GL1X · GenesisL1 explorer

MolNFT v1 · #106122 · protein

Crystal structure of PKM2-K422R mutant bound with fbp

4RPP · Pyruvate kinase pkm: “Crystal structure of PKM2-K422R mutant bound with fbp”. X-ray diffraction, 1 ligand (FBP), 20 pockets (best druggability 0.87). MolNFT v1 #106122 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
4RPP
Type
protein
Length
1,623 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pyruvate kinase pkm
EC
2.7.1.40
UniProt
P14618
Ligands
FBP
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 4 distinct chains · 48% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APyruvate kinase pkm (EC 2.7.1.40)protein41148% helix, 16% strandP14618
BPyruvate kinase pkm (EC 2.7.1.40)protein40847% helix, 16% strandP14618
CPyruvate kinase pkm (EC 2.7.1.40)protein39649% helix, 16% strandP14618
DPyruvate kinase pkm (EC 2.7.1.40)protein40849% helix, 16% strandP14618

Ligands and binding sites

  • FBP · 1,6-di-O-phosphono-beta-D-fructofuranose · ligand · 4 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13900.870.9551empty
23890.860.9443empty
37040.740.8054empty
4580.590.9121empty
51270.590.8529FBP

Interfaces

5 interfaces between chains.

  • A–B · 2516 Ų buried · 41 hydrogen bonds · protein-protein
  • C–D · 2454 Ų buried · 35 hydrogen bonds · protein-protein
  • B–D · 1168 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 1136 Ų buried · 20 hydrogen bonds · protein-protein
  • A–D · 14 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4RPP · crystal structure of PKM2-K422R mutant bound with FBP · the same entry in another collection · chain A against A, TM-score 1.00

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