Antimony in PDB 8cgs: Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
Enzymatic activity of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
All present enzymatic activity of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion:
1.20.9.1;
Protein crystallography data
The structure of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion, PDB code: 8cgs
was solved by
F.Engrola,
M.A.S.Correia,
M.J.Romao,
T.Santos-Silva,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
116.27 /
1.84
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
90.378,
109.21,
117.342,
97.71,
90.06,
96.28
|
R / Rfree (%)
|
15.4 /
18.9
|
Other elements in 8cgs:
The structure of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion also contains other interesting chemical elements:
Antimony Binding Sites:
The binding sites of Antimony atom in the Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
(pdb code 8cgs). This binding sites where shown within
5.0 Angstroms radius around Antimony atom.
In total 4 binding sites of Antimony where determined in the
Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion, PDB code: 8cgs:
Jump to Antimony binding site number:
1;
2;
3;
4;
Antimony binding site 1 out
of 4 in 8cgs
Go back to
Antimony Binding Sites List in 8cgs
Antimony binding site 1 out
of 4 in the Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
Mono view
Stereo pair view
|
A full contact list of Antimony with other atoms in the Sb binding
site number 1 of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Sb5010
b:27.6
occ:0.38
|
SB02
|
A:UJI5010
|
0.0
|
27.6
|
0.4
|
O04
|
A:UJI5010
|
1.8
|
36.3
|
1.0
|
O05
|
A:UJI5010
|
1.9
|
35.8
|
1.0
|
O01
|
A:UJI5010
|
2.0
|
28.9
|
1.0
|
O03
|
A:UJI5010
|
2.0
|
35.0
|
1.0
|
O
|
A:O5003
|
2.1
|
23.9
|
1.0
|
MO
|
A:4MO5004
|
3.5
|
19.4
|
1.0
|
ND2
|
A:ASN196
|
3.7
|
17.6
|
1.0
|
OE2
|
A:GLU203
|
3.7
|
21.3
|
1.0
|
O
|
A:HOH5155
|
3.8
|
31.4
|
1.0
|
NE2
|
A:HIS195
|
3.9
|
19.0
|
1.0
|
NH2
|
A:ARG419
|
3.9
|
21.5
|
1.0
|
O
|
A:HOH5181
|
4.1
|
23.9
|
1.0
|
ND1
|
A:HIS423
|
4.1
|
14.1
|
1.0
|
N
|
A:HIS423
|
4.1
|
12.9
|
1.0
|
NZ
|
A:LYS385
|
4.4
|
16.1
|
1.0
|
CE1
|
A:HIS195
|
4.4
|
19.5
|
1.0
|
NH1
|
A:ARG419
|
4.4
|
18.7
|
1.0
|
CA
|
A:GLY422
|
4.6
|
15.0
|
1.0
|
CB
|
A:HIS423
|
4.6
|
14.8
|
1.0
|
S12
|
A:MGD5001
|
4.6
|
15.5
|
1.0
|
CZ
|
A:ARG419
|
4.7
|
19.9
|
1.0
|
CD
|
A:GLU203
|
4.7
|
18.7
|
1.0
|
N
|
A:GLY422
|
4.8
|
14.8
|
1.0
|
CG
|
A:ASN196
|
4.8
|
16.2
|
1.0
|
S13
|
A:MGD5002
|
4.8
|
14.8
|
1.0
|
CB
|
A:HIS166
|
4.8
|
14.5
|
1.0
|
CG
|
A:HIS423
|
4.9
|
14.4
|
1.0
|
OE1
|
A:GLU203
|
4.9
|
17.6
|
1.0
|
C
|
A:GLY422
|
4.9
|
13.8
|
1.0
|
S12
|
A:MGD5002
|
5.0
|
16.9
|
1.0
|
CA
|
A:HIS423
|
5.0
|
14.3
|
1.0
|
|
Antimony binding site 2 out
of 4 in 8cgs
Go back to
Antimony Binding Sites List in 8cgs
Antimony binding site 2 out
of 4 in the Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
Mono view
Stereo pair view
|
A full contact list of Antimony with other atoms in the Sb binding
site number 2 of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Sb5109
b:29.9
occ:0.39
|
SB02
|
C:UJI5109
|
0.0
|
29.9
|
0.4
|
O04
|
C:UJI5109
|
1.8
|
41.9
|
1.0
|
O05
|
C:UJI5109
|
1.9
|
41.9
|
1.0
|
O03
|
C:UJI5109
|
2.0
|
38.6
|
1.0
|
O01
|
C:UJI5109
|
2.0
|
33.8
|
1.0
|
O
|
C:O5103
|
2.1
|
28.2
|
1.0
|
MO
|
C:4MO5104
|
3.6
|
18.4
|
1.0
|
ND2
|
C:ASN196
|
3.7
|
14.9
|
1.0
|
OE2
|
C:GLU203
|
3.7
|
21.2
|
1.0
|
O
|
C:HOH5223
|
3.7
|
30.5
|
1.0
|
NE2
|
C:HIS195
|
3.9
|
15.6
|
1.0
|
NH2
|
C:ARG419
|
3.9
|
20.6
|
1.0
|
O
|
C:HOH5218
|
4.0
|
23.6
|
1.0
|
N
|
C:HIS423
|
4.1
|
13.2
|
1.0
|
ND1
|
C:HIS423
|
4.1
|
14.3
|
1.0
|
CE1
|
C:HIS195
|
4.4
|
14.9
|
1.0
|
NZ
|
C:LYS385
|
4.4
|
14.8
|
1.0
|
NH1
|
C:ARG419
|
4.5
|
18.8
|
1.0
|
CB
|
C:HIS423
|
4.5
|
14.9
|
1.0
|
CA
|
C:GLY422
|
4.6
|
14.4
|
1.0
|
S12
|
C:MGD5101
|
4.7
|
14.0
|
1.0
|
CZ
|
C:ARG419
|
4.7
|
17.9
|
1.0
|
CD
|
C:GLU203
|
4.7
|
18.3
|
1.0
|
N
|
C:GLY422
|
4.7
|
14.4
|
1.0
|
CB
|
C:HIS166
|
4.8
|
14.6
|
1.0
|
CG
|
C:ASN196
|
4.8
|
14.9
|
1.0
|
S13
|
C:MGD5102
|
4.8
|
12.9
|
1.0
|
CG
|
C:HIS423
|
4.8
|
13.4
|
1.0
|
C
|
C:GLY422
|
4.9
|
13.5
|
1.0
|
CA
|
C:HIS423
|
4.9
|
13.9
|
1.0
|
S12
|
C:MGD5102
|
5.0
|
14.8
|
1.0
|
OE1
|
C:GLU203
|
5.0
|
16.6
|
1.0
|
|
Antimony binding site 3 out
of 4 in 8cgs
Go back to
Antimony Binding Sites List in 8cgs
Antimony binding site 3 out
of 4 in the Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
Mono view
Stereo pair view
|
A full contact list of Antimony with other atoms in the Sb binding
site number 3 of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Sb5009
b:25.4
occ:0.37
|
SB02
|
E:UJI5009
|
0.0
|
25.4
|
0.4
|
O04
|
E:UJI5009
|
1.8
|
37.4
|
1.0
|
O05
|
E:UJI5009
|
1.9
|
33.4
|
1.0
|
O01
|
E:UJI5009
|
2.0
|
28.4
|
1.0
|
O03
|
E:UJI5009
|
2.0
|
33.4
|
1.0
|
O
|
E:O5003
|
2.2
|
26.6
|
1.0
|
MO
|
E:4MO5004
|
3.5
|
19.2
|
1.0
|
ND2
|
E:ASN196
|
3.7
|
18.9
|
1.0
|
OE2
|
E:GLU203
|
3.7
|
21.2
|
1.0
|
NE2
|
E:HIS195
|
3.9
|
18.1
|
1.0
|
O
|
E:HOH5107
|
3.9
|
29.0
|
1.0
|
NH2
|
E:ARG419
|
3.9
|
21.4
|
1.0
|
O
|
E:HOH5118
|
4.1
|
24.3
|
1.0
|
N
|
E:HIS423
|
4.2
|
14.3
|
1.0
|
ND1
|
E:HIS423
|
4.2
|
14.8
|
1.0
|
NH1
|
E:ARG419
|
4.4
|
18.3
|
1.0
|
CE1
|
E:HIS195
|
4.4
|
17.9
|
1.0
|
NZ
|
E:LYS385
|
4.5
|
18.3
|
1.0
|
CB
|
E:HIS423
|
4.5
|
15.4
|
1.0
|
CA
|
E:GLY422
|
4.6
|
14.7
|
1.0
|
CZ
|
E:ARG419
|
4.6
|
18.6
|
1.0
|
CD
|
E:GLU203
|
4.7
|
18.7
|
1.0
|
S12
|
E:MGD5001
|
4.7
|
15.4
|
1.0
|
N
|
E:GLY422
|
4.7
|
15.6
|
1.0
|
CG
|
E:ASN196
|
4.8
|
18.7
|
1.0
|
CB
|
E:HIS166
|
4.8
|
14.9
|
1.0
|
S13
|
E:MGD5002
|
4.8
|
12.4
|
1.0
|
CG
|
E:HIS423
|
4.8
|
15.0
|
1.0
|
CA
|
E:HIS423
|
4.9
|
14.4
|
1.0
|
OE1
|
E:GLU203
|
5.0
|
17.2
|
1.0
|
C
|
E:GLY422
|
5.0
|
14.3
|
1.0
|
S12
|
E:MGD5002
|
5.0
|
15.8
|
1.0
|
|
Antimony binding site 4 out
of 4 in 8cgs
Go back to
Antimony Binding Sites List in 8cgs
Antimony binding site 4 out
of 4 in the Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion
Mono view
Stereo pair view
|
A full contact list of Antimony with other atoms in the Sb binding
site number 4 of Crystal Structure of Arsenite Oxidase From Alcaligenes Faecalis (Af Aio) Bound to Antimony Oxyanion within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Sb5010
b:29.9
occ:0.39
|
SB02
|
G:UJI5010
|
0.0
|
29.9
|
0.4
|
O04
|
G:UJI5010
|
1.8
|
37.5
|
1.0
|
O05
|
G:UJI5010
|
1.9
|
38.0
|
1.0
|
O01
|
G:UJI5010
|
2.0
|
37.7
|
1.0
|
O03
|
G:UJI5010
|
2.0
|
34.9
|
1.0
|
O
|
G:O5003
|
2.0
|
25.5
|
1.0
|
MO
|
G:4MO5004
|
3.5
|
19.7
|
1.0
|
ND2
|
G:ASN196
|
3.6
|
20.1
|
1.0
|
OE2
|
G:GLU203
|
3.7
|
21.7
|
1.0
|
O
|
G:HOH5110
|
3.8
|
31.3
|
1.0
|
NH2
|
G:ARG419
|
3.9
|
18.9
|
1.0
|
O
|
G:HOH5113
|
4.0
|
24.1
|
1.0
|
NE2
|
G:HIS195
|
4.0
|
17.5
|
1.0
|
N
|
G:HIS423
|
4.2
|
14.2
|
1.0
|
ND1
|
G:HIS423
|
4.3
|
17.8
|
1.0
|
NH1
|
G:ARG419
|
4.4
|
19.1
|
1.0
|
NZ
|
G:LYS385
|
4.4
|
17.4
|
1.0
|
CE1
|
G:HIS195
|
4.5
|
17.7
|
1.0
|
CA
|
G:GLY422
|
4.6
|
16.6
|
1.0
|
CZ
|
G:ARG419
|
4.6
|
17.8
|
1.0
|
CD
|
G:GLU203
|
4.7
|
20.6
|
1.0
|
S12
|
G:MGD5001
|
4.7
|
15.6
|
1.0
|
CB
|
G:HIS423
|
4.7
|
16.6
|
1.0
|
N
|
G:GLY422
|
4.7
|
16.6
|
1.0
|
CG
|
G:ASN196
|
4.7
|
18.6
|
1.0
|
S13
|
G:MGD5002
|
4.8
|
15.3
|
1.0
|
CB
|
G:HIS166
|
4.8
|
14.7
|
1.0
|
OE1
|
G:GLU203
|
4.9
|
20.0
|
1.0
|
C
|
G:GLY422
|
4.9
|
15.3
|
1.0
|
S12
|
G:MGD5002
|
4.9
|
16.1
|
1.0
|
|
Reference:
F.Engrola,
M.A.S.Correia,
M.J.Romao,
T.Santos-Silva.
Arsenite Oxidase in Complex with Antimonite and Arsenite Oxyanions - Insights Into the Catalytic Mechanism To Be Published.
Page generated: Thu Oct 10 13:19:39 2024
|