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Structure of Trypanosoma brucei brucei adenosine kinase in complex with adenosine and AMPPNP

Analyse Structure of Trypanosoma brucei brucei adenosine kinase in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4N09
Type
protein
Length
1,377 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.6
Source
Trypanosoma brucei brucei
Molecule
Adenosine kinase
EC
2.7.1.20
UniProt
Q584S0
Ligands
ADN, ADP
Pockets
13 · best druggability 0.81

Structure

x-ray diffraction · resolution 2.6 · 2 distinct chains · 43% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CAdenosine kinase (EC 2.7.1.20)protein34543% helix, 22% strandQ584S0
DAdenosine kinase (EC 2.7.1.20)protein34243% helix, 23% strandQ584S0

Ligands and binding sites

  • ADN · Adenosine · ligand · 4 copies · chains A, B, C, D
  • ADP · Adenosine-5'-diphosphate · ligand · 4 copies · chains A, B, C, D
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A, B

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

Pockets

13 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16230.810.8675ADN, ADP
25840.790.8563ADN, ADP, EDO
36700.790.8476ADN, ADP, EDO
46120.760.8277ADN, ADP
55150.750.8369empty

Interfaces

3 interfaces between chains.

  • A–B · 951 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 676 Ų buried · 7 hydrogen bonds · protein-protein
  • B–D · 635 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 4N09 · Structure of trypanosoma brucei brucei adenosine kinase in complex with adenosine and… · the same entry in another collection · chain A against A, TM-score 1.00

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