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Crystal structure of streptogramin a acetyltransferase vata from staphylococcus aureus in complex with streptogramin analog F1037 (47)

Analyse Crystal structure of streptogramin a acetyltransferase vata from staphylococcus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6X3C
Type
protein
Length
1,231 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Virginiamycin a acetyltransferase
EC
2.3.1.-
UniProt
P26839
Ligands
SXA, O7S, MG, PO4, CL, SO4
Pockets
13 · best druggability 0.81

Structure

x-ray diffraction · 5 distinct chains · 22% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVirginiamycin a acetyltransferase (EC 2.3.1.-)protein20724% helix, 20% strandP26839
BVirginiamycin a acetyltransferase (EC 2.3.1.-)protein20422% helix, 21% strandP26839
CVirginiamycin a acetyltransferase (EC 2.3.1.-)protein20521% helix, 20% strandP26839
D, FVirginiamycin a acetyltransferase (EC 2.3.1.-)protein20621% helix, 20% strandP26839
EVirginiamycin a acetyltransferase (EC 2.3.1.-)protein20323% helix, 21% strandP26839

Ligands and binding sites

  • SXA · Thioacetic acid S-{2-[3-(2-hydroxy-3,3-dimethyl-4-phosphonooxy-butyrylamino)-propionylamino]-ethyl} ester · ligand · 6 copies · chains A, F, B, C, D, E
  • O7S · (3r,4r,5e,10e,12e,14s,16r,26ar)-16-fluoro-14-hydroxy-12-methyl-3-(propan-2-yl)-4-(prop-2-en-1-yl)-3,4,8,9, 14,15,16,17,24,25,26,26A-dodecahydro-1H,7H,22H-21,18-(azeno)pyrrolo[2,1-C][1,8,4, 19]dioxadiazacyclotetracosine-1,7,22-trione · ligand · 6 copies · chains A, E, B, D, C, F
  • MG · Magnesium ion · metal · 2 copies · chains B, C, D, A, E, F
  • PO4 · Phosphate ion · ion · 14 copies · chains A, B, D, C, E, F
  • CL · Chloride ion · ion · 6 copies · chains A, C, D, E, F
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, D

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

Pockets

13 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111460.810.82108O7S, CL, SXA
25850.770.8360SXA, O7S
35930.760.8258SXA, O7S
49080.760.7979PO4, CL
55500.750.8263SXA, O7S, CL

Interfaces

9 interfaces between chains.

  • B–C · 1424 Ų buried · 18 hydrogen bonds · protein-protein
  • E–F · 1417 Ų buried · 13 hydrogen bonds · protein-protein
  • A–F · 1404 Ų buried · 13 hydrogen bonds · protein-protein
  • A–E · 1403 Ų buried · 16 hydrogen bonds · protein-protein
  • B–D · 1393 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 6X3C · Crystal structure of streptogramin A acetyltransferase VatA from Staphylococcus aureus in… · the same entry in another collection · chain F against F, TM-score 1.00
  • P26839 · AlphaFold monomer V2.0 prediction for virginiamycin a acetyltransferase (P26839) · a predicted model of the same protein · chain C against A, TM-score 0.99

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