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Iron in PDB 8aio: Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)

Enzymatic activity of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)

All present enzymatic activity of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi):
1.12.7.2;

Protein crystallography data

The structure of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi), PDB code: 8aio was solved by J.Duan, E.Hofmann, T.Happe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.03 / 1.52
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 87.6, 72.16, 103.21, 90, 101.94, 90
R / Rfree (%) 16.7 / 19.2

Other elements in 8aio:

The structure of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) also contains other interesting chemical elements:

Magnesium (Mg) 4 atoms
Chlorine (Cl) 2 atoms

Iron Binding Sites:

Pages:

>>> Page 1 <<< Page 2, Binding sites: 11 - 20; Page 3, Binding sites: 21 - 30; Page 4, Binding sites: 31 - 40;

Binding sites:

The binding sites of Iron atom in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) (pdb code 8aio). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 40 binding sites of Iron where determined in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi), PDB code: 8aio:
Jump to Iron binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Iron binding site 1 out of 40 in 8aio

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Iron binding site 1 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe601

b:19.4
occ:0.82
FE1 A:MHX601 0.0 19.4 0.8
C3 A:MHX601 1.7 12.7 0.8
C4 A:MHX601 1.8 21.1 0.8
C5 A:MHX601 1.9 20.3 0.8
S2 A:MHX601 2.3 19.4 0.8
S1 A:MHX601 2.3 19.9 0.8
SG A:CYS503 2.5 18.0 1.0
FE2 A:MHX601 2.6 20.6 0.8
O3 A:MHX601 2.9 19.0 0.8
O5 A:MHX601 3.0 19.0 0.8
N4 A:MHX601 3.1 12.3 0.8
HB3 A:CYS503 3.4 19.7 1.0
CB A:CYS503 3.4 16.4 1.0
C1 A:MHX601 3.4 17.8 0.8
C2 A:MHX601 3.5 20.5 0.8
HB2 A:CYS503 3.5 19.7 1.0
C7 A:MHX601 3.8 21.3 0.8
N1 A:MHX601 3.8 20.5 0.8
C6 A:MHX601 3.9 21.2 0.8
HE1 A:MET353 3.9 22.0 0.1
HE3 A:LYS358 4.0 20.7 1.0
C A:MHX601 4.0 21.0 0.6
HD2 A:PRO231 4.1 26.6 1.0
FE4 A:SF4602 4.1 18.9 1.0
HB1 A:ALA230 4.2 21.6 1.0
HA2 A:GLY418 4.3 22.9 1.0
S2 A:SF4602 4.3 19.1 1.0
HG3 A:PRO354 4.4 21.4 1.0
HG2 A:PRO354 4.4 21.4 1.0
HD2 A:PRO354 4.4 21.2 1.0
HE2 A:MET353 4.5 22.0 0.1
CE A:MET353 4.6 18.4 0.1
HG2 A:PRO231 4.6 25.6 1.0
HE3 A:MET353 4.6 22.0 0.1
O7 A:MHX601 4.7 21.3 0.8
CG A:PRO354 4.7 17.9 1.0
N6 A:MHX601 4.7 15.9 0.8
HE2 A:LYS358 4.8 20.7 1.0
CE A:LYS358 4.8 17.2 1.0
HB3 A:PHE417 4.9 22.8 1.0
CA A:CYS503 4.9 16.5 1.0
CD A:PRO354 4.9 17.7 1.0
CD A:PRO231 5.0 22.2 1.0
HB2 A:ALA230 5.0 21.6 1.0

Iron binding site 2 out of 40 in 8aio

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Iron binding site 2 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe601

b:20.6
occ:0.82
FE2 A:MHX601 0.0 20.6 0.8
C7 A:MHX601 1.8 21.3 0.8
C A:MHX601 1.8 21.0 0.6
C6 A:MHX601 1.9 21.2 0.8
C5 A:MHX601 2.0 20.3 0.8
S2 A:MHX601 2.3 19.4 0.8
S1 A:MHX601 2.3 19.9 0.8
FE1 A:MHX601 2.6 19.4 0.8
O5 A:MHX601 2.9 19.0 0.8
O7 A:MHX601 2.9 21.3 0.8
O A:MHX601 2.9 18.6 0.6
N6 A:MHX601 3.0 15.9 0.8
HG2 A:PRO324 3.2 28.2 1.0
N1 A:MHX601 3.4 20.5 0.8
HD2 A:PHE417 3.4 26.5 1.0
C1 A:MHX601 3.5 17.8 0.8
C2 A:MHX601 3.5 20.5 0.8
HD2 A:PRO324 3.6 25.6 1.0
HB2 A:PRO324 3.7 23.3 1.0
C4 A:MHX601 3.8 21.1 0.8
C3 A:MHX601 3.8 12.7 0.8
CG A:PRO324 3.9 23.5 1.0
HE3 A:LYS358 4.0 20.7 1.0
HB3 A:PHE417 4.1 22.8 1.0
HD2 A:PRO231 4.1 26.6 1.0
HZ2 A:LYS358 4.2 20.2 1.0
HB2 A:CYS299 4.2 26.1 1.0
CD A:PRO324 4.2 21.4 1.0
CB A:PRO324 4.3 19.4 1.0
CD2 A:PHE417 4.3 22.1 1.0
HG2 A:PRO231 4.4 25.6 1.0
HE2 A:MET353 4.5 22.0 0.1
HE1 A:MET353 4.6 22.0 0.1
SG A:CYS503 4.7 18.0 1.0
HG3 A:PRO324 4.7 28.2 1.0
HG22 A:ILE268 4.7 26.3 1.0
NZ A:LYS358 4.7 16.8 1.0
HZ3 A:LYS358 4.8 20.2 1.0
CE A:LYS358 4.8 17.2 1.0
N4 A:MHX601 4.8 12.3 0.8
O3 A:MHX601 4.8 19.0 0.8
HB3 A:PRO324 4.8 23.3 1.0
HG21 A:ILE268 4.9 26.3 1.0
HD3 A:PRO324 4.9 25.6 1.0
CD A:PRO231 4.9 22.2 1.0
O A:CYS299 4.9 21.4 1.0
H A:GLN325 4.9 21.3 1.0
CB A:PHE417 4.9 19.0 1.0
HD3 A:PRO231 5.0 26.6 1.0
CE A:MET353 5.0 18.4 0.1
HE2 A:PHE417 5.0 24.4 1.0
HB2 A:SER323 5.0 23.5 1.0

Iron binding site 3 out of 40 in 8aio

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Iron binding site 3 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe602

b:18.0
occ:0.94
FE1 A:SF4602 0.0 18.0 0.9
SG A:CYS355 2.3 20.4 1.0
S2 A:SF4602 2.3 19.1 1.0
S4 A:SF4602 2.3 18.1 1.0
S3 A:SF4602 2.3 19.3 1.0
FE3 A:SF4602 2.7 18.2 1.0
FE2 A:SF4602 2.7 17.9 1.0
FE4 A:SF4602 2.7 18.9 1.0
HB2 A:CYS355 2.9 25.7 1.0
CB A:CYS355 3.2 21.4 1.0
HD2 A:PRO301 3.7 19.7 1.0
O A:HOH756 3.8 18.7 1.0
HB3 A:CYS355 3.8 25.7 1.0
HB3 A:SER357 3.8 23.5 1.0
S1 A:SF4602 3.8 18.4 1.0
O3 A:MHX601 3.9 19.0 0.8
HG2 A:LYS358 4.0 19.8 1.0
HG2 A:PRO301 4.1 21.7 1.0
HA A:CYS355 4.2 24.1 1.0
HE2 A:LYS358 4.3 20.7 1.0
CA A:CYS355 4.3 20.1 1.0
H A:SER357 4.4 22.8 1.0
H A:GLY302 4.4 20.1 1.0
HB2 A:SER357 4.5 23.5 1.0
CD A:PRO301 4.6 16.4 1.0
CB A:SER357 4.6 19.6 1.0
C3 A:MHX601 4.6 12.7 0.8
H A:LYS358 4.7 23.2 1.0
SG A:CYS300 4.7 17.9 1.0
SG A:CYS503 4.7 18.0 1.0
SG A:CYS499 4.7 18.3 1.0
CG A:PRO301 4.8 18.1 1.0
HA A:CYS300 4.8 22.3 1.0
HA3 A:GLY506 4.8 22.2 1.0
CG A:LYS358 4.9 16.5 1.0
HG3 A:LYS358 4.9 19.8 1.0
HA A:CYS503 4.9 19.8 1.0
HA A:CYS193 5.0 21.3 1.0

Iron binding site 4 out of 40 in 8aio

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Iron binding site 4 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe602

b:17.9
occ:1.00
FE2 A:SF4602 0.0 17.9 1.0
S1 A:SF4602 2.3 18.4 1.0
S3 A:SF4602 2.3 19.3 1.0
SG A:CYS499 2.3 18.3 1.0
S4 A:SF4602 2.3 18.1 1.0
FE1 A:SF4602 2.7 18.0 0.9
FE3 A:SF4602 2.7 18.2 1.0
FE4 A:SF4602 2.7 18.9 1.0
HB2 A:CYS499 2.9 22.5 1.0
CB A:CYS499 3.2 18.8 1.0
H A:CYS499 3.4 21.0 1.0
HA2 A:GLY506 3.5 22.2 1.0
HB3 A:ALA498 3.8 23.5 1.0
N A:CYS499 3.8 17.5 1.0
HA A:CYS503 3.8 19.8 1.0
S2 A:SF4602 3.9 19.1 1.0
HB3 A:CYS499 3.9 22.5 1.0
HA3 A:GLY506 4.0 22.2 1.0
CA A:CYS499 4.1 16.0 1.0
O A:HOH756 4.1 18.7 1.0
CA A:GLY506 4.2 18.5 1.0
H A:ALA498 4.3 21.8 1.0
H A:GLY507 4.4 21.4 1.0
HB2 A:CYS193 4.4 24.3 1.0
SG A:CYS355 4.6 20.4 1.0
HA A:CYS499 4.7 19.2 1.0
HB2 A:CYS355 4.7 25.7 1.0
C A:ALA498 4.7 18.1 1.0
SG A:CYS300 4.7 17.9 1.0
CB A:ALA498 4.7 19.6 1.0
HE21 A:GLN195 4.7 28.1 1.0
CA A:CYS503 4.8 16.5 1.0
N A:ALA498 4.8 18.2 1.0
SG A:CYS503 4.9 18.0 1.0
HA A:CYS193 5.0 21.3 1.0
CA A:ALA498 5.0 18.9 1.0

Iron binding site 5 out of 40 in 8aio

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Iron binding site 5 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 5 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe602

b:18.2
occ:1.00
FE3 A:SF4602 0.0 18.2 1.0
S4 A:SF4602 2.2 18.1 1.0
S2 A:SF4602 2.3 19.1 1.0
SG A:CYS300 2.3 17.9 1.0
S1 A:SF4602 2.3 18.4 1.0
FE1 A:SF4602 2.7 18.0 0.9
FE2 A:SF4602 2.7 17.9 1.0
FE4 A:SF4602 2.7 18.9 1.0
H A:ALA498 3.2 21.8 1.0
HB2 A:CYS300 3.3 21.4 1.0
CB A:CYS300 3.3 17.9 1.0
HB3 A:ALA498 3.5 23.5 1.0
HA A:CYS300 3.5 22.3 1.0
H A:GLY302 3.6 20.1 1.0
HD2 A:PRO301 3.6 19.7 1.0
S3 A:SF4602 3.8 19.3 1.0
CA A:CYS300 3.9 18.6 1.0
N A:ALA498 4.1 18.2 1.0
H A:CYS499 4.1 21.0 1.0
HB3 A:CYS300 4.2 21.4 1.0
CB A:ALA498 4.3 19.6 1.0
HA3 A:GLY302 4.4 19.4 1.0
C A:CYS300 4.4 19.3 1.0
HA A:MET497 4.4 19.6 1.0
N A:GLY302 4.4 16.8 1.0
HB2 A:ALA498 4.4 23.5 1.0
CD A:PRO301 4.4 16.4 1.0
H A:TRP303 4.5 21.5 1.0
N A:PRO301 4.5 17.9 1.0
HB3 A:MET497 4.5 24.2 1.0
C2 A:MHX601 4.7 20.5 0.8
SG A:CYS499 4.7 18.3 1.0
CA A:ALA498 4.7 18.9 1.0
SG A:CYS503 4.7 18.0 1.0
N A:CYS499 4.8 17.5 1.0
HG2 A:PRO301 4.8 21.7 1.0
SG A:CYS355 4.8 20.4 1.0
SD A:MET497 4.8 19.1 1.0
CA A:GLY302 4.9 16.2 1.0
HB2 A:CYS499 4.9 22.5 1.0

Iron binding site 6 out of 40 in 8aio

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Iron binding site 6 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 6 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe602

b:18.9
occ:1.00
FE4 A:SF4602 0.0 18.9 1.0
S3 A:SF4602 2.2 19.3 1.0
S1 A:SF4602 2.3 18.4 1.0
S2 A:SF4602 2.3 19.1 1.0
SG A:CYS503 2.3 18.0 1.0
FE1 A:SF4602 2.7 18.0 0.9
FE3 A:SF4602 2.7 18.2 1.0
FE2 A:SF4602 2.7 17.9 1.0
HA A:CYS503 2.8 19.8 1.0
CB A:CYS503 3.3 16.4 1.0
CA A:CYS503 3.4 16.5 1.0
HB3 A:CYS503 3.5 19.7 1.0
C3 A:MHX601 3.8 12.7 0.8
O3 A:MHX601 3.9 19.0 0.8
S4 A:SF4602 3.9 18.1 1.0
N A:CYS503 3.9 16.6 1.0
HB2 A:CYS355 4.1 25.7 1.0
H A:CYS503 4.1 20.0 1.0
HB2 A:CYS503 4.1 19.7 1.0
FE1 A:MHX601 4.1 19.4 0.8
C2 A:MHX601 4.2 20.5 0.8
S2 A:MHX601 4.3 19.4 0.8
HB2 A:CYS499 4.4 22.5 1.0
HG2 A:PRO354 4.4 21.4 1.0
C A:GLY502 4.7 19.5 1.0
SG A:CYS355 4.7 20.4 1.0
HB2 A:CYS300 4.7 21.4 1.0
SD A:MET497 4.7 19.1 1.0
HA3 A:GLY506 4.7 22.2 1.0
C A:CYS503 4.8 16.6 1.0
SG A:CYS300 4.8 17.9 1.0
CB A:CYS355 4.8 21.4 1.0
HB3 A:MET497 4.8 24.2 1.0
HA A:CYS300 4.9 22.3 1.0
SG A:CYS499 4.9 18.3 1.0
HD2 A:PRO301 4.9 19.7 1.0
H A:CYS499 4.9 21.0 1.0

Iron binding site 7 out of 40 in 8aio

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Iron binding site 7 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 7 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe603

b:18.9
occ:1.00
FE1 A:SF4603 0.0 18.9 1.0
S4 A:SF4603 2.3 19.4 1.0
SG A:CYS193 2.3 19.4 1.0
S3 A:SF4603 2.3 18.5 1.0
S2 A:SF4603 2.3 18.2 1.0
FE2 A:SF4603 2.8 17.9 1.0
FE3 A:SF4603 2.8 19.4 1.0
FE4 A:SF4603 2.8 18.9 1.0
H A:CYS193 3.0 22.2 1.0
HG21 A:THR161 3.2 22.9 1.0
H A:GLY194 3.3 20.2 1.0
H A:GLN195 3.5 21.2 1.0
N A:CYS193 3.6 18.5 1.0
CB A:CYS193 3.7 20.2 1.0
N A:GLY194 3.8 16.8 1.0
HB2 A:LEU191 3.9 21.7 1.0
HB3 A:CYS193 3.9 24.3 1.0
S1 A:SF4603 4.0 19.5 1.0
H A:LEU191 4.0 22.0 1.0
CA A:CYS193 4.0 17.7 1.0
HB2 A:GLN195 4.1 21.7 1.0
CG2 A:THR161 4.1 19.1 1.0
H A:LEU192 4.1 23.5 1.0
HG23 A:THR161 4.2 22.9 1.0
H A:CYS196 4.2 23.2 1.0
C A:CYS193 4.2 17.9 1.0
N A:GLN195 4.3 17.7 1.0
HB2 A:CYS193 4.4 24.3 1.0
N A:LEU192 4.4 19.6 1.0
HG22 A:THR161 4.5 22.9 1.0
C A:LEU192 4.7 20.4 1.0
N A:LEU191 4.7 18.3 1.0
SG A:CYS190 4.7 19.1 1.0
CB A:LEU191 4.7 18.1 1.0
CA A:GLY194 4.7 19.9 1.0
SG A:CYS196 4.7 18.9 1.0
HG A:LEU191 4.7 21.2 1.0
HA2 A:GLY194 4.8 23.8 1.0
HA A:LEU192 4.8 22.1 1.0
HD11 A:LEU191 4.8 25.4 1.0
SG A:CYS157 4.8 17.9 1.0
HA A:CYS157 4.8 16.6 1.0
HG2 A:GLN195 4.9 25.3 1.0
CB A:GLN195 4.9 18.1 1.0
CA A:LEU192 4.9 18.4 1.0
C A:LEU191 5.0 20.4 1.0
C A:GLY194 5.0 15.8 1.0
HA A:CYS193 5.0 21.3 1.0
N A:CYS196 5.0 19.4 1.0

Iron binding site 8 out of 40 in 8aio

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Iron binding site 8 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 8 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe603

b:17.9
occ:1.00
FE2 A:SF4603 0.0 17.9 1.0
S3 A:SF4603 2.3 18.5 1.0
S1 A:SF4603 2.3 19.5 1.0
SG A:CYS157 2.3 17.9 1.0
S4 A:SF4603 2.3 19.4 1.0
FE4 A:SF4603 2.7 18.9 1.0
FE3 A:SF4603 2.7 19.4 1.0
FE1 A:SF4603 2.8 18.9 1.0
HB2 A:CYS157 3.0 17.6 1.0
CB A:CYS157 3.2 14.7 1.0
HB1 A:ALA165 3.3 23.2 1.0
HA A:CYS157 3.6 16.6 1.0
HG21 A:THR161 3.8 22.9 1.0
H A:MET166 3.9 21.6 1.0
HG1 A:THR163 3.9 25.4 1.0
S2 A:SF4603 3.9 18.2 1.0
CA A:CYS157 4.0 13.9 1.0
HB3 A:CYS157 4.0 17.6 1.0
HB2 A:MET166 4.1 27.4 1.0
H A:ALA165 4.1 25.3 1.0
OG1 A:THR163 4.1 21.2 1.0
HG1 A:THR161 4.2 24.5 1.0
CB A:ALA165 4.3 19.3 1.0
OG1 A:THR161 4.3 20.4 1.0
HG23 A:THR161 4.3 22.9 1.0
HB3 A:CYS196 4.4 23.9 1.0
N A:MET166 4.4 18.0 1.0
CG2 A:THR161 4.5 19.1 1.0
HB3 A:MET166 4.5 27.4 1.0
HB3 A:ALA165 4.7 23.2 1.0
H A:LEU191 4.7 22.0 1.0
N A:ALA165 4.7 21.1 1.0
CB A:MET166 4.7 22.9 1.0
HA A:CYS190 4.7 25.0 1.0
HB2 A:ALA165 4.8 23.2 1.0
SG A:CYS193 4.8 19.4 1.0
C A:CYS157 4.9 17.7 1.0
CA A:ALA165 4.9 21.8 1.0
H A:CYS196 4.9 23.2 1.0
SG A:CYS196 4.9 18.9 1.0
C A:ALA165 4.9 21.4 1.0
SG A:CYS190 4.9 19.1 1.0
O A:CYS157 5.0 19.6 1.0

Iron binding site 9 out of 40 in 8aio

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Iron binding site 9 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 9 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe603

b:19.4
occ:1.00
FE3 A:SF4603 0.0 19.4 1.0
S2 A:SF4603 2.3 18.2 1.0
S4 A:SF4603 2.3 19.4 1.0
S1 A:SF4603 2.3 19.5 1.0
SG A:CYS196 2.3 18.9 1.0
FE2 A:SF4603 2.7 17.9 1.0
FE4 A:SF4603 2.8 18.9 1.0
FE1 A:SF4603 2.8 18.9 1.0
HB3 A:CYS196 3.0 23.9 1.0
H A:CYS196 3.1 23.2 1.0
CB A:CYS196 3.3 19.9 1.0
HE2 A:MET166 3.7 26.0 1.0
H A:GLY194 3.8 20.2 1.0
N A:CYS196 3.9 19.4 1.0
S3 A:SF4603 3.9 18.5 1.0
HD11 A:LEU140 4.0 38.8 1.0
HB2 A:CYS196 4.0 23.9 1.0
HB2 A:MET166 4.1 27.4 1.0
HD13 A:LEU140 4.1 38.8 1.0
HB2 A:CYS157 4.1 17.6 1.0
HA2 A:GLY194 4.2 23.8 1.0
CA A:CYS196 4.2 18.9 1.0
H A:GLN195 4.3 21.2 1.0
N A:GLY194 4.4 16.8 1.0
CD1 A:LEU140 4.5 32.3 1.0
N A:GLN195 4.6 17.7 1.0
CE A:MET166 4.6 21.6 1.0
HE3 A:MET166 4.6 26.0 1.0
CA A:GLY194 4.6 19.9 1.0
SG A:CYS190 4.7 19.1 1.0
SG A:CYS193 4.7 19.4 1.0
SG A:CYS157 4.7 17.9 1.0
HD21 A:LEU140 4.8 36.4 1.0
HA A:CYS196 4.8 22.7 1.0
C A:GLY194 4.8 15.8 1.0
CB A:CYS157 4.9 14.7 1.0
H A:ILE197 4.9 21.8 1.0
H A:CYS193 4.9 22.2 1.0
HB2 A:GLN195 4.9 21.7 1.0
HD22 A:LEU140 4.9 36.4 1.0
HE1 A:MET166 5.0 26.0 1.0
CB A:MET166 5.0 22.9 1.0

Iron binding site 10 out of 40 in 8aio

Go back to Iron Binding Sites List in 8aio
Iron binding site 10 out of 40 in the Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 10 of Co-Bound [Fefe]-Hydrogenase I From Clostridium Pasteurianum (Cpi) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe603

b:18.9
occ:1.00
FE4 A:SF4603 0.0 18.9 1.0
S1 A:SF4603 2.3 19.5 1.0
S3 A:SF4603 2.3 18.5 1.0
SG A:CYS190 2.3 19.1 1.0
S2 A:SF4603 2.3 18.2 1.0
FE2 A:SF4603 2.7 17.9 1.0
FE3 A:SF4603 2.8 19.4 1.0
FE1 A:SF4603 2.8 18.9 1.0
H A:LEU192 3.2 23.5 1.0
H A:LEU191 3.3 22.0 1.0
HA A:CYS190 3.4 25.0 1.0
HB1 A:ALA165 3.4 23.2 1.0
CB A:CYS190 3.4 19.7 1.0
HB2 A:CYS190 3.5 23.6 1.0
HD11 A:LEU140 3.7 38.8 1.0
CA A:CYS190 3.8 20.8 1.0
N A:LEU191 3.8 18.3 1.0
S4 A:SF4603 3.9 19.4 1.0
N A:LEU192 3.9 19.6 1.0
HD1 A:PHE185 4.0 23.8 1.0
H A:CYS193 4.1 22.2 1.0
HA A:LEU192 4.1 22.1 1.0
HB2 A:ALA165 4.1 23.2 1.0
CB A:ALA165 4.2 19.3 1.0
C A:CYS190 4.2 21.9 1.0
HB3 A:CYS190 4.2 23.6 1.0
CD1 A:LEU140 4.5 32.3 1.0
H A:GLY194 4.6 20.2 1.0
CA A:LEU192 4.6 18.4 1.0
HB3 A:ALA165 4.6 23.2 1.0
HD13 A:LEU140 4.6 38.8 1.0
HD23 A:LEU192 4.6 24.2 1.0
CD1 A:PHE185 4.7 19.8 1.0
HD12 A:LEU140 4.8 38.8 1.0
N A:CYS193 4.8 18.5 1.0
HB2 A:LEU191 4.8 21.7 1.0
SG A:CYS157 4.8 17.9 1.0
CA A:LEU191 4.8 20.5 1.0
C A:LEU191 4.8 20.4 1.0
HE1 A:PHE185 4.8 30.0 1.0
SG A:CYS196 4.9 18.9 1.0
HB3 A:PHE185 5.0 26.2 1.0
SG A:CYS193 5.0 19.4 1.0

Reference:

J.Duan, A.Hemschemeier, D.J.Burr, S.T.Stripp, E.Hofmann, T.Happe. Cyanide Binding to [Fefe]-Hydrogenase Stabilizes the Alternative Configuration of the Proton Transfer Pathway. Angew.Chem.Int.Ed.Engl. 2022.
ISSN: ESSN 1521-3773
PubMed: 36464641
DOI: 10.1002/ANIE.202216903
Page generated: Fri Aug 9 17:33:29 2024

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