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Crystal structure of effect protein avrptob complexed with kinase pto

Analyse Crystal structure of effect protein avrptob complexed with kinase pto in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3HGK
Type
protein
Length
1,458 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein kinase; Effector protein HOPAB2
EC
6.3.2.-
UniProt
Q40234, Q8RSY1
Pockets
18 · best druggability 0.85

Structure

x-ray diffraction · 4 distinct chains · 39% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DProtein kinaseprotein28835% helix, 12% strandQ40234
BProtein kinaseprotein28837% helix, 15% strandQ40234
CProtein kinaseprotein28637% helix, 16% strandQ40234
E, F, G, HEffector protein HOPAB2 (EC 6.3.2.-)protein7765% helix, 3% strandQ8RSY1

Pockets

18 pockets found on a 1 Å grid, 15 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17270.850.88107empty
27470.850.8893empty
32910.760.8942empty
43010.750.8744empty
55170.720.8156empty

Interfaces

15 interfaces between chains.

  • C–G · 1004 Ų buried · 7 hydrogen bonds · protein-protein
  • B–E · 986 Ų buried · 6 hydrogen bonds · protein-protein
  • D–H · 934 Ų buried · 8 hydrogen bonds · protein-protein
  • A–F · 930 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 845 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified (phosphorylation).

Compared structures

  • 3HGK · crystal structure of effect protein AvrptoB complexed with kinase Pto · the same entry in another collection · chain H against H, TM-score 1.00
  • Q8RSY1 · AlphaFold monomer V2.0 prediction for effector protein HOPAB2 (Q8RSY1) · a predicted model of the same protein · chain E against A, TM-score 0.96

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