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Iron in PDB 6gal: Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10

Enzymatic activity of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10

All present enzymatic activity of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10:
1.12.99.6;

Protein crystallography data

The structure of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10, PDB code: 6gal was solved by S.B.Carr, F.A.Armstrong, R.M.Evans, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 92.12 / 1.25
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 94.906, 95.224, 183.910, 90.00, 90.00, 90.00
R / Rfree (%) 12 / 14.7

Other elements in 6gal:

The structure of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 also contains other interesting chemical elements:

Nickel (Ni) 2 atoms
Magnesium (Mg) 2 atoms
Chlorine (Cl) 2 atoms

Iron Binding Sites:

Pages:

>>> Page 1 <<< Page 2, Binding sites: 11 - 20; Page 3, Binding sites: 21 - 24;

Binding sites:

The binding sites of Iron atom in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 (pdb code 6gal). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 24 binding sites of Iron where determined in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10, PDB code: 6gal:
Jump to Iron binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Iron binding site 1 out of 24 in 6gal

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Iron binding site 1 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe401

b:7.4
occ:1.00
FE1 S:SF4401 0.0 7.4 1.0
SG S:CYS215 2.3 7.5 1.0
S2 S:SF4401 2.3 7.9 1.0
S3 S:SF4401 2.3 7.2 1.0
S4 S:SF4401 2.3 7.8 1.0
FE3 S:SF4401 2.7 7.6 1.0
FE4 S:SF4401 2.7 7.3 1.0
FE2 S:SF4401 2.8 7.1 1.0
H S:LEU216 3.0 6.4 1.0
HB2 S:PHE196 3.4 8.6 1.0
CB S:CYS215 3.4 7.5 1.0
HB2 S:CYS215 3.4 7.6 1.0
H S:TYR217 3.5 7.6 1.0
HA S:CYS215 3.6 7.0 1.0
HD1 S:PHE196 3.7 8.9 1.0
N S:LEU216 3.8 6.3 1.0
HB2 S:TYR217 3.9 8.0 1.0
HB2 S:ARG192 3.9 7.7 1.0
CA S:CYS215 3.9 6.9 1.0
S1 S:SF4401 3.9 7.5 1.0
N S:TYR217 4.2 7.7 1.0
HB3 S:CYS215 4.2 7.3 1.0
CB S:PHE196 4.3 8.5 1.0
C S:CYS215 4.3 6.2 1.0
CD1 S:PHE196 4.4 9.3 1.0
HE1 S:HIS187 4.4 8.5 1.0
ND1 S:HIS187 4.5 8.0 1.0
HB3 S:ARG192 4.5 7.8 1.0
HB2 S:LEU216 4.6 7.1 1.0
CB S:TYR217 4.6 7.8 1.0
HB3 S:CYS221 4.6 6.9 1.0
CB S:ARG192 4.6 7.7 1.0
HB3 S:TYR217 4.7 7.9 1.0
O S:ARG192 4.7 8.2 1.0
CG S:PHE196 4.7 8.6 1.0
HB3 S:PHE196 4.7 8.4 1.0
CA S:LEU216 4.8 7.0 1.0
C S:LEU216 4.8 7.1 1.0
HA S:TYR217 4.8 7.1 1.0
H S:PHE196 4.8 7.6 1.0
HA S:ARG193 4.8 7.8 1.0
CE1 S:HIS187 4.8 8.5 1.0
CA S:TYR217 4.8 7.2 1.0
HD2 S:ARG193 4.9 9.8 1.0
SG S:CYS190 4.9 7.4 1.0
SG S:CYS221 4.9 7.1 1.0
C S:ARG192 5.0 7.4 1.0

Iron binding site 2 out of 24 in 6gal

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Iron binding site 2 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe401

b:7.1
occ:1.00
FE2 S:SF4401 0.0 7.1 1.0
S4 S:SF4401 2.3 7.8 1.0
SG S:CYS221 2.3 7.1 1.0
S1 S:SF4401 2.3 7.5 1.0
S3 S:SF4401 2.3 7.2 1.0
FE4 S:SF4401 2.7 7.3 1.0
FE3 S:SF4401 2.7 7.6 1.0
FE1 S:SF4401 2.8 7.4 1.0
HB3 S:CYS221 3.1 6.9 1.0
CB S:CYS221 3.3 6.8 1.0
HD12 S:ILE243 3.5 7.3 1.0
HD3 S:PRO224 3.5 7.3 1.0
HB2 S:CYS221 3.5 6.7 1.0
HD13 S:ILE243 3.6 7.6 1.0
HA3 S:GLY223 3.8 7.2 1.0
H S:GLY223 3.8 6.8 1.0
HG12 S:ILE243 3.8 7.2 1.0
S2 S:SF4401 3.9 7.9 1.0
CD1 S:ILE243 3.9 7.5 1.0
H S:LEU216 4.0 6.4 1.0
HB2 S:LEU216 4.0 7.1 1.0
HG22 S:ILE243 4.4 7.0 1.0
CG1 S:ILE243 4.4 7.0 1.0
CD S:PRO224 4.4 7.5 1.0
H S:CYS249 4.5 6.1 1.0
N S:GLY223 4.5 7.0 1.0
CA S:GLY223 4.6 7.4 1.0
ND1 S:HIS187 4.6 8.0 1.0
CA S:CYS221 4.6 6.3 1.0
HA S:TYR217 4.7 7.1 1.0
H S:TYR217 4.7 7.6 1.0
SG S:CYS215 4.7 7.5 1.0
HB2 S:HIS187 4.7 7.9 1.0
N S:TYR217 4.7 7.7 1.0
SG S:CYS190 4.8 7.4 1.0
HD11 S:ILE243 4.8 7.2 1.0
HD2 S:PRO224 4.8 7.5 1.0
N S:LEU216 4.8 6.3 1.0
HB2 S:TYR217 4.9 8.0 1.0
HG21 S:ILE186 4.9 8.9 1.0
HG3 S:PRO224 4.9 8.1 1.0
C S:CYS221 4.9 6.3 1.0
CB S:LEU216 4.9 7.2 1.0
C S:LEU216 4.9 7.1 1.0
HA2 S:GLY248 5.0 6.5 1.0
O S:CYS221 5.0 7.6 1.0

Iron binding site 3 out of 24 in 6gal

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Iron binding site 3 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe401

b:7.6
occ:1.00
FE3 S:SF4401 0.0 7.6 1.0
ND1 S:HIS187 2.1 8.0 1.0
S1 S:SF4401 2.3 7.5 1.0
S4 S:SF4401 2.3 7.8 1.0
S2 S:SF4401 2.3 7.9 1.0
FE4 S:SF4401 2.7 7.3 1.0
FE1 S:SF4401 2.7 7.4 1.0
FE2 S:SF4401 2.7 7.1 1.0
CE1 S:HIS187 3.0 8.5 1.0
HE1 S:HIS187 3.1 8.5 1.0
CG S:HIS187 3.2 8.7 1.0
HB2 S:HIS187 3.3 7.9 1.0
HA S:HIS187 3.4 7.4 1.0
HD3 S:PRO224 3.5 7.3 1.0
HG3 S:PRO224 3.6 8.1 1.0
CB S:HIS187 3.6 8.2 1.0
HD3 S:ARG193 3.8 9.8 1.0
S3 S:SF4401 3.9 7.2 1.0
HD2 S:ARG193 4.0 9.8 1.0
HB3 S:CYS190 4.0 7.2 1.0
CA S:HIS187 4.0 7.5 1.0
NE2 S:HIS187 4.1 9.2 1.0
CD2 S:HIS187 4.3 9.3 1.0
CD S:PRO224 4.3 7.5 1.0
CG S:PRO224 4.3 8.1 1.0
CD S:ARG193 4.3 9.8 1.0
HA3 S:GLY223 4.3 7.2 1.0
HG2 S:ARG193 4.4 9.2 1.0
HB2 S:PHE196 4.4 8.6 1.0
HB2 S:CYS190 4.4 7.4 1.0
CB S:CYS190 4.5 7.3 1.0
HD1 S:PHE196 4.5 8.9 1.0
HB3 S:HIS187 4.5 8.1 1.0
SG S:CYS215 4.7 7.5 1.0
SG S:CYS190 4.7 7.4 1.0
HG2 S:PRO224 4.7 8.2 1.0
CD1 S:PHE196 4.7 9.3 1.0
SG S:CYS221 4.8 7.1 1.0
N S:PRO224 4.9 7.6 1.0
O S:HIS187 4.9 9.5 1.0
HE2 S:HIS187 4.9 9.3 0.0
CG S:ARG193 4.9 9.4 1.0
HB2 S:TYR217 4.9 8.0 1.0
HA S:ARG193 5.0 7.8 1.0
CG S:PHE196 5.0 8.6 1.0

Iron binding site 4 out of 24 in 6gal

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Iron binding site 4 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe401

b:7.3
occ:1.00
FE4 S:SF4401 0.0 7.3 1.0
S2 S:SF4401 2.3 7.9 1.0
SG S:CYS190 2.3 7.4 1.0
S3 S:SF4401 2.3 7.2 1.0
S1 S:SF4401 2.3 7.5 1.0
FE3 S:SF4401 2.7 7.6 1.0
FE2 S:SF4401 2.7 7.1 1.0
FE1 S:SF4401 2.7 7.4 1.0
HB3 S:CYS190 3.0 7.2 1.0
CB S:CYS190 3.1 7.3 1.0
HB2 S:ARG192 3.2 7.7 1.0
HB2 S:CYS190 3.3 7.4 1.0
HD13 S:ILE243 3.4 7.6 1.0
HG22 S:ILE243 3.4 7.0 1.0
H S:ARG192 3.9 6.2 1.0
S4 S:SF4401 3.9 7.8 1.0
HA S:HIS187 4.1 7.4 1.0
CB S:ARG192 4.2 7.7 1.0
CD1 S:ILE243 4.2 7.5 1.0
HG2 S:ARG193 4.3 9.2 1.0
HD12 S:ILE243 4.3 7.3 1.0
CG2 S:ILE243 4.4 7.0 1.0
HG12 S:ILE243 4.5 7.2 1.0
ND1 S:HIS187 4.5 8.0 1.0
CA S:CYS190 4.5 6.9 1.0
H S:LEU216 4.6 6.4 1.0
HB3 S:ARG192 4.6 7.8 1.0
HD2 S:ARG192 4.7 7.7 1.0
HG23 S:ILE243 4.7 7.1 1.0
N S:ARG192 4.7 6.6 1.0
C S:ARG192 4.7 7.4 1.0
CA S:ARG192 4.7 7.3 1.0
HG21 S:ILE186 4.7 8.9 1.0
SG S:CYS221 4.8 7.1 1.0
HG3 S:ARG192 4.8 7.9 1.0
HG21 S:ILE243 4.8 7.1 1.0
N S:ARG193 4.8 7.2 1.0
CG1 S:ILE243 4.8 7.0 1.0
HA S:CYS190 4.9 7.0 1.0
H S:ARG193 4.9 7.4 1.0
HA S:ARG193 4.9 7.8 1.0
HA S:CYS215 4.9 7.0 1.0
HD11 S:ILE243 4.9 7.2 1.0
SG S:CYS215 4.9 7.5 1.0
C S:CYS190 5.0 6.9 1.0
CG S:ARG192 5.0 8.1 1.0

Iron binding site 5 out of 24 in 6gal

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Iron binding site 5 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 5 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe402

b:7.6
occ:1.00
FE1 S:F3S402 0.0 7.6 1.0
S2 S:F3S402 2.2 7.8 1.0
S1 S:F3S402 2.3 7.9 1.0
S3 S:F3S402 2.3 7.5 1.0
SG S:CYS252 2.3 8.0 1.0
FE3 S:F3S402 2.7 7.3 1.0
FE4 S:F3S402 2.7 7.5 1.0
H S:CYS252 3.0 6.8 1.0
HB3 S:CYS252 3.4 7.9 1.0
CB S:CYS252 3.4 8.0 1.0
O L:HOH960 3.8 8.5 1.0
N S:CYS252 3.8 7.2 1.0
HD22 S:ASN228 3.8 7.4 0.0
S4 S:F3S402 3.9 8.0 1.0
O S:HOH581 4.0 7.9 1.0
H S:ALA253 4.0 7.4 1.0
HG2 S:PRO242 4.1 5.8 1.0
CA S:CYS252 4.1 7.2 1.0
HB2 S:CYS252 4.2 7.8 1.0
H S:CYS149 4.3 2.9 1.0
H S:LEU250 4.4 6.4 1.0
HE3 L:LYS226 4.5 8.2 1.0
N S:ALA253 4.5 7.4 1.0
H S:GLY251 4.5 7.5 1.0
O L:HOH967 4.5 8.1 1.0
C S:CYS252 4.5 7.2 1.0
ND2 S:ASN228 4.6 7.7 1.0
SG S:CYS230 4.7 7.7 1.0
HD21 S:ASN228 4.7 7.4 0.0
SG S:CYS249 4.7 7.2 1.0
HB1 S:ALA253 4.7 8.6 1.0
HZ1 L:LYS226 4.7 9.0 1.0
HG22 S:THR226 4.8 8.0 1.0
HD3 L:LYS226 4.8 7.6 1.0
HD2 L:LYS226 4.8 7.6 1.0
HB2 S:LEU250 4.8 6.6 1.0
HA2 S:GLY148 4.9 6.9 1.0
HZ2 S:TRP235 4.9 6.6 1.0
C S:GLY251 5.0 7.3 1.0
HA S:CYS252 5.0 7.6 1.0

Iron binding site 6 out of 24 in 6gal

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Iron binding site 6 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 6 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe402

b:7.3
occ:1.00
FE3 S:F3S402 0.0 7.3 1.0
S4 S:F3S402 2.2 8.0 1.0
S1 S:F3S402 2.3 7.9 1.0
S3 S:F3S402 2.3 7.5 1.0
SG S:CYS249 2.3 7.2 1.0
FE1 S:F3S402 2.7 7.6 1.0
FE4 S:F3S402 2.7 7.5 1.0
HB2 S:CYS249 3.2 6.8 1.0
HA S:CYS249 3.2 6.8 1.0
CB S:CYS249 3.2 6.8 1.0
H S:GLY251 3.3 7.5 1.0
H S:LEU250 3.4 6.4 1.0
H S:CYS252 3.5 6.8 1.0
HG13 S:ILE186 3.7 9.1 1.0
CA S:CYS249 3.7 6.8 1.0
HG22 S:THR226 3.8 8.0 1.0
S2 S:F3S402 3.8 7.8 1.0
HG2 S:PRO242 3.9 5.8 1.0
N S:LEU250 4.1 6.4 1.0
HB3 S:CYS249 4.1 6.8 1.0
N S:GLY251 4.2 7.5 1.0
C S:CYS249 4.3 6.8 1.0
HD12 S:ILE186 4.4 8.5 1.0
N S:CYS252 4.4 7.2 1.0
HA2 S:GLY251 4.4 7.3 1.0
HB2 S:PRO242 4.5 6.1 1.0
HG21 S:THR226 4.5 8.1 1.0
CG1 S:ILE186 4.6 8.9 1.0
CG2 S:THR226 4.6 8.0 1.0
HG22 S:ILE186 4.6 8.9 1.0
CG S:PRO242 4.8 5.9 1.0
CA S:GLY251 4.8 7.0 1.0
SG S:CYS252 4.8 8.0 1.0
HG1 S:THR226 4.8 8.1 0.0
H S:ALA253 4.8 7.4 1.0
HD2 S:PRO242 4.8 6.3 1.0
HD22 S:ASN228 4.8 7.4 0.0
SG S:CYS230 4.8 7.7 1.0
CD1 S:ILE186 4.9 8.5 1.0
N S:CYS249 4.9 6.3 1.0
HB2 S:CYS230 5.0 7.5 1.0
HB3 S:CYS252 5.0 7.9 1.0
HB S:THR226 5.0 8.4 1.0
HG12 S:ILE186 5.0 8.6 1.0

Iron binding site 7 out of 24 in 6gal

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Iron binding site 7 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 7 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe402

b:7.5
occ:1.00
FE4 S:F3S402 0.0 7.5 1.0
S4 S:F3S402 2.2 8.0 1.0
S2 S:F3S402 2.2 7.8 1.0
SG S:CYS230 2.3 7.7 1.0
S3 S:F3S402 2.3 7.5 1.0
FE1 S:F3S402 2.7 7.6 1.0
FE3 S:F3S402 2.7 7.3 1.0
HB2 S:CYS230 3.2 7.5 1.0
CB S:CYS230 3.3 7.3 1.0
HD12 S:ILE186 3.4 8.5 1.0
HB3 S:CYS230 3.4 7.1 1.0
HD22 S:ASN228 3.4 7.4 0.0
HE1 S:TRP235 3.5 6.5 1.0
HG2 S:PRO242 3.7 5.8 1.0
HD2 S:PRO242 3.8 6.3 1.0
ND2 S:ASN228 3.9 7.7 1.0
S1 S:F3S402 4.0 7.9 1.0
HB3 S:ASN228 4.1 7.6 1.0
HG13 S:ILE186 4.2 9.1 1.0
CD1 S:ILE186 4.2 8.5 1.0
HD21 S:ASN228 4.2 7.4 0.0
O S:HOH581 4.3 7.9 1.0
HD11 S:ILE186 4.3 8.5 1.0
NE1 S:TRP235 4.3 6.6 1.0
H S:CYS230 4.4 6.8 1.0
CD S:PRO242 4.5 6.4 1.0
CG S:PRO242 4.5 5.9 1.0
CG S:ASN228 4.6 7.5 1.0
HD2 S:PHE241 4.6 6.9 1.0
CA S:CYS230 4.7 7.1 1.0
HD3 S:PRO242 4.7 6.2 1.0
CB S:ASN228 4.7 7.5 1.0
HB2 S:ASN228 4.7 7.5 1.0
CG1 S:ILE186 4.7 8.9 1.0
HZ2 S:TRP235 4.7 6.6 1.0
SG S:CYS252 4.8 8.0 1.0
SG S:CYS249 4.8 7.2 1.0
HD2 L:LYS226 4.8 7.6 1.0
HD13 S:ILE186 4.9 8.5 1.0
HB2 S:PHE241 5.0 6.5 1.0
HA S:CYS230 5.0 7.1 1.0

Iron binding site 8 out of 24 in 6gal

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Iron binding site 8 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 8 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe403

b:7.7
occ:1.00
FE1 S:SF3403 0.0 7.7 1.0
SG S:CYS115 2.3 8.2 1.0
S1 S:SF3403 2.3 7.5 1.0
S3 S:SF3403 2.3 7.5 1.0
S2 S:SF3403 2.3 7.7 1.0
FE4 S:SF3403 2.6 7.5 1.0
FE3 S:SF3403 2.8 7.4 1.0
FE7 S:SF3403 2.8 8.2 1.0
HB2 S:CYS115 3.2 8.6 1.0
H S:CYS115 3.2 7.2 1.0
CB S:CYS115 3.3 8.3 1.0
H S:CYS17 3.6 7.4 1.0
O S:HOH525 3.9 9.9 1.0
HB3 S:CYS120 3.9 7.3 1.0
N S:CYS115 4.0 7.6 1.0
SG S:CYS19 4.0 7.5 1.0
HA S:GLU16 4.0 8.0 1.0
HB3 S:CYS115 4.1 8.1 1.0
O S:HOH576 4.2 7.5 1.0
CA S:CYS115 4.2 8.0 1.0
HB2 S:CYS120 4.3 7.3 1.0
SG S:CYS120 4.4 7.7 1.0
CB S:CYS120 4.4 6.9 1.0
HB2 S:GLU16 4.4 8.6 1.0
HB3 S:GLU16 4.5 8.8 1.0
HA S:CYS115 4.5 8.0 1.0
HA2 S:GLY77 4.6 8.1 1.0
N S:CYS17 4.6 7.5 1.0
SG S:CYS20 4.6 8.3 1.0
HE21 S:GLN122 4.7 7.5 0.0
H S:GLY77 4.7 7.9 1.0
SG S:CYS17 4.7 7.0 1.0
SG S:CYS149 4.8 6.9 1.0
CB S:GLU16 4.8 8.9 1.0
CA S:GLU16 4.8 8.0 1.0
H S:CYS19 4.9 6.4 1.0
HB3 S:CYS17 4.9 6.5 1.0
HA3 S:GLY113 5.0 7.3 1.0

Iron binding site 9 out of 24 in 6gal

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Iron binding site 9 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 9 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe403

b:7.4
occ:1.00
FE3 S:SF3403 0.0 7.4 1.0
SG S:CYS149 2.3 6.9 1.0
S3 S:SF3403 2.3 7.5 1.0
S1 S:SF3403 2.3 7.5 1.0
SG S:CYS120 2.3 7.7 1.0
FE1 S:SF3403 2.8 7.7 1.0
HB2 S:CYS149 3.2 7.0 1.0
CB S:CYS149 3.3 7.2 1.0
HA S:CYS149 3.4 6.1 1.0
CB S:CYS120 3.5 6.9 1.0
HB3 S:CYS120 3.5 7.3 1.0
FE4 S:SF3403 3.6 7.5 1.0
HB2 S:CYS120 3.6 7.3 1.0
HB S:THR114 3.7 7.8 1.0
H S:CYS115 3.8 7.2 1.0
HG2 L:ARG74 3.8 6.1 1.0
CA S:CYS149 4.0 6.2 1.0
FE7 S:SF3403 4.0 8.2 1.0
HG3 L:ARG74 4.0 6.1 1.0
SG S:CYS115 4.0 8.2 1.0
H S:VAL121 4.1 6.8 1.0
SG S:CYS19 4.1 7.5 1.0
HB3 S:CYS149 4.1 7.0 1.0
HE L:ARG74 4.2 6.1 1.0
HZ2 S:TRP258 4.3 7.6 1.0
CG L:ARG74 4.4 6.1 1.0
H S:THR114 4.4 6.8 1.0
N S:CYS115 4.4 7.6 1.0
CB S:THR114 4.6 7.8 1.0
S2 S:SF3403 4.7 7.7 1.0
HE1 S:TRP258 4.7 6.7 1.0
C S:CYS149 4.8 6.2 1.0
HB3 L:ARG74 4.9 5.8 1.0
CA S:CYS120 4.9 7.1 1.0
HB S:VAL121 4.9 7.6 1.0
HD2 L:HIS229 4.9 6.0 1.0
O S:GLY148 4.9 7.9 1.0
N S:VAL121 4.9 7.0 1.0
HA S:CYS120 5.0 7.3 1.0
HG21 S:THR114 5.0 7.8 1.0

Iron binding site 10 out of 24 in 6gal

Go back to Iron Binding Sites List in 6gal
Iron binding site 10 out of 24 in the Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 10 of Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10 within 5.0Å range:
probe atom residue distance (Å) B Occ
S:Fe403

b:7.5
occ:1.00
FE4 S:SF3403 0.0 7.5 1.0
SG S:CYS17 2.3 7.0 1.0
S3 S:SF3403 2.3 7.5 1.0
S2 S:SF3403 2.3 7.7 1.0
SG S:CYS19 2.3 7.5 1.0
FE1 S:SF3403 2.6 7.7 1.0
H S:CYS19 2.8 6.4 1.0
FE7 S:SF3403 2.8 8.2 1.0
H S:CYS17 2.9 7.4 1.0
HB3 S:CYS17 3.3 6.5 1.0
CB S:CYS17 3.4 6.4 1.0
HE2 L:HIS229 3.4 6.2 0.0
HB3 S:CYS19 3.4 7.0 1.0
CB S:CYS19 3.4 7.0 1.0
FE3 S:SF3403 3.6 7.4 1.0
N S:CYS19 3.7 6.7 1.0
S1 S:SF3403 3.7 7.5 1.0
N S:CYS17 3.7 7.5 1.0
CA S:CYS17 3.9 6.8 1.0
H S:THR18 4.0 7.4 1.0
CA S:CYS19 4.1 7.2 1.0
HG3 L:ARG74 4.1 6.1 1.0
NE2 L:HIS229 4.2 6.4 1.0
HB2 S:CYS17 4.2 6.5 1.0
N S:THR18 4.2 7.2 1.0
H S:CYS20 4.2 6.5 1.0
C S:CYS17 4.2 6.9 1.0
HB2 S:CYS19 4.2 7.2 1.0
SG S:CYS149 4.4 6.9 1.0
O S:HOH576 4.5 7.5 1.0
HD2 L:HIS229 4.5 6.0 1.0
SG S:CYS115 4.6 8.2 1.0
HB2 S:GLU16 4.7 8.6 1.0
HA S:GLU16 4.7 8.0 1.0
CD2 L:HIS229 4.8 6.2 1.0
N S:CYS20 4.8 6.5 1.0
C S:THR18 4.8 7.1 1.0
HB3 L:ARG74 4.8 5.8 1.0
C S:CYS19 4.9 6.6 1.0
HA S:CYS17 4.9 7.0 1.0
HA S:CYS19 4.9 7.1 1.0
HA3 L:GLY77 4.9 7.9 1.0
C S:GLU16 4.9 8.6 1.0
CG L:ARG74 5.0 6.1 1.0

Reference:

R.M.Evans, P.A.Ash, S.E.Beaton, E.J.Brooke, K.A.Vincent, S.B.Carr, F.A.Armstrong. Mechanistic Exploitation of A Self-Repairing, Blocked Proton Transfer Pathway in An O2-Tolerant [Nife]-Hydrogenase. J. Am. Chem. Soc. V. 140 10208 2018.
ISSN: ESSN 1520-5126
PubMed: 30070475
DOI: 10.1021/JACS.8B04798
Page generated: Tue Aug 6 19:13:36 2024

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