6YG6: MKK7 (MAP2K7) covalently

Crystal structure of MKK7 (MAP2K7) covalently bound with type-II inhibitor TL10-105. Determined by X-ray diffraction at 2.15 Å resolution. Released 12 Aug 2020.

Method
X-ray diffraction
Resolution
2.15 Å
Organism
Homo sapiens
Chains
2
Atoms
4,807
Mol. weight
71.5 kDa
Ligands
OQ8
Released
12 Aug 2020

Explore 6YG6 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6YG6 contains 37 α-helices and 24 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 19 helices, 13 β-strands

ElementResiduesLengthSheet
β-strand120-12451
β-strand127-13151
α-helix133-1353
β-strand136-14161
β-strand149-15571
β-strand161-16881
α-helix169-1702
α-helix173-18715
β-strand19512
α-helix196-1972
β-strand198-20361
β-strand207-21371
α-helix214-2152
β-strand217-21822
α-helix219-2268
α-helix229-2313
α-helix232-25322
α-helix262-2643
β-strand265-26732
β-strand273-27532
β-strand29513
α-helix302-3054
α-helix318-33316
β-strand33913
α-helix344-35310
α-helix355-3562
α-helix358-3603
α-helix367-37610
α-helix381-3833
α-helix387-3915
α-helix394-4018
α-helix406-41510
Chain B: 18 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand121-12444
β-strand127-13044
α-helix133-1353
β-strand136-14165
β-strand149-15575
β-strand161-16885
α-helix173-18715
β-strand19516
α-helix196-1972
β-strand198-20365
β-strand207-21375
α-helix214-2152
β-strand217-21826
α-helix219-2268
α-helix229-2313
α-helix232-25322
α-helix262-2643
β-strand265-26736
β-strand273-27536
α-helix302-3054
α-helix318-33316
α-helix344-35310
α-helix355-3562
α-helix358-3603
α-helix367-37610
α-helix381-3833
α-helix387-3904
α-helix394-4018
α-helix406-41510

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Dual specificity mitogen-activated protein kinase kinase 7A, Bprotein307Homo sapiensO14733 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>6YG6_1 Dual specificity mitogen-activated protein kinase kinase 7 (chains A, B)
SMKQTGYLTIGGQRYQAEINDLENLGEMGSGTCGQVWKMRFRKTGHVIAVKQMRRSGNKE
ENKRILMDLDVVLKSHDCPYIVQCFGTFITNTDVFIAMELMGTCAEKLKKRMQGPIPERI
LGKMTVAIVKALYYLKEKHGVIHRDVKPSNILLDERGQIKLCDFGISGRLVDDKAKDRSA
GCAAYMAPERIDPPDPTKPDYDIRADVWSLGISLVELATGQFPYKNCKTDFEVLTKVLQE
EPPLLPGHMGFSGDFQSFVKDCLTKDHRKRPKYNKLLEHSFIKRYETLEVDVASWFKDVM
AKTESPR

Ligands and cofactors

IDNameFormulaCopies
OQ8~{N}-[4-[(4-ethylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl]-4-methyl-3-[…C33 H40 F3 N7 O32

Water and common crystallization additives (EDO) are not listed.

Primary citation

Catalytic Domain Plasticity of MKK7 Reveals Structural Mechanisms of Allosteric Activation and Diverse Targeting Opportunities. Schroder, M., Tan, L., Wang, J. et al. Cell Chem Biol (2020) 27:1285-1295.e4. DOI 10.1016/j.chembiol.2020.07.014 · PubMed

Other PDB entries of the same protein (UniProt O14733 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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