scPDB - 4twr entry

Protein Data Bank Entry:

PDB ID : 4twr

Resolution :1.900 Å

Experimental Method : X-ray

Deposition Date : 2014-07-01

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	NAD binding site:NAD-dependent epimerase/dehydratase:UDP-glucose 4-epimerase
ID:	Q2YKG6_BRUA2
AC:	Q2YKG6
Organism:	Brucella abortus
Reign:	Bacteria
TaxID:	359391
EC Number:	/

Chains:

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

Ligand binding site composition:

B-Factor:	30.764
Number of residues:	50
Including
Standard Amino Acids:	47
Non Standard Amino Acids:	1
Water Molecules:	2
Cofactors:
Metals:	ZN

Cavity properties

Ligandability	Volume (Å3)
0.990	1498.500

% Hydrophobic	% Polar
38.96	61.04
According to VolSite

Ligand :

HET Code:	NAD
Formula:	C21H26N7O14P2
Molecular weight:	662.417 g/mol
DrugBank ID:	-
Buried Surface Area:	77.55 %
Polar Surface area:	343.54 Å2

Number of
H-Bond Acceptors:	18
H-Bond Donors:	6
Rings:	5
Aromatic rings:	3
Anionic atoms:	2
Cationic atoms:	1
Rule of Five Violation:	3
Rotatable Bonds:	11

Mass center Coordinates

X	Y	Z
-3.22714	-11.8579	-17.4415

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
O2A	N	PHE- 14	2.78	176.28	H-Bond (Protein Donor)	false
O2N	N	ILE- 15	2.98	167.18	H-Bond (Protein Donor)	false
C3N	CD1	ILE- 15	4.07	0	Hydrophobic	false
O3B	OD2	ASP- 34	2.65	153.82	H-Bond (Ligand Donor)	false
O3B	OD1	ASP- 34	3.19	126.89	H-Bond (Ligand Donor)	false
O2B	OD1	ASP- 34	2.71	159.82	H-Bond (Ligand Donor)	false
N3A	N	ASN- 35	3.17	145.23	H-Bond (Protein Donor)	false
O1A	OG1	THR- 38	2.73	159.04	H-Bond (Protein Donor)	false
O2B	N	THR- 38	3.14	169.78	H-Bond (Protein Donor)	false
C2B	CB	THR- 38	4.31	0	Hydrophobic	false
O2B	N	GLY- 39	3.07	151.14	H-Bond (Protein Donor)	false
N6A	OD1	ASP- 53	2.97	144.17	H-Bond (Ligand Donor)	false
N1A	N	ILE- 54	2.93	164.62	H-Bond (Protein Donor)	false
C4D	CB	PHE- 75	4.11	0	Hydrophobic	false
C1B	CB	ALA- 76	4.48	0	Hydrophobic	false
C3D	CB	ALA- 77	4.23	0	Hydrophobic	false
N7A	ND2	ASN- 94	3.25	145.6	H-Bond (Protein Donor)	false
N6A	OD1	ASN- 94	3	157.52	H-Bond (Ligand Donor)	false
O3D	O	SER- 117	3.37	146.28	H-Bond (Ligand Donor)	false
C5N	CB	SER- 119	3.92	0	Hydrophobic	false
O2D	NZ	LYS- 147	2.67	136.78	H-Bond (Protein Donor)	false
C5N	CE2	TYR- 170	3.47	0	Hydrophobic	false
C3N	CB	ALA- 173	4.39	0	Hydrophobic	false
O7N	N	ALA- 173	2.93	156.98	H-Bond (Protein Donor)	false
O2A	NE2	HIS- 186	2.8	157.59	H-Bond (Protein Donor)	false
O5B	O	HOH- 575	3.04	156.48	H-Bond (Protein Donor)	false
N7N	O	HOH- 587	2.99	161.77	H-Bond (Ligand Donor)	false