scPDB - 2zl9 entry

Protein Data Bank Entry:

PDB ID : 2zl9

Resolution :1.900 Å

Experimental Method : X-ray

Deposition Date : 2008-04-04

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Vitamin D3 receptor
ID:	VDR_RAT
AC:	P13053
Organism:	Rattus norvegicus
Reign:	Eukaryota
TaxID:	10116
EC Number:	/

Chains:

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

Ligand binding site composition:

B-Factor:	35.015
Number of residues:	51
Including
Standard Amino Acids:	48
Non Standard Amino Acids:	0
Water Molecules:	3
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
2.042	654.750

% Hydrophobic	% Polar
73.71	26.29
According to VolSite

Ligand :

HET Code:	VDA
Formula:	C28H46O5S
Molecular weight:	494.727 g/mol
DrugBank ID:	-
Buried Surface Area:	75.64 %
Polar Surface area:	115.45 Å2

Number of
H-Bond Acceptors:	6
H-Bond Donors:	4
Rings:	3
Aromatic rings:	0
Anionic atoms:	0
Cationic atoms:	0
Rule of Five Violation:	0
Rotatable Bonds:	10

Mass center Coordinates

X	Y	Z
13.0212	4.48406	23.6902

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
O5	O	THR- 142	3.37	138.84	H-Bond (Ligand Donor)	false
O2	OH	TYR- 143	2.73	132.59	H-Bond (Protein Donor)	false
C2	CE2	TYR- 143	4.29	0	Hydrophobic	false
C3	CZ	TYR- 143	4.35	0	Hydrophobic	false
C30	CE2	TYR- 143	4.15	0	Hydrophobic	false
C31	CD2	TYR- 143	3.6	0	Hydrophobic	false
C3	CE2	TYR- 147	3.94	0	Hydrophobic	false
C30	CE2	TYR- 147	4.01	0	Hydrophobic	false
C4	CZ	PHE- 150	4.35	0	Hydrophobic	false
C30	CE1	PHE- 150	4.05	0	Hydrophobic	false
C3	CZ	PHE- 150	4.29	0	Hydrophobic	false
C29	CD1	LEU- 223	3.39	0	Hydrophobic	false
C11	CD2	LEU- 226	4.25	0	Hydrophobic	false
C12	CD1	LEU- 226	4.34	0	Hydrophobic	false
C18	CD2	LEU- 226	4.41	0	Hydrophobic	false
C29	CB	LEU- 226	3.52	0	Hydrophobic	false
C2	CD2	LEU- 229	4.38	0	Hydrophobic	false
C10	CD2	LEU- 229	4.01	0	Hydrophobic	false
C18	CD1	LEU- 229	4.34	0	Hydrophobic	false
C6	CD1	LEU- 229	3.84	0	Hydrophobic	false
C18	CG2	VAL- 230	3.68	0	Hydrophobic	false
C23	CG2	VAL- 230	3.95	0	Hydrophobic	false
C27	CG2	VAL- 230	3.7	0	Hydrophobic	false
C30	CE2	TYR- 232	4.15	0	Hydrophobic	false
C1	CB	SER- 233	4.5	0	Hydrophobic	false
O1	OG	SER- 233	2.62	156.29	H-Bond (Ligand Donor)	false
C16	CD1	ILE- 264	3.98	0	Hydrophobic	false
C10	CG2	ILE- 267	4.08	0	Hydrophobic	false
C15	CG2	ILE- 267	4.03	0	Hydrophobic	false
C15	CG	MET- 268	4.07	0	Hydrophobic	false
C1	CG	ARG- 270	3.89	0	Hydrophobic	false
O1	NH1	ARG- 270	2.74	152.15	H-Bond (Protein Donor)	false
O5	NH1	ARG- 270	2.94	167.53	H-Bond (Protein Donor)	false
C10	CB	SER- 271	4.01	0	Hydrophobic	false
C5	CB	SER- 271	3.65	0	Hydrophobic	false
O2	OG	SER- 274	2.92	162.06	H-Bond (Ligand Donor)	false
C3	CB	SER- 274	4.08	0	Hydrophobic	false
C9	CD2	TRP- 282	3.3	0	Hydrophobic	false
C11	CE3	TRP- 282	4.16	0	Hydrophobic	false
C4	SG	CYS- 284	3.37	0	Hydrophobic	false
C11	CB	TYR- 291	4.16	0	Hydrophobic	false
C20	CG1	VAL- 296	4.04	0	Hydrophobic	false
C12	CG2	VAL- 296	3.57	0	Hydrophobic	false
S22	CB	ALA- 299	4.41	0	Hydrophobic	false
C29	CB	ALA- 299	3.99	0	Hydrophobic	false
O3	NE2	HIS- 301	2.61	160.54	H-Bond (Ligand Donor)	false
C21	CD2	LEU- 305	3.91	0	Hydrophobic	false
O3	NE2	HIS- 393	2.92	142.59	H-Bond (Protein Donor)	false
C28	CE1	TYR- 397	4	0	Hydrophobic	false
C28	CG1	VAL- 414	4.14	0	Hydrophobic	false
C28	CE1	PHE- 418	3.78	0	Hydrophobic	false
O5	O	HOH- 504	2.73	157.97	H-Bond (Protein Donor)	false