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Crystal structure of divalent ion tolerance protein CUTA1 from ehrlichia chaffeensis

Analyse Crystal structure of divalent ion tolerance protein CUTA1 from ehrlichia… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4IYQ
Type
protein
Length
321 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Divalent ion tolerance protein CUTA1
UniProt
Q2GG79
Ligands
CA
Pockets
4 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 36% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CDivalent ion tolerance protein CUTA1protein10736% helix, 40% strandQ2GG79

Ligands and binding sites

  • CA · Calcium ion · metal · 5 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11650.840.9828empty
21090.490.8017empty
3940.490.8118empty
4950.470.8115empty

Interfaces

3 interfaces between chains.

  • B–C · 1062 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1009 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 968 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 4IYQ · Crystal structure of divalent ion tolerance protein CutA1 from Ehrlichia chaffeensis · the same entry in another collection · chain A against A, TM-score 1.00

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