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Crystal structure of caenorhabditis elegans acdh-11 in complex with C11-CoA

Analyse Crystal structure of caenorhabditis elegans acdh-11 in complex with C11-CoA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Y9J
Type
protein
Length
1,185 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein acdh-11, isoform B
EC
1.3.8.9
UniProt
Q3T978
Ligands
FAD, UCC
Pockets
14 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 56% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein acdh-11, isoform B (EC 1.3.8.9)protein59256% helix, 13% strandQ3T978
BProtein acdh-11, isoform B (EC 1.3.8.9)protein59356% helix, 13% strandQ3T978

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
  • UCC · S-{(3S,5R,9R)-1-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]-3,5,9-trihydroxy-8,8-dimethyl-3,5-dioxido-10,14-dioxo-2,4,6-trioxa-11,15-diaza-3lambda~5~,5lambda~5~-diphosphaheptadecan-17-yl} undecanethioate · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18820.840.86111FAD, UCC
210600.840.8570empty
310480.840.85121FAD, UCC
41060.440.7831empty
5670.430.8117empty

Interfaces

1 interface between chains.

  • A–B · 4731 Ų buried · 96 hydrogen bonds · protein-protein

Compared structures

  • 4Y9J · Crystal Structure of Caenorhabditis elegans ACDH-11 in complex with C11-CoA · the same entry in another collection · chain A against A, TM-score 1.00

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