GL1X · GenesisL1 explorer

MolNFT v1 · #63124 · protein

Crystal structure of human mkp-2

3EZZ · Dual specificity protein phosphatase 4: “Crystal structure of human mkp-2”. X-ray diffraction, 1 ligand (SO4), 6 pockets (best druggability 0.76). MolNFT v1 #63124 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
3EZZ
Type
protein
Length
864 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dual specificity protein phosphatase 4
EC
3.1.3.48, 3.1.3.16
UniProt
Q13115
Ligands
SO4
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FDual specificity protein phosphatase 4 (EC 3.1.3.48, 3.1.3.16)protein14442% helix, 15% strandQ13115

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 9 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17720.760.8172empty
21230.470.7930SO4
31310.440.7729SO4
41040.370.7421empty
5560.360.7916empty

Interfaces

7 interfaces between chains.

  • E–F · 530 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 529 Ų buried · 6 hydrogen bonds · protein-protein
  • B–E · 468 Ų buried · 9 hydrogen bonds · protein-protein
  • A–E · 434 Ų buried · 2 hydrogen bonds · protein-protein
  • B–D · 373 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3EZZ · Crystal Structure of human MKP-2 · the same entry in another collection · chain F against F, TM-score 1.00
  • Q13115 · AlphaFold monomer V2.0 prediction for dual specificity protein phosphatase 4 (Q13115) · a predicted model of the same protein · chain E against A, TM-score 0.98

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