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Structure of aspergillus fumigatus udp-galactopyranose mutase mutant Y104A

Analyse Structure of aspergillus fumigatus udp-galactopyranose mutase mutant Y104A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4U8J
Type
protein
Length
2,020 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Udp-galactopyranose mutase
EC
5.4.99.9
UniProt
Q4W1X2
Ligands
FDA, SO4
Pockets
17 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DUdp-galactopyranose mutase (EC 5.4.99.9)protein50537% helix, 23% strandQ4W1X2

Ligands and binding sites

  • FDA · Dihydroflavine-adenine dinucleotide · ligand · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 23 copies · chains A, B, C, D
  • EDO · 1,2-ethanediol · additive · 13 copies · chains A, C, B, D

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

Pockets

17 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110300.800.8186FDA, EDO
210180.790.8185FDA, EDO
311940.780.8091FDA, EDO
411880.780.8091FDA, EDO
5990.770.9838empty

Interfaces

6 interfaces between chains.

  • B–D · 1219 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 1217 Ų buried · 21 hydrogen bonds · protein-protein
  • A–D · 911 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 898 Ų buried · 2 hydrogen bonds · protein-protein
  • C–D · 41 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4U8J · Structure of Aspergillus fumigatus UDP-Galactopyranose mutase mutant Y104A · the same entry in another collection · chain A against A, TM-score 1.00

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