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1.1 resolution structure of ybff, a new esterase from escherichia COLI: a unique substrate-binding crevice generated by domain arrangement

Analyse 1.1 resolution structure of ybff, a new esterase from escherichia COLI: a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3BF8
Type
protein
Length
509 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Esterase ybff
EC
3.1.-.-
UniProt
J7QD06
Pockets
6 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEsterase ybff (EC 3.1.-.-)protein25540% helix, 15% strandJ7QD06
BEsterase ybff (EC 3.1.-.-)protein25442% helix, 15% strandJ7QD06

Ligands and binding sites

  • MLA · Malonic acid · 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18460.770.8065empty
2610.690.9622MLA
3600.680.9522MLA
41050.370.7421empty
5800.370.7620empty

Interfaces

1 interface between chains.

  • A–B · 726 Ų buried · 18 hydrogen bonds · protein-protein

Compared structures

  • 3BF8 · 1.1 resolution structure of ybfF, a new esterase from Escherichia coli: a unique… · the same entry in another collection · chain A against A, TM-score 1.00

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