA]
Reaction:
1.
L-seryl-[protein] + ATP = O-phospho-L-seryl-[protein] + ADP + H
+
2.
L-threonyl-[protein] + ATP = O-phospho-L-threonyl-[protein] + ADP + H
+
L-seryl-[protein]
+
ATP
=
O-phospho-L-seryl-[protein]
Bound ligand (Het Group name =
ADP
)
corresponds exactly
+
ADP
+
H(+)
L-threonyl-[protein]
+
ATP
=
O-phospho-L-threonyl-[protein]
Bound ligand (Het Group name =
ADP
)
corresponds exactly
+
ADP
+
H(+)
Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
reference
Structure
19
:675-690 (2011)
PubMed id:
21565702
Briefly bound to activate: transient binding of a second catalytic magnesium activates the structure and dynamics of CDK2 kinase for catalysis.
Z.Q.Bao,
D.M.Jacobsen,
M.A.Young.
ABSTRACT
No abstract given.
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