Uniprot accession / id : Q3UMW7  OR   Uniprot accession / id : Q16644
 
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Entry Information
Entry status  (1)
REL
(5)
 
Experimental methods  (1)
X-ray diffraction
(5)
 
Authors  (44)
Barf T
(2)
Barker J
(2)
Cheng RKY
(2)
Felicetti B
(2)
Hesterkamp T
(2)
Kaptein A
(2)
Kazemier B
(2)
Oubrie A
(2)
Palan S
(2)
Schultz-Fademrecht C
(2)
Whittaker M
(2)
de Roos J
(2)
van Hoek M
(2)
van de Kar B
(2)
van der Heijden R
(2)
Borsboom J
(1)
Cheng R
(1)
Croll TI
(1)
Demont D
(1)
Goorden R
(1)
Heijden R
(1)
Hoek M
(1)
Hofstra C
(1)
Hoogenboom N
(1)
Hornberg J
(1)
Kar B
(1)
Klop H
(1)
Lommerse J
(1)
Read RJ
(1)
Roos J
(1)
Scheffers M
(1)
Scheich C
(1)
Seegers N
(1)
Smeets R
(1)
Someren R
(1)
Toogood-Johnson I
(1)
Versteegh J
(1)
Wilde S
(1)
Zeeland M
(1)
de Kimpe V
(1)
de Wilde S
(1)
de Zwart E
(1)
van Someren R
(1)
van Zeeland M
(1)
 
Homo / hetero assembly  (1)
homo
(5)
 
Assembly composition  (1)
protein structure
(5)
 
Assembly polymer count  (1)
monomer
(5)
 
Resolution distribution
1.5 - 2
(3)
2.0 - 2.5
(2)
 
Release year distribution
2005 - 2010
(2)
2010 - 2015
(3)
2020 - 2025
(1)
 
Journal  (4)
Bioorg Med Chem Lett
(2)
Acta Crystallogr D Struct Biol
(1)
Protein Sci
(1)
To be published
(1)
 
Macromolecules
Organism superkingdom  (1)
Eukaryota
(5)
 
Organism name  (1)
Homo sapiens
(5)
 
Molecule name  (8)
3pK
(5)
Chromosome 3p kinase
(5)
MAP kinase-activated protein kinase 3
(5)
MAPK-activated protein kinase 3
(5)
MAPKAP kinase 3
(5)
MAPKAP-K3
(5)
MAPKAPK-3
(5)
MK-3
(5)
 
Molecule type  (1)
Protein
(5)
 
Gene names  (1)
MAPKAPK3
(5)
 
Interacting ligands  (4)
P4O : 2-(2-QUINOLIN-3-YLPYRIDIN-4-YL)-1,5,6,7-TETRAHYDRO-4H-PYRROLO[3,2-C]PYRIDIN-4-ONE
(2)
05B : 2'-[2-(1,3-benzodioxol-5-yl)pyrimidin-4-yl]-5',6'-dihydrospiro[piperidine-4,7'-pyrrolo[3,2-c]pyridin]-4'(1'H)-one
(1)
F10 : 2-[2-(2-FLUOROPHENYL)PYRIDIN-4-YL]-1,5,6,7-TETRAHYDRO-4H-PYRROLO[3,2-C]PYRIDIN-4-ONE
(1)
I85 : N-{4-[(3S)-4'-oxo-1',4',5',6'-tetrahydrospiro[piperidine-3,7'-pyrrolo[3,2-c]pyridin]-2'-yl]pyridin-2-yl}-3-(trifluoromethyl)benzamide
(1)
 
Function and Biology
EC number / name  (1)
2.7.11.1 : Non-specific serine/threonine protein kinase
(5)
 
Biological function  (2)
ATP binding
(5)
protein kinase activity
(5)
 
Biological process  (1)
protein phosphorylation
(5)
 
Representative Structures
Representative Structures
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Entries 1 to 5 of 5
Entries 1 to 5 of 5
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Re-refinement of MK3-inhibitor complex
Croll TI, Read RJ
Acta Crystallogr D Struct Biol (2021) [PMID: 33825704  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: P4O    P4O   
Assembly name: MAP kinase-activated protein kinase 3 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-172538 (Preferred)   search this ID
PDBe-KB: Q16644   
X-ray diffraction
1.9Å resolution
Released: 12 Jan 2022
Model geometry
Fit model/data
7nrb
7nrb
7nrb
High resolution crystal structure of mitogen-activated protein kinase-activated protein kinase 3/inhibitor 2 complex
Cheng RKY, Barker J, Palan S, Felicetti B, Whittaker M, Hesterkamp T
To be published
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: F10    F10   
Assembly name: MAP kinase-activated protein kinase 3 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-172538 (Preferred)   search this ID
PDBe-KB: Q16644   
X-ray diffraction
2Å resolution
Released: 26 Jan 2010
Model geometry
Fit model/data
3fxw
3fxw
3fxw
High resolution crystal structure of mitogen-activated protein kinase-activated protein kinase 3 (MK3)-inhibitor complex
Cheng RKY, Barker J, Palan S, Felicetti B, Whittaker M, Hesterkamp T
Protein Sci (2010) [PMID: 19937655  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: P4O    P4O   
Assembly name: MAP kinase-activated protein kinase 3 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-172538 (Preferred)   search this ID
PDBe-KB: Q16644   
X-ray diffraction
1.9Å resolution
Released: 15 Dec 2009
Model geometry
Fit model/data
3fhr
3fhr
3fhr
MK3 kinase bound to Compound 5b
Oubrie A, Kazemier B
Bioorg Med Chem Lett (2011) [PMID: 21565500  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: 05B    05B   
Assembly name: MAP kinase-activated protein kinase 3 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-172538 (Preferred)   search this ID
PDBe-KB: Q16644   
X-ray diffraction
2.09Å resolution
Released: 25 May 2011
Model geometry
Fit model/data
3r1n
3r1n
3r1n
Novel ATP-competitive MK2 inhibitors with potent biochemical and cell-based activity throughout the series
Oubrie A, Kazemier B
Bioorg Med Chem Lett (2012) [PMID: 22119462  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: I85    I85   
Assembly name: MAP kinase-activated protein kinase 3 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-172538 (Preferred)   search this ID
PDBe-KB: Q16644   
X-ray diffraction
2.25Å resolution
Released: 14 Dec 2011
Model geometry
Fit model/data
3she
3she
3she
Entries 1 to 5 of 5
Entries 1 to 5 of 5