Manganese in PDB 4j25: Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Protein crystallography data
The structure of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H), PDB code: 4j25
was solved by
J.S.Scotti,
M.A.Mcdonough,
C.J.Schofield,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
62.13 /
1.97
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
45.330,
62.160,
132.830,
91.84,
94.70,
90.08
|
R / Rfree (%)
|
21.2 /
25.7
|
Manganese Binding Sites:
The binding sites of Manganese atom in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
(pdb code 4j25). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 8 binding sites of Manganese where determined in the
Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H), PDB code: 4j25:
Jump to Manganese binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Manganese binding site 1 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 1 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn401
b:21.3
occ:1.00
|
NE2
|
A:HIS183
|
2.1
|
13.7
|
1.0
|
O2'
|
A:OGA402
|
2.1
|
24.2
|
1.0
|
OD1
|
A:ASP126
|
2.2
|
15.3
|
1.0
|
O2
|
A:OGA402
|
2.2
|
24.2
|
1.0
|
NE2
|
A:HIS124
|
2.2
|
19.5
|
1.0
|
O
|
A:HOH503
|
2.2
|
14.9
|
1.0
|
C2
|
A:OGA402
|
2.7
|
26.3
|
1.0
|
C1
|
A:OGA402
|
2.8
|
26.8
|
1.0
|
CE1
|
A:HIS183
|
3.0
|
13.7
|
1.0
|
CE1
|
A:HIS124
|
3.0
|
20.1
|
1.0
|
CG
|
A:ASP126
|
3.1
|
16.9
|
1.0
|
CD2
|
A:HIS183
|
3.2
|
14.0
|
1.0
|
CD2
|
A:HIS124
|
3.2
|
20.1
|
1.0
|
OD2
|
A:ASP126
|
3.3
|
17.6
|
1.0
|
O1
|
A:OGA402
|
4.0
|
25.8
|
1.0
|
N1
|
A:OGA402
|
4.1
|
27.6
|
1.0
|
ND1
|
A:HIS183
|
4.1
|
13.9
|
1.0
|
ND1
|
A:HIS124
|
4.2
|
21.1
|
1.0
|
CG
|
A:HIS183
|
4.2
|
14.1
|
1.0
|
CG
|
A:HIS124
|
4.3
|
21.3
|
1.0
|
CB
|
A:ASP126
|
4.5
|
18.7
|
1.0
|
CE2
|
A:TYR121
|
4.7
|
31.6
|
1.0
|
C4
|
A:OGA402
|
4.7
|
27.4
|
1.0
|
CZ
|
A:PHE176
|
4.9
|
15.4
|
1.0
|
CA
|
A:ASP126
|
4.9
|
19.9
|
1.0
|
CZ
|
A:TYR121
|
5.0
|
32.9
|
1.0
|
|
Manganese binding site 2 out
of 8 in 4j25
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Manganese Binding Sites List in 4j25
Manganese binding site 2 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn401
b:19.6
occ:1.00
|
O2
|
B:OGA402
|
2.1
|
24.0
|
1.0
|
NE2
|
B:HIS183
|
2.1
|
17.6
|
1.0
|
OD1
|
B:ASP126
|
2.2
|
19.7
|
1.0
|
NE2
|
B:HIS124
|
2.2
|
20.7
|
1.0
|
O
|
B:HOH518
|
2.3
|
21.9
|
1.0
|
O2'
|
B:OGA402
|
2.3
|
24.8
|
1.0
|
C2
|
B:OGA402
|
2.8
|
27.0
|
1.0
|
C1
|
B:OGA402
|
2.8
|
27.1
|
1.0
|
CE1
|
B:HIS183
|
3.1
|
16.4
|
1.0
|
CG
|
B:ASP126
|
3.1
|
21.1
|
1.0
|
CE1
|
B:HIS124
|
3.1
|
20.7
|
1.0
|
CD2
|
B:HIS183
|
3.2
|
16.0
|
1.0
|
CD2
|
B:HIS124
|
3.2
|
20.3
|
1.0
|
OD2
|
B:ASP126
|
3.4
|
22.3
|
1.0
|
O1
|
B:OGA402
|
4.1
|
25.5
|
1.0
|
N1
|
B:OGA402
|
4.1
|
27.3
|
1.0
|
ND1
|
B:HIS183
|
4.2
|
14.5
|
1.0
|
ND1
|
B:HIS124
|
4.2
|
22.3
|
1.0
|
CG
|
B:HIS183
|
4.3
|
14.5
|
1.0
|
CG
|
B:HIS124
|
4.3
|
21.8
|
1.0
|
CB
|
B:ASP126
|
4.5
|
23.3
|
1.0
|
CE1
|
B:TYR121
|
4.7
|
31.6
|
1.0
|
C4
|
B:OGA402
|
4.8
|
26.9
|
1.0
|
CZ
|
B:PHE176
|
4.9
|
14.5
|
1.0
|
CA
|
B:ASP126
|
4.9
|
26.7
|
1.0
|
N
|
B:ASP126
|
5.0
|
25.5
|
1.0
|
|
Manganese binding site 3 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 3 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn401
b:20.1
occ:1.00
|
OD1
|
C:ASP126
|
2.1
|
21.8
|
1.0
|
NE2
|
C:HIS124
|
2.2
|
23.2
|
1.0
|
O2
|
C:OGA402
|
2.2
|
26.0
|
1.0
|
O2'
|
C:OGA402
|
2.2
|
26.4
|
1.0
|
NE2
|
C:HIS183
|
2.2
|
19.8
|
1.0
|
O
|
C:HOH508
|
2.3
|
23.5
|
1.0
|
C2
|
C:OGA402
|
2.8
|
26.1
|
1.0
|
C1
|
C:OGA402
|
2.8
|
27.8
|
1.0
|
CE1
|
C:HIS124
|
2.9
|
21.2
|
1.0
|
CG
|
C:ASP126
|
3.1
|
23.4
|
1.0
|
CE1
|
C:HIS183
|
3.1
|
19.6
|
1.0
|
CD2
|
C:HIS183
|
3.3
|
18.9
|
1.0
|
CD2
|
C:HIS124
|
3.3
|
22.8
|
1.0
|
OD2
|
C:ASP126
|
3.3
|
25.5
|
1.0
|
O1
|
C:OGA402
|
4.0
|
29.8
|
1.0
|
O
|
C:HOH588
|
4.0
|
38.2
|
1.0
|
N1
|
C:OGA402
|
4.1
|
27.1
|
1.0
|
ND1
|
C:HIS124
|
4.1
|
22.5
|
1.0
|
ND1
|
C:HIS183
|
4.3
|
18.4
|
1.0
|
CG
|
C:HIS124
|
4.3
|
23.3
|
1.0
|
CG
|
C:HIS183
|
4.4
|
17.7
|
1.0
|
CB
|
C:ASP126
|
4.5
|
23.5
|
1.0
|
CE2
|
C:TYR121
|
4.7
|
30.0
|
1.0
|
C4
|
C:OGA402
|
4.7
|
25.6
|
1.0
|
CA
|
C:ASP126
|
4.8
|
26.7
|
1.0
|
CZ2
|
C:TRP198
|
4.9
|
25.4
|
1.0
|
CZ
|
C:PHE176
|
4.9
|
17.0
|
1.0
|
N
|
C:ASP126
|
5.0
|
26.5
|
1.0
|
CZ
|
C:TYR121
|
5.0
|
32.8
|
1.0
|
|
Manganese binding site 4 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 4 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 4 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn401
b:17.6
occ:1.00
|
OD1
|
D:ASP126
|
2.2
|
19.5
|
1.0
|
NE2
|
D:HIS183
|
2.2
|
17.0
|
1.0
|
O2'
|
D:OGA402
|
2.2
|
26.6
|
1.0
|
O
|
D:HOH505
|
2.3
|
18.7
|
1.0
|
O2
|
D:OGA402
|
2.3
|
25.9
|
1.0
|
NE2
|
D:HIS124
|
2.3
|
20.1
|
1.0
|
C2
|
D:OGA402
|
2.8
|
27.4
|
1.0
|
C1
|
D:OGA402
|
2.9
|
28.6
|
1.0
|
CG
|
D:ASP126
|
3.1
|
21.3
|
1.0
|
CE1
|
D:HIS183
|
3.1
|
17.2
|
1.0
|
CD2
|
D:HIS183
|
3.2
|
17.3
|
1.0
|
CE1
|
D:HIS124
|
3.2
|
20.1
|
1.0
|
CD2
|
D:HIS124
|
3.3
|
21.8
|
1.0
|
OD2
|
D:ASP126
|
3.3
|
21.0
|
1.0
|
N1
|
D:OGA402
|
4.1
|
28.4
|
1.0
|
O1
|
D:OGA402
|
4.1
|
30.1
|
1.0
|
ND1
|
D:HIS183
|
4.2
|
18.3
|
1.0
|
CG
|
D:HIS183
|
4.3
|
18.9
|
1.0
|
ND1
|
D:HIS124
|
4.3
|
20.8
|
1.0
|
CG
|
D:HIS124
|
4.4
|
21.4
|
1.0
|
CB
|
D:ASP126
|
4.5
|
21.3
|
1.0
|
C4
|
D:OGA402
|
4.6
|
28.0
|
1.0
|
O
|
D:HOH520
|
4.7
|
32.5
|
1.0
|
CE2
|
D:TYR121
|
4.7
|
33.3
|
1.0
|
CA
|
D:ASP126
|
4.9
|
21.6
|
1.0
|
CZ
|
D:PHE176
|
4.9
|
14.7
|
1.0
|
CZ2
|
D:TRP198
|
5.0
|
19.2
|
1.0
|
|
Manganese binding site 5 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 5 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 5 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mn401
b:20.1
occ:1.00
|
O2
|
E:OGA402
|
2.1
|
23.7
|
1.0
|
O2'
|
E:OGA402
|
2.2
|
26.1
|
1.0
|
NE2
|
E:HIS183
|
2.2
|
20.2
|
1.0
|
OD1
|
E:ASP126
|
2.2
|
23.9
|
1.0
|
NE2
|
E:HIS124
|
2.2
|
24.9
|
1.0
|
O
|
E:HOH509
|
2.3
|
21.4
|
1.0
|
C2
|
E:OGA402
|
2.8
|
25.6
|
1.0
|
C1
|
E:OGA402
|
2.8
|
26.5
|
1.0
|
CE1
|
E:HIS124
|
3.1
|
23.0
|
1.0
|
CG
|
E:ASP126
|
3.1
|
23.7
|
1.0
|
CE1
|
E:HIS183
|
3.1
|
20.7
|
1.0
|
CD2
|
E:HIS183
|
3.2
|
19.8
|
1.0
|
CD2
|
E:HIS124
|
3.3
|
24.8
|
1.0
|
OD2
|
E:ASP126
|
3.3
|
23.5
|
1.0
|
O1
|
E:OGA402
|
4.0
|
28.7
|
1.0
|
N1
|
E:OGA402
|
4.1
|
24.9
|
1.0
|
O
|
E:HOH504
|
4.2
|
27.5
|
1.0
|
ND1
|
E:HIS183
|
4.2
|
20.7
|
1.0
|
ND1
|
E:HIS124
|
4.2
|
21.6
|
1.0
|
O
|
E:HOH516
|
4.2
|
33.2
|
1.0
|
CG
|
E:HIS183
|
4.3
|
20.1
|
1.0
|
CG
|
E:HIS124
|
4.4
|
23.3
|
1.0
|
CB
|
E:ASP126
|
4.5
|
25.6
|
1.0
|
CZ2
|
E:TRP198
|
4.6
|
23.1
|
1.0
|
C4
|
E:OGA402
|
4.7
|
25.3
|
1.0
|
CE2
|
E:TYR121
|
4.8
|
24.3
|
1.0
|
O
|
E:HOH530
|
4.8
|
29.2
|
1.0
|
CA
|
E:ASP126
|
4.9
|
28.1
|
1.0
|
CZ
|
E:TYR121
|
5.0
|
24.9
|
1.0
|
|
Manganese binding site 6 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 6 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 6 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
F:Mn401
b:29.1
occ:1.00
|
O1
|
F:OGA402
|
2.1
|
30.8
|
1.0
|
NE2
|
F:HIS183
|
2.1
|
29.3
|
1.0
|
OD1
|
F:ASP126
|
2.2
|
34.8
|
1.0
|
O2'
|
F:OGA402
|
2.2
|
29.9
|
1.0
|
O
|
F:HOH506
|
2.3
|
25.3
|
1.0
|
NE2
|
F:HIS124
|
2.3
|
33.4
|
1.0
|
C1
|
F:OGA402
|
2.8
|
31.1
|
1.0
|
C2
|
F:OGA402
|
2.8
|
28.8
|
1.0
|
CE1
|
F:HIS183
|
2.9
|
30.2
|
1.0
|
CG
|
F:ASP126
|
3.1
|
36.7
|
1.0
|
CD2
|
F:HIS183
|
3.2
|
28.1
|
1.0
|
CD2
|
F:HIS124
|
3.2
|
34.4
|
1.0
|
CE1
|
F:HIS124
|
3.3
|
33.4
|
1.0
|
OD2
|
F:ASP126
|
3.4
|
34.5
|
1.0
|
O2
|
F:OGA402
|
4.0
|
31.3
|
1.0
|
ND1
|
F:HIS183
|
4.1
|
29.8
|
1.0
|
N1
|
F:OGA402
|
4.1
|
28.6
|
1.0
|
CG
|
F:HIS183
|
4.3
|
28.5
|
1.0
|
ND1
|
F:HIS124
|
4.4
|
34.4
|
1.0
|
CG
|
F:HIS124
|
4.4
|
35.1
|
1.0
|
CB
|
F:ASP126
|
4.5
|
38.8
|
1.0
|
CE2
|
F:TYR121
|
4.7
|
38.4
|
1.0
|
C4
|
F:OGA402
|
4.8
|
28.4
|
1.0
|
CZ2
|
F:TRP198
|
4.9
|
36.3
|
1.0
|
CA
|
F:ASP126
|
4.9
|
40.5
|
1.0
|
CZ
|
F:PHE176
|
4.9
|
30.1
|
1.0
|
|
Manganese binding site 7 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 7 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 7 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Mn401
b:25.5
occ:1.00
|
NE2
|
G:HIS124
|
2.1
|
29.6
|
1.0
|
NE2
|
G:HIS183
|
2.2
|
29.8
|
1.0
|
O
|
G:HOH505
|
2.2
|
36.5
|
1.0
|
OD1
|
G:ASP126
|
2.2
|
28.7
|
1.0
|
O1
|
G:OGA402
|
2.4
|
31.2
|
1.0
|
O2'
|
G:OGA402
|
2.4
|
30.9
|
1.0
|
CE1
|
G:HIS124
|
3.0
|
29.9
|
1.0
|
C2
|
G:OGA402
|
3.0
|
31.5
|
1.0
|
CD2
|
G:HIS183
|
3.1
|
30.2
|
1.0
|
C1
|
G:OGA402
|
3.1
|
32.1
|
1.0
|
CG
|
G:ASP126
|
3.1
|
28.7
|
1.0
|
CE1
|
G:HIS183
|
3.1
|
28.6
|
1.0
|
CD2
|
G:HIS124
|
3.2
|
28.8
|
1.0
|
OD2
|
G:ASP126
|
3.4
|
30.8
|
1.0
|
ND1
|
G:HIS124
|
4.1
|
28.6
|
1.0
|
CG
|
G:HIS124
|
4.2
|
27.9
|
1.0
|
ND1
|
G:HIS183
|
4.2
|
28.1
|
1.0
|
CG
|
G:HIS183
|
4.3
|
29.4
|
1.0
|
N1
|
G:OGA402
|
4.3
|
30.5
|
1.0
|
O2
|
G:OGA402
|
4.3
|
32.1
|
1.0
|
O
|
G:HOH509
|
4.3
|
29.3
|
1.0
|
CB
|
G:ASP126
|
4.5
|
27.5
|
1.0
|
CE2
|
G:TYR121
|
4.6
|
33.4
|
1.0
|
CZ2
|
G:TRP198
|
4.8
|
30.7
|
1.0
|
CA
|
G:ASP126
|
4.8
|
28.9
|
1.0
|
CZ
|
G:TYR121
|
4.9
|
32.8
|
1.0
|
C4
|
G:OGA402
|
4.9
|
30.3
|
1.0
|
CZ
|
G:PHE176
|
5.0
|
30.5
|
1.0
|
|
Manganese binding site 8 out
of 8 in 4j25
Go back to
Manganese Binding Sites List in 4j25
Manganese binding site 8 out
of 8 in the Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H)
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 8 of Crystal Structure of A Pseudomonas Putida Prolyl-4-Hydroxylase (P4H) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
H:Mn401
b:19.8
occ:1.00
|
O
|
H:HOH502
|
2.1
|
26.7
|
1.0
|
NE2
|
H:HIS183
|
2.1
|
22.1
|
1.0
|
OD1
|
H:ASP126
|
2.2
|
20.4
|
1.0
|
NE2
|
H:HIS124
|
2.2
|
21.3
|
1.0
|
O2'
|
H:OGA402
|
2.3
|
29.0
|
1.0
|
O1
|
H:OGA402
|
2.3
|
27.7
|
1.0
|
C2
|
H:OGA402
|
2.9
|
29.5
|
1.0
|
C1
|
H:OGA402
|
2.9
|
29.8
|
1.0
|
CD2
|
H:HIS183
|
3.1
|
22.2
|
1.0
|
CG
|
H:ASP126
|
3.1
|
21.4
|
1.0
|
CE1
|
H:HIS124
|
3.1
|
22.9
|
1.0
|
CE1
|
H:HIS183
|
3.1
|
20.9
|
1.0
|
CD2
|
H:HIS124
|
3.2
|
22.8
|
1.0
|
OD2
|
H:ASP126
|
3.3
|
22.3
|
1.0
|
N1
|
H:OGA402
|
4.2
|
30.8
|
1.0
|
O2
|
H:OGA402
|
4.2
|
32.1
|
1.0
|
ND1
|
H:HIS183
|
4.2
|
21.8
|
1.0
|
ND1
|
H:HIS124
|
4.2
|
23.3
|
1.0
|
CG
|
H:HIS183
|
4.2
|
23.5
|
1.0
|
CG
|
H:HIS124
|
4.3
|
24.1
|
1.0
|
CB
|
H:ASP126
|
4.5
|
23.1
|
1.0
|
CE2
|
H:TYR121
|
4.7
|
27.9
|
1.0
|
CZ2
|
H:TRP198
|
4.8
|
25.1
|
1.0
|
C4
|
H:OGA402
|
4.8
|
29.4
|
1.0
|
CA
|
H:ASP126
|
4.9
|
25.6
|
1.0
|
CZ
|
H:TYR121
|
4.9
|
29.1
|
1.0
|
OH
|
H:TYR121
|
5.0
|
29.4
|
1.0
|
|
Reference:
J.S.Scotti,
I.K.H.Leung,
W.Ge,
M.A.Bentley,
J.Paps,
H.B.Kramer,
J.Lee,
W.Aik,
H.Choi,
S.M.Paulsen,
L.A.H.Bowman,
N.D.Loik,
S.Horita,
C.H.Ho,
N.J.Kershaw,
C.M.Tang,
T.D.W.Claridge,
G.M.Preston,
M.A.Mcdonough,
C.J.Schofield.
Human Oxygen Sensing May Have Origins in Prokaryotic Elongation Factor Tu Prolyl-Hydroxylation Proc.Natl.Acad.Sci.Usa V. 111 13331 2014.
ISSN: ISSN 0027-8424
PubMed: 25197067
DOI: 10.1073/PNAS.1409916111
Page generated: Sat Oct 5 19:56:51 2024
|