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Braf kinase domain B3AC loop deletion mutant in complex with AZ628

Analyse Braf kinase domain B3AC loop deletion mutant in complex with AZ628 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5HID
Type
protein
Length
526 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
B1E
Pockets
7 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASERINE/THREONINE-protein kinase B-RAF (EC 2.7.11.1)protein25743% helix, 18% strandP15056
BSERINE/THREONINE-protein kinase B-RAF (EC 2.7.11.1)protein26941% helix, 17% strandP15056

Ligands and binding sites

  • B1E · 3-(2-cyanopropan-2-yl)-N-{4-methyl-3-[(3-methyl-4-oxo-3,4-dihydroquinazolin-6-yl)amino]phenyl}benzamide · ligand · 2 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 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, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17920.740.7973B1E
25180.680.7851B1E
31110.570.8519empty
41470.550.8126empty
5510.480.8614empty

Interfaces

1 interface between chains.

  • A–B · 1222 Ų buried · 18 hydrogen bonds · protein-protein

Compared structures

  • 5HID · BRAF Kinase domain b3aC loop deletion mutant in complex with AZ628 · 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 0.94

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