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Structure of a hyperthermostable carbonic anhydrase identified from an active hydrothermal vent chimney

Analyse Structure of a hyperthermostable carbonic anhydrase identified from an active… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6EKI
Type
protein
Length
1,332 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carbonic anhydrase
EC
4.2.1.1
Ligands
ZN
Pockets
11 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 18% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FCarbonic anhydrase (EC 4.2.1.1)protein22218% helix, 39% strand—

Ligands and binding sites

  • ZN · Zinc ion · metal · 6 copies · chains A, B, C, D, E, F

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

Pockets

11 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18620.740.7890empty
2500.721.0016empty
38470.680.7578empty
45800.680.7859empty
53820.570.7546empty

Interfaces

7 interfaces between chains.

  • B–F · 1044 Ų buried · 19 hydrogen bonds · protein-protein
  • C–E · 1028 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 563 Ų buried · 16 hydrogen bonds · protein-protein
  • B–D · 533 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 313 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 6EKI · Structure of a hyperthermostable carbonic anhydrase identified from an active… · the same entry in another collection · chain A against A, TM-score 1.00

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