Cobalt in PDB 6h9e: Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12
Enzymatic activity of Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12
All present enzymatic activity of Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12:
5.4.99.1;
Protein crystallography data
The structure of Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12, PDB code: 6h9e
was solved by
K.Gruber,
V.Csitkovits,
C.Kratky,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
40.41 /
1.82
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
63.890,
112.620,
108.350,
90.00,
95.69,
90.00
|
R / Rfree (%)
|
13.7 /
16.8
|
Cobalt Binding Sites:
The binding sites of Cobalt atom in the Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12
(pdb code 6h9e). This binding sites where shown within
5.0 Angstroms radius around Cobalt atom.
In total 2 binding sites of Cobalt where determined in the
Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12, PDB code: 6h9e:
Jump to Cobalt binding site number:
1;
2;
Cobalt binding site 1 out
of 2 in 6h9e
Go back to
Cobalt Binding Sites List in 6h9e
Cobalt binding site 1 out
of 2 in the Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12
 Mono view
 Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 1 of Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co201
b:7.3
occ:1.00
|
CO
|
A:B12201
|
0.0
|
7.3
|
1.0
|
N21
|
A:B12201
|
1.9
|
6.8
|
1.0
|
N24
|
A:B12201
|
1.9
|
6.3
|
1.0
|
N23
|
A:B12201
|
1.9
|
7.9
|
1.0
|
N22
|
A:B12201
|
1.9
|
5.3
|
1.0
|
C6'
|
B:FWK501
|
2.1
|
6.8
|
1.0
|
NE2
|
A:HIS16
|
2.2
|
9.0
|
1.0
|
C19
|
A:B12201
|
2.8
|
6.1
|
1.0
|
C1
|
A:B12201
|
2.9
|
7.8
|
1.0
|
C9
|
A:B12201
|
2.9
|
5.7
|
1.0
|
C11
|
A:B12201
|
2.9
|
7.3
|
1.0
|
C4
|
A:B12201
|
2.9
|
9.0
|
1.0
|
C14
|
A:B12201
|
3.0
|
4.5
|
1.0
|
C16
|
A:B12201
|
3.0
|
4.5
|
1.0
|
C6
|
A:B12201
|
3.0
|
5.1
|
1.0
|
CE1
|
A:HIS16
|
3.1
|
8.4
|
1.0
|
C5'
|
B:FWK501
|
3.1
|
9.5
|
1.0
|
C10
|
A:B12201
|
3.2
|
5.8
|
1.0
|
CD2
|
A:HIS16
|
3.3
|
6.6
|
1.0
|
C5
|
A:B12201
|
3.4
|
7.5
|
1.0
|
C15
|
A:B12201
|
3.4
|
5.4
|
1.0
|
C20
|
A:B12201
|
3.5
|
6.8
|
1.0
|
C18
|
A:B12201
|
4.1
|
4.6
|
1.0
|
C2
|
A:B12201
|
4.1
|
8.9
|
1.0
|
C8
|
A:B12201
|
4.2
|
6.2
|
1.0
|
C12
|
A:B12201
|
4.2
|
6.7
|
1.0
|
C3
|
A:B12201
|
4.2
|
7.5
|
1.0
|
C13
|
A:B12201
|
4.2
|
6.4
|
1.0
|
C17
|
A:B12201
|
4.2
|
5.6
|
1.0
|
ND1
|
A:HIS16
|
4.3
|
8.6
|
1.0
|
C7
|
A:B12201
|
4.3
|
5.8
|
1.0
|
CG
|
A:HIS16
|
4.4
|
6.8
|
1.0
|
C4'
|
B:FWK501
|
4.5
|
10.3
|
1.0
|
C26
|
A:B12201
|
4.6
|
6.2
|
1.0
|
C46
|
A:B12201
|
4.7
|
7.4
|
1.0
|
C48
|
A:B12201
|
4.8
|
7.6
|
1.0
|
O
|
B:HOH776
|
4.8
|
5.7
|
1.0
|
C3'
|
B:FWK501
|
4.9
|
9.6
|
1.0
|
C35
|
A:B12201
|
4.9
|
7.4
|
1.0
|
C41
|
A:B12201
|
4.9
|
5.1
|
1.0
|
C53
|
A:B12201
|
4.9
|
6.2
|
1.0
|
C54
|
A:B12201
|
4.9
|
5.2
|
1.0
|
|
Cobalt binding site 2 out
of 2 in 6h9e
Go back to
Cobalt Binding Sites List in 6h9e
Cobalt binding site 2 out
of 2 in the Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12
 Mono view
 Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 2 of Structure of Glutamate Mutase Reconstituted with Homo-Coenzyme B12 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Co201
b:8.0
occ:1.00
|
CO
|
C:B12201
|
0.0
|
8.0
|
1.0
|
N21
|
C:B12201
|
1.9
|
6.3
|
1.0
|
N24
|
C:B12201
|
1.9
|
7.1
|
1.0
|
N23
|
C:B12201
|
1.9
|
7.7
|
1.0
|
N22
|
C:B12201
|
1.9
|
7.1
|
1.0
|
C6'
|
D:FWK501
|
2.1
|
6.7
|
1.0
|
NE2
|
C:HIS16
|
2.2
|
7.0
|
1.0
|
C19
|
C:B12201
|
2.8
|
6.8
|
1.0
|
C11
|
C:B12201
|
2.9
|
4.9
|
1.0
|
C1
|
C:B12201
|
2.9
|
7.0
|
1.0
|
C9
|
C:B12201
|
2.9
|
8.0
|
1.0
|
C4
|
C:B12201
|
2.9
|
7.2
|
1.0
|
C14
|
C:B12201
|
2.9
|
5.8
|
1.0
|
C16
|
C:B12201
|
3.0
|
5.8
|
1.0
|
C6
|
C:B12201
|
3.0
|
7.0
|
1.0
|
CE1
|
C:HIS16
|
3.0
|
9.1
|
1.0
|
C5'
|
D:FWK501
|
3.1
|
8.5
|
1.0
|
C10
|
C:B12201
|
3.2
|
5.1
|
1.0
|
CD2
|
C:HIS16
|
3.3
|
6.3
|
1.0
|
C15
|
C:B12201
|
3.4
|
6.8
|
1.0
|
C5
|
C:B12201
|
3.4
|
7.5
|
1.0
|
C20
|
C:B12201
|
3.6
|
7.4
|
1.0
|
C18
|
C:B12201
|
4.1
|
4.5
|
1.0
|
C2
|
C:B12201
|
4.2
|
8.6
|
1.0
|
C12
|
C:B12201
|
4.2
|
5.8
|
1.0
|
C13
|
C:B12201
|
4.2
|
6.5
|
1.0
|
C3
|
C:B12201
|
4.2
|
6.5
|
1.0
|
C8
|
C:B12201
|
4.2
|
6.3
|
1.0
|
ND1
|
C:HIS16
|
4.2
|
7.3
|
1.0
|
C17
|
C:B12201
|
4.2
|
5.6
|
1.0
|
C7
|
C:B12201
|
4.3
|
6.0
|
1.0
|
CG
|
C:HIS16
|
4.4
|
5.7
|
1.0
|
C4'
|
D:FWK501
|
4.5
|
9.1
|
1.0
|
C26
|
C:B12201
|
4.6
|
7.2
|
1.0
|
C48
|
C:B12201
|
4.7
|
7.2
|
1.0
|
C46
|
C:B12201
|
4.7
|
6.8
|
1.0
|
O
|
D:HOH796
|
4.8
|
7.7
|
1.0
|
C53
|
C:B12201
|
4.9
|
6.9
|
1.0
|
C3'
|
D:FWK501
|
4.9
|
9.4
|
1.0
|
C35
|
C:B12201
|
4.9
|
7.3
|
1.0
|
C54
|
C:B12201
|
4.9
|
6.1
|
1.0
|
C41
|
C:B12201
|
5.0
|
8.3
|
1.0
|
|
Reference:
C.Csitkovits,
A.Lyskowski,
S.Gschoesser,
C.Kratky,
B.Kraeutler,
K.Gruber.
Structures of Glutamate Mutase Reconstituted with Homo- and Bishomo-Coenzyme B12 To Be Published.
Page generated: Tue Jul 30 18:38:01 2024
|