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Human cyclin-dependent kinase 2 in complex with roscovitine

Analyse Human cyclin-dependent kinase 2 in complex with roscovitine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2A4L
Type
protein
Length
286 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Homo sapiens cyclin-dependent kinase 2
EC
2.7.1.37
Ligands
RRC
Pockets
2 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHomo sapiens cyclin-dependent kinase 2 (EC 2.7.1.37)protein28634% helix, 15% strand—

Ligands and binding sites

  • RRC · R-roscovitine · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13500.730.8446RRC
2650.300.7416empty

Compared structures

  • 2A4L · Human cyclin-dependent kinase 2 in complex with roscovitine · the same entry in another collection · chain A against A, TM-score 1.00

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