Potassium in PDB 1jdb: Carbamoyl Phosphate Synthetase From Escherichia Coli
Enzymatic activity of Carbamoyl Phosphate Synthetase From Escherichia Coli
All present enzymatic activity of Carbamoyl Phosphate Synthetase From Escherichia Coli:
6.3.5.5;
Protein crystallography data
The structure of Carbamoyl Phosphate Synthetase From Escherichia Coli, PDB code: 1jdb
was solved by
J.B.Thoden,
H.M.Holden,
G.Wesenberg,
F.M.Raushel,
I.Rayment,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.00 /
2.10
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
143.800,
167.700,
323.000,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
17.9 /
n/a
|
Other elements in 1jdb:
The structure of Carbamoyl Phosphate Synthetase From Escherichia Coli also contains other interesting chemical elements:
Potassium Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
20;
Page 3, Binding sites: 21 -
29;
Binding sites:
The binding sites of Potassium atom in the Carbamoyl Phosphate Synthetase From Escherichia Coli
(pdb code 1jdb). This binding sites where shown within
5.0 Angstroms radius around Potassium atom.
In total 29 binding sites of Potassium where determined in the
Carbamoyl Phosphate Synthetase From Escherichia Coli, PDB code: 1jdb:
Jump to Potassium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Potassium binding site 1 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 1 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 1 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K1075
b:11.3
occ:1.00
|
OE1
|
B:GLU214
|
2.5
|
10.9
|
1.0
|
OD1
|
B:ASN235
|
2.6
|
20.4
|
1.0
|
O
|
B:ILE241
|
2.6
|
14.7
|
1.0
|
O
|
B:ALA238
|
2.8
|
18.5
|
1.0
|
O
|
B:ASP237
|
2.8
|
11.5
|
1.0
|
OG
|
B:SER246
|
2.8
|
10.9
|
1.0
|
C
|
B:ALA238
|
3.5
|
14.8
|
1.0
|
CG
|
B:ASN235
|
3.5
|
18.5
|
1.0
|
C
|
B:ASP237
|
3.6
|
9.6
|
1.0
|
CD
|
B:GLU214
|
3.6
|
25.1
|
1.0
|
CB
|
B:ASN235
|
3.8
|
16.8
|
1.0
|
C
|
B:ILE241
|
3.8
|
16.5
|
1.0
|
CB
|
B:SER246
|
3.8
|
5.6
|
1.0
|
CB
|
B:GLU214
|
4.0
|
7.3
|
1.0
|
CG
|
B:GLU214
|
4.2
|
6.8
|
1.0
|
N
|
B:ALA238
|
4.2
|
3.9
|
1.0
|
O2'
|
B:ADP1093
|
4.2
|
11.5
|
1.0
|
CA
|
B:ALA238
|
4.3
|
6.0
|
1.0
|
N
|
B:MET239
|
4.3
|
17.9
|
1.0
|
O
|
B:HIS242
|
4.3
|
17.4
|
1.0
|
C
|
B:HIS242
|
4.4
|
11.6
|
1.0
|
CB
|
B:ASP237
|
4.4
|
17.0
|
1.0
|
N
|
B:ILE241
|
4.4
|
15.6
|
1.0
|
CB
|
B:ILE241
|
4.4
|
20.2
|
1.0
|
N
|
B:THR243
|
4.4
|
13.8
|
1.0
|
CA
|
B:ILE241
|
4.4
|
14.6
|
1.0
|
CA
|
B:THR243
|
4.5
|
5.5
|
1.0
|
CA
|
B:ASP237
|
4.5
|
9.8
|
1.0
|
CA
|
B:MET239
|
4.5
|
8.4
|
1.0
|
OE2
|
B:GLU214
|
4.5
|
18.1
|
1.0
|
CG2
|
B:THR243
|
4.7
|
10.8
|
1.0
|
ND2
|
B:ASN235
|
4.7
|
12.2
|
1.0
|
N
|
B:HIS242
|
4.8
|
12.5
|
1.0
|
CG2
|
B:ILE241
|
4.9
|
4.6
|
1.0
|
N
|
B:GLY240
|
5.0
|
23.7
|
1.0
|
N
|
B:ASP237
|
5.0
|
13.0
|
1.0
|
|
Potassium binding site 2 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 2 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 2 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K1076
b:17.1
occ:1.00
|
OE1
|
B:GLU298
|
2.7
|
12.7
|
1.0
|
O
|
B:MET299
|
2.8
|
16.9
|
1.0
|
O
|
B:HOH1100
|
2.8
|
20.3
|
1.0
|
O
|
B:HOH1105
|
2.8
|
38.8
|
1.0
|
O
|
B:HOH1097
|
2.8
|
23.5
|
1.0
|
OE2
|
B:GLU126
|
3.2
|
30.9
|
1.0
|
O
|
B:ALA125
|
3.3
|
21.7
|
1.0
|
OD1
|
B:ASN300
|
3.4
|
15.3
|
1.0
|
O
|
B:HOH1162
|
3.5
|
23.5
|
1.0
|
MN
|
B:MN1073
|
3.8
|
15.8
|
1.0
|
CD
|
B:GLU298
|
3.8
|
23.6
|
1.0
|
C
|
B:MET299
|
3.8
|
17.1
|
1.0
|
CD
|
B:GLU126
|
3.8
|
47.3
|
1.0
|
C
|
B:ALA125
|
4.1
|
18.1
|
1.0
|
OE1
|
B:GLU126
|
4.2
|
20.4
|
1.0
|
N
|
B:MET299
|
4.2
|
8.8
|
1.0
|
CB
|
B:GLU298
|
4.3
|
7.0
|
1.0
|
NH1
|
B:ARG128
|
4.3
|
15.0
|
1.0
|
CA
|
B:GLU126
|
4.4
|
7.7
|
1.0
|
CG
|
B:ASN300
|
4.4
|
27.9
|
1.0
|
NH2
|
B:ARG128
|
4.5
|
17.2
|
1.0
|
CZ
|
B:ARG128
|
4.5
|
21.0
|
1.0
|
N
|
B:ASN300
|
4.5
|
12.0
|
1.0
|
CA
|
B:ASN300
|
4.5
|
12.7
|
1.0
|
N
|
B:GLU126
|
4.6
|
23.0
|
1.0
|
O
|
B:HOH1256
|
4.6
|
9.8
|
1.0
|
CG
|
B:GLU298
|
4.6
|
5.1
|
1.0
|
OE2
|
B:GLU298
|
4.7
|
13.8
|
1.0
|
O3B
|
B:ADP1093
|
4.7
|
10.7
|
1.0
|
CA
|
B:MET299
|
4.7
|
15.2
|
1.0
|
O
|
B:HOH1254
|
4.8
|
12.8
|
1.0
|
CB
|
B:ALA125
|
4.8
|
13.7
|
1.0
|
CG
|
B:GLU126
|
4.9
|
10.7
|
1.0
|
CD
|
B:PRO301
|
4.9
|
14.7
|
1.0
|
|
Potassium binding site 3 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 3 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 3 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K1077
b:28.2
occ:1.00
|
OE1
|
B:GLN284
|
2.6
|
13.8
|
1.0
|
OE1
|
B:GLU216
|
2.8
|
18.4
|
1.0
|
O3
|
B:PO41078
|
2.8
|
6.5
|
1.0
|
O
|
B:HOH1099
|
3.1
|
2.3
|
1.0
|
OG1
|
B:THR243
|
3.2
|
10.8
|
1.0
|
CD
|
B:GLN284
|
3.4
|
13.3
|
1.0
|
OD1
|
B:ASN282
|
3.5
|
42.7
|
1.0
|
O
|
B:HOH1101
|
3.5
|
9.4
|
1.0
|
MN
|
B:MN1074
|
3.6
|
14.2
|
1.0
|
CD
|
B:GLU216
|
3.7
|
43.0
|
1.0
|
O
|
B:HOH1098
|
3.8
|
16.2
|
1.0
|
ND2
|
B:ASN282
|
3.9
|
45.0
|
1.0
|
CG
|
B:GLN284
|
3.9
|
12.1
|
1.0
|
P
|
B:PO41078
|
4.0
|
14.6
|
1.0
|
O2
|
B:PO41078
|
4.0
|
15.8
|
1.0
|
CG
|
B:ASN282
|
4.1
|
24.9
|
1.0
|
OG
|
B:SER306
|
4.2
|
20.8
|
1.0
|
CB
|
B:THR243
|
4.2
|
10.7
|
1.0
|
ND2
|
B:ASN300
|
4.2
|
13.3
|
1.0
|
CG2
|
B:THR243
|
4.4
|
10.8
|
1.0
|
NE2
|
B:GLN284
|
4.4
|
9.8
|
1.0
|
OE2
|
B:GLU216
|
4.5
|
18.9
|
1.0
|
NH1
|
B:ARG305
|
4.5
|
8.1
|
1.0
|
CG
|
B:GLU216
|
4.6
|
35.0
|
1.0
|
OE2
|
B:GLU298
|
4.7
|
13.8
|
1.0
|
O4
|
B:PO41078
|
4.7
|
14.4
|
1.0
|
CB
|
B:SER306
|
4.8
|
9.1
|
1.0
|
|
Potassium binding site 4 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 4 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 4 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K1081
b:22.9
occ:1.00
|
OE1
|
B:GLU760
|
2.7
|
24.6
|
1.0
|
O
|
B:VAL786
|
2.7
|
17.5
|
1.0
|
O
|
B:GLU782
|
2.8
|
18.0
|
1.0
|
ND1
|
B:HIS780
|
2.9
|
21.2
|
1.0
|
O
|
B:GLN783
|
2.9
|
29.2
|
1.0
|
OG
|
B:SER791
|
2.9
|
17.5
|
1.0
|
C
|
B:GLN783
|
3.4
|
28.1
|
1.0
|
CB
|
B:GLU760
|
3.6
|
15.0
|
1.0
|
C
|
B:GLU782
|
3.6
|
23.7
|
1.0
|
CD
|
B:GLU760
|
3.6
|
19.6
|
1.0
|
CG
|
B:HIS780
|
3.8
|
33.0
|
1.0
|
C
|
B:VAL786
|
3.8
|
29.1
|
1.0
|
CB
|
B:HIS780
|
3.9
|
20.2
|
1.0
|
CE1
|
B:HIS780
|
3.9
|
17.3
|
1.0
|
CB
|
B:SER791
|
4.0
|
17.1
|
1.0
|
N
|
B:ALA784
|
4.1
|
18.7
|
1.0
|
CG
|
B:GLU760
|
4.1
|
37.6
|
1.0
|
CB
|
B:VAL786
|
4.2
|
42.4
|
1.0
|
CA
|
B:GLN783
|
4.2
|
34.5
|
1.0
|
N
|
B:GLN783
|
4.2
|
22.6
|
1.0
|
O2'
|
B:ADP1094
|
4.2
|
21.5
|
1.0
|
CA
|
B:ALA784
|
4.2
|
19.2
|
1.0
|
N
|
B:VAL786
|
4.3
|
28.3
|
1.0
|
CB
|
B:GLU782
|
4.4
|
13.3
|
1.0
|
CA
|
B:VAL786
|
4.4
|
14.2
|
1.0
|
O
|
B:HIS787
|
4.5
|
18.1
|
1.0
|
OE2
|
B:GLU760
|
4.5
|
28.6
|
1.0
|
CA
|
B:GLU782
|
4.5
|
8.5
|
1.0
|
C
|
B:HIS787
|
4.6
|
13.7
|
1.0
|
N
|
B:SER788
|
4.6
|
15.0
|
1.0
|
CA
|
B:SER788
|
4.7
|
10.5
|
1.0
|
O
|
B:HOH1666
|
4.7
|
15.7
|
1.0
|
CG1
|
B:VAL786
|
4.8
|
23.4
|
1.0
|
CA
|
B:GLU760
|
4.9
|
17.2
|
1.0
|
C
|
B:ALA784
|
4.9
|
23.0
|
1.0
|
N
|
B:HIS787
|
4.9
|
20.7
|
1.0
|
N
|
B:GLY785
|
4.9
|
23.9
|
1.0
|
|
Potassium binding site 5 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 5 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 5 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K1083
b:35.9
occ:1.00
|
O
|
B:HOH1275
|
2.6
|
52.9
|
1.0
|
OG1
|
B:THR142
|
2.8
|
16.6
|
1.0
|
O
|
B:HOH1272
|
2.8
|
29.6
|
1.0
|
O
|
B:ALA143
|
2.9
|
23.8
|
1.0
|
O
|
B:THR142
|
3.1
|
16.8
|
1.0
|
O
|
B:HOH1274
|
3.1
|
19.1
|
1.0
|
C
|
B:ALA143
|
3.6
|
20.9
|
1.0
|
C
|
B:THR142
|
3.6
|
9.9
|
1.0
|
O
|
B:HOH1273
|
3.7
|
37.8
|
1.0
|
CB
|
B:THR142
|
4.0
|
21.3
|
1.0
|
N
|
B:ARG144
|
4.1
|
15.1
|
1.0
|
CA
|
B:ARG144
|
4.1
|
17.6
|
1.0
|
CA
|
B:THR142
|
4.2
|
30.3
|
1.0
|
N
|
B:THR142
|
4.3
|
18.3
|
1.0
|
N
|
B:ALA143
|
4.4
|
17.1
|
1.0
|
OD1
|
B:ASP132
|
4.5
|
51.5
|
1.0
|
CA
|
B:ALA143
|
4.5
|
6.7
|
1.0
|
O
|
B:HOH1266
|
4.7
|
41.1
|
1.0
|
O
|
B:HOH1276
|
4.7
|
28.4
|
1.0
|
N
|
B:SER145
|
4.8
|
22.0
|
1.0
|
O
|
B:HOH1334
|
4.8
|
15.0
|
1.0
|
OD2
|
B:ASP132
|
4.9
|
55.4
|
1.0
|
C
|
B:ARG144
|
4.9
|
30.0
|
1.0
|
OG
|
B:SER145
|
5.0
|
24.9
|
1.0
|
|
Potassium binding site 6 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 6 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 6 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K1084
b:49.0
occ:1.00
|
O
|
B:GLY111
|
2.8
|
43.3
|
1.0
|
OG1
|
B:THR113
|
2.9
|
61.2
|
1.0
|
O
|
B:ASP83
|
2.9
|
23.7
|
1.0
|
C
|
B:GLY111
|
3.7
|
31.2
|
1.0
|
C
|
B:ASP83
|
3.8
|
13.5
|
1.0
|
N
|
B:THR113
|
3.8
|
21.8
|
1.0
|
CB
|
B:THR113
|
4.0
|
39.4
|
1.0
|
CA
|
B:ASP83
|
4.0
|
10.8
|
1.0
|
CB
|
B:ASP83
|
4.4
|
27.3
|
1.0
|
OD1
|
B:ASP83
|
4.4
|
40.7
|
1.0
|
C
|
B:VAL112
|
4.4
|
45.8
|
1.0
|
CA
|
B:VAL112
|
4.4
|
30.1
|
1.0
|
N
|
B:VAL112
|
4.4
|
48.8
|
1.0
|
CA
|
B:THR113
|
4.5
|
58.7
|
1.0
|
O
|
B:HOH1220
|
4.5
|
40.1
|
1.0
|
CA
|
B:GLY111
|
4.7
|
41.6
|
1.0
|
CG
|
B:ASP83
|
5.0
|
52.1
|
1.0
|
|
Potassium binding site 7 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 7 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 7 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:K383
b:23.6
occ:1.00
|
O
|
C:HOH435
|
2.6
|
22.9
|
1.0
|
O
|
C:HOH434
|
2.6
|
22.9
|
1.0
|
O
|
C:ASP112
|
2.7
|
14.9
|
1.0
|
O
|
C:HIS16
|
2.8
|
20.0
|
1.0
|
O
|
C:HOH433
|
3.0
|
35.8
|
1.0
|
O
|
B:HOH1649
|
3.1
|
22.1
|
1.0
|
O
|
C:HOH438
|
3.9
|
39.6
|
1.0
|
C
|
C:ASP112
|
3.9
|
11.8
|
1.0
|
C
|
C:HIS16
|
4.0
|
15.2
|
1.0
|
NH2
|
B:ARG493
|
4.2
|
9.2
|
1.0
|
O
|
B:HOH1925
|
4.3
|
33.8
|
1.0
|
CL
|
C:CL384
|
4.4
|
24.4
|
1.0
|
O
|
B:HOH1488
|
4.4
|
13.2
|
1.0
|
CA
|
C:GLY17
|
4.4
|
14.4
|
1.0
|
O
|
C:HOH432
|
4.4
|
15.8
|
1.0
|
CB
|
C:ASP112
|
4.5
|
17.0
|
1.0
|
CA
|
C:ILE113
|
4.5
|
12.3
|
1.0
|
CZ
|
B:ARG493
|
4.6
|
21.7
|
1.0
|
O
|
C:HOH437
|
4.6
|
42.3
|
1.0
|
N
|
C:GLY17
|
4.7
|
13.8
|
1.0
|
N
|
C:ILE113
|
4.8
|
22.4
|
1.0
|
NH1
|
B:ARG493
|
4.8
|
17.1
|
1.0
|
CA
|
C:ASP112
|
4.9
|
13.0
|
1.0
|
CG2
|
C:ILE113
|
4.9
|
8.6
|
1.0
|
O
|
B:HOH1654
|
4.9
|
44.8
|
1.0
|
|
Potassium binding site 8 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 8 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 8 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:K1075
b:15.1
occ:1.00
|
OE1
|
E:GLU214
|
2.6
|
19.0
|
1.0
|
OG
|
E:SER246
|
2.6
|
13.3
|
1.0
|
O
|
E:ILE241
|
2.7
|
12.5
|
1.0
|
OD1
|
E:ASN235
|
2.7
|
16.5
|
1.0
|
O
|
E:ASP237
|
2.9
|
16.2
|
1.0
|
O
|
E:ALA238
|
2.9
|
13.9
|
1.0
|
C
|
E:ASP237
|
3.6
|
13.7
|
1.0
|
C
|
E:ALA238
|
3.6
|
18.7
|
1.0
|
CG
|
E:ASN235
|
3.7
|
16.4
|
1.0
|
CB
|
E:SER246
|
3.7
|
4.1
|
1.0
|
CD
|
E:GLU214
|
3.7
|
44.9
|
1.0
|
C
|
E:ILE241
|
3.8
|
29.4
|
1.0
|
CB
|
E:ASN235
|
3.9
|
10.9
|
1.0
|
CB
|
E:GLU214
|
4.1
|
7.8
|
1.0
|
N
|
E:ALA238
|
4.2
|
12.1
|
1.0
|
CG
|
E:GLU214
|
4.3
|
19.4
|
1.0
|
CA
|
E:ALA238
|
4.3
|
9.1
|
1.0
|
O
|
E:HIS242
|
4.3
|
14.3
|
1.0
|
CB
|
E:ASP237
|
4.3
|
9.6
|
1.0
|
O2'
|
E:ADP1095
|
4.4
|
15.3
|
1.0
|
N
|
E:MET239
|
4.4
|
11.5
|
1.0
|
C
|
E:HIS242
|
4.4
|
6.4
|
1.0
|
CB
|
E:ILE241
|
4.4
|
8.0
|
1.0
|
CA
|
E:ASP237
|
4.4
|
8.8
|
1.0
|
N
|
E:THR243
|
4.4
|
18.5
|
1.0
|
N
|
E:ILE241
|
4.5
|
11.0
|
1.0
|
CA
|
E:ILE241
|
4.5
|
20.9
|
1.0
|
CA
|
E:THR243
|
4.5
|
21.2
|
1.0
|
CA
|
E:MET239
|
4.5
|
20.0
|
1.0
|
OE2
|
E:GLU214
|
4.7
|
28.3
|
1.0
|
N
|
E:HIS242
|
4.8
|
17.6
|
1.0
|
CG2
|
E:THR243
|
4.9
|
14.4
|
1.0
|
ND2
|
E:ASN235
|
4.9
|
14.7
|
1.0
|
N
|
E:ASP237
|
4.9
|
16.2
|
1.0
|
CG2
|
E:ILE241
|
4.9
|
4.0
|
1.0
|
|
Potassium binding site 9 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 9 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 9 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:K1076
b:18.7
occ:1.00
|
O
|
E:HOH1223
|
2.6
|
37.6
|
1.0
|
O
|
E:MET299
|
2.8
|
18.3
|
1.0
|
OE1
|
E:GLU298
|
2.9
|
12.8
|
1.0
|
O
|
E:HOH1218
|
2.9
|
20.6
|
1.0
|
OE2
|
E:GLU126
|
3.0
|
25.4
|
1.0
|
O
|
E:ALA125
|
3.1
|
15.1
|
1.0
|
O
|
E:HOH1215
|
3.2
|
21.8
|
1.0
|
OD1
|
E:ASN300
|
3.4
|
14.8
|
1.0
|
O
|
E:HOH1281
|
3.5
|
20.5
|
1.0
|
CD
|
E:GLU126
|
3.7
|
32.4
|
1.0
|
CD
|
E:GLU298
|
3.8
|
11.5
|
1.0
|
C
|
E:MET299
|
3.9
|
8.6
|
1.0
|
C
|
E:ALA125
|
3.9
|
16.7
|
1.0
|
MN
|
E:MN1073
|
3.9
|
15.7
|
1.0
|
OE1
|
E:GLU126
|
4.3
|
23.5
|
1.0
|
N
|
E:MET299
|
4.3
|
19.6
|
1.0
|
NH1
|
E:ARG128
|
4.3
|
14.7
|
1.0
|
CG
|
E:ASN300
|
4.4
|
19.4
|
1.0
|
CA
|
E:GLU126
|
4.4
|
10.3
|
1.0
|
N
|
E:GLU126
|
4.4
|
17.5
|
1.0
|
O
|
E:HOH1372
|
4.4
|
13.9
|
1.0
|
CB
|
E:GLU298
|
4.5
|
8.1
|
1.0
|
CA
|
E:ASN300
|
4.6
|
27.2
|
1.0
|
CG
|
E:GLU298
|
4.6
|
10.6
|
1.0
|
N
|
E:ASN300
|
4.6
|
19.0
|
1.0
|
CZ
|
E:ARG128
|
4.7
|
14.3
|
1.0
|
OE2
|
E:GLU298
|
4.7
|
8.0
|
1.0
|
CG
|
E:GLU126
|
4.7
|
15.9
|
1.0
|
CB
|
E:ALA125
|
4.7
|
8.7
|
1.0
|
NH2
|
E:ARG128
|
4.8
|
20.1
|
1.0
|
CA
|
E:MET299
|
4.8
|
9.0
|
1.0
|
O3B
|
E:ADP1095
|
4.8
|
17.8
|
1.0
|
CA
|
E:ALA125
|
4.8
|
12.2
|
1.0
|
CD
|
E:PRO301
|
4.9
|
25.8
|
1.0
|
|
Potassium binding site 10 out
of 29 in 1jdb
Go back to
Potassium Binding Sites List in 1jdb
Potassium binding site 10 out
of 29 in the Carbamoyl Phosphate Synthetase From Escherichia Coli
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 10 of Carbamoyl Phosphate Synthetase From Escherichia Coli within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:K1077
b:28.2
occ:1.00
|
OE1
|
E:GLN284
|
2.7
|
26.6
|
1.0
|
O3
|
E:PO41078
|
2.7
|
7.5
|
1.0
|
OE1
|
E:GLU216
|
2.9
|
30.7
|
1.0
|
O
|
E:HOH1217
|
2.9
|
1.7
|
1.0
|
OG1
|
E:THR243
|
3.2
|
14.0
|
1.0
|
CD
|
E:GLN284
|
3.5
|
30.6
|
1.0
|
OD1
|
E:ASN282
|
3.6
|
41.1
|
1.0
|
O
|
E:HOH1219
|
3.6
|
13.2
|
1.0
|
CD
|
E:GLU216
|
3.6
|
57.3
|
1.0
|
O
|
E:HOH1216
|
3.6
|
13.9
|
1.0
|
MN
|
E:MN1074
|
3.6
|
14.8
|
1.0
|
ND2
|
E:ASN282
|
3.8
|
47.4
|
1.0
|
P
|
E:PO41078
|
3.9
|
16.7
|
1.0
|
CG
|
E:GLN284
|
3.9
|
15.7
|
1.0
|
O2
|
E:PO41078
|
3.9
|
9.5
|
1.0
|
CG
|
E:ASN282
|
4.0
|
20.6
|
1.0
|
CB
|
E:THR243
|
4.2
|
14.1
|
1.0
|
ND2
|
E:ASN300
|
4.2
|
18.2
|
1.0
|
OG
|
E:SER306
|
4.2
|
25.5
|
1.0
|
CG
|
E:GLU216
|
4.3
|
48.5
|
1.0
|
CG2
|
E:THR243
|
4.4
|
14.4
|
1.0
|
OE2
|
E:GLU216
|
4.4
|
39.2
|
1.0
|
NH1
|
E:ARG305
|
4.6
|
14.3
|
1.0
|
NE2
|
E:GLN284
|
4.6
|
12.8
|
1.0
|
O4
|
E:PO41078
|
4.6
|
12.9
|
1.0
|
OE2
|
E:GLU298
|
4.7
|
8.0
|
1.0
|
CB
|
E:SER306
|
4.7
|
19.5
|
1.0
|
O1
|
E:PO41078
|
4.9
|
9.6
|
1.0
|
|
Reference:
J.B.Thoden,
F.M.Raushel,
M.M.Benning,
I.Rayment,
H.M.Holden.
The Structure of Carbamoyl Phosphate Synthetase Determined to 2.1 A Resolution. Acta Crystallogr.,Sect.D V. 55 8 1999.
ISSN: ISSN 0907-4449
PubMed: 10089390
DOI: 10.1107/S0907444998006234
Page generated: Mon Aug 12 04:38:16 2024
|