7PQV: MEK1

MEK1 in complex with compound 7. Determined by X-ray diffraction at 2.13 Å resolution. Released 16 Mar 2022.

Method
X-ray diffraction
Resolution
2.13 Å
Organism
Homo sapiens
Chains
1
Atoms
2,674
Mol. weight
39.02 kDa
Ligands
80C, CA, MG
Released
16 Mar 2022

Explore 7PQV in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7PQV contains 19 α-helices and 9 β-strands across 1 chain. 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, 9 β-strands

ElementResiduesLengthSheet
α-helix44-5815
α-helix65-673
β-strand68-7691
β-strand81-8771
β-strand92-10091
α-helix105-11410
α-helix115-1195
β-strand12612
β-strand129-13461
β-strand138-14361
β-strand15012
α-helix151-1588
α-helix163-18422
α-helix193-1953
β-strand196-19832
β-strand204-20632
α-helix213-2197
α-helix232-2354
α-helix243-25816
α-helix265-2673
α-helix268-2747
α-helix310-31910
α-helix321-3233
α-helix325-3262
α-helix332-34110
α-helix352-3565
α-helix359-3668
α-helix371-3799

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Dual specificity mitogen-activated protein kinase kinase 1Aprotein344Homo sapiensQ02750 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>7PQV_1 Dual specificity mitogen-activated protein kinase kinase 1 (chains A)
ELELDEQQRKRLEAFLTQKQKVGELKDDDFEKISELGAGNGGVVFKVSHKPSGLVMARKL
IHLEIKPAIRNQIIRELQVLHECNSPYIVGFYGAFYSDGEISICMEHMDGGSLDQVLKKA
GRIPEQILGKVSIAVIKGLTYLREKHKIMHRDVKPSNILVNSRGEIKLCDFGVSGQLIDS
MANSFVGTRSYMSPERLQGTHYSVQSDIWSMGLSLVEMAVGRYPIPPPDAKELELMFGCQ
VEGDAAETPPRPRTPGRPLNKFGMDSRPPMAIFELLDYIVNEPPPKLPSGVFSLEFQDFV
NKCLIKNPAERADLKQLMVHAFIKRSDAEEVDFAGWLCSTIGLN

Ligands and cofactors

IDNameFormulaCopies
80C8-(2-chloranyl-4-methoxy-phenyl)-7-fluoranyl-1-piperidin-4-yl-imidazo[4,5-c]qui…C22 H20 Cl F N4 O1
CACalcium ionCa2
MGMagnesium ionMg1

Primary citation

Discovery of MAP855, an Efficacious and Selective MEK1/2 Inhibitor with an ATP-Competitive Mode of Action. Poddutoori, R., Aardalen, K., Aithal, K. et al. J Med Chem (2022) 65:4350-4366. DOI 10.1021/acs.jmedchem.1c02192 · PubMed

Other PDB entries of the same protein (UniProt Q02750 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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