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MolNFT v1 · #64169 · protein

Polo-like kinase 1 polo box domain in complex with ac-lhspta-NH2 peptide

3FVH · SERINE/THREONINE-protein kinase PLK1: “Polo-like kinase 1 polo box domain in complex with ac-lhspta-NH2 peptide”. X-ray diffraction, 2 ligands (ACE, NH2), 3 pockets (best druggability 0.43). MolNFT v1 #64169 on GenesisL1: 3D…

PDB
3FVH
Type
protein
Length
238 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SERINE/THREONINE-protein kinase PLK1; Acetyl-leu-his-ser-phosphothr-ala-NH2 peptide
EC
2.7.11.21
UniProt
P53350
Ligands
ACE, NH2
Pockets
3 · best druggability 0.43

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASERINE/THREONINE-protein kinase PLK1 (EC 2.7.11.21)protein23334% helix, 28% strandP53350
BAcetyl-leu-his-ser-phosphothr-ala-NH2 peptideprotein50% helix, 20% strand—

Ligands and binding sites

  • ACE · Acetyl group · 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1570.430.8318empty
2600.370.7918empty
3790.290.7219empty

Interfaces

1 interface between chains.

  • A–B · 414 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 3FVH · Polo-like kinase 1 Polo box domain in complex with Ac-LHSpTA-NH2 peptide · the same entry in another collection · chain A against A, TM-score 1.00

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