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Crystal structure of the tetratricopeptide repeat (tpr) motif of human dual specificity protein kinase MPS1

Analyse Crystal structure of the tetratricopeptide repeat (tpr) motif of human dual… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4H7Y
Type
protein
Length
556 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dual specificity protein kinase ttk
EC
2.7.12.1
UniProt
P33981
Pockets
7 · best druggability 0.75

Structure

x-ray diffraction · 3 distinct chains · 74% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADual specificity protein kinase ttk (EC 2.7.12.1)protein14173% helix, 1% strandP33981
BDual specificity protein kinase ttk (EC 2.7.12.1)protein13974% helix, 1% strandP33981
C, DDual specificity protein kinase ttk (EC 2.7.12.1)protein13875% helix, 1% strandP33981

Pockets

7 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18720.750.7972empty
26600.700.7857empty
31110.520.8323empty
4980.370.7524empty
5770.350.7616empty

Interfaces

5 interfaces between chains.

  • A–D · 970 Ų buried · 16 hydrogen bonds · protein-protein
  • B–C · 940 Ų buried · 18 hydrogen bonds · protein-protein
  • A–B · 751 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 71 Ų buried · 1 hydrogen bond · protein-protein
  • B–D · 51 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4H7Y · Crystal structure of the tetratricopeptide repeat (TPR) motif of human dual specificity… · the same entry in another collection · chain A against A, TM-score 1.00

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