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Syk catalytic domain in complex with a potent pyridopyrimidinone inhibitor

Analyse Syk catalytic domain in complex with a potent pyridopyrimidinone inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PX6
Type
protein
Length
262 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tyrosine-protein kinase syk
EC
2.7.10.2
UniProt
P43405
Ligands
2X6
Pockets
2 · best druggability 0.62

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein kinase syk (EC 2.7.10.2)protein26242% helix, 23% strandP43405

Ligands and binding sites

  • 2X6 · 7-{[(1R,2S)-2-aminocyclohexyl]amino}-5-(1H-indol-7-ylamino)pyrido[4,3-d]pyrimidin-4(3H)-one · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12970.620.79332X6
2540.270.7414empty

Compared structures

  • 4PX6 · SYK catalytic domain in complex with a potent pyridopyrimidi inhibitor · the same entry in another collection · chain A against A, TM-score 1.00
  • P43405 · AlphaFold monomer V2.0 prediction for tyrosine-protein kinase syk (P43405) · a predicted model of the same protein · chain A against A, TM-score 0.92

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