scPDB - 4qbg entry

Protein Data Bank Entry:

PDB ID : 4qbg

Resolution :1.370 Å

Experimental Method : X-ray

Deposition Date : 2014-05-08

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Adenylate kinase
ID:	KAD_BACSU
AC:	P16304
Organism:	Bacillus subtilis
Reign:	Bacteria
TaxID:	224308
EC Number:	/

Chains:

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

Ligand binding site composition:

B-Factor:	20.060
Number of residues:	63
Including
Standard Amino Acids:	55
Non Standard Amino Acids:	1
Water Molecules:	7
Cofactors:
Metals:	MG

Cavity properties

Ligandability	Volume (Å3)
0.088	894.375

% Hydrophobic	% Polar
29.43	70.57
According to VolSite

Ligand :

HET Code:	AP5
Formula:	C20H24N10O22P5
Molecular weight:	911.327 g/mol
DrugBank ID:	DB01717
Buried Surface Area:	65.69 %
Polar Surface area:	543.69 Å2

Number of
H-Bond Acceptors:	30
H-Bond Donors:	6
Rings:	6
Aromatic rings:	4
Anionic atoms:	5
Cationic atoms:	0
Rule of Five Violation:	3
Rotatable Bonds:	16

Mass center Coordinates

X	Y	Z
16.8728	-11.362	5.114

Binding mode :

What is Poseview ?

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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
O3B	N	GLY- 10	3.05	148.07	H-Bond (Protein Donor)	false
O3A	N	GLY- 12	3.21	131.82	H-Bond (Protein Donor)	false
O1B	N	GLY- 12	3.11	134.28	H-Bond (Protein Donor)	false
O1B	NZ	LYS- 13	2.88	163.29	H-Bond (Protein Donor)	false
O1B	N	LYS- 13	2.87	160.82	H-Bond (Protein Donor)	false
O1D	NZ	LYS- 13	2.53	160.3	H-Bond (Protein Donor)	false
O1B	NZ	LYS- 13	2.88	0	Ionic (Protein Cationic)	false
O1D	NZ	LYS- 13	2.53	0	Ionic (Protein Cationic)	false
O2B	N	GLY- 14	2.98	156.64	H-Bond (Protein Donor)	false
O1A	N	THR- 15	2.94	151.5	H-Bond (Protein Donor)	false
O1A	OG1	THR- 15	2.72	164.91	H-Bond (Protein Donor)	false
N7B	OG1	THR- 31	2.78	160.52	H-Bond (Protein Donor)	false
C1J	CD2	PHE- 35	4.06	0	Hydrophobic	false
C4J	CG1	ILE- 53	3.97	0	Hydrophobic	false
C1J	CG1	ILE- 53	3.73	0	Hydrophobic	false
O2J	O	GLU- 57	2.59	156.47	H-Bond (Ligand Donor)	false
C2J	CD2	LEU- 58	4.4	0	Hydrophobic	false
C1J	CG2	VAL- 59	4.13	0	Hydrophobic	false
N3B	N	VAL- 59	2.97	140.94	H-Bond (Protein Donor)	false
N6B	O	GLY- 85	2.95	137.26	H-Bond (Ligand Donor)	false
O1D	NH1	ARG- 88	3.49	156.29	H-Bond (Protein Donor)	false
O2D	NH1	ARG- 88	3.32	132.19	H-Bond (Protein Donor)	false
O2E	NH2	ARG- 88	2.83	160.79	H-Bond (Protein Donor)	false
N7B	NH2	ARG- 88	3.39	129.19	H-Bond (Protein Donor)	false
O2E	CZ	ARG- 88	3.78	0	Ionic (Protein Cationic)	false
N6B	OE1	GLN- 92	3.01	170.4	H-Bond (Ligand Donor)	false
N1B	NE2	GLN- 92	2.98	164.74	H-Bond (Protein Donor)	false
C4F	CB	ARG- 123	4.23	0	Hydrophobic	false
C1F	CD	ARG- 123	4.33	0	Hydrophobic	false
DuAr	CZ	ARG- 123	3.56	3.34	Pi/Cation	false
C5F	CD2	LEU- 124	3.86	0	Hydrophobic	false
O2A	NH2	ARG- 127	3.41	121.2	H-Bond (Protein Donor)	false
O1G	NH2	ARG- 127	2.89	140.06	H-Bond (Protein Donor)	false
O1G	NH1	ARG- 127	2.82	146.41	H-Bond (Protein Donor)	false
O1G	CZ	ARG- 127	3.27	0	Ionic (Protein Cationic)	false
O3G	NH1	ARG- 171	3.4	120.43	H-Bond (Protein Donor)	false
O2D	NH1	ARG- 171	3.17	172.84	H-Bond (Protein Donor)	false
N6A	O	GLN- 199	2.84	177.68	H-Bond (Ligand Donor)	false
O2B	MG	MG- 303	2.11	0	Metal Acceptor	false
O2G	MG	MG- 303	2.03	0	Metal Acceptor	false
O2E	O	HOH- 407	2.72	179.97	H-Bond (Protein Donor)	false
O3J	O	HOH- 412	2.63	159.42	H-Bond (Ligand Donor)	false
O3J	O	HOH- 452	2.89	179.99	H-Bond (Protein Donor)	false
O1E	O	HOH- 560	2.79	153.67	H-Bond (Protein Donor)	false