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Crystal structure of PLK1 polo-box domain in complex with pl-55

Analyse Crystal structure of PLK1 polo-box domain in complex with pl-55 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4LKL
Type
protein
Length
220 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SERINE/THREONINE-protein kinase PLK1; Pl-55
EC
2.7.11.21
UniProt
P53350
Ligands
ACE, ADM, NH2
Pockets
2 · best druggability 0.42

Structure

x-ray diffraction · 2 distinct chains · 30% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASERINE/THREONINE-protein kinase PLK1 (EC 2.7.11.21)protein21430% helix, 30% strandP53350
BPl-55protein60% helix, 17% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains A, B
  • ADM · Adamantane · ligand · chains A, B
  • NH2 · Amino group · ion · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1550.420.8322empty
2570.320.7612empty

Interfaces

1 interface between chains.

  • A–B · 475 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent, 1 modified (covalent ligand, phosphorylation).

Compared structures

  • 4LKL · Crystal structure of Plk1 Polo-box domain in complex with PL-55 · the same entry in another collection · chain A against A, TM-score 1.00

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