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Crystal structure of the shikimate kinase + 3-dehydroquinate dehydratase + 3-dehydroshikimate dehydrogenase domains of ARO1 from candida albicans

Analyse Crystal structure of the shikimate kinase + 3-dehydroquinate dehydratase +… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TBV
Type
protein
Length
2,719 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pentafunctional arom polypeptide
Ligands
MG, CL
Pockets
20 · best druggability 0.76

Structure

x-ray diffraction · 4 distinct chains · 46% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APentafunctional arom polypeptideprotein68245% helix, 19% strand—
BPentafunctional arom polypeptideprotein67946% helix, 18% strand—
CPentafunctional arom polypeptideprotein67846% helix, 18% strand—
DPentafunctional arom polypeptideprotein68046% helix, 19% strand—

Ligands and binding sites

  • MG · Magnesium ion · metal · 4 copies · chains A, B, C, D
  • CL · Chloride ion · ion · 2 copies · chains A, D
  • GOL · Glycerol · additive · 13 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 17 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18550.760.8082GOL
29090.760.79101empty
38330.750.7976empty
46710.730.8055empty
53130.650.8138empty

Interfaces

3 interfaces between chains.

  • A–B · 884 Ų buried · 7 hydrogen bonds · protein-protein
  • B–D · 608 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 95 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 7TBV · Crystal structure of the shikimate kinase + 3-dehydroquinate dehydratase +… · the same entry in another collection · chain A against A, TM-score 1.00

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