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Structure of the mycobacterium tuberculosis aps kinase cysc in complex with ADP

Analyse Structure of the mycobacterium tuberculosis aps kinase cysc in complex with ADP in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4BZP
Type
protein
Length
346 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional enzyme CYSN/CYSC
EC
2.7.1.25
UniProt
Q10600
Ligands
ADP
Pockets
5 · best druggability 0.70

Structure

x-ray diffraction · 1 distinct chain · 45% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BBifunctional enzyme CYSN/CYSC (EC 2.7.1.25)protein17345% helix, 14% strandQ10600

Ligands and binding sites

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

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14410.700.8148ADP
24210.680.8048ADP
31210.420.7617empty
41050.410.7717empty
5570.320.7612empty

Interfaces

1 interface between chains.

  • A–B · 727 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 4BZP · Structure of the Mycobacterium tuberculosis APS kinase CysC in complex with ADP · the same entry in another collection · chain A against A, TM-score 1.00

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