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CDK9/CYCLIN T in complex with CAN508

Analyse CDK9/CYCLIN T in complex with CAN508 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TN8
Type
protein
Length
557 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cyclin-dependent kinase 9; Cyclin-T1
EC
2.7.11.22, 2.7.11.23
UniProt
P50750, O60563
Ligands
F18, PO4
Pockets
10 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 49% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACyclin-dependent kinase 9 (EC 2.7.11.22, 2.7.11.23)protein30537% helix, 14% strandP50750
BCyclin-T1protein25263% helix, 0% strandO60563

Ligands and binding sites

  • F18 · 4-[(E)-(3,5-diamino-1H-pyrazol-4-yl)diazenyl]phenol · ligand · chains A
  • PO4 · Phosphate ion · ion · 3 copies · chains B, A
  • GOL · Glycerol · additive · 2 copies · chains B, A

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

Pockets

10 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11740.700.8824F18
21620.500.7820empty
31420.480.7821empty
41020.450.7914empty
51260.450.7720GOL

Interfaces

1 interface between chains.

  • A–B · 938 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (phosphorylation).

Compared structures

  • 3TN8 · CDK9/cyclin T in complex with CAN508 · the same entry in another collection · chain A against A, TM-score 1.00
  • P50750 · AlphaFold monomer V2.0 prediction for cyclin-dependent kinase 9 (P50750) · a predicted model of the same protein · chain A against A, TM-score 0.99
  • O60563 · AlphaFold monomer V2.0 prediction for cyclin-T1 (O60563) · a predicted model of the same protein · chain B against A, TM-score 0.98

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