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Human B-RAF kinase in complex with an amide linked pyrazolopyridine inhibitor

Analyse Human B-RAF kinase in complex with an amide linked pyrazolopyridine inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3SKC
Type
protein
Length
536 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SERINE/THREONINE-protein kinase B-RAF
EC
2.7.11.1
UniProt
P15056
Ligands
BR2
Pockets
7 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 39% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASERINE/THREONINE-protein kinase B-RAF (EC 2.7.11.1)protein26040% helix, 15% strandP15056
BSERINE/THREONINE-protein kinase B-RAF (EC 2.7.11.1)protein27639% helix, 14% strandP15056

Ligands and binding sites

  • BR2 · 2,6-difluoro-N-[(5S)-3-methoxy-5H-pyrazolo[3,4-b]pyridin-5-yl]-3-[(phenylsulfonyl)amino]benzamide · ligand · 2 copies · chains A, B

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

Pockets

7 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16900.780.8372BR2
24900.700.8052BR2
3910.680.9329empty
42500.560.7834empty
52020.560.7927empty

Interfaces

1 interface between chains.

  • A–B · 1172 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 3SKC · Human B-Raf Kinase in Complex with an Amide Linked Pyrazolopyridine Inhibitor · the same entry in another collection · chain A against A, TM-score 1.00
  • P15056 · AlphaFold monomer V2.0 prediction for SERINE/THREONINE-protein kinase B-RAF (P15056) · a predicted model of the same protein · chain A against A, TM-score 0.98

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