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Crystal structure of ketosteroid isomerase Y16AD103A from pseudomonas putida

Analyse Crystal structure of ketosteroid isomerase Y16AD103A from pseudomonas putida in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3T8N
Type
protein
Length
516 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Steroid delta-isomerase
EC
5.3.3.1
UniProt
P07445
Ligands
EDT, SO4
Pockets
6 · best druggability 0.74

Structure

x-ray diffraction · 4 distinct chains · 29% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASteroid delta-isomerase (EC 5.3.3.1)protein12930% helix, 40% strandP07445
BSteroid delta-isomerase (EC 5.3.3.1)protein13029% helix, 39% strandP07445
DSteroid delta-isomerase (EC 5.3.3.1)protein12730% helix, 38% strandP07445
FSteroid delta-isomerase (EC 5.3.3.1)protein13028% helix, 39% strandP07445

Ligands and binding sites

  • EDT · {[-(bis-carboxymethyl-amino)-ethyl]-carboxymethyl-amino}-acetic acid · ligand · chains D, F
  • SO4 · Sulfate ion · ion · 5 copies · chains A, D

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
12150.740.8828empty
22480.720.8632empty
31950.720.8729empty
42280.690.8532empty
5700.330.7516SO4

Interfaces

2 interfaces between chains.

  • A–B · 1088 Ų buried · 20 hydrogen bonds · protein-protein
  • D–F · 1078 Ų buried · 19 hydrogen bonds · protein-protein

Compared structures

  • 3T8N · Crystal structure of ketosteroid isomerase Y16AD103A from Pseudomonas putida · the same entry in another collection · chain A against A, TM-score 1.00

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