scPDB - 1ipe entry

Protein Data Bank Entry:

PDB ID : 1ipe

Resolution :2.500 Å

Experimental Method : X-ray

Deposition Date : 2001-05-09

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Tropinone reductase 2
ID:	TRN2_DATST
AC:	P50163
Organism:	Datura stramonium
Reign:	Eukaryota
TaxID:	4076
EC Number:	1.1.1.236

Chains:

Chain Name:	Percentage of Residues within binding site
A	100 %

Ligand binding site composition:

B-Factor:	11.260
Number of residues:	49
Including
Standard Amino Acids:	48
Non Standard Amino Acids:	0
Water Molecules:	1
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
1.028	975.375

% Hydrophobic	% Polar
49.48	50.52
According to VolSite

Ligand :

HET Code:	NDP
Formula:	C21H26N7O17P3
Molecular weight:	741.389 g/mol
DrugBank ID:	DB02338
Buried Surface Area:	78.09 %
Polar Surface area:	404.9 Å2

Number of
H-Bond Acceptors:	22
H-Bond Donors:	5
Rings:	5
Aromatic rings:	2
Anionic atoms:	4
Cationic atoms:	0
Rule of Five Violation:	2
Rotatable Bonds:	13

Mass center Coordinates

X	Y	Z
3.98715	23.4266	151.255

Binding mode :

What is Poseview ?

2D View
3D View

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

Ligand	Protein		Interaction
Atom	Atom	Residue	Distance (Å)	Angle (°)	Type
O3B	N	SER- 18	3.45	134.46	H-Bond (Protein Donor)	false
O3B	OG	SER- 18	2.74	147.14	H-Bond (Protein Donor)	false
C3B	CB	ARG- 19	4.44	0	Hydrophobic	false
O1X	CZ	ARG- 19	3.74	0	Ionic (Protein Cationic)	false
O2X	CZ	ARG- 19	3.56	0	Ionic (Protein Cationic)	false
O1X	NH1	ARG- 19	3.09	130.15	H-Bond (Protein Donor)	false
O2X	NH2	ARG- 19	2.65	153.39	H-Bond (Protein Donor)	false
O2N	N	ILE- 21	2.99	142.2	H-Bond (Protein Donor)	false
C5D	CB	ILE- 21	4.25	0	Hydrophobic	false
C4D	CD1	ILE- 21	4.47	0	Hydrophobic	false
O2X	NH2	ARG- 41	3.15	155.86	H-Bond (Protein Donor)	false
O3X	N	ARG- 41	2.99	139.27	H-Bond (Protein Donor)	false
O3X	NE	ARG- 41	2.74	167.11	H-Bond (Protein Donor)	false
O3X	NH2	ARG- 41	3.25	133.03	H-Bond (Protein Donor)	false
O3X	CZ	ARG- 41	3.42	0	Ionic (Protein Cationic)	false
N6A	OD1	ASP- 66	3.11	131.55	H-Bond (Ligand Donor)	false
N1A	N	LEU- 67	2.91	157.71	H-Bond (Protein Donor)	false
O3D	O	ASN- 94	2.63	123.9	H-Bond (Ligand Donor)	false
C1B	CB	ALA- 95	4.28	0	Hydrophobic	false
C4D	CG2	ILE- 144	4.12	0	Hydrophobic	false
C5N	CB	SER- 146	3.68	0	Hydrophobic	false
O2D	OH	TYR- 159	2.55	157.91	H-Bond (Protein Donor)	false
O3D	NZ	LYS- 163	3.15	128.43	H-Bond (Protein Donor)	false
O2D	NZ	LYS- 163	2.78	156.31	H-Bond (Protein Donor)	false
C5N	CB	PRO- 189	3.81	0	Hydrophobic	false
O7N	N	ILE- 192	2.9	166.48	H-Bond (Protein Donor)	false
N7N	O	ILE- 192	3.28	132.43	H-Bond (Ligand Donor)	false
O1N	OG1	THR- 194	2.5	171.61	H-Bond (Protein Donor)	false
O2A	OG	SER- 195	2.97	162.91	H-Bond (Protein Donor)	false
O2N	O	HOH- 276	2.96	151.9	H-Bond (Protein Donor)	false