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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

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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 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

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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

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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

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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

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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

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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

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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

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