Calcium in PDB 1jkv: Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Enzymatic activity of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
All present enzymatic activity of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide:
1.11.1.6;
Protein crystallography data
The structure of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide, PDB code: 1jkv
was solved by
V.V.Barynin,
M.M.Whittaker,
S.V.Antonyuk,
V.S.Lamzin,
P.M.Harrison,
P.J.Artymiuk,
J.W.Whittaker,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
17.00 /
1.39
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
74.210,
95.550,
106.110,
90.00,
106.18,
90.00
|
R / Rfree (%)
|
10.4 /
13
|
Other elements in 1jkv:
The structure of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
(pdb code 1jkv). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 6 binding sites of Calcium where determined in the
Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide, PDB code: 1jkv:
Jump to Calcium binding site number:
1;
2;
3;
4;
5;
6;
Calcium binding site 1 out
of 6 in 1jkv
Go back to
Calcium Binding Sites List in 1jkv
Calcium binding site 1 out
of 6 in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 1 of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca4272
b:14.0
occ:1.00
|
OD1
|
F:ASN218
|
2.2
|
18.3
|
1.0
|
O
|
F:SER220
|
2.4
|
11.7
|
1.0
|
OD1
|
A:ASP61
|
2.4
|
12.4
|
1.0
|
O
|
F:GLY222
|
2.4
|
13.0
|
1.0
|
OD1
|
A:ASP57
|
2.4
|
11.3
|
1.0
|
OD2
|
A:ASP57
|
2.4
|
12.9
|
1.0
|
O
|
F:HOH9361
|
2.6
|
18.4
|
1.0
|
CG
|
A:ASP57
|
2.8
|
11.7
|
1.0
|
OD2
|
A:ASP61
|
2.9
|
15.1
|
1.0
|
CG
|
A:ASP61
|
3.0
|
11.5
|
1.0
|
CG
|
F:ASN218
|
3.4
|
15.6
|
1.0
|
C
|
F:GLY222
|
3.4
|
12.6
|
1.0
|
C
|
F:SER220
|
3.5
|
10.6
|
1.0
|
OG
|
F:SER225
|
3.9
|
13.9
|
1.0
|
N
|
F:GLY222
|
4.1
|
11.9
|
1.0
|
N
|
F:SER220
|
4.2
|
10.1
|
1.0
|
CA
|
F:GLY222
|
4.2
|
12.1
|
1.0
|
CA
|
F:SER220
|
4.3
|
10.0
|
1.0
|
CB
|
A:ASP57
|
4.3
|
10.1
|
1.0
|
ND2
|
F:ASN218
|
4.3
|
17.2
|
1.0
|
CB
|
F:ASN218
|
4.4
|
13.5
|
1.0
|
CB
|
F:SER220
|
4.4
|
9.9
|
1.0
|
N
|
F:ASP223
|
4.4
|
14.1
|
1.0
|
CA
|
F:ASN218
|
4.4
|
13.0
|
1.0
|
C
|
F:ASP221
|
4.4
|
12.6
|
1.0
|
CA
|
F:ASP223
|
4.5
|
14.3
|
1.0
|
N
|
F:ASP221
|
4.5
|
11.0
|
1.0
|
O
|
A:ASP57
|
4.5
|
10.2
|
1.0
|
CB
|
A:ASP61
|
4.5
|
10.0
|
1.0
|
O
|
F:HOH9403
|
4.6
|
23.1
|
1.0
|
C
|
F:ASN218
|
4.7
|
13.2
|
1.0
|
O
|
A:HOH5318
|
4.7
|
13.7
|
1.0
|
OH
|
F:TYR241
|
4.7
|
16.7
|
1.0
|
CA
|
F:ASP221
|
4.8
|
11.6
|
1.0
|
CB
|
F:SER225
|
4.8
|
12.4
|
1.0
|
N
|
F:PHE219
|
4.9
|
11.7
|
1.0
|
C
|
A:ASP57
|
4.9
|
9.5
|
1.0
|
N
|
F:SER225
|
5.0
|
12.1
|
1.0
|
C
|
F:ASP223
|
5.0
|
13.7
|
1.0
|
|
Calcium binding site 2 out
of 6 in 1jkv
Go back to
Calcium Binding Sites List in 1jkv
Calcium binding site 2 out
of 6 in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 2 of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ca5272
b:13.2
occ:1.00
|
OD1
|
C:ASN218
|
2.2
|
19.1
|
1.0
|
O
|
C:SER220
|
2.3
|
10.7
|
1.0
|
O
|
C:GLY222
|
2.4
|
11.7
|
1.0
|
OD1
|
B:ASP61
|
2.4
|
12.0
|
1.0
|
OD2
|
B:ASP57
|
2.4
|
11.2
|
1.0
|
OD1
|
B:ASP57
|
2.4
|
10.3
|
1.0
|
O
|
C:HOH6343
|
2.5
|
16.6
|
1.0
|
CG
|
B:ASP57
|
2.8
|
10.2
|
1.0
|
OD2
|
B:ASP61
|
2.9
|
14.3
|
1.0
|
CG
|
B:ASP61
|
3.0
|
10.1
|
1.0
|
CG
|
C:ASN218
|
3.4
|
15.6
|
1.0
|
C
|
C:GLY222
|
3.4
|
12.1
|
1.0
|
C
|
C:SER220
|
3.5
|
10.1
|
1.0
|
OG
|
C:SER225
|
3.9
|
12.8
|
1.0
|
N
|
C:GLY222
|
4.0
|
11.3
|
1.0
|
N
|
C:SER220
|
4.2
|
10.2
|
1.0
|
CA
|
C:GLY222
|
4.2
|
12.3
|
1.0
|
CA
|
C:SER220
|
4.2
|
9.4
|
1.0
|
CB
|
B:ASP57
|
4.3
|
9.4
|
1.0
|
ND2
|
C:ASN218
|
4.3
|
17.2
|
1.0
|
CB
|
C:ASN218
|
4.3
|
12.9
|
1.0
|
CA
|
C:ASN218
|
4.4
|
12.5
|
1.0
|
CB
|
C:SER220
|
4.4
|
8.8
|
1.0
|
N
|
C:ASP223
|
4.4
|
12.8
|
1.0
|
C
|
C:ASP221
|
4.4
|
11.6
|
1.0
|
N
|
C:ASP221
|
4.5
|
10.6
|
1.0
|
CB
|
B:ASP61
|
4.5
|
8.8
|
1.0
|
CA
|
C:ASP223
|
4.5
|
12.7
|
1.0
|
O
|
B:ASP57
|
4.5
|
9.8
|
1.0
|
O
|
C:HOH6391
|
4.6
|
22.0
|
1.0
|
C
|
C:ASN218
|
4.6
|
13.0
|
1.0
|
O
|
B:HOH9308
|
4.7
|
12.5
|
1.0
|
CA
|
C:ASP221
|
4.7
|
10.9
|
1.0
|
OH
|
C:TYR241
|
4.8
|
16.4
|
1.0
|
N
|
C:PHE219
|
4.8
|
11.4
|
1.0
|
CB
|
C:SER225
|
4.9
|
13.0
|
1.0
|
C
|
B:ASP57
|
4.9
|
9.4
|
1.0
|
C
|
C:ASP223
|
5.0
|
12.7
|
1.0
|
OG
|
C:SER220
|
5.0
|
9.9
|
1.0
|
N
|
C:GLY224
|
5.0
|
11.8
|
1.0
|
|
Calcium binding site 3 out
of 6 in 1jkv
Go back to
Calcium Binding Sites List in 1jkv
Calcium binding site 3 out
of 6 in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 3 of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Ca6272
b:17.0
occ:1.00
|
OD1
|
B:ASN218
|
2.2
|
20.6
|
1.0
|
O
|
B:SER220
|
2.3
|
14.2
|
1.0
|
O
|
B:GLY222
|
2.3
|
15.3
|
1.0
|
OD1
|
C:ASP61
|
2.4
|
15.2
|
1.0
|
OD2
|
C:ASP57
|
2.4
|
16.0
|
1.0
|
OD1
|
C:ASP57
|
2.4
|
13.4
|
1.0
|
O
|
B:HOH9400
|
2.5
|
22.9
|
1.0
|
CG
|
C:ASP57
|
2.8
|
13.3
|
1.0
|
OD2
|
C:ASP61
|
2.9
|
16.7
|
1.0
|
CG
|
C:ASP61
|
3.1
|
13.9
|
1.0
|
CG
|
B:ASN218
|
3.4
|
18.9
|
1.0
|
C
|
B:GLY222
|
3.4
|
15.4
|
1.0
|
C
|
B:SER220
|
3.5
|
13.2
|
1.0
|
OG
|
B:SER225
|
3.9
|
16.1
|
1.0
|
N
|
B:GLY222
|
4.0
|
14.9
|
1.0
|
N
|
B:SER220
|
4.2
|
13.0
|
1.0
|
CA
|
B:GLY222
|
4.2
|
14.6
|
1.0
|
CA
|
B:SER220
|
4.2
|
12.9
|
1.0
|
ND2
|
B:ASN218
|
4.2
|
21.4
|
1.0
|
CB
|
C:ASP57
|
4.3
|
12.5
|
1.0
|
CB
|
B:SER220
|
4.3
|
12.8
|
1.0
|
CB
|
B:ASN218
|
4.4
|
16.4
|
1.0
|
N
|
B:ASP223
|
4.4
|
16.1
|
1.0
|
CA
|
B:ASN218
|
4.4
|
15.3
|
1.0
|
C
|
B:ASP221
|
4.4
|
15.2
|
1.0
|
O
|
B:HOH9414
|
4.5
|
24.5
|
1.0
|
N
|
B:ASP221
|
4.5
|
13.7
|
1.0
|
CA
|
B:ASP223
|
4.5
|
16.5
|
1.0
|
O
|
C:ASP57
|
4.5
|
12.4
|
1.0
|
CB
|
C:ASP61
|
4.6
|
11.9
|
1.0
|
C
|
B:ASN218
|
4.7
|
16.2
|
1.0
|
O
|
C:HOH6327
|
4.7
|
15.6
|
1.0
|
CA
|
B:ASP221
|
4.7
|
14.4
|
1.0
|
OH
|
B:TYR241
|
4.8
|
19.8
|
1.0
|
CB
|
B:SER225
|
4.8
|
15.8
|
1.0
|
N
|
B:PHE219
|
4.9
|
13.6
|
1.0
|
OG
|
B:SER220
|
4.9
|
14.0
|
1.0
|
C
|
C:ASP57
|
5.0
|
11.8
|
1.0
|
|
Calcium binding site 4 out
of 6 in 1jkv
Go back to
Calcium Binding Sites List in 1jkv
Calcium binding site 4 out
of 6 in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 4 of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Ca7272
b:18.0
occ:1.00
|
OD1
|
E:ASN218
|
2.2
|
20.2
|
1.0
|
O
|
E:GLY222
|
2.4
|
16.7
|
1.0
|
O
|
E:SER220
|
2.4
|
15.2
|
1.0
|
OD1
|
D:ASP61
|
2.4
|
16.3
|
1.0
|
OD2
|
D:ASP57
|
2.4
|
16.5
|
1.0
|
OD1
|
D:ASP57
|
2.5
|
15.8
|
1.0
|
O
|
E:HOH8380
|
2.6
|
22.2
|
1.0
|
CG
|
D:ASP57
|
2.8
|
13.7
|
1.0
|
OD2
|
D:ASP61
|
2.9
|
18.2
|
1.0
|
CG
|
D:ASP61
|
3.0
|
15.0
|
1.0
|
CG
|
E:ASN218
|
3.4
|
18.9
|
1.0
|
C
|
E:GLY222
|
3.5
|
17.3
|
1.0
|
C
|
E:SER220
|
3.6
|
14.0
|
1.0
|
OG
|
E:SER225
|
3.9
|
17.9
|
1.0
|
N
|
E:GLY222
|
4.1
|
15.6
|
1.0
|
N
|
E:SER220
|
4.2
|
13.6
|
1.0
|
CA
|
E:GLY222
|
4.3
|
16.4
|
1.0
|
ND2
|
E:ASN218
|
4.3
|
21.7
|
1.0
|
CA
|
E:SER220
|
4.3
|
13.6
|
1.0
|
CB
|
E:ASN218
|
4.3
|
16.6
|
1.0
|
CB
|
D:ASP57
|
4.3
|
12.8
|
1.0
|
CA
|
E:ASN218
|
4.4
|
16.3
|
1.0
|
N
|
E:ASP223
|
4.4
|
18.1
|
1.0
|
CB
|
E:SER220
|
4.5
|
13.9
|
1.0
|
CA
|
E:ASP223
|
4.5
|
19.1
|
1.0
|
C
|
E:ASP221
|
4.5
|
15.3
|
1.0
|
O
|
D:ASP57
|
4.5
|
13.2
|
1.0
|
O
|
E:HOH8423
|
4.5
|
27.1
|
1.0
|
CB
|
D:ASP61
|
4.5
|
13.1
|
1.0
|
N
|
E:ASP221
|
4.6
|
13.7
|
1.0
|
C
|
E:ASN218
|
4.7
|
17.3
|
1.0
|
OH
|
E:TYR241
|
4.7
|
21.6
|
1.0
|
O
|
D:HOH7341
|
4.7
|
17.3
|
1.0
|
CA
|
E:ASP221
|
4.8
|
15.0
|
1.0
|
CB
|
E:SER225
|
4.9
|
16.7
|
1.0
|
N
|
E:PHE219
|
4.9
|
15.0
|
1.0
|
C
|
D:ASP57
|
5.0
|
12.2
|
1.0
|
|
Calcium binding site 5 out
of 6 in 1jkv
Go back to
Calcium Binding Sites List in 1jkv
Calcium binding site 5 out
of 6 in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 5 of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Ca8272
b:17.5
occ:1.00
|
OD1
|
D:ASN218
|
2.2
|
20.6
|
1.0
|
O
|
D:GLY222
|
2.3
|
16.3
|
1.0
|
O
|
D:SER220
|
2.4
|
14.1
|
1.0
|
OD1
|
E:ASP61
|
2.4
|
16.2
|
1.0
|
OD2
|
E:ASP57
|
2.4
|
17.0
|
1.0
|
OD1
|
E:ASP57
|
2.4
|
14.2
|
1.0
|
O
|
D:HOH7389
|
2.5
|
21.7
|
1.0
|
CG
|
E:ASP57
|
2.8
|
13.8
|
1.0
|
OD2
|
E:ASP61
|
2.9
|
17.8
|
1.0
|
CG
|
E:ASP61
|
3.0
|
14.1
|
1.0
|
CG
|
D:ASN218
|
3.4
|
18.8
|
1.0
|
C
|
D:GLY222
|
3.4
|
16.0
|
1.0
|
C
|
D:SER220
|
3.5
|
13.2
|
1.0
|
OG
|
D:SER225
|
3.9
|
17.1
|
1.0
|
N
|
D:GLY222
|
4.0
|
14.8
|
1.0
|
CA
|
D:GLY222
|
4.2
|
15.4
|
1.0
|
N
|
D:SER220
|
4.2
|
13.1
|
1.0
|
ND2
|
D:ASN218
|
4.2
|
19.6
|
1.0
|
CA
|
D:SER220
|
4.3
|
12.8
|
1.0
|
CB
|
E:ASP57
|
4.3
|
11.9
|
1.0
|
N
|
D:ASP223
|
4.3
|
16.8
|
1.0
|
CB
|
D:ASN218
|
4.4
|
16.4
|
1.0
|
CB
|
D:SER220
|
4.4
|
13.1
|
1.0
|
CA
|
D:ASN218
|
4.4
|
16.2
|
1.0
|
C
|
D:ASP221
|
4.4
|
14.4
|
1.0
|
CA
|
D:ASP223
|
4.5
|
16.9
|
1.0
|
O
|
E:ASP57
|
4.5
|
13.2
|
1.0
|
N
|
D:ASP221
|
4.5
|
13.2
|
1.0
|
CB
|
E:ASP61
|
4.5
|
12.8
|
1.0
|
O
|
D:HOH7405
|
4.6
|
24.0
|
1.0
|
O
|
E:HOH8326
|
4.7
|
16.3
|
1.0
|
C
|
D:ASN218
|
4.7
|
16.6
|
1.0
|
OH
|
D:TYR241
|
4.7
|
20.3
|
1.0
|
CA
|
D:ASP221
|
4.8
|
13.2
|
1.0
|
CB
|
D:SER225
|
4.8
|
16.9
|
1.0
|
N
|
D:PHE219
|
4.9
|
14.8
|
1.0
|
C
|
E:ASP57
|
5.0
|
11.8
|
1.0
|
C
|
D:ASP223
|
5.0
|
16.7
|
1.0
|
|
Calcium binding site 6 out
of 6 in 1jkv
Go back to
Calcium Binding Sites List in 1jkv
Calcium binding site 6 out
of 6 in the Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 6 of Crystal Structure of Manganese Catalase From Lactobacillus Plantarum Complexed with Azide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
F:Ca9272
b:18.6
occ:1.00
|
OD1
|
A:ASN218
|
2.2
|
20.8
|
1.0
|
O
|
A:SER220
|
2.3
|
14.7
|
1.0
|
O
|
A:GLY222
|
2.3
|
16.3
|
1.0
|
OD1
|
F:ASP61
|
2.4
|
15.7
|
1.0
|
OD1
|
F:ASP57
|
2.4
|
14.4
|
1.0
|
OD2
|
F:ASP57
|
2.5
|
15.7
|
1.0
|
O
|
A:HOH5396
|
2.5
|
23.4
|
1.0
|
CG
|
F:ASP57
|
2.8
|
14.2
|
1.0
|
OD2
|
F:ASP61
|
2.9
|
17.2
|
1.0
|
CG
|
F:ASP61
|
3.0
|
14.7
|
1.0
|
CG
|
A:ASN218
|
3.4
|
19.0
|
1.0
|
C
|
A:GLY222
|
3.4
|
15.7
|
1.0
|
C
|
A:SER220
|
3.5
|
14.1
|
1.0
|
OG
|
A:SER225
|
3.9
|
15.9
|
1.0
|
N
|
A:GLY222
|
4.0
|
15.3
|
1.0
|
N
|
A:SER220
|
4.2
|
13.2
|
1.0
|
CA
|
A:GLY222
|
4.2
|
16.0
|
1.0
|
CA
|
A:SER220
|
4.2
|
12.7
|
1.0
|
ND2
|
A:ASN218
|
4.3
|
21.1
|
1.0
|
CB
|
A:ASN218
|
4.3
|
16.8
|
1.0
|
CB
|
F:ASP57
|
4.3
|
12.5
|
1.0
|
N
|
A:ASP223
|
4.3
|
15.6
|
1.0
|
CA
|
A:ASN218
|
4.3
|
15.5
|
1.0
|
CB
|
A:SER220
|
4.4
|
13.5
|
1.0
|
C
|
A:ASP221
|
4.4
|
15.2
|
1.0
|
CA
|
A:ASP223
|
4.5
|
16.3
|
1.0
|
N
|
A:ASP221
|
4.5
|
13.7
|
1.0
|
O
|
A:HOH5383
|
4.5
|
22.3
|
1.0
|
CB
|
F:ASP61
|
4.5
|
11.6
|
1.0
|
O
|
F:ASP57
|
4.6
|
12.9
|
1.0
|
C
|
A:ASN218
|
4.6
|
16.0
|
1.0
|
OH
|
A:TYR241
|
4.7
|
21.2
|
1.0
|
CA
|
A:ASP221
|
4.7
|
14.9
|
1.0
|
O
|
F:HOH9333
|
4.7
|
16.0
|
1.0
|
CB
|
A:SER225
|
4.8
|
15.8
|
1.0
|
N
|
A:PHE219
|
4.8
|
14.1
|
1.0
|
C
|
F:ASP57
|
5.0
|
11.7
|
1.0
|
|
Reference:
V.V.Barynin,
M.M.Whittaker,
S.V.Antonyuk,
V.S.Lamzin,
P.M.Harrison,
P.J.Artymiuk,
J.W.Whittaker.
Crystal Structure of Manganese Catalase From Lactobacillus Plantarum. Structure V. 9 725 2001.
ISSN: ISSN 0969-2126
PubMed: 11587647
DOI: 10.1016/S0969-2126(01)00628-1
Page generated: Thu Jul 11 10:48:28 2024
|