scPDB - 3pft entry

Protein Data Bank Entry:

PDB ID : 3pft

Resolution :1.600 Å

Experimental Method : X-ray

Deposition Date : 2010-10-29

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Flavin reductase
ID:	B6CDL6_9MYCO
AC:	B6CDL6
Organism:	Mycobacterium goodii
Reign:	Bacteria
TaxID:	134601
EC Number:	/

Chains:

Chain Name:	Percentage of Residues within binding site
A	3 %
B	97 %

Ligand binding site composition:

B-Factor:	18.402
Number of residues:	33
Including
Standard Amino Acids:	31
Non Standard Amino Acids:	0
Water Molecules:	2
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
0.893	870.750

% Hydrophobic	% Polar
40.31	59.69
According to VolSite

Ligand :

HET Code:	FMN
Formula:	C17H19N4O9P
Molecular weight:	454.328 g/mol
DrugBank ID:	DB03247
Buried Surface Area:	64.71 %
Polar Surface area:	217.05 Å2

Number of
H-Bond Acceptors:	12
H-Bond Donors:	4
Rings:	3
Aromatic rings:	1
Anionic atoms:	2
Cationic atoms:	0
Rule of Five Violation:	1
Rotatable Bonds:	7

Mass center Coordinates

X	Y	Z
60.5206	32.7075	28.2771

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
O2'	N	ALA- 37	3.17	131.83	H-Bond (Protein Donor)	false
C9	CB	ALA- 37	4.45	0	Hydrophobic	false
O4	N	SER- 39	3.24	131.15	H-Bond (Protein Donor)	false
N5	N	SER- 39	2.95	147	H-Bond (Protein Donor)	false
C6	CB	SER- 39	3.65	0	Hydrophobic	false
O4	OG1	THR- 40	2.69	177.23	H-Bond (Protein Donor)	false
O4	N	THR- 40	3.43	122.08	H-Bond (Protein Donor)	false
N3	O	ALA- 54	2.71	171.06	H-Bond (Ligand Donor)	false
O2	N	GLN- 56	2.66	169.48	H-Bond (Protein Donor)	false
O1P	OG	SER- 59	2.62	155.1	H-Bond (Protein Donor)	false
O2P	N	THR- 60	2.67	165.93	H-Bond (Protein Donor)	false
O2P	OG1	THR- 60	2.74	170.48	H-Bond (Protein Donor)	false
O1P	OG1	THR- 61	3.15	138.46	H-Bond (Protein Donor)	false
O1P	N	THR- 61	3.14	149.51	H-Bond (Protein Donor)	false
O3P	OG1	THR- 61	2.72	146.34	H-Bond (Protein Donor)	false
C8M	CD	ARG- 85	4.15	0	Hydrophobic	false
C1'	CB	ALA- 88	4.48	0	Hydrophobic	false
C3'	CB	ALA- 88	3.88	0	Hydrophobic	false
C8M	CB	ALA- 88	3.44	0	Hydrophobic	false
O3'	O	ALA- 88	2.53	165.56	H-Bond (Ligand Donor)	false
C5'	CD	LYS- 90	4.05	0	Hydrophobic	false
O5'	NZ	LYS- 90	3.38	132.05	H-Bond (Protein Donor)	false
O3P	CZ	ARG- 94	3.74	0	Ionic (Protein Cationic)	false
O3P	NH2	ARG- 94	2.74	161.08	H-Bond (Protein Donor)	false
C7M	CE1	PHE- 151	3.57	0	Hydrophobic	false
C7M	CZ	PHE- 156	3.56	0	Hydrophobic	false