scPDB - 1ozp entry

Protein Data Bank Entry:

PDB ID : 1ozp

Resolution :1.700 Å

Experimental Method : X-ray

Deposition Date : 2003-04-09

Activity from ChEMBL: What is pChEMBL ?

	Min	Mean	Median	Standard Deviation	Max	Count
pChEMBL:

List of CHEMBLId :

Binding Site :

Uniprot Annotation

Name:	Mycothiol acetyltransferase
ID:	MSHD_MYCTU
AC:	P9WJM7
Organism:	Mycobacterium tuberculosis
Reign:	Bacteria
TaxID:	83332
EC Number:	2.3.1.189

Chains:

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

Ligand binding site composition:

B-Factor:	14.778
Number of residues:	41
Including
Standard Amino Acids:	38
Non Standard Amino Acids:	0
Water Molecules:	3
Cofactors:
Metals:

Cavity properties

Ligandability	Volume (Å3)
0.891	1005.750

% Hydrophobic	% Polar
37.25	62.75
According to VolSite

Ligand :

HET Code:	ACO
Formula:	C23H34N7O17P3S
Molecular weight:	805.539 g/mol
DrugBank ID:	-
Buried Surface Area:	57.08 %
Polar Surface area:	429.68 Å2

Number of
H-Bond Acceptors:	22
H-Bond Donors:	5
Rings:	3
Aromatic rings:	2
Anionic atoms:	4
Cationic atoms:	0
Rule of Five Violation:	2
Rotatable Bonds:	20

Mass center Coordinates

X	Y	Z
6.86776	20.2955	20.1653

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
C6P	CB	ALA- 173	4.1	0	Hydrophobic	false
C6P	CZ	PHE- 174	3.35	0	Hydrophobic	false
C2P	CZ	PHE- 174	3.9	0	Hydrophobic	false
CH3	CG1	VAL- 235	4.03	0	Hydrophobic	false
CEP	CD2	LEU- 238	3.83	0	Hydrophobic	false
N4P	O	LEU- 238	2.75	153.66	H-Bond (Ligand Donor)	false
O	N	LEU- 238	2.99	146.46	H-Bond (Protein Donor)	false
CEP	CG2	VAL- 240	3.8	0	Hydrophobic	false
O9P	N	VAL- 240	2.99	171.1	H-Bond (Protein Donor)	false
CAP	CG	GLN- 245	4.23	0	Hydrophobic	false
O9P	NE2	GLN- 245	3.33	125.71	H-Bond (Protein Donor)	false
O5A	N	ARG- 246	2.94	171.32	H-Bond (Protein Donor)	false
O2A	N	GLY- 248	2.89	144.3	H-Bond (Protein Donor)	false
O3A	N	GLY- 250	3.45	120.34	H-Bond (Protein Donor)	false
O4A	N	GLY- 250	2.87	147.5	H-Bond (Protein Donor)	false
O1A	N	GLN- 251	3.01	155.21	H-Bond (Protein Donor)	false
CH3	CB	LEU- 281	4.02	0	Hydrophobic	false
S1P	CG2	VAL- 283	4.01	0	Hydrophobic	false
O5P	ND2	ASN- 287	2.77	151.24	H-Bond (Protein Donor)	false
C1B	CB	ALA- 289	4.35	0	Hydrophobic	false
CDP	CB	ALA- 289	4.09	0	Hydrophobic	false
CDP	CB	ALA- 290	3.86	0	Hydrophobic	false
N3A	NH1	ARG- 292	2.92	131.29	H-Bond (Protein Donor)	false
C1B	CD	ARG- 292	4.03	0	Hydrophobic	false
C4B	CB	ARG- 292	4.01	0	Hydrophobic	false
C5B	CB	THR- 293	4.12	0	Hydrophobic	false
S1P	CE2	TYR- 294	4.34	0	Hydrophobic	false
CH3	CZ	TYR- 294	4.17	0	Hydrophobic	false
O	OH	TYR- 294	3.47	120.27	H-Bond (Protein Donor)	false
O4A	O	HOH- 604	2.61	179.96	H-Bond (Protein Donor)	false