1.850 Å
X-ray
2000-07-12
Name: | Adenylate kinase |
---|---|
ID: | KAD_ECOLI |
AC: | P69441 |
Organism: | Escherichia coli |
Reign: | Bacteria |
TaxID: | 83333 |
EC Number: | / |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 100 % |
B-Factor: | 10.908 |
---|---|
Number of residues: | 60 |
Including | |
Standard Amino Acids: | 60 |
Non Standard Amino Acids: | 0 |
Water Molecules: | 0 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.246 | 928.125 |
% Hydrophobic | % Polar |
---|---|
38.18 | 61.82 |
According to VolSite |
HET Code: | AP5 |
---|---|
Formula: | C20H24N10O22P5 |
Molecular weight: | 911.327 g/mol |
DrugBank ID: | DB01717 |
Buried Surface Area: | 78.42 % |
Polar Surface area: | 543.69 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 30 |
H-Bond Donors: | 6 |
Rings: | 6 |
Aromatic rings: | 4 |
Anionic atoms: | 5 |
Cationic atoms: | 0 |
Rule of Five Violation: | 3 |
Rotatable Bonds: | 16 |
X | Y | Z |
---|---|---|
-2.39349 | 0.248123 | 2.4934 |
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 |
O3B | N | VAL- 10 | 3.46 | 137.16 | H-Bond (Protein Donor) |
O2G | N | VAL- 10 | 2.84 | 148.05 | H-Bond (Protein Donor) |
O3A | N | GLY- 12 | 2.94 | 140.56 | H-Bond (Protein Donor) |
O1B | N | GLY- 12 | 3.05 | 126.39 | H-Bond (Protein Donor) |
O1B | N | LYS- 13 | 2.85 | 159.87 | H-Bond (Protein Donor) |
O1B | NZ | LYS- 13 | 3.3 | 160.39 | H-Bond (Protein Donor) |
O1B | NZ | LYS- 13 | 3.3 | 0 | Ionic (Protein Cationic) |
O1G | NZ | LYS- 13 | 2.91 | 0 | Ionic (Protein Cationic) |
O2G | NZ | LYS- 13 | 3.59 | 0 | Ionic (Protein Cationic) |
O2B | N | GLY- 14 | 2.71 | 167.91 | H-Bond (Protein Donor) |
O1A | OG1 | THR- 15 | 2.61 | 163.41 | H-Bond (Protein Donor) |
O1A | N | THR- 15 | 2.95 | 141.32 | H-Bond (Protein Donor) |
N7B | OG1 | THR- 31 | 2.76 | 168.32 | H-Bond (Protein Donor) |
C1J | CD1 | LEU- 35 | 4.28 | 0 | Hydrophobic |
O1E | NH2 | ARG- 36 | 3.07 | 143.95 | H-Bond (Protein Donor) |
O1E | NH1 | ARG- 36 | 2.95 | 150.59 | H-Bond (Protein Donor) |
O1E | CZ | ARG- 36 | 3.45 | 0 | Ionic (Protein Cationic) |
C4J | CE | MET- 53 | 4.27 | 0 | Hydrophobic |
O2J | O | LYS- 57 | 2.81 | 150.79 | H-Bond (Ligand Donor) |
C2J | CD2 | LEU- 58 | 4.04 | 0 | Hydrophobic |
C1J | CG2 | VAL- 59 | 4.42 | 0 | Hydrophobic |
N3B | N | VAL- 59 | 3 | 148.11 | H-Bond (Protein Donor) |
N6B | O | GLY- 85 | 2.65 | 141.06 | H-Bond (Ligand Donor) |
O1G | NH2 | ARG- 88 | 3.49 | 154.9 | H-Bond (Protein Donor) |
O2E | NH1 | ARG- 88 | 3.19 | 125.32 | H-Bond (Protein Donor) |
N6B | OE1 | GLN- 92 | 3 | 165.6 | H-Bond (Ligand Donor) |
N1B | NE2 | GLN- 92 | 3.27 | 145.94 | H-Bond (Protein Donor) |
C4F | CD | ARG- 119 | 4.42 | 0 | Hydrophobic |
C1F | CD | ARG- 119 | 4.31 | 0 | Hydrophobic |
DuAr | CZ | ARG- 119 | 3.6 | 6.18 | Pi/Cation |
O2A | CZ | ARG- 123 | 3.47 | 0 | Ionic (Protein Cationic) |
O1D | NH2 | ARG- 123 | 3.48 | 126.45 | H-Bond (Protein Donor) |
O2D | NH1 | ARG- 123 | 3.35 | 147.21 | H-Bond (Protein Donor) |
C3F | CG | ARG- 123 | 3.29 | 0 | Hydrophobic |
C3F | CG2 | VAL- 132 | 3.95 | 0 | Hydrophobic |
O3F | O | TYR- 133 | 2.93 | 139.92 | H-Bond (Ligand Donor) |
C1F | CB | HIS- 134 | 4.11 | 0 | Hydrophobic |
O2F | ND2 | ASN- 138 | 3.25 | 149.21 | H-Bond (Protein Donor) |
O1D | CZ | ARG- 156 | 3.42 | 0 | Ionic (Protein Cationic) |
O1D | NH2 | ARG- 156 | 2.56 | 147.77 | H-Bond (Protein Donor) |
O1D | NH2 | ARG- 167 | 3.26 | 130.36 | H-Bond (Protein Donor) |
O1D | NH1 | ARG- 167 | 2.93 | 143.31 | H-Bond (Protein Donor) |
O1D | CZ | ARG- 167 | 3.46 | 0 | Ionic (Protein Cationic) |
N6A | O | LYS- 200 | 2.51 | 123.67 | H-Bond (Ligand Donor) |