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MolNFT v1 · #157962 · protein

Crystal structure of nonphosphorylated, HPK1 kinase domain in complex with sunitinib in the inactive state.

6NFY · Mitogen-activated protein kinase kinase kinase kinase 1: “Crystal structure of nonphosphorylated, HPK1 kinase domain in complex with sunitinib in the inactive state.”. X-ray diffraction, 1 ligand (B49), 7 pockets (best druggability…

PDB
6NFY
Type
protein
Length
567 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mitogen-activated protein kinase kinase kinase kinase 1
EC
2.7.11.1
UniProt
Q92918
Ligands
B49
Pockets
7 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMitogen-activated protein kinase kinase kinase kinase 1 (EC 2.7.11.1)protein28240% helix, 18% strandQ92918
BMitogen-activated protein kinase kinase kinase kinase 1 (EC 2.7.11.1)protein28536% helix, 20% strandQ92918

Ligands and binding sites

  • B49 · N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fluoro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide · 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, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13480.810.9043empty
23170.650.8143B49
33190.650.8138empty
42530.610.8032B49
52280.530.7727empty

Interfaces

1 interface between chains.

  • A–B · 2331 Ų buried · 27 hydrogen bonds · protein-protein

Compared structures

  • 6NFY · Crystal structure of nonphosphorylated, HPK1 kinase domain in complex with sunitinib in… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q92918 · AlphaFold monomer V2.0 prediction for mitogen-activated protein kinase kinase kinase… · a predicted model of the same protein · chain B against A, TM-score 0.92

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