1.900 Å
X-ray
2009-06-01
Name: | 3-oxoacyl-[acyl-carrier-protein] synthase 2 |
---|---|
ID: | FABF_ECOLI |
AC: | P0AAI5 |
Organism: | Escherichia coli |
Reign: | Bacteria |
TaxID: | 83333 |
EC Number: | 2.3.1.179 |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 20.904 |
---|---|
Number of residues: | 38 |
Including | |
Standard Amino Acids: | 34 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 4 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
1.242 | 452.250 |
% Hydrophobic | % Polar |
---|---|
56.72 | 43.28 |
According to VolSite |
HET Code: | N3A |
---|---|
Formula: | C24H26NO7 |
Molecular weight: | 440.466 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 56.26 % |
Polar Surface area: | 146.99 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 7 |
H-Bond Donors: | 4 |
Rings: | 4 |
Aromatic rings: | 1 |
Anionic atoms: | 1 |
Cationic atoms: | 0 |
Rule of Five Violation: | 0 |
Rotatable Bonds: | 5 |
X | Y | Z |
---|---|---|
-3.46953 | 69.4175 | 68.1453 |
Represent the protein/ligand binding mode, centered on the ligand
Dashed lines represents hydrogen bonds and metal interactions
Green residue labels for amino acids with hydrophobic contacts (green lines) to the ligand
Ligand | Protein | Interaction | |||
---|---|---|---|---|---|
Atom | Atom | Residue | Distance (Å) | Angle (°) | Type |
N28 | O | THR- 270 | 2.85 | 176.17 | H-Bond (Ligand Donor) |
C2 | CB | SER- 271 | 4.07 | 0 | Hydrophobic |
O33 | NE2 | HIS- 303 | 3.07 | 144.01 | H-Bond (Protein Donor) |
O20 | OG1 | THR- 307 | 2.77 | 172.54 | H-Bond (Protein Donor) |
C3 | CB | THR- 307 | 3.7 | 0 | Hydrophobic |
C18 | CB | THR- 307 | 4.34 | 0 | Hydrophobic |
O19 | N | ALA- 309 | 2.83 | 155.57 | H-Bond (Protein Donor) |
O32 | NE2 | HIS- 340 | 3.23 | 120.96 | H-Bond (Protein Donor) |
O33 | NE2 | HIS- 340 | 2.74 | 174.17 | H-Bond (Protein Donor) |
O33 | O | HOH- 574 | 3.01 | 177.41 | H-Bond (Protein Donor) |