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Crystal structure of bovine pancreatic carboxypeptidase a complexed with D-N-hydroxyaminocarbonyl phenylalanine at 2.3 a

Analyse Crystal structure of bovine pancreatic carboxypeptidase a complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1HDQ
Type
protein
Length
307 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carboxypeptidase a
EC
3.4.17.1
UniProt
P00730
Ligands
INF, ZN
Pockets
2 · best druggability 0.62

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACarboxypeptidase a (EC 3.4.17.1)protein30740% helix, 18% strandP00730

Ligands and binding sites

  • INF · D-[(N-hydroxyamino)carbonyl]phenylalanine · ligand · chains A
  • ZN · Zinc ion · metal · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11600.620.8427INF
2520.290.7514empty

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 1HDQ · Crystal structure of bovine pancreatic carboxypeptidase A complexed with… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00730 · AlphaFold monomer V2.0 prediction for carboxypeptidase A1 (P00730) · a predicted model of the same protein · chain A against A, TM-score 1.00

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