Potassium in PDB 4tlx: Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Protein crystallography data
The structure of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn, PDB code: 4tlx
was solved by
J.W.Setser,
C.L.Drennan,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
49.82 /
2.23
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
84.150,
156.906,
163.639,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
18.7 /
21.4
|
Potassium Binding Sites:
The binding sites of Potassium atom in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
(pdb code 4tlx). This binding sites where shown within
5.0 Angstroms radius around Potassium atom.
In total 9 binding sites of Potassium where determined in the
Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn, PDB code: 4tlx:
Jump to Potassium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
Potassium binding site 1 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 1 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 1 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K504
b:44.8
occ:1.00
|
O
|
A:SER33
|
2.6
|
28.5
|
1.0
|
O
|
A:LEU30
|
2.8
|
26.7
|
1.0
|
O
|
A:ALA35
|
3.2
|
47.6
|
1.0
|
O
|
A:GLU31
|
3.3
|
25.3
|
1.0
|
C
|
A:SER33
|
3.7
|
31.4
|
1.0
|
C
|
A:GLU31
|
3.8
|
29.3
|
1.0
|
C
|
A:LEU30
|
3.9
|
28.2
|
1.0
|
CA
|
A:GLU31
|
3.9
|
28.3
|
1.0
|
N
|
A:SER33
|
4.3
|
27.5
|
1.0
|
C
|
A:ALA35
|
4.3
|
38.6
|
1.0
|
N
|
A:GLU31
|
4.4
|
26.4
|
1.0
|
CA
|
A:SER33
|
4.5
|
34.4
|
1.0
|
C
|
A:PRO34
|
4.6
|
30.9
|
1.0
|
CB
|
A:SER33
|
4.7
|
36.0
|
1.0
|
N
|
A:PRO34
|
4.8
|
29.9
|
1.0
|
N
|
A:GLU32
|
4.8
|
26.2
|
1.0
|
O
|
A:PRO34
|
4.8
|
37.8
|
1.0
|
N
|
A:ALA35
|
4.8
|
35.7
|
1.0
|
C
|
A:GLU32
|
4.8
|
30.7
|
1.0
|
CA
|
A:PRO34
|
4.9
|
35.3
|
1.0
|
|
Potassium binding site 2 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 2 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 2 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K505
b:45.3
occ:1.00
|
O
|
A:GLU115
|
2.7
|
28.3
|
1.0
|
O
|
A:LEU118
|
2.8
|
38.7
|
1.0
|
O
|
A:HIS120
|
2.8
|
41.4
|
1.0
|
O
|
A:HOH743
|
2.9
|
47.3
|
1.0
|
O
|
A:HOH676
|
3.3
|
37.4
|
1.0
|
O
|
A:SER116
|
3.6
|
27.3
|
1.0
|
C
|
A:LEU118
|
3.7
|
34.1
|
1.0
|
OE2
|
A:GLU121
|
3.7
|
55.0
|
1.0
|
CB
|
A:LEU118
|
3.8
|
28.2
|
1.0
|
K
|
A:K506
|
3.8
|
58.1
|
1.0
|
C
|
A:GLU115
|
3.9
|
30.0
|
1.0
|
C
|
A:HIS120
|
4.0
|
41.4
|
1.0
|
C
|
A:SER116
|
4.0
|
28.3
|
1.0
|
CA
|
A:SER116
|
4.1
|
32.7
|
1.0
|
CA
|
A:LEU118
|
4.1
|
33.5
|
1.0
|
N
|
A:LEU118
|
4.3
|
30.1
|
1.0
|
O
|
A:ALA119
|
4.3
|
44.2
|
1.0
|
N
|
A:SER116
|
4.5
|
27.6
|
1.0
|
C
|
A:ALA119
|
4.5
|
36.6
|
1.0
|
OE1
|
A:GLU115
|
4.5
|
31.1
|
1.0
|
CD
|
A:GLU115
|
4.5
|
35.4
|
1.0
|
CD
|
A:GLU121
|
4.5
|
58.5
|
1.0
|
CA
|
A:GLU121
|
4.6
|
39.1
|
1.0
|
OE2
|
A:GLU115
|
4.6
|
41.7
|
1.0
|
N
|
A:ALA119
|
4.7
|
31.3
|
1.0
|
N
|
A:GLU121
|
4.7
|
39.6
|
1.0
|
N
|
A:HIS120
|
4.8
|
36.7
|
1.0
|
C
|
A:LYS117
|
4.9
|
31.9
|
1.0
|
N
|
A:LYS117
|
4.9
|
29.2
|
1.0
|
|
Potassium binding site 3 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 3 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 3 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K506
b:58.1
occ:1.00
|
O
|
A:LEU118
|
2.6
|
38.7
|
1.0
|
O
|
A:SER116
|
2.8
|
27.3
|
1.0
|
C
|
A:LEU118
|
3.7
|
34.1
|
1.0
|
O
|
A:LYS117
|
3.8
|
29.2
|
1.0
|
K
|
A:K505
|
3.8
|
45.3
|
1.0
|
C
|
A:SER116
|
4.0
|
28.3
|
1.0
|
C
|
A:LYS117
|
4.1
|
31.9
|
1.0
|
CA
|
A:ALA119
|
4.2
|
35.7
|
1.0
|
O
|
A:ALA119
|
4.3
|
44.2
|
1.0
|
N
|
A:ALA119
|
4.3
|
31.3
|
1.0
|
O
|
A:HOH743
|
4.4
|
47.3
|
1.0
|
C
|
A:ALA119
|
4.6
|
36.6
|
1.0
|
N
|
A:LEU118
|
4.6
|
30.1
|
1.0
|
CA
|
A:LYS117
|
4.6
|
30.0
|
1.0
|
CA
|
A:LEU118
|
4.8
|
33.5
|
1.0
|
N
|
A:LYS117
|
4.8
|
29.2
|
1.0
|
|
Potassium binding site 4 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 4 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 4 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K504
b:49.9
occ:1.00
|
O
|
B:SER33
|
2.6
|
37.6
|
1.0
|
O
|
B:LEU30
|
2.9
|
25.9
|
1.0
|
O
|
B:ALA35
|
3.2
|
45.0
|
1.0
|
O
|
B:GLU31
|
3.3
|
34.4
|
1.0
|
C
|
B:SER33
|
3.8
|
38.1
|
1.0
|
C
|
B:GLU31
|
3.8
|
33.1
|
1.0
|
CA
|
B:GLU31
|
3.9
|
30.2
|
1.0
|
C
|
B:LEU30
|
4.0
|
29.9
|
1.0
|
C
|
B:ALA35
|
4.3
|
45.8
|
1.0
|
N
|
B:SER33
|
4.3
|
29.2
|
1.0
|
N
|
B:GLU31
|
4.5
|
28.2
|
1.0
|
CA
|
B:SER33
|
4.5
|
34.3
|
1.0
|
C
|
B:PRO34
|
4.7
|
44.4
|
1.0
|
CB
|
B:SER33
|
4.7
|
33.2
|
1.0
|
N
|
B:GLU32
|
4.8
|
33.1
|
1.0
|
N
|
B:PRO34
|
4.8
|
40.4
|
1.0
|
O
|
B:PRO34
|
4.8
|
51.7
|
1.0
|
N
|
B:ALA35
|
4.8
|
43.8
|
1.0
|
C
|
B:GLU32
|
4.9
|
30.6
|
1.0
|
CA
|
B:PRO34
|
4.9
|
40.2
|
1.0
|
|
Potassium binding site 5 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 5 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 5 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K505
b:54.6
occ:1.00
|
O
|
B:LEU118
|
2.8
|
40.5
|
1.0
|
O
|
B:GLU115
|
2.9
|
32.7
|
1.0
|
O
|
B:HIS120
|
3.1
|
49.5
|
1.0
|
O
|
B:HOH660
|
3.4
|
42.6
|
1.0
|
O
|
B:SER116
|
3.4
|
32.6
|
1.0
|
OE2
|
B:GLU121
|
3.6
|
67.4
|
1.0
|
C
|
B:LEU118
|
3.8
|
37.4
|
1.0
|
C
|
B:SER116
|
3.9
|
32.8
|
1.0
|
C
|
B:GLU115
|
3.9
|
35.7
|
1.0
|
CA
|
B:SER116
|
4.0
|
34.1
|
1.0
|
CB
|
B:LEU118
|
4.1
|
36.0
|
1.0
|
C
|
B:HIS120
|
4.3
|
45.3
|
1.0
|
CA
|
B:LEU118
|
4.4
|
36.0
|
1.0
|
N
|
B:LEU118
|
4.4
|
33.0
|
1.0
|
O
|
B:ALA119
|
4.4
|
55.0
|
1.0
|
N
|
B:SER116
|
4.4
|
31.0
|
1.0
|
CD
|
B:GLU121
|
4.4
|
63.0
|
1.0
|
OE1
|
B:GLU115
|
4.6
|
38.6
|
1.0
|
CD
|
B:GLU115
|
4.6
|
38.0
|
1.0
|
OE2
|
B:GLU115
|
4.6
|
41.3
|
1.0
|
C
|
B:ALA119
|
4.7
|
46.2
|
1.0
|
CA
|
B:GLU121
|
4.8
|
43.0
|
1.0
|
N
|
B:LYS117
|
4.8
|
35.1
|
1.0
|
C
|
B:LYS117
|
4.9
|
31.4
|
1.0
|
N
|
B:ALA119
|
4.9
|
35.9
|
1.0
|
OE1
|
B:GLU121
|
5.0
|
61.4
|
1.0
|
N
|
B:GLU121
|
5.0
|
41.0
|
1.0
|
|
Potassium binding site 6 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 6 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 6 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:K504
b:58.9
occ:1.00
|
O
|
C:SER33
|
2.8
|
50.0
|
1.0
|
O
|
C:LEU30
|
3.0
|
41.7
|
1.0
|
O
|
C:ALA35
|
3.3
|
59.7
|
1.0
|
O
|
C:GLU31
|
3.4
|
44.7
|
1.0
|
C
|
C:GLU31
|
3.9
|
42.1
|
1.0
|
CA
|
C:GLU31
|
4.0
|
38.0
|
1.0
|
C
|
C:SER33
|
4.0
|
50.1
|
1.0
|
C
|
C:LEU30
|
4.1
|
41.7
|
1.0
|
C
|
C:ALA35
|
4.4
|
61.9
|
1.0
|
N
|
C:GLU31
|
4.5
|
39.0
|
1.0
|
N
|
C:SER33
|
4.6
|
41.4
|
1.0
|
CA
|
C:SER33
|
4.7
|
48.0
|
1.0
|
C
|
C:PRO34
|
4.8
|
55.2
|
1.0
|
O
|
C:PRO34
|
4.9
|
58.8
|
1.0
|
N
|
C:GLU32
|
4.9
|
40.4
|
1.0
|
CB
|
C:SER33
|
5.0
|
42.0
|
1.0
|
N
|
C:PRO34
|
5.0
|
50.4
|
1.0
|
|
Potassium binding site 7 out
of 9 in 4tlx
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Potassium Binding Sites List in 4tlx
Potassium binding site 7 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 7 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:K505
b:57.7
occ:1.00
|
O
|
C:GLU115
|
2.8
|
42.1
|
1.0
|
O
|
C:LEU118
|
2.9
|
46.1
|
1.0
|
O
|
C:HIS120
|
2.9
|
63.5
|
1.0
|
O
|
C:SER116
|
3.6
|
49.7
|
1.0
|
OE1
|
C:GLU121
|
3.6
|
72.6
|
1.0
|
C
|
C:LEU118
|
3.8
|
47.9
|
1.0
|
C
|
C:GLU115
|
3.9
|
41.5
|
1.0
|
CB
|
C:LEU118
|
4.0
|
40.0
|
1.0
|
C
|
C:SER116
|
4.0
|
44.7
|
1.0
|
O
|
C:HOH719
|
4.0
|
41.5
|
1.0
|
C
|
C:HIS120
|
4.1
|
58.2
|
1.0
|
CD
|
C:GLU121
|
4.1
|
72.8
|
1.0
|
CA
|
C:SER116
|
4.1
|
38.7
|
1.0
|
O
|
C:ALA119
|
4.3
|
55.4
|
1.0
|
CA
|
C:LEU118
|
4.3
|
41.3
|
1.0
|
OE2
|
C:GLU121
|
4.4
|
74.3
|
1.0
|
OE2
|
C:GLU115
|
4.5
|
45.4
|
1.0
|
N
|
C:LEU118
|
4.5
|
40.0
|
1.0
|
N
|
C:SER116
|
4.5
|
34.2
|
1.0
|
CD
|
C:GLU115
|
4.5
|
41.5
|
1.0
|
CA
|
C:GLU121
|
4.6
|
57.4
|
1.0
|
C
|
C:ALA119
|
4.6
|
51.1
|
1.0
|
OE1
|
C:GLU115
|
4.7
|
43.7
|
1.0
|
N
|
C:GLU121
|
4.8
|
57.5
|
1.0
|
CG
|
C:GLU121
|
4.9
|
67.7
|
1.0
|
N
|
C:ALA119
|
4.9
|
47.1
|
1.0
|
N
|
C:HIS120
|
5.0
|
49.5
|
1.0
|
C
|
C:LYS117
|
5.0
|
42.5
|
1.0
|
N
|
C:LYS117
|
5.0
|
43.0
|
1.0
|
|
Potassium binding site 8 out
of 9 in 4tlx
Go back to
Potassium Binding Sites List in 4tlx
Potassium binding site 8 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 8 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:K504
b:46.3
occ:1.00
|
O
|
D:SER33
|
2.7
|
41.8
|
1.0
|
O
|
D:LEU30
|
2.8
|
33.6
|
1.0
|
O
|
D:ALA35
|
3.1
|
46.8
|
1.0
|
O
|
D:GLU31
|
3.4
|
38.3
|
1.0
|
C
|
D:SER33
|
3.8
|
40.7
|
1.0
|
C
|
D:GLU31
|
3.9
|
36.0
|
1.0
|
C
|
D:LEU30
|
3.9
|
35.0
|
1.0
|
CA
|
D:GLU31
|
4.0
|
31.9
|
1.0
|
C
|
D:ALA35
|
4.2
|
48.1
|
1.0
|
N
|
D:GLU31
|
4.5
|
30.4
|
1.0
|
N
|
D:SER33
|
4.5
|
35.5
|
1.0
|
CA
|
D:SER33
|
4.6
|
40.7
|
1.0
|
C
|
D:PRO34
|
4.7
|
44.8
|
1.0
|
CB
|
D:SER33
|
4.7
|
39.4
|
1.0
|
O
|
D:PRO34
|
4.8
|
48.4
|
1.0
|
N
|
D:ALA35
|
4.8
|
44.1
|
1.0
|
N
|
D:PRO34
|
4.8
|
44.6
|
1.0
|
N
|
D:GLU32
|
4.9
|
32.4
|
1.0
|
CA
|
D:PRO34
|
4.9
|
50.5
|
1.0
|
CA
|
D:ALA36
|
5.0
|
54.4
|
1.0
|
C
|
D:GLU32
|
5.0
|
33.8
|
1.0
|
|
Potassium binding site 9 out
of 9 in 4tlx
Go back to
Potassium Binding Sites List in 4tlx
Potassium binding site 9 out
of 9 in the Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 9 of Kutzneria Sp. 744 Ornithine N-Hydroxylase, Ktzi-Fadred-Nadp+-L-Orn within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:K505
b:51.9
occ:1.00
|
O
|
D:HIS120
|
2.8
|
54.6
|
1.0
|
O
|
D:LEU118
|
2.9
|
44.9
|
1.0
|
O
|
D:GLU115
|
2.9
|
43.3
|
1.0
|
OE2
|
D:GLU121
|
3.5
|
64.8
|
1.0
|
O
|
D:SER116
|
3.7
|
41.2
|
1.0
|
C
|
D:LEU118
|
3.8
|
45.8
|
1.0
|
CB
|
D:LEU118
|
4.0
|
41.6
|
1.0
|
C
|
D:HIS120
|
4.0
|
53.0
|
1.0
|
C
|
D:GLU115
|
4.0
|
40.5
|
1.0
|
C
|
D:SER116
|
4.1
|
42.6
|
1.0
|
CA
|
D:SER116
|
4.2
|
38.1
|
1.0
|
O
|
D:ALA119
|
4.2
|
52.5
|
1.0
|
CA
|
D:LEU118
|
4.3
|
42.1
|
1.0
|
CD
|
D:GLU121
|
4.4
|
65.2
|
1.0
|
CA
|
D:GLU121
|
4.5
|
50.7
|
1.0
|
N
|
D:LEU118
|
4.5
|
39.1
|
1.0
|
C
|
D:ALA119
|
4.5
|
46.6
|
1.0
|
OE1
|
D:GLU115
|
4.5
|
43.0
|
1.0
|
CD
|
D:GLU115
|
4.6
|
44.2
|
1.0
|
N
|
D:SER116
|
4.6
|
34.1
|
1.0
|
OE2
|
D:GLU115
|
4.6
|
48.8
|
1.0
|
N
|
D:GLU121
|
4.7
|
52.1
|
1.0
|
N
|
D:ALA119
|
4.9
|
51.2
|
1.0
|
N
|
D:HIS120
|
4.9
|
46.5
|
1.0
|
|
Reference:
J.W.Setser,
J.R.Heemstra,
C.T.Walsh,
C.L.Drennan.
Crystallographic Evidence For Drastic Conformational Changes in the Active Site of A Flavin-Dependent N-Hydroxylase. Biochemistry 2014.
ISSN: ISSN 0006-2960
PubMed: 25184411
DOI: 10.1021/BI500655Q
Page generated: Mon Aug 12 12:05:36 2024
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