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X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in a ternary complex with U0126, ADP and MG2P

Analyse X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3EQH
Type
protein
Length
314 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dual specificity mitogen-activated protein kinase kinase 1
EC
2.7.12.2
UniProt
Q02750
Ligands
5BM, ADP, MG, CA, NA
Pockets
4 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADual specificity mitogen-activated protein kinase kinase 1 (EC 2.7.12.2)protein31446% helix, 14% strandQ02750

Ligands and binding sites

  • 5BM · (2Z)-bis{amino[(2-aminophenyl)sulfanyl]methylidene}butanedinitrile · ligand · chains A
  • ADP · Adenosine-5'-diphosphate · ligand · chains A
  • MG · Magnesium ion · metal · chains A
  • CA · Calcium ion · metal · chains A
  • NA · Sodium ion · metal · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17120.800.84645BM, ADP, MG
21780.530.7919empty
31160.490.8027empty
4550.420.8221empty

Compared structures

  • 3EQH · X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in a… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q02750 · AlphaFold monomer V2.0 prediction for dual specificity mitogen- activated protein kinase… · a predicted model of the same protein · chain A against A, TM-score 0.98

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