scPDB - 2c91 entry

Protein Data Bank Entry:

PDB ID : 2c91

Resolution :2.300 Å

Experimental Method : X-ray

Deposition Date : 2005-12-08

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Aflatoxin B1 aldehyde reductase member 2
ID:	ARK72_MOUSE
AC:	Q8CG76
Organism:	Mus musculus
Reign:	Eukaryota
TaxID:	10090
EC Number:	/

Chains:

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

Ligand binding site composition:

B-Factor:	34.676
Number of residues:	58
Including
Standard Amino Acids:	54
Non Standard Amino Acids:	0
Water Molecules:	4
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
0.797	1117.125

% Hydrophobic	% Polar
45.32	54.68
According to VolSite

Ligand :

HET Code:	NAP
Formula:	C21H25N7O17P3
Molecular weight:	740.381 g/mol
DrugBank ID:	DB03461
Buried Surface Area:	80.45 %
Polar Surface area:	405.54 Å2

Number of
H-Bond Acceptors:	21
H-Bond Donors:	5
Rings:	5
Aromatic rings:	3
Anionic atoms:	4
Cationic atoms:	1
Rule of Five Violation:	2
Rotatable Bonds:	13

Mass center Coordinates

X	Y	Z
16.6315	15.2175	54.1118

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
C3D	CE	MET- 13	3.95	0	Hydrophobic	false
C2D	CB	MET- 13	4.1	0	Hydrophobic	false
C5N	CE	MET- 13	3.53	0	Hydrophobic	false
O3D	N	MET- 13	3.48	161.87	H-Bond (Protein Donor)	false
O2D	OD2	ASP- 40	2.74	170.13	H-Bond (Ligand Donor)	false
C2D	CZ	TYR- 45	4.11	0	Hydrophobic	false
N7N	OG	SER- 139	3.02	139.2	H-Bond (Ligand Donor)	false
O7N	ND2	ASN- 140	2.72	164.69	H-Bond (Protein Donor)	false
N7N	OE1	GLN- 165	3.06	162	H-Bond (Ligand Donor)	false
DuAr	DuAr	TYR- 193	3.95	0	Aromatic Face/Face	false
C5N	CB	TYR- 193	4.09	0	Hydrophobic	false
O2N	ND2	ASN- 194	2.67	139.91	H-Bond (Protein Donor)	false
O1A	N	LEU- 196	2.91	147.14	H-Bond (Protein Donor)	false
O1A	N	GLY- 198	2.8	141.36	H-Bond (Protein Donor)	false
N3A	NZ	LYS- 204	2.9	161.04	H-Bond (Protein Donor)	false
O2X	NZ	LYS- 204	2.94	152.52	H-Bond (Protein Donor)	false
O2X	NZ	LYS- 204	2.94	0	Ionic (Protein Cationic)	false
O3X	NZ	LYS- 204	3.57	0	Ionic (Protein Cationic)	false
O3B	NH2	ARG- 218	3.36	131.89	H-Bond (Protein Donor)	false
O1N	NH2	ARG- 218	2.88	164.47	H-Bond (Protein Donor)	false
O2N	NH2	ARG- 218	3.49	130.63	H-Bond (Protein Donor)	false
O2N	NH1	ARG- 218	2.86	163.21	H-Bond (Protein Donor)	false
O1X	N	ARG- 218	3.06	128.26	H-Bond (Protein Donor)	false
O1N	CZ	ARG- 218	3.87	0	Ionic (Protein Cationic)	false
O2N	CZ	ARG- 218	3.6	0	Ionic (Protein Cationic)	false
C4D	CG2	ILE- 282	3.37	0	Hydrophobic	false
C2B	CB	SER- 286	4.4	0	Hydrophobic	false
O3X	OG	SER- 286	2.53	147.24	H-Bond (Protein Donor)	false
O3X	NE2	GLN- 290	2.9	173.67	H-Bond (Protein Donor)	false
N7A	ND2	ASN- 294	3.04	163.32	H-Bond (Protein Donor)	false
N6A	OD1	ASN- 294	3.15	172.2	H-Bond (Ligand Donor)	false