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Crystal structure of alpha carbonic anhydrase from schistosoma mansoni bound to 1-(4-fluorophenyl)-3-(4-SULPHAMOYLPHENYL)SELENOUREA

Analyse Crystal structure of alpha carbonic anhydrase from schistosoma mansoni bound to… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7BM4
Type
protein
Length
552 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carbonic anhydrase
EC
4.2.1.1
UniProt
A0A3Q0KSG2
Ligands
U3N, NAG, ZN
Pockets
6 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 15% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCarbonic anhydrase (EC 4.2.1.1)protein27615% helix, 29% strandA0A3Q0KSG2

Ligands and binding sites

  • U3N · 1-(4-fluorophenyl)-3-(4-sulfamoylphenyl)selenourea · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1840.730.9638GOL
24300.620.7660empty
31500.550.8125U3N
41460.540.8123U3N
5660.290.7426empty

Interfaces

1 interface between chains.

  • A–B · 1101 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 glycan, 2 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7BM4 · Crystal structure of alpha Carbonic anhydrase from Schistosoma mansoni bound to… · the same entry in another collection · chain B against B, TM-score 1.00

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