scPDB - 3b3f entry

Protein Data Bank Entry:

PDB ID : 3b3f

Resolution :2.200 Å

Experimental Method : X-ray

Deposition Date : 2007-10-22

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Histone-arginine methyltransferase CARM1
ID:	CARM1_RAT
AC:	Q4AE70
Organism:	Rattus norvegicus
Reign:	Eukaryota
TaxID:	10116
EC Number:	/

Chains:

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

Ligand binding site composition:

B-Factor:	30.687
Number of residues:	39
Including
Standard Amino Acids:	36
Non Standard Amino Acids:	0
Water Molecules:	3
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
0.298	735.750

% Hydrophobic	% Polar
34.86	65.14
According to VolSite

Ligand :

HET Code:	SAH
Formula:	C14H20N6O5S
Molecular weight:	384.411 g/mol
DrugBank ID:	DB01752
Buried Surface Area:	78.3 %
Polar Surface area:	212.38 Å2

Number of
H-Bond Acceptors:	10
H-Bond Donors:	4
Rings:	3
Aromatic rings:	2
Anionic atoms:	1
Cationic atoms:	1
Rule of Five Violation:	1
Rotatable Bonds:	7

Mass center Coordinates

X	Y	Z
23.246	21.7434	116.202

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
C2'	CE1	TYR- 150	4.34	0	Hydrophobic	false
C2'	CE1	PHE- 151	4.23	0	Hydrophobic	false
SD	CE1	TYR- 154	3.85	0	Hydrophobic	false
C3'	CG	TYR- 154	3.42	0	Hydrophobic	false
C2'	CD2	TYR- 154	3.71	0	Hydrophobic	false
O3'	NE2	GLN- 160	3.3	149.51	H-Bond (Protein Donor)	false
CB	CE	MET- 163	4.25	0	Hydrophobic	false
SD	SD	MET- 163	3.34	0	Hydrophobic	false
O	CZ	ARG- 169	3.58	0	Ionic (Protein Cationic)	false
OXT	CZ	ARG- 169	3.51	0	Ionic (Protein Cationic)	false
O	NH1	ARG- 169	2.75	158.37	H-Bond (Protein Donor)	false
OXT	NH2	ARG- 169	2.91	149.38	H-Bond (Protein Donor)	false
OXT	NH1	ARG- 169	3.26	133.43	H-Bond (Protein Donor)	false
N	O	GLY- 193	3	169.45	H-Bond (Ligand Donor)	false
O3'	OE2	GLU- 215	3.12	121.43	H-Bond (Ligand Donor)	false
O3'	OE1	GLU- 215	2.79	163.15	H-Bond (Ligand Donor)	false
O2'	OE2	GLU- 215	2.74	165.94	H-Bond (Ligand Donor)	false
N3	N	ALA- 216	3.32	131.08	H-Bond (Protein Donor)	false
N1	N	VAL- 243	3.05	162.81	H-Bond (Protein Donor)	false
N6	OE1	GLU- 244	3.09	159.88	H-Bond (Ligand Donor)	false
CG	CB	GLU- 258	4.3	0	Hydrophobic	false
C5'	SD	MET- 269	3.66	0	Hydrophobic	false
C4'	CE	MET- 269	4.21	0	Hydrophobic	false
C1'	CE	MET- 269	4.33	0	Hydrophobic	false
N6	OG	SER- 272	3.21	122.39	H-Bond (Ligand Donor)	false
N	O	HOH- 486	2.81	169.73	H-Bond (Ligand Donor)	false
OXT	O	HOH- 497	2.78	179.96	H-Bond (Protein Donor)	false