Uniprot accession / id : Q62073  OR   Uniprot accession / id : O43318
 
Filter by :
Entry Information
Entry status  (1)
REL
(24)
 
Experimental methods  (1)
X-ray diffraction
(24)
 
Authors  (179)
Gurbani D
(8)
Westover KD
(8)
Gray NS
(7)
Hunter JC
(7)
Tan L
(7)
Du G
(6)
Ficarro SB
(6)
Fukami TA
(6)
Griffin JD
(6)
Ide M
(6)
Irie M
(6)
Jones DS
(6)
Kashiwagi H
(6)
Li L
(6)
Marto JA
(6)
Matsuura T
(6)
Miura T
(6)
Morikami K
(6)
Morishima K
(6)
Mowafy S
(6)
Muraoka T
(6)
Nakamura M
(6)
Nishihara M
(6)
Rao S
(6)
Sorger PK
(6)
Tam CP
(6)
Weisberg EL
(6)
Mulvihill MJ
(5)
Albertella M
(3)
Bittner M
(3)
Cooke A
(3)
Crew AP
(3)
Hornberger KR
(3)
Kamikawa T
(3)
Kleinberg A
(3)
Liu J
(3)
Maresca P
(3)
Maskos K
(3)
May E
(3)
Meyn P
(3)
Moertl M
(3)
Romashko D
(3)
Tokar B
(3)
Wang J
(3)
Wilde VL
(3)
Babiss L
(2)
Berger DM
(2)
Bruseker YB
(2)
Cuozzo JW
(2)
Damen E
(2)
Dong H
(2)
Gray MJ
(2)
Heijne EH
(2)
Hekking KFW
(2)
Hupp CD
(2)
Jestel A
(2)
Keefe AD
(2)
Li AH
(2)
McRiner AJ
(2)
Medeiros MR
(2)
Mueller G
(2)
Muller G
(2)
Müller G
(2)
Peick W
(2)
Renzetti LM
(2)
Siu K
(2)
Tanowitz M
(2)
Tarrant J
(2)
Thomson HA
(2)
Veerman JJN
(2)
Weng F
(2)
Winkel R
(2)
Zech B
(2)
Zhang Y
(2)
van Bruggen W
(2)
van Rijnsbergen P
(2)
Bell A
(1)
Bera AK
(1)
Bess K
(1)
Bodoor K
(1)
Bouzan A
(1)
Brenneisen S
(1)
Brown DG
(1)
Brown K
(1)
Buhrlage SJ
(1)
Byth KF
(1)
Campany K
(1)
Campbell PL
(1)
Carlson DA
(1)
Cheetham GM
(1)
Chen H
(1)
Chen X
(1)
Chen Z
(1)
Chenal G
(1)
Choi HG
(1)
Cohen P
(1)
Dedi N
(1)
Demirci S
(1)
Deng X
(1)
Derbyshire ER
(1)
 
More...
 
Homo / hetero assembly  (1)
homo
(24)
 
Assembly composition  (1)
protein structure
(24)
 
Assembly polymer count  (1)
monomer
(24)
 
Resolution distribution
1.5 - 2
(4)
2.0 - 2.5
(11)
2.5 - 3
(8)
3.0 - 3.5
(1)
 
Release year distribution
2005 - 2010
(1)
2010 - 2015
(6)
2015 - 2020
(13)
2020 - 2025
(4)
 
Journal  (9)
Bioorg Med Chem
(9)
Bioorg Med Chem Lett
(3)
Chem Pharm Bull (Tokyo)
(3)
ACS Med Chem Lett
(2)
J Med Chem
(2)
To be published
(2)
ACS Chem Biol
(1)
Cell Chem Biol
(1)
J Mol Biol
(1)
 
Macromolecules
Organism superkingdom  (1)
Eukaryota
(24)
 
Organism name  (1)
Homo sapiens
(24)
 
Molecule name  (7)
Mitogen-activated protein kinase kinase kinase 7
(24)
TGF-beta-activated kinase 1
(24)
Transforming growth factor-beta-activated kinase 1
(24)
Mitogen-activated protein kinase kinase kinase 7-interacting protein 1
(23)
TAK1-binding protein 1
(23)
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1
(23)
TGF-beta-activated kinase 1-binding protein 1
(23)
 
Molecule type  (1)
Protein
(24)
 
Gene names  (4)
MAP3K7
(24)
TAK1
(24)
MAP3K7IP1
(23)
TAB1
(23)
 
Interacting ligands  (26)
EDO : 1,2-ETHANEDIOL
(3)
DMS : DIMETHYL SULFOXIDE
(2)
GOL : GLYCEROL
(2)
1FM : (3S,5Z,8S,9S,11E)-8,9,16-trihydroxy-14-methoxy-3-methyl-3,4,9,10-tetrahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione
(1)
1UH : 2-(1-benzothiophen-7-yl)-4-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]furo[2,3-c]pyridin-7-amine
(1)
1UL : 1-(4-{4-[7-amino-2-(1,2,3-benzothiadiazol-7-yl)furo[2,3-c]pyridin-4-yl]-1H-pyrazol-1-yl}piperidin-1-yl)ethanone
(1)
1UO : trans-4-{4-[7-amino-2-(1,2,3-benzothiadiazol-7-yl)-3-chlorofuro[2,3-c]pyridin-4-yl]-1H-pyrazol-1-yl}cyclohexanol
(1)
5KW : 2-chloro-N-{2-[(5-chloro-2-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)oxy]phenyl}acetamide
(1)
6H3 : N-{2-[(5-chloro-2-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)amino]phenyl}propanamide
(1)
6H4 : N-{2-[(5-chloro-2-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)oxy]phenyl}prop-2-enamide
(1)
6HF : N-(4-((2-((4-(4-methylpiperazin-1-yl)phenyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)phenyl)acrylamide
(1)
6JV : N-(2-methoxy-4-{[3-(4-methylpiperazin-1-yl)propyl]carbamoyl}phenyl)-4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-7-carboxamide
(1)
6KC : N-[5-(4-methylpiperazine-1-carbonyl)[1,1'-biphenyl]-2-yl]-4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-7-carboxamide
(1)
6KD : N-(2-isopropoxy-3-(4-methylpiperazine-1-carbonyl)phenyl)-4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-7-carboxamide
(1)
6L4 : ~{N}-[2-[5-chloranyl-2-[(1-methylpyrazol-4-yl)amino]pyrimidin-4-yl]oxyphenyl]prop-2-enamide
(1)
6V3 : 1-(4-((1H-pyrrolo[2,3-b]pyridin-4-yl)oxy)phenyl)-3-(5-(4-methylpiperazin-1-yl)naphthalen-2-yl)urea
(1)
6V4 : N-(2-isopropoxy-4-(4-methylpiperazine-1-carbonyl)phenyl)-2-(3-(3-phenylureido)phenyl)thiazole-4-carboxamide
(1)
6V5 : N-(2-isopropoxy-4-(4-methylpiperazine-1-carbonyl)phenyl)-2-(3-(phenylcarbamoyl)phenyl)thiazole-4-carboxamide
(1)
A1IED : 6-[5-[6-(4-oxidanylcyclohexyl)oxy-1~{H}-pyrrolo[2,3-b]pyridin-5-yl]-1,2-oxazol-3-yl]pyridine-2-carboxamide
(1)
ADN : ADENOSINE
(1)
EDH : N~1~-(1-propyl-1,3-dihydro-2H-benzimidazol-2-ylidene)benzene-1,3-dicarboxamide
(1)
NG2 : N-{4-[(4-ethylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}-4-methyl-3-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)benzamide
(1)
T92 : 2-[(5-chloro-2-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)amino]phenyl prop-2-enoate
(1)
URW : 2-[[5-[[2-[bis(fluoranyl)methoxy]phenyl]methyl-[(2~{R})-1-(methylamino)-1-oxidanylidene-propan-2-yl]carbamoyl]-1~{H}-imidazol-2-yl]carbonyl]isoindole-5-carboxamide
(1)
UWZ : ~{N}-[[2-[bis(fluoranyl)methoxy]phenyl]methyl]-~{N}-[2-(methylamino)-2-oxidanylidene-ethyl]-2-pyrrolidin-1-ylcarbonyl-1~{H}-imidazole-4-carboxamide
(1)
YIY : (1E)-1-[5-TERT-BUTYL-2-(3-FLUOROPHENYL)-1H-PYRAZOL-3-YLIDENE]-3-(4-PYRIDIN-3-YLOXYPHENYL)UREA
(1)
 
Function and Biology
EC number / name  (1)
2.7.11.25 : Mitogen-activated protein kinase kinase kinase
(24)
 
Biological function  (2)
ATP binding
(24)
protein kinase activity
(24)
 
Biological process  (1)
protein phosphorylation
(24)
 
Sequence and Structure classification
CATH class  (2)
Alpha Beta
(20)
Mainly Alpha
(20)
 
CATH topology  (2)
Phosphorylase Kinase; domain 1
(20)
Transferase(Phosphotransferase); domain 1
(20)
 
Pfam accession / name  (1)
PF07714 : PK_Tyr_Ser-Thr
(24)
 
Experimental Information
Diffraction protocol  (1)
Single wavelength
(24)
 
Diffraction radiation source type  (2)
Synchrotron
(23)
Rotating anode
(1)
 
Diffraction source  (11)
APS BEAMLINE 19-ID
(8)
SLS BEAMLINE X06SA
(3)
SLS BEAMLINE X10SA
(3)
ESRF BEAMLINE MASSIF-1
(2)
PHOTON FACTORY BEAMLINE BL-17A
(2)
APS BEAMLINE 17-ID
(1)
PHOTON FACTORY BEAMLINE AR-NW12A
(1)
PHOTON FACTORY BEAMLINE BL-5A
(1)
RIGAKU FR-E+ DW
(1)
SRS BEAMLINE PX14.1
(1)
SSRF BEAMLINE BL19U1
(1)
 
Synchrotron site  (6)
APS
(9)
SLS
(6)
Photon Factory
(4)
ESRF
(2)
SRS
(1)
SSRF
(1)
 
Diffraction detector type  (2)
CCD
(16)
Pixel
(8)
 
Refinement software  (4)
REFMAC
(11)
PHENIX
(9)
BUSTER
(3)
CNS
(1)
 
Representative Structures
Representative Structures
100%
95%
90%
70%
50%
40%
30%
Entries 1 to 10 of 24
Entries 1 to 10 of 24
 Select all entries on this page
Crystal structure of compound 8 bound to TAK1-TAB
Brown DG, Phillips C
To be published
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: YIY    YIY   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.49Å resolution
Released: 23 May 2012
Model geometry
Fit model/data
2yiy
2yiy
2yiy
Crystal Structure of type II inhibitor NG25 bound to TAK1-TAB1
Gurbani D, Hunter JC, Tan L, Westover KD
J Med Chem (2015) [PMID: 25075558  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: NG2    NG2   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.393Å resolution
Released: 30 Jul 2014
Model geometry
Fit model/data
4o91
4o91
4o91
Crystal Structure of (1R,4R)-4-{4-[7-amino-2-(1,2,3-benzothiadiazol-7-yl)-3-chlorofuro[2,3-c]pyridin-4-yl]-1H-pyrazol-1-yl}cyclohexan-1-ol bound to TAK1-TAB1
Wang J, Hornberger KR, Crew AP, Jestel A, Maskos K, Moertl M
Bioorg Med Chem Lett (2013) [PMID: 23856049  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: 1UO    1UO    EDO   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.55Å resolution
Released: 3 Jul 2013
Model geometry
Fit model/data
4l53
4l53
4l53
Crystal Structure of 2-(1-benzothiophen-7-yl)-4-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]furo[2,3-c]pyridin-7-amine bound to TAK1-TAB1
Wang J, Hornberger KR, Crew AP, Steinbacher S, Maskos K, Moertl M
Bioorg Med Chem Lett (2013) [PMID: 23850198  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: 1UH    1UH   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.68Å resolution
Released: 19 Jun 2013
Model geometry
Fit model/data
4l3p
4l3p
4l3p
Irreversible Inhibition of TAK1 Kinase by 5Z-7-Oxozeaenol
Larsen NA, Ferguson AD, Wu J
ACS Chem Biol (2013) [PMID: 23272696  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: 1FM    EDO    1FM   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.2Å resolution
Released: 23 Jan 2013
Model geometry
Fit model/data
4gs6
4gs6
4gs6
Crystal Structure of 1-(4-{4-[7-amino-2-(1,2,3-benzothiadiazol-7-yl)furo[2,3-c]pyridin-4-yl]-1H-pyrazol-1-yl}piperidin-1-yl)ethan-1-one bound to TAK1-TAB1
Wang J, Hornberger KR, Crew AP, Jestel A, Maskos K, Moertl M
Bioorg Med Chem Lett (2013) [PMID: 23850198  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: 1UL    1UL   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.54Å resolution
Released: 3 Jul 2013
Model geometry
Fit model/data
4l52
4l52
4l52
Crystal structure of human TAK1 kinase domain fused with TAB1
Liu J, Sun W, Gao J
To be published
Source organism: Homo sapiens  
Assembly composition: protein only structure
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.05Å resolution
Released: 20 Sep 2023
Model geometry
Fit model/data
8gw3
8gw3
8gw3
Crystal structure of human TAK1/TAB1 fusion protein in complex with compound S1
Scheufler C, Lammens A
J Med Chem (2024) [PMID: 39576936  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: A1IED    EDO   
Modified residues: SEP    TPO    SEP    TPO   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
2.402Å resolution
Released: 4 Dec 2024
Model geometry
Fit model/data
9fpd
9fpd
9fpd
Structure of TAK1 in complex with compound 22
Veerman JJN, Bruseker YB, Damen E, Heijne EH, van Bruggen W, Hekking KFW, Winkel R, Hupp CD, Keefe AD, Liu J, Thomson HA, Zhang Y, Cuozzo JW, McRiner AJ, Mulvihill MJ, van Rijnsbergen P, Zech B, Renzetti LM, Babiss L, Mueller G
ACS Med Chem Lett (2021) [PMID: 33859795  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: GOL    DMS    DMS    UWZ   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
1.98Å resolution
Released: 7 Apr 2021
Model geometry
Fit model/data
7nti
7nti
7nti
Structure of TAK1 in complex with compound 54
Veerman JJN, Bruseker YB, Damen E, Heijne EH, van Bruggen W, Hekking KFW, Winkel R, Hupp CD, Keefe AD, Liu J, Thomson HA, Zhang Y, Cuozzo JW, McRiner AJ, Mulvihill MJ, van Rijnsbergen P, Zech B, Renzetti LM, Babiss L, Mueller G
ACS Med Chem Lett (2021) [PMID: 33859795  ]
Source organism: Homo sapiens  
Assembly composition: protein only structure
Bound ligands: GOL    DMS    DMS    URW   
Assembly name: Mitogen-activated protein kinase kinase kinase 7, TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Preferred)   search this complex
PDBe complex ID: PDB-CPX-128894 (Preferred)   search this ID
PDBe-KB: Q15750    O43318   
X-ray diffraction
1.97Å resolution
Released: 7 Apr 2021
Model geometry
Fit model/data
7nth
7nth
7nth
Entries 1 to 10 of 24
Entries 1 to 10 of 24