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Zinc in PDB 6jf3: Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii

Enzymatic activity of Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii

All present enzymatic activity of Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii:
3.5.1.88;

Protein crystallography data

The structure of Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii, PDB code: 6jf3 was solved by I.H.Lee, T.H.Ho, L.W.Kang, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.99 / 2.01
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 39.728, 70.786, 110.859, 90.00, 90.00, 90.00
R / Rfree (%) 20 / 26.2

Zinc Binding Sites:

The binding sites of Zinc atom in the Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii (pdb code 6jf3). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii, PDB code: 6jf3:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 6jf3

Go back to Zinc Binding Sites List in 6jf3
Zinc binding site 1 out of 2 in the Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn201

b:41.6
occ:1.00
NE2 A:HIS145 2.2 36.9 1.0
O4 A:BB2202 2.2 45.6 1.0
NE2 A:HIS149 2.2 35.1 1.0
SG A:CYS103 2.4 43.3 1.0
O2 A:BB2202 2.5 48.9 1.0
C3 A:BB2202 2.8 49.5 1.0
N1 A:BB2202 3.0 49.8 1.0
CD2 A:HIS145 3.1 34.0 1.0
CD2 A:HIS149 3.1 34.5 1.0
CE1 A:HIS145 3.2 39.7 1.0
CE1 A:HIS149 3.2 33.2 1.0
NE2 A:GLN55 3.3 25.4 1.0
CB A:CYS103 3.3 47.2 1.0
O A:HOH311 3.4 36.6 1.0
CA A:CYS103 3.8 42.9 1.0
CD A:GLN55 4.0 28.2 1.0
OE1 A:GLN55 4.2 26.4 1.0
C5 A:BB2202 4.2 50.7 1.0
CG A:HIS145 4.3 31.6 1.0
ND1 A:HIS145 4.3 35.4 1.0
CG A:HIS149 4.3 29.5 1.0
ND1 A:HIS149 4.3 30.2 1.0
N A:LEU104 4.3 52.5 1.0
C6 A:BB2202 4.4 52.5 1.0
O A:HOH309 4.5 42.0 1.0
C A:CYS103 4.5 49.7 1.0
C7 A:BB2202 4.8 49.8 1.0
OE1 A:GLU146 4.8 31.1 1.0
OE2 A:GLU146 4.9 31.0 1.0
O A:GLY102 4.9 46.2 1.0
N A:CYS103 5.0 47.1 1.0

Zinc binding site 2 out of 2 in 6jf3

Go back to Zinc Binding Sites List in 6jf3
Zinc binding site 2 out of 2 in the Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn201

b:31.8
occ:1.00
NE2 B:HIS145 2.2 27.3 1.0
NE2 B:HIS149 2.2 25.9 1.0
O2 B:BB2202 2.3 34.4 1.0
O4 B:BB2202 2.3 33.5 1.0
SG B:CYS103 2.3 31.1 1.0
C3 B:BB2202 2.9 36.1 1.0
N1 B:BB2202 3.0 33.1 1.0
CD2 B:HIS145 3.0 28.5 1.0
CE1 B:HIS149 3.1 28.6 1.0
CD2 B:HIS149 3.2 25.4 1.0
NE2 B:GLN55 3.2 23.5 1.0
CE1 B:HIS145 3.2 28.5 1.0
CB B:CYS103 3.3 31.2 1.0
O B:HOH312 3.4 27.1 1.0
CD B:GLN55 3.8 28.3 1.0
CA B:CYS103 3.9 31.6 1.0
OE1 B:GLN55 4.1 27.6 1.0
CG B:HIS145 4.2 26.7 1.0
ND1 B:HIS149 4.2 27.1 1.0
ND1 B:HIS145 4.3 29.2 1.0
CG B:HIS149 4.3 24.0 1.0
C5 B:BB2202 4.3 36.8 1.0
N B:LEU104 4.5 35.1 1.0
OE1 B:GLU146 4.5 35.0 1.0
O B:HOH309 4.6 26.8 1.0
C B:CYS103 4.6 32.6 1.0
C6 B:BB2202 4.6 37.8 1.0
OE2 B:GLU146 4.8 42.1 1.0
C7 B:BB2202 4.9 38.9 1.0
CG B:GLN55 4.9 25.0 1.0
O B:GLY102 5.0 41.1 1.0

Reference:

I.H.Lee, T.H.Ho, L.W.Kang. Actinonin Bound Crystal Structure of Class I Type B Peptide Deformylase From Acinetobacter Baumannii To Be Published.
Page generated: Thu Aug 21 16:22:35 2025

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