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Crystal structure of the MK2H peptide homodimer.

Analyse Crystal structure of the MK2H peptide homodimer. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DXR
Type
protein
Length
176 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MK2H protein
Ligands
SO4
Pockets
1 · best druggability 0.46

Structure

x-ray diffraction · 3 distinct chains · 23% helix, 36% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMK2H proteinprotein4821% helix, 33% strand—
B, DMK2H proteinprotein4323% helix, 37% strand—
CMK2H proteinprotein4224% helix, 38% strand—

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 5 copies · chains B, A, C, D
  • CXS · 3-cyclohexyl-1-propylsulfonic acid · additive · chains C, D

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

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1680.460.8316empty

Interfaces

6 interfaces between chains.

  • A–B · 2231 Ų buried · 50 hydrogen bonds · protein-protein
  • C–D · 2210 Ų buried · 50 hydrogen bonds · protein-protein
  • A–D · 242 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 190 Ų buried · 0 hydrogen bonds · protein-protein
  • A–C · 171 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 7DXR · Crystal structure of the mk2h peptide homodimer. · the same entry in another collection · chain A against A, TM-score 1.00

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