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sc-PDB

An Annotated Database of Druggable Binding Sites from the Protein DataBank

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Protein Data Bank Entry:

4c68

1.380 Å

X-ray

2013-09-17

Interactomes:
Molecular Function:
Binding Site :

Uniprot Annotation

Name:Glycylpeptide N-tetradecanoyltransferase
ID:A5K1A2_PLAVS
AC:A5K1A2
Organism:Plasmodium vivax
Reign:Eukaryota
TaxID:126793
EC Number:/


Chains:

Chain Name:Percentage of Residues
within binding site
C100 %


Ligand binding site composition:

B-Factor:11.760
Number of residues:61
Including
Standard Amino Acids: 56
Non Standard Amino Acids: 1
Water Molecules: 4
Cofactors:
Metals: MG

Cavity properties

LigandabilityVolume (Å3)
1.4691117.125

% Hydrophobic% Polar
52.2747.73
According to VolSite

Ligand :
4c68_3 Structure
HET Code: NHW
Formula: C36H60N7O17P3S
Molecular weight: 987.885 g/mol
DrugBank ID: -
Buried Surface Area:71.46 %
Polar Surface area: 429.68 Å2
Number of
H-Bond Acceptors: 22
H-Bond Donors: 5
Rings: 3
Aromatic rings: 2
Anionic atoms: 4
Cationic atoms: 0
Rule of Five Violation: 2
Rotatable Bonds: 33

Mass center Coordinates

XYZ
-10.283111.7922-87.1724


Binding mode :
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Binding mode
BioSolveIT Image generated by PoseView
Protein
Binding Site
Ligand
Interaction pattern
hydrophobic (CA)
aromatic (CZ)
hydrogen bond acceptor (O)
hydrogen bond acceptor/donor (OG)
hydrogen bond donor (N)
positively ionized (NZ)
negatively ionized (OD1)
metal (ZN)

Legend:

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

Image generated using PoseView by BioSolveIT
BioSolveIT


LigandProteinInteraction
AtomAtomResidueDistance
(Å)
Angle (°)Type
O7ANPHE- 302.82129.03H-Bond
(Protein Donor)
N3ANE1TRP- 313.34144.33H-Bond
(Protein Donor)
O7ANTRP- 312.76169.14H-Bond
(Protein Donor)
C6MCZ2TRP- 313.930Hydrophobic
C8MCH2TRP- 313.720Hydrophobic
C2CZTYR- 953.990Hydrophobic
C6CD1TYR- 953.660Hydrophobic
C2CG2VAL- 963.680Hydrophobic
C6CG2VAL- 964.050Hydrophobic
C7MCG1VAL- 1603.950Hydrophobic
CBMCG2VAL- 1603.990Hydrophobic
C4MCG1VAL- 1604.010Hydrophobic
CAMCG2VAL- 1603.980Hydrophobic
N4OLEU- 1632.74139.66H-Bond
(Ligand Donor)
C13CD2LEU- 1634.170Hydrophobic
C14CGLEU- 1633.650Hydrophobic
C3MCBLEU- 1633.660Hydrophobic
C5MCD2LEU- 1633.820Hydrophobic
O1MNLEU- 1632.95158.53H-Bond
(Protein Donor)
O9NVAL- 1652.96170.76H-Bond
(Protein Donor)
C14CG2VAL- 1653.80Hydrophobic
C10CDARG- 1703.690Hydrophobic
O4ANSER- 1712.81153.85H-Bond
(Protein Donor)
O1ANARG- 1732.83142.1H-Bond
(Protein Donor)
O9ANH1ARG- 1732.98146.65H-Bond
(Protein Donor)
O9ANH2ARG- 1732.9151.2H-Bond
(Protein Donor)
C5XCDARG- 1734.480Hydrophobic
O9ACZARG- 1733.40Ionic
(Protein Cationic)
C12CBALA- 1753.920Hydrophobic
C14CBALA- 1754.150Hydrophobic
O2ANALA- 1752.76168.8H-Bond
(Protein Donor)
C4XCGPRO- 1763.850Hydrophobic
CAMCG2ILE- 1794.320Hydrophobic
C5MCD1ILE- 1793.80Hydrophobic
C8MCG2ILE- 1794.120Hydrophobic
CBMCG2ILE- 1824.190Hydrophobic
CBMCBTHR- 1834.210Hydrophobic
CCMCG2THR- 1834.040Hydrophobic
CEMCG2ILE- 1864.10Hydrophobic
CDMCD1ILE- 1863.660Hydrophobic
C9MCBALA- 1943.820Hydrophobic
CDMCBALA- 1943.670Hydrophobic
C2MCBTYR- 1964.180Hydrophobic
C4MCD2TYR- 1963.810Hydrophobic
C6MCD2TYR- 1964.050Hydrophobic
C7MCGTYR- 1964.150Hydrophobic
C8MCE1TYR- 1963.770Hydrophobic
S1CBALA- 1983.850Hydrophobic
C2XCD2LEU- 2024.490Hydrophobic
CAMCD2TYR- 3934.450Hydrophobic
C9MCD2TYR- 3933.70Hydrophobic
CCMCD1TYR- 3933.560Hydrophobic