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Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion CO2 capture

Analyse Surface residue engineering of bovine carbonic anhydrase to an extreme… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4CNW
Type
protein
Length
515 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carbonic anhydrase 2
EC
4.2.1.1
UniProt
P00921
Ligands
ZN, CA
Pockets
5 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 12% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACarbonic anhydrase 2 (EC 4.2.1.1)protein25712% helix, 30% strandP00921
BCarbonic anhydrase 2 (EC 4.2.1.1)protein25813% helix, 30% strandP00921

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • CA · Calcium ion · metal · chains B

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14490.660.7851empty
21540.540.8024empty
31250.520.8123empty
41510.450.7519empty
5910.320.7324empty

Interfaces

1 interface between chains.

  • A–B · 333 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 4CNW · Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00921 · AlphaFold monomer V2.0 prediction for carbonic anhydrase 2 (P00921) · a predicted model of the same protein · chain A against A, TM-score 0.99

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