Zinc in PDB 9g3t: Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans
Protein crystallography data
The structure of Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans, PDB code: 9g3t
was solved by
B.Claushuis,
F.Wojtalla,
H.Van Leeuwen,
J.Corver,
U.Baumann,
P.Hensbergen,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
62.81 /
1.60
|
Space group
|
P 41 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
125.622,
125.622,
63.483,
90,
90,
90
|
R / Rfree (%)
|
15.7 /
17.7
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans
(pdb code 9g3t). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the
Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans, PDB code: 9g3t:
Jump to Zinc binding site number:
1;
2;
Zinc binding site 1 out
of 2 in 9g3t
Go back to
Zinc Binding Sites List in 9g3t
Zinc binding site 1 out
of 2 in the Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans
 Mono view
 Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn701
b:21.9
occ:1.00
|
OE1
|
A:GLU197
|
2.0
|
22.7
|
0.6
|
OE1
|
A:GLU197
|
2.0
|
20.8
|
0.4
|
NE2
|
A:HIS157
|
2.1
|
20.9
|
1.0
|
NE2
|
A:HIS153
|
2.2
|
20.3
|
1.0
|
O4
|
A:BCN702
|
2.2
|
29.7
|
0.8
|
O22
|
A:BCN702
|
2.2
|
25.2
|
0.8
|
N1
|
A:BCN702
|
2.3
|
30.1
|
0.8
|
CD
|
A:GLU197
|
2.8
|
19.8
|
0.4
|
HO4
|
A:BCN702
|
2.8
|
35.7
|
0.8
|
H52
|
A:BCN702
|
2.8
|
52.1
|
0.8
|
C1
|
A:BCN702
|
2.9
|
43.0
|
0.8
|
C2
|
A:BCN702
|
2.9
|
42.6
|
0.8
|
OE2
|
A:GLU197
|
2.9
|
23.4
|
0.4
|
CD
|
A:GLU197
|
2.9
|
26.6
|
0.6
|
C4
|
A:BCN702
|
2.9
|
40.9
|
0.8
|
C5
|
A:BCN702
|
3.0
|
43.4
|
0.8
|
CD2
|
A:HIS153
|
3.0
|
19.7
|
1.0
|
C3
|
A:BCN702
|
3.1
|
37.2
|
0.8
|
HD2
|
A:HIS153
|
3.1
|
23.6
|
1.0
|
CD2
|
A:HIS157
|
3.1
|
21.5
|
1.0
|
CE1
|
A:HIS157
|
3.1
|
25.5
|
1.0
|
H12
|
A:BCN702
|
3.1
|
51.6
|
0.8
|
H42
|
A:BCN702
|
3.2
|
49.1
|
0.8
|
H51
|
A:BCN702
|
3.2
|
52.1
|
0.8
|
OE2
|
A:GLU197
|
3.2
|
26.2
|
0.6
|
CE1
|
A:HIS153
|
3.2
|
20.6
|
1.0
|
HD2
|
A:HIS157
|
3.3
|
25.8
|
1.0
|
HE1
|
A:HIS157
|
3.3
|
30.6
|
1.0
|
H31
|
A:BCN702
|
3.5
|
44.7
|
0.8
|
HE1
|
A:HIS153
|
3.5
|
24.7
|
1.0
|
H11
|
A:BCN702
|
3.8
|
51.6
|
0.8
|
H41
|
A:BCN702
|
3.8
|
49.1
|
0.8
|
H32
|
A:BCN702
|
3.9
|
44.7
|
0.8
|
O21
|
A:BCN702
|
4.1
|
33.5
|
0.8
|
HA
|
A:GLU197
|
4.1
|
22.4
|
1.0
|
CG
|
A:HIS153
|
4.2
|
15.7
|
1.0
|
ND1
|
A:HIS157
|
4.2
|
19.5
|
1.0
|
CG
|
A:HIS157
|
4.2
|
19.9
|
1.0
|
ND1
|
A:HIS153
|
4.3
|
19.4
|
1.0
|
CG
|
A:GLU197
|
4.3
|
21.0
|
0.6
|
HB3
|
A:ALA200
|
4.3
|
21.0
|
1.0
|
CG
|
A:GLU197
|
4.3
|
21.7
|
0.4
|
HG2
|
A:GLU197
|
4.4
|
25.3
|
0.6
|
C6
|
A:BCN702
|
4.4
|
51.6
|
0.8
|
H61
|
A:BCN702
|
4.6
|
62.0
|
0.8
|
HB3
|
A:GLU197
|
4.6
|
24.8
|
0.4
|
HG3
|
A:GLU197
|
4.7
|
26.1
|
0.4
|
HE1
|
A:PHE191
|
4.7
|
29.3
|
1.0
|
HB1
|
A:ALA200
|
4.7
|
21.0
|
1.0
|
H62
|
A:BCN702
|
4.8
|
62.0
|
0.8
|
HG2
|
A:GLU197
|
4.8
|
26.1
|
0.4
|
CB
|
A:ALA200
|
4.9
|
17.5
|
1.0
|
CB
|
A:GLU197
|
4.9
|
20.6
|
0.4
|
HG3
|
A:GLU197
|
4.9
|
25.3
|
0.6
|
CA
|
A:GLU197
|
4.9
|
18.7
|
0.4
|
HB2
|
A:ALA200
|
5.0
|
21.0
|
1.0
|
CA
|
A:GLU197
|
5.0
|
18.6
|
0.6
|
|
Zinc binding site 2 out
of 2 in 9g3t
Go back to
Zinc Binding Sites List in 9g3t
Zinc binding site 2 out
of 2 in the Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans
 Mono view
 Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn302
b:19.8
occ:1.00
|
O4
|
B:BCN303
|
2.0
|
28.5
|
1.0
|
OE1
|
B:GLU197
|
2.1
|
23.6
|
1.0
|
NE2
|
B:HIS157
|
2.1
|
20.1
|
1.0
|
O21
|
B:BCN303
|
2.2
|
26.5
|
1.0
|
NE2
|
B:HIS153
|
2.2
|
19.4
|
1.0
|
N1
|
B:BCN303
|
2.4
|
25.5
|
1.0
|
HO4
|
B:BCN303
|
2.6
|
34.2
|
1.0
|
H51
|
B:BCN303
|
2.9
|
45.1
|
1.0
|
C2
|
B:BCN303
|
2.9
|
50.2
|
1.0
|
C4
|
B:BCN303
|
2.9
|
35.5
|
1.0
|
CD2
|
B:HIS153
|
3.0
|
18.0
|
1.0
|
CD
|
B:GLU197
|
3.0
|
29.6
|
1.0
|
C1
|
B:BCN303
|
3.0
|
34.5
|
1.0
|
HD2
|
B:HIS153
|
3.0
|
21.7
|
1.0
|
C3
|
B:BCN303
|
3.0
|
31.1
|
1.0
|
CD2
|
B:HIS157
|
3.1
|
23.0
|
1.0
|
CE1
|
B:HIS157
|
3.1
|
21.1
|
1.0
|
C5
|
B:BCN303
|
3.2
|
37.6
|
1.0
|
OE2
|
B:GLU197
|
3.2
|
34.2
|
1.0
|
HD2
|
B:HIS157
|
3.2
|
27.6
|
1.0
|
CE1
|
B:HIS153
|
3.3
|
19.2
|
1.0
|
HE1
|
B:HIS157
|
3.3
|
25.3
|
1.0
|
H11
|
B:BCN303
|
3.4
|
41.5
|
1.0
|
H41
|
B:BCN303
|
3.5
|
42.6
|
1.0
|
H32
|
B:BCN303
|
3.5
|
37.4
|
1.0
|
HE1
|
B:HIS153
|
3.5
|
23.1
|
1.0
|
H52
|
B:BCN303
|
3.6
|
45.1
|
1.0
|
H42
|
B:BCN303
|
3.7
|
42.6
|
1.0
|
H12
|
B:BCN303
|
3.8
|
41.5
|
1.0
|
H31
|
B:BCN303
|
3.9
|
37.4
|
1.0
|
O22
|
B:BCN303
|
4.1
|
38.5
|
1.0
|
CG
|
B:HIS153
|
4.2
|
15.4
|
1.0
|
HA
|
B:GLU197
|
4.2
|
20.7
|
1.0
|
ND1
|
B:HIS157
|
4.2
|
20.4
|
1.0
|
CG
|
B:HIS157
|
4.2
|
18.2
|
1.0
|
ND1
|
B:HIS153
|
4.3
|
18.1
|
1.0
|
O
|
B:HOH404
|
4.3
|
33.3
|
1.0
|
HB3
|
B:ALA200
|
4.3
|
18.6
|
1.0
|
CG
|
B:GLU197
|
4.4
|
17.8
|
1.0
|
C6
|
B:BCN303
|
4.5
|
54.1
|
1.0
|
H61
|
B:BCN303
|
4.6
|
64.9
|
1.0
|
HE1
|
B:PHE191
|
4.6
|
24.6
|
1.0
|
HB3
|
B:GLU197
|
4.7
|
23.7
|
1.0
|
HB1
|
B:ALA200
|
4.8
|
18.6
|
1.0
|
HG3
|
B:GLU197
|
4.8
|
21.3
|
1.0
|
CB
|
B:ALA200
|
4.9
|
15.5
|
1.0
|
CB
|
B:GLU197
|
4.9
|
19.8
|
1.0
|
HB2
|
B:ALA200
|
5.0
|
18.6
|
1.0
|
HG2
|
B:GLU197
|
5.0
|
21.3
|
1.0
|
CA
|
B:GLU197
|
5.0
|
17.3
|
1.0
|
|
Reference:
B.Claushuis,
F.Wojtalla,
H.Van Leeuwen,
J.Corver,
U.Baumann,
P.Hensbergen.
Structure of the Pro-Pro Endopeptidase (Ppep-3) E153A Y189F From Geobacillus Thermodenitrificans To Be Published.
Page generated: Fri Aug 22 17:51:59 2025
|