Logo scPDB

sc-PDB

An Annotated Database of Druggable Binding Sites from the Protein DataBank

Logo CNRS Logo Unistra
Protein Data Bank Entry:

2nmt

2.900 Å

X-ray

1998-07-14

Interactomes:
Molecular Function:
Binding Site :

Uniprot Annotation

Name:Glycylpeptide N-tetradecanoyltransferase
ID:NMT_YEAST
AC:P14743
Organism:Saccharomyces cerevisiae
Reign:Eukaryota
TaxID:559292
EC Number:2.3.1.97


Chains:

Chain Name:Percentage of Residues
within binding site
A100 %


Ligand binding site composition:

B-Factor:48.940
Number of residues:55
Including
Standard Amino Acids: 53
Non Standard Amino Acids: 1
Water Molecules: 1
Cofactors:
Metals:

Cavity properties

LigandabilityVolume (Å3)
0.8871653.750

% Hydrophobic% Polar
49.3950.61
According to VolSite

Ligand :
2nmt_1 Structure
HET Code: NHM
Formula: C36H60N7O17P3S
Molecular weight: 987.885 g/mol
DrugBank ID: DB02271
Buried Surface Area:70.96 %
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
18.719622.03275.9672


Binding mode :
What is Poseview ?
  • 2D View
  • 3D View
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
O8AND1HIS- 382.58136.17H-Bond
(Protein Donor)
O7ANPHE- 403.34171.59H-Bond
(Protein Donor)
N3ANE1TRP- 413.24153.54H-Bond
(Protein Donor)
O9ANTRP- 412.62176.46H-Bond
(Protein Donor)
C8MCH2TRP- 414.080Hydrophobic
C6MCZ2TRP- 414.280Hydrophobic
C6CD1TYR- 1033.40Hydrophobic
C2CZTYR- 1034.150Hydrophobic
C6CG2VAL- 1043.370Hydrophobic
C2CG2VAL- 1044.060Hydrophobic
C4MCD1ILE- 1494.360Hydrophobic
CBMCG1VAL- 1664.280Hydrophobic
CDMCG1VAL- 1664.230Hydrophobic
C7MCG2ILE- 1683.890Hydrophobic
C2MCG2ILE- 1684.160Hydrophobic
C4MCG2ILE- 1683.930Hydrophobic
CAMCG1ILE- 1683.740Hydrophobic
O1MNLEU- 1713.09175.14H-Bond
(Protein Donor)
N4OLEU- 1712.69123.53H-Bond
(Ligand Donor)
C13CD2LEU- 1714.010Hydrophobic
C4MCD2LEU- 1713.80Hydrophobic
C14CGLEU- 1713.510Hydrophobic
O9NVAL- 1732.75169.57H-Bond
(Protein Donor)
C14CG2VAL- 1733.450Hydrophobic
C10CDARG- 1784.210Hydrophobic
O5ANSER- 1792.69149.14H-Bond
(Protein Donor)
O7ACZARG- 1813.760Ionic
(Protein Cationic)
O2ANARG- 1812.84125.42H-Bond
(Protein Donor)
O1ANLEU- 1823.2132.89H-Bond
(Protein Donor)
C12CBTHR- 1834.380Hydrophobic
C1XCG2THR- 1834.220Hydrophobic
C4XCBTHR- 1834.480Hydrophobic
O1ANTHR- 1833.05153.78H-Bond
(Protein Donor)
O1AOG1THR- 1832.82156.4H-Bond
(Protein Donor)
C4XCGPRO- 1843.860Hydrophobic
CAMCG2ILE- 1874.420Hydrophobic
C7MCG2ILE- 1874.370Hydrophobic
C6MCD1ILE- 1873.620Hydrophobic
CAMCG2ILE- 1904.360Hydrophobic
CCMCG2THR- 1913.560Hydrophobic
CDMCG1VAL- 1944.120Hydrophobic
C9MCBALA- 2023.730Hydrophobic
CBMCBALA- 2023.540Hydrophobic
C7MCGTYR- 2044.160Hydrophobic
C2MCBTYR- 2044.110Hydrophobic
C3MCD2TYR- 2044.490Hydrophobic
C8MCD1TYR- 2043.790Hydrophobic
C5MCD2TYR- 2043.520Hydrophobic
S1CBALA- 2064.160Hydrophobic
C9MCBPHE- 4253.80Hydrophobic
C8MCD1PHE- 4254.170Hydrophobic
CCMCD2PHE- 4253.680Hydrophobic