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Crystal structure of aclacinomycin methylesterase (rdmc) with bound product analogue, 10-decarboxymethylaclacinomycin a (dcma)

Analyse Crystal structure of aclacinomycin methylesterase (rdmc) with bound product… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1Q0Z
Type
protein
Length
297 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aclacinomycin methylesterase
UniProt
Q54528
Ligands
AKA, SO4
Pockets
1 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAclacinomycin methylesteraseprotein29743% helix, 16% strandQ54528

Ligands and binding sites

  • AKA · 10-decarboxymethylaclacinomycin A (dcmaa) · ligand · chains A
  • SO4 · Sulfate ion · ion · chains A
  • 1PE · Pentaethylene glycol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15280.820.8865AKA, SO4, 1PE

Compared structures

  • 1Q0Z · Crystal structure of aclacinomycin methylesterase (RdmC) with bound product analogue… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q54528 · AlphaFold monomer V2.0 prediction for aclacinomycin methylesterase rdmc (Q54528) · a predicted model of the same protein · chain A against A, TM-score 1.00

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