scPDB - 1e1n entry

Protein Data Bank Entry:

PDB ID : 1e1n

Resolution :2.400 Å

Experimental Method : X-ray

Deposition Date : 2000-05-09

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	NADPH:adrenodoxin oxidoreductase, mitochondrial
ID:	ADRO_BOVIN
AC:	P08165
Organism:	Bos taurus
Reign:	Eukaryota
TaxID:	9913
EC Number:	1.18.1.6

Chains:

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

Ligand binding site composition:

B-Factor:	30.226
Number of residues:	64
Including
Standard Amino Acids:	58
Non Standard Amino Acids:	0
Water Molecules:	6
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
1.169	1495.125

% Hydrophobic	% Polar
49.21	50.79
According to VolSite

Ligand :

HET Code:	FAD
Formula:	C27H31N9O15P2
Molecular weight:	783.534 g/mol
DrugBank ID:	DB03147
Buried Surface Area:	71.32 %
Polar Surface area:	381.7 Å2

Number of
H-Bond Acceptors:	22
H-Bond Donors:	7
Rings:	6
Aromatic rings:	3
Anionic atoms:	2
Cationic atoms:	0
Rule of Five Violation:	3
Rotatable Bonds:	13

Mass center Coordinates

X	Y	Z
15.52	2.0694	10.5219

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
C4'	CG	PRO- 16	3.85	0	Hydrophobic	false
O1P	N	ALA- 17	2.5	150.8	H-Bond (Protein Donor)	false
O3B	OE1	GLU- 38	2.71	162.09	H-Bond (Ligand Donor)	false
O2B	OE1	GLU- 38	3.27	151.09	H-Bond (Ligand Donor)	false
N3A	N	LYS- 39	3.03	135.47	H-Bond (Protein Donor)	false
O2A	N	LEU- 46	3.1	153.22	H-Bond (Protein Donor)	false
C8M	CD1	LEU- 46	3.82	0	Hydrophobic	false
N6A	O	VAL- 82	2.9	153.62	H-Bond (Ligand Donor)	false
N1A	N	VAL- 82	2.96	143.88	H-Bond (Protein Donor)	false
C1B	CB	TYR- 102	4.48	0	Hydrophobic	false
C8M	CD	ARG- 124	4.29	0	Hydrophobic	false
C7M	CG1	VAL- 127	3.93	0	Hydrophobic	false
C7	CG2	VAL- 156	3.66	0	Hydrophobic	false
C8M	CE2	TYR- 331	3.48	0	Hydrophobic	false
C8M	CH2	TRP- 367	4.09	0	Hydrophobic	false
C3'	CZ2	TRP- 367	3.39	0	Hydrophobic	false
C5'	CE2	TRP- 367	3.67	0	Hydrophobic	false
O2P	N	TRP- 367	3.07	161.3	H-Bond (Protein Donor)	false
O3'	O	GLY- 374	3.11	161.94	H-Bond (Ligand Donor)	false
N1	N	ILE- 376	3.45	142.23	H-Bond (Protein Donor)	false
O2	N	ILE- 376	2.85	162.35	H-Bond (Protein Donor)	false
C2'	CG1	ILE- 376	3.82	0	Hydrophobic	false
O3'	OG1	THR- 379	3.41	151.42	H-Bond (Protein Donor)	false
O1P	O	HOH- 2004	2.7	179.99	H-Bond (Protein Donor)	false
O3B	O	HOH- 2012	3.08	127.66	H-Bond (Protein Donor)	false
O1A	O	HOH- 2032	2.69	179.94	H-Bond (Protein Donor)	false
O4	O	HOH- 2049	3.35	142.12	H-Bond (Protein Donor)	false
O2P	O	HOH- 2119	2.68	179.97	H-Bond (Protein Donor)	false