2.300 Å
X-ray
2003-08-13
Name: | Tyrosine-protein phosphatase non-receptor type 1 |
---|---|
ID: | PTN1_HUMAN |
AC: | P18031 |
Organism: | Homo sapiens |
Reign: | Eukaryota |
TaxID: | 9606 |
EC Number: | 3.1.3.48 |
Chain Name: | Percentage of Residues within binding site |
---|---|
A | 78 % |
B | 22 % |
B-Factor: | 32.875 |
---|---|
Number of residues: | 53 |
Including | |
Standard Amino Acids: | 49 |
Non Standard Amino Acids: | 1 |
Water Molecules: | 3 |
Cofactors: | |
Metals: |
Ligandability | Volume (Å3) |
---|---|
0.846 | 945.000 |
% Hydrophobic | % Polar |
---|---|
39.29 | 60.71 |
According to VolSite |
HET Code: | 600 |
---|---|
Formula: | C43H38F2N4O7P2 |
Molecular weight: | 822.729 g/mol |
DrugBank ID: | - |
Buried Surface Area: | 61.25 % |
Polar Surface area: | 198.83 Å2 |
Number of | |
---|---|
H-Bond Acceptors: | 10 |
H-Bond Donors: | 0 |
Rings: | 7 |
Aromatic rings: | 7 |
Anionic atoms: | 4 |
Cationic atoms: | 0 |
Rule of Five Violation: | 3 |
Rotatable Bonds: | 14 |
X | Y | Z |
---|---|---|
37.5621 | 43.5767 | 51.0844 |
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 |
O58 | O | HOH- 25 | 2.65 | 178 | H-Bond (Protein Donor) |
O81 | O | HOH- 184 | 2.75 | 179.96 | H-Bond (Protein Donor) |
O80 | NE | ARG- 524 | 3.15 | 174.84 | H-Bond (Protein Donor) |
O81 | NE | ARG- 524 | 3.43 | 121.87 | H-Bond (Protein Donor) |
O81 | NH2 | ARG- 524 | 2.74 | 139.05 | H-Bond (Protein Donor) |
O80 | CZ | ARG- 524 | 3.97 | 0 | Ionic (Protein Cationic) |
O81 | CZ | ARG- 524 | 3.46 | 0 | Ionic (Protein Cationic) |
C30 | CD1 | TYR- 546 | 4.45 | 0 | Hydrophobic |
C35 | CG | TYR- 546 | 3.49 | 0 | Hydrophobic |
C3 | CE1 | TYR- 546 | 3.43 | 0 | Hydrophobic |
C41 | CB | ARG- 547 | 4.41 | 0 | Hydrophobic |
N46 | N | ASP- 548 | 3.3 | 164.63 | H-Bond (Protein Donor) |
C61 | CB | ASP- 548 | 4.43 | 0 | Hydrophobic |
C25 | CB | ASP- 548 | 3.61 | 0 | Hydrophobic |
C35 | CG2 | VAL- 549 | 3.86 | 0 | Hydrophobic |
C10 | CG2 | VAL- 549 | 4.2 | 0 | Hydrophobic |
C20 | CG2 | VAL- 549 | 4.07 | 0 | Hydrophobic |
C76 | CZ | PHE- 552 | 3.62 | 0 | Hydrophobic |
F53 | CB | ASP- 681 | 3.36 | 0 | Hydrophobic |
F53 | CE2 | PHE- 682 | 3.57 | 0 | Hydrophobic |
F54 | CE1 | PHE- 682 | 3.4 | 0 | Hydrophobic |
C14 | CZ | PHE- 682 | 3.41 | 0 | Hydrophobic |
O57 | N | SER- 716 | 2.96 | 132.94 | H-Bond (Protein Donor) |
C35 | CB | ALA- 717 | 4.42 | 0 | Hydrophobic |
C14 | CB | ALA- 717 | 3.62 | 0 | Hydrophobic |
C10 | CB | ALA- 717 | 3.36 | 0 | Hydrophobic |
O57 | N | ALA- 717 | 2.75 | 170.11 | H-Bond (Protein Donor) |
C10 | CD1 | ILE- 719 | 3.9 | 0 | Hydrophobic |
C15 | CG1 | ILE- 719 | 3.8 | 0 | Hydrophobic |
C23 | CD1 | ILE- 719 | 4.19 | 0 | Hydrophobic |
O56 | N | ILE- 719 | 2.96 | 153.45 | H-Bond (Protein Donor) |
O56 | N | GLY- 720 | 2.63 | 169.51 | H-Bond (Protein Donor) |
O57 | CZ | ARG- 721 | 3.91 | 0 | Ionic (Protein Cationic) |
O58 | CZ | ARG- 721 | 3.65 | 0 | Ionic (Protein Cationic) |
O57 | NH2 | ARG- 721 | 3.03 | 168.32 | H-Bond (Protein Donor) |
O58 | N | ARG- 721 | 2.91 | 173.74 | H-Bond (Protein Donor) |
O58 | NE | ARG- 721 | 2.86 | 162.64 | H-Bond (Protein Donor) |
C62 | CE | MET- 758 | 3.65 | 0 | Hydrophobic |
C76 | CB | MET- 758 | 3.89 | 0 | Hydrophobic |
C63 | SD | MET- 758 | 3.44 | 0 | Hydrophobic |
C15 | CG | GLN- 762 | 4.2 | 0 | Hydrophobic |
F54 | CG | GLN- 762 | 3.58 | 0 | Hydrophobic |
C6 | CB | ALA- 1017 | 4.41 | 0 | Hydrophobic |
C44 | CB | ALA- 1018 | 4.11 | 0 | Hydrophobic |
C6 | CB | ALA- 1018 | 3.61 | 0 | Hydrophobic |
C32 | CG | GLN- 1021 | 4.42 | 0 | Hydrophobic |
C44 | CG | GLN- 1021 | 3.55 | 0 | Hydrophobic |
C20 | CG | GLN- 1021 | 3.54 | 0 | Hydrophobic |
C45 | CG | GLN- 1021 | 3.75 | 0 | Hydrophobic |