Magnesium in PDB 7kkt: Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Enzymatic activity of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
All present enzymatic activity of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site:
4.3.3.7;
Protein crystallography data
The structure of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site, PDB code: 7kkt
was solved by
S.Saran,
M.Majdi Yazdi,
D.A.R.Sanders,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
49.13 /
1.71
|
Space group
|
C 2 2 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
85.02,
225.47,
200.42,
90,
90,
90
|
R / Rfree (%)
|
16.4 /
19.5
|
Magnesium Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
18;
Binding sites:
The binding sites of Magnesium atom in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
(pdb code 7kkt). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 18 binding sites of Magnesium where determined in the
Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site, PDB code: 7kkt:
Jump to Magnesium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Magnesium binding site 1 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 1 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg302
b:20.2
occ:1.00
|
O
|
A:HOH432
|
2.0
|
26.7
|
1.0
|
O
|
A:HOH464
|
2.1
|
24.8
|
1.0
|
O
|
A:HOH491
|
2.1
|
19.3
|
1.0
|
O
|
A:HOH443
|
4.1
|
23.1
|
1.0
|
OD1
|
A:ASP102
|
4.2
|
21.1
|
1.0
|
O
|
A:VAL75
|
4.3
|
18.0
|
1.0
|
O
|
A:THR73
|
4.4
|
21.3
|
1.0
|
OD2
|
A:ASP102
|
4.4
|
16.9
|
1.0
|
O
|
A:CYS70
|
4.4
|
16.2
|
1.0
|
CG
|
A:ASP102
|
4.7
|
19.9
|
1.0
|
O
|
A:HOH447
|
4.9
|
20.3
|
1.0
|
|
Magnesium binding site 2 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 2 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg303
b:44.5
occ:1.00
|
O
|
A:HOH649
|
3.3
|
34.3
|
1.0
|
CB
|
A:ALA220
|
3.9
|
16.5
|
1.0
|
CZ
|
A:PHE224
|
4.2
|
18.3
|
1.0
|
CE2
|
A:PHE224
|
4.2
|
15.9
|
1.0
|
O
|
A:HOH497
|
4.7
|
26.8
|
1.0
|
CA
|
A:ALA220
|
4.8
|
15.0
|
1.0
|
|
Magnesium binding site 3 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 3 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg304
b:16.3
occ:1.00
|
O
|
A:HOH459
|
3.0
|
26.4
|
1.0
|
N
|
A:VAL107
|
3.2
|
15.9
|
1.0
|
N
|
A:GLY82
|
3.2
|
20.2
|
1.0
|
O
|
A:LEU105
|
3.4
|
19.2
|
1.0
|
O
|
F:HOH421
|
3.4
|
30.2
|
1.0
|
CA
|
A:GLY82
|
3.6
|
16.9
|
1.0
|
N
|
A:ALA81
|
3.7
|
14.8
|
1.0
|
CB
|
A:VAL107
|
3.8
|
16.7
|
1.0
|
C
|
A:LEU105
|
3.8
|
13.9
|
1.0
|
CA
|
A:SER106
|
3.8
|
17.7
|
1.0
|
CG1
|
A:VAL107
|
3.9
|
17.4
|
1.0
|
C
|
A:SER106
|
4.0
|
13.8
|
1.0
|
N
|
A:SER106
|
4.0
|
14.2
|
1.0
|
CA
|
A:VAL107
|
4.1
|
16.8
|
1.0
|
CA
|
A:GLY80
|
4.1
|
17.6
|
1.0
|
CG
|
A:LEU105
|
4.2
|
12.9
|
1.0
|
C
|
A:ALA81
|
4.3
|
21.4
|
1.0
|
CD2
|
A:LEU105
|
4.3
|
15.8
|
1.0
|
C
|
A:GLY80
|
4.3
|
12.8
|
1.0
|
CD2
|
A:TYR137
|
4.4
|
19.5
|
1.0
|
CB
|
A:LEU105
|
4.5
|
13.8
|
1.0
|
CA
|
A:ALA81
|
4.6
|
19.7
|
1.0
|
C
|
A:GLY82
|
4.7
|
16.4
|
1.0
|
CA
|
A:LEU105
|
4.8
|
14.5
|
1.0
|
CE2
|
A:TYR137
|
4.9
|
16.1
|
1.0
|
CA
|
A:GLY46
|
4.9
|
20.1
|
1.0
|
O
|
A:GLY82
|
4.9
|
17.0
|
1.0
|
O
|
A:VAL45
|
5.0
|
19.8
|
1.0
|
|
Magnesium binding site 4 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 4 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg303
b:42.1
occ:1.00
|
O
|
A:HOH605
|
2.5
|
36.9
|
1.0
|
OG
|
B:SER0
|
2.6
|
21.6
|
1.0
|
O
|
A:HOH634
|
3.1
|
36.8
|
1.0
|
O
|
B:HOH641
|
3.2
|
38.2
|
1.0
|
CB
|
B:SER0
|
3.4
|
19.8
|
1.0
|
CD
|
B:ARG184
|
3.5
|
13.6
|
1.0
|
CA
|
B:SER0
|
3.9
|
15.8
|
1.0
|
CG
|
B:ARG184
|
3.9
|
16.9
|
1.0
|
CD
|
A:LYS294
|
4.0
|
34.1
|
1.0
|
CB
|
A:LYS294
|
4.3
|
22.2
|
1.0
|
CG
|
A:LYS294
|
4.5
|
21.4
|
1.0
|
O
|
B:SER0
|
4.6
|
19.2
|
1.0
|
C
|
B:SER0
|
4.8
|
22.1
|
1.0
|
NH1
|
B:ARG184
|
4.8
|
17.8
|
1.0
|
NE
|
B:ARG184
|
4.9
|
16.5
|
1.0
|
CE
|
A:LYS294
|
4.9
|
40.3
|
1.0
|
N
|
B:SER0
|
4.9
|
17.8
|
1.0
|
CB
|
B:ARG184
|
4.9
|
15.0
|
1.0
|
O
|
B:GLY-1
|
4.9
|
18.1
|
1.0
|
|
Magnesium binding site 5 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 5 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 5 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg304
b:42.5
occ:1.00
|
OG
|
B:SER251
|
2.8
|
21.9
|
1.0
|
O
|
B:HOH521
|
2.9
|
27.0
|
1.0
|
CE
|
E:LYS113
|
3.5
|
38.8
|
1.0
|
O
|
B:HOH611
|
3.5
|
25.8
|
1.0
|
CA
|
B:SER251
|
3.6
|
13.9
|
1.0
|
N
|
B:SER251
|
3.7
|
16.5
|
1.0
|
CB
|
B:SER251
|
3.7
|
19.0
|
1.0
|
O
|
B:HOH605
|
3.8
|
37.4
|
1.0
|
O
|
B:HOH584
|
4.0
|
19.4
|
1.0
|
NZ
|
E:LYS113
|
4.0
|
53.5
|
1.0
|
C
|
B:GLU250
|
4.3
|
20.6
|
1.0
|
CD
|
E:LYS113
|
4.6
|
28.4
|
1.0
|
O
|
E:HOH596
|
4.6
|
40.1
|
1.0
|
O
|
B:GLU250
|
4.8
|
17.5
|
1.0
|
CB
|
E:LYS113
|
4.8
|
17.7
|
1.0
|
CA
|
B:GLU250
|
4.9
|
16.1
|
1.0
|
O
|
E:LYS113
|
5.0
|
15.5
|
1.0
|
|
Magnesium binding site 6 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 6 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 6 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg305
b:16.5
occ:1.00
|
O
|
B:HOH491
|
3.1
|
26.7
|
1.0
|
N
|
B:VAL107
|
3.2
|
12.9
|
1.0
|
N
|
B:GLY82
|
3.2
|
18.6
|
1.0
|
O
|
B:LEU105
|
3.3
|
19.1
|
1.0
|
CA
|
B:GLY82
|
3.7
|
18.5
|
1.0
|
N
|
B:ALA81
|
3.7
|
15.3
|
1.0
|
CB
|
B:VAL107
|
3.7
|
14.2
|
1.0
|
O
|
E:HOH402
|
3.7
|
28.1
|
1.0
|
C
|
B:LEU105
|
3.8
|
16.2
|
1.0
|
CA
|
B:SER106
|
3.8
|
13.8
|
1.0
|
CG1
|
B:VAL107
|
3.9
|
16.1
|
1.0
|
C
|
B:SER106
|
3.9
|
12.8
|
1.0
|
N
|
B:SER106
|
4.0
|
12.2
|
1.0
|
CA
|
B:VAL107
|
4.0
|
17.7
|
1.0
|
CG
|
B:LEU105
|
4.1
|
15.9
|
1.0
|
CA
|
B:GLY80
|
4.2
|
19.2
|
1.0
|
CD2
|
B:LEU105
|
4.3
|
18.1
|
1.0
|
C
|
B:ALA81
|
4.3
|
18.6
|
1.0
|
CD2
|
B:TYR137
|
4.3
|
18.8
|
1.0
|
C
|
B:GLY80
|
4.4
|
16.6
|
1.0
|
CB
|
B:LEU105
|
4.5
|
16.2
|
1.0
|
CA
|
B:ALA81
|
4.6
|
14.5
|
1.0
|
C
|
B:GLY82
|
4.7
|
19.1
|
1.0
|
CA
|
B:LEU105
|
4.8
|
15.4
|
1.0
|
CE2
|
B:TYR137
|
4.9
|
19.1
|
1.0
|
O
|
B:GLY82
|
4.9
|
16.1
|
1.0
|
|
Magnesium binding site 7 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 7 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 7 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg302
b:17.4
occ:1.00
|
O
|
C:HOH424
|
3.2
|
24.8
|
1.0
|
N
|
C:VAL107
|
3.2
|
14.1
|
1.0
|
N
|
C:GLY82
|
3.3
|
17.6
|
1.0
|
O
|
C:LEU105
|
3.4
|
17.0
|
1.0
|
O
|
D:HOH422
|
3.5
|
29.3
|
1.0
|
CA
|
C:GLY82
|
3.7
|
20.1
|
1.0
|
CB
|
C:VAL107
|
3.7
|
14.0
|
1.0
|
N
|
C:ALA81
|
3.8
|
17.0
|
1.0
|
CG1
|
C:VAL107
|
3.8
|
15.0
|
1.0
|
C
|
C:LEU105
|
3.8
|
16.6
|
1.0
|
CA
|
C:SER106
|
3.9
|
15.8
|
1.0
|
N
|
C:SER106
|
4.0
|
12.1
|
1.0
|
C
|
C:SER106
|
4.0
|
15.2
|
1.0
|
CA
|
C:VAL107
|
4.0
|
13.5
|
1.0
|
CG
|
C:LEU105
|
4.1
|
16.0
|
1.0
|
CA
|
C:GLY80
|
4.2
|
14.7
|
1.0
|
CD2
|
C:TYR137
|
4.3
|
17.8
|
1.0
|
CD2
|
C:LEU105
|
4.3
|
15.4
|
1.0
|
C
|
C:ALA81
|
4.4
|
17.1
|
1.0
|
C
|
C:GLY80
|
4.4
|
15.3
|
1.0
|
CB
|
C:LEU105
|
4.5
|
11.6
|
1.0
|
O
|
C:HOH404
|
4.6
|
35.2
|
1.0
|
CA
|
C:ALA81
|
4.7
|
14.1
|
1.0
|
C
|
C:GLY82
|
4.7
|
20.8
|
1.0
|
CE2
|
C:TYR137
|
4.8
|
20.2
|
1.0
|
CA
|
C:LEU105
|
4.9
|
14.0
|
1.0
|
CA
|
C:GLY46
|
5.0
|
20.5
|
1.0
|
O
|
C:GLY82
|
5.0
|
17.2
|
1.0
|
|
Magnesium binding site 8 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 8 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 8 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg303
b:19.3
occ:1.00
|
O
|
C:HOH446
|
2.0
|
23.8
|
1.0
|
O
|
C:HOH483
|
2.1
|
19.7
|
1.0
|
O
|
C:HOH461
|
2.1
|
22.0
|
1.0
|
O
|
C:HOH451
|
4.0
|
23.9
|
1.0
|
OD1
|
C:ASP102
|
4.2
|
20.7
|
1.0
|
O
|
C:VAL75
|
4.3
|
17.8
|
1.0
|
OD2
|
C:ASP102
|
4.3
|
17.3
|
1.0
|
O
|
C:THR73
|
4.3
|
19.9
|
1.0
|
O
|
C:CYS70
|
4.5
|
15.3
|
1.0
|
CG
|
C:ASP102
|
4.7
|
24.1
|
1.0
|
O
|
C:HOH485
|
4.7
|
19.0
|
1.0
|
|
Magnesium binding site 9 out
of 18 in 7kkt
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Magnesium Binding Sites List in 7kkt
Magnesium binding site 9 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 9 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg302
b:47.5
occ:1.00
|
O
|
D:HOH500
|
2.1
|
42.1
|
1.0
|
O
|
D:HOH491
|
2.3
|
44.6
|
1.0
|
OE2
|
D:GLU64
|
4.5
|
39.9
|
1.0
|
OE1
|
D:GLU64
|
4.6
|
48.0
|
1.0
|
O
|
D:HOH593
|
4.6
|
52.8
|
1.0
|
CD
|
D:GLU64
|
5.0
|
32.2
|
1.0
|
|
Magnesium binding site 10 out
of 18 in 7kkt
Go back to
Magnesium Binding Sites List in 7kkt
Magnesium binding site 10 out
of 18 in the Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 10 of Dihydrodipicolinate Synthase (Dhdps) From C.Jejuni, N84D Mutant with Pyruvate Bound in the Active Site and R,R-Bislysine Bound at the Allosteric Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg303
b:17.7
occ:1.00
|
O
|
D:HOH517
|
2.9
|
31.3
|
1.0
|
N
|
D:VAL107
|
3.2
|
16.4
|
1.0
|
N
|
D:GLY82
|
3.3
|
19.6
|
1.0
|
O
|
D:LEU105
|
3.4
|
19.3
|
1.0
|
O
|
C:HOH415
|
3.6
|
31.1
|
1.0
|
CA
|
D:GLY82
|
3.7
|
19.6
|
1.0
|
CB
|
D:VAL107
|
3.8
|
18.6
|
1.0
|
N
|
D:ALA81
|
3.8
|
15.2
|
1.0
|
C
|
D:LEU105
|
3.8
|
13.9
|
1.0
|
CA
|
D:SER106
|
3.9
|
14.4
|
1.0
|
CG1
|
D:VAL107
|
3.9
|
15.6
|
1.0
|
C
|
D:SER106
|
4.0
|
13.3
|
1.0
|
N
|
D:SER106
|
4.0
|
13.3
|
1.0
|
CA
|
D:VAL107
|
4.1
|
15.7
|
1.0
|
CA
|
D:GLY80
|
4.1
|
17.7
|
1.0
|
CG
|
D:LEU105
|
4.2
|
17.1
|
1.0
|
CD2
|
D:LEU105
|
4.3
|
20.0
|
1.0
|
C
|
D:GLY80
|
4.3
|
17.9
|
1.0
|
CD2
|
D:TYR137
|
4.3
|
18.3
|
1.0
|
C
|
D:ALA81
|
4.4
|
24.2
|
1.0
|
CB
|
D:LEU105
|
4.5
|
14.6
|
1.0
|
CA
|
D:ALA81
|
4.7
|
15.1
|
1.0
|
C
|
D:GLY82
|
4.7
|
15.9
|
1.0
|
CE2
|
D:TYR137
|
4.8
|
19.9
|
1.0
|
CA
|
D:LEU105
|
4.8
|
13.9
|
1.0
|
O
|
D:VAL45
|
4.9
|
24.1
|
1.0
|
CA
|
D:GLY46
|
4.9
|
18.3
|
1.0
|
O
|
D:GLY82
|
5.0
|
16.6
|
1.0
|
|
Reference:
S.Saran,
M.Majdi Yazdi,
D.R.J.Palmer,
D.A.R.Sanders.
A Tight Dimer Interface N84 Residue, Plays A Critical Role in the Transmission of the Allosteric Inhibition Signals in Cj.Dhdps To Be Published.
Page generated: Wed Oct 2 22:22:39 2024
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