Atomistry » Iron » PDB 1m6z-1mko » 1mhy
Atomistry »
  Iron »
    PDB 1m6z-1mko »
      1mhy »

Iron in PDB 1mhy: Methane Monooxygenase Hydroxylase

Enzymatic activity of Methane Monooxygenase Hydroxylase

All present enzymatic activity of Methane Monooxygenase Hydroxylase:
1.14.13.25;

Protein crystallography data

The structure of Methane Monooxygenase Hydroxylase, PDB code: 1mhy was solved by N.Elango, R.Radhakrishnan, W.A.Froland, B.J.Waller, C.A.Earhart, J.D.Lipscomb, D.H.Ohlendorf, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 5.00 / 2.00
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 264.490, 71.190, 139.440, 90.00, 90.00, 90.00
R / Rfree (%) 13.7 / n/a

Iron Binding Sites:

The binding sites of Iron atom in the Methane Monooxygenase Hydroxylase (pdb code 1mhy). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Methane Monooxygenase Hydroxylase, PDB code: 1mhy:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 1mhy

Go back to Iron Binding Sites List in 1mhy
Iron binding site 1 out of 2 in the Methane Monooxygenase Hydroxylase


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Methane Monooxygenase Hydroxylase within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Fe801

b:14.1
occ:1.00
H2 D:HOH803 1.2 0.0 1.0
HD1 D:HIS147 1.3 0.0 1.0
H1 D:HOH803 1.7 0.0 1.0
O D:HOH803 1.7 11.5 1.0
OE1 D:GLU114 1.9 12.8 1.0
OE1 D:GLU144 2.0 12.5 1.0
O D:HOH804 2.2 14.8 1.0
ND1 D:HIS147 2.2 8.7 1.0
O D:HOH805 2.2 13.0 1.0
H1 D:HOH805 2.5 0.0 1.0
H1 D:HOH804 2.7 0.0 1.0
CD D:GLU114 2.9 16.4 1.0
H2 D:HOH804 3.0 0.0 1.0
CD D:GLU144 3.0 15.3 1.0
FE D:FE802 3.0 21.1 1.0
CE1 D:HIS147 3.1 9.4 1.0
H2 D:HOH805 3.2 0.0 1.0
OE2 D:GLU144 3.2 12.0 1.0
CG D:HIS147 3.3 10.1 1.0
OE2 D:GLU114 3.4 17.8 1.0
CB D:HIS147 3.7 9.6 1.0
OE1 D:GLU243 3.7 31.2 1.0
H1 D:HOH806 3.8 0.0 1.0
HD1 D:HIS246 3.9 0.0 1.0
OE2 D:GLU243 4.2 18.1 1.0
CG D:GLU114 4.2 13.2 1.0
O D:HOH806 4.2 27.8 1.0
NE2 D:HIS147 4.3 9.7 1.0
CE1 D:HIS246 4.4 17.5 1.0
CD2 D:HIS147 4.4 8.6 1.0
O D:HOH807 4.4 59.0 1.0
CD D:GLU243 4.4 28.3 1.0
H2 D:HOH807 4.4 0.0 1.0
CG D:GLU144 4.4 8.9 1.0
ND1 D:HIS246 4.5 16.9 1.0
CB D:GLU114 4.6 14.3 1.0
CA D:GLU144 4.6 9.3 1.0
OE2 D:GLU209 4.6 26.3 1.0
CA D:GLU114 4.7 12.7 1.0
CG1 D:VAL239 4.8 19.7 1.0
CB D:GLU144 4.8 9.9 1.0
O D:ASP143 4.9 13.2 1.0

Iron binding site 2 out of 2 in 1mhy

Go back to Iron Binding Sites List in 1mhy
Iron binding site 2 out of 2 in the Methane Monooxygenase Hydroxylase


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Methane Monooxygenase Hydroxylase within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Fe802

b:21.1
occ:1.00
HD1 D:HIS246 1.3 0.0 1.0
H1 D:HOH804 1.7 0.0 1.0
H2 D:HOH803 1.8 0.0 1.0
OE2 D:GLU243 1.9 18.1 1.0
OE2 D:GLU209 2.0 26.3 1.0
O D:HOH803 2.0 11.5 1.0
O D:HOH804 2.2 14.8 1.0
ND1 D:HIS246 2.3 16.9 1.0
OE2 D:GLU144 2.3 12.0 1.0
H1 D:HOH803 2.4 0.0 1.0
CD D:GLU243 2.8 28.3 1.0
H2 D:HOH804 2.9 0.0 1.0
FE D:FE801 3.0 14.1 1.0
CD D:GLU209 3.0 24.9 1.0
CE1 D:HIS246 3.0 17.5 1.0
OE1 D:GLU243 3.1 31.2 1.0
CD D:GLU144 3.2 15.3 1.0
CG D:HIS246 3.4 20.4 1.0
HE22 D:GLN140 3.5 0.0 1.0
OE1 D:GLU144 3.5 12.5 1.0
CG D:GLU209 3.6 22.6 1.0
HD1 D:HIS147 3.9 0.0 1.0
CB D:HIS246 3.9 19.9 1.0
NE2 D:GLN140 3.9 14.1 1.0
O D:HOH805 4.0 13.0 1.0
OE1 D:GLU209 4.0 23.9 1.0
HE21 D:GLN140 4.2 0.0 1.0
NE2 D:HIS246 4.2 16.1 1.0
H1 D:HOH806 4.2 0.0 1.0
CG D:GLU243 4.2 28.2 1.0
CD2 D:HIS246 4.4 15.0 1.0
ND1 D:HIS147 4.5 8.7 1.0
H2 D:HOH805 4.5 0.0 1.0
H1 D:HOH805 4.6 0.0 1.0
OE1 D:GLU114 4.6 12.8 1.0
CG D:GLU144 4.6 8.9 1.0
CE1 D:HIS147 4.6 9.4 1.0
CD D:GLN140 4.7 18.8 1.0
O D:HOH806 4.8 27.8 1.0
O D:HOH807 4.8 59.0 1.0
CB D:GLU209 4.8 20.9 1.0
H2 D:HOH809 4.9 0.0 1.0
CG D:GLN140 5.0 14.0 1.0

Reference:

N.Elango, R.Radhakrishnan, W.A.Froland, B.J.Wallar, C.A.Earhart, J.D.Lipscomb, D.H.Ohlendorf. Crystal Structure of the Hydroxylase Component of Methane Monooxygenase From Methylosinus Trichosporium OB3B Protein Sci. V. 6 556 1997.
ISSN: ISSN 0961-8368
PubMed: 9070438
Page generated: Sat Aug 3 10:41:33 2024

Last articles

Zn in 9J0N
Zn in 9J0O
Zn in 9J0P
Zn in 9FJX
Zn in 9EKB
Zn in 9C0F
Zn in 9CAH
Zn in 9CH0
Zn in 9CH3
Zn in 9CH1
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy