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Crystal structure of the kinetoplastid kinetochore protein trypanosoma brucei KKT3 divergent polo-box domain

Analyse Crystal structure of the kinetoplastid kinetochore protein trypanosoma brucei… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
8A0K
Type
protein
Length
815 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein kinase, putative
UniProt
Q38DT1
Pockets
13 · best druggability 0.78

Structure

x-ray diffraction · 4 distinct chains · 20% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein kinase, putativeprotein20619% helix, 32% strandQ38DT1
BProtein kinase, putativeprotein20619% helix, 31% strandQ38DT1
CProtein kinase, putativeprotein20022% helix, 33% strandQ38DT1
DProtein kinase, putativeprotein20320% helix, 32% strandQ38DT1

Ligands and binding sites

  • PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains A, C, 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110630.780.7977PEG
23330.550.7552empty
31870.470.7631empty
41310.440.7730empty
5500.430.8318empty

Interfaces

4 interfaces between chains.

  • A–C · 636 Ų buried · 3 hydrogen bonds · protein-protein
  • B–D · 549 Ų buried · 14 hydrogen bonds · protein-protein
  • A–D · 54 Ų buried · 1 hydrogen bond · protein-protein
  • A–B · 40 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 8A0K · crystal structure of the kinetoplastid kinetochore protein Trypanosoma brucei KKT3… · the same entry in another collection · chain A against A, TM-score 1.00

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