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Iron in PDB 9f47: Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii

Protein crystallography data

The structure of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii, PDB code: 9f47 was solved by J.Duan, A.Rutz, E.Hofmann, T.Happe, G.Kurisu, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.26 / 2.90
Space group P 42 21 2
Cell size a, b, c (Å), α, β, γ (°) 169, 169, 127, 90, 90, 90
R / Rfree (%) 24.2 / 29.8

Other elements in 9f47:

The structure of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii also contains other interesting chemical elements:

Zinc (Zn) 2 atoms
Chlorine (Cl) 10 atoms

Iron Binding Sites:

Pages:

>>> Page 1 <<< Page 2, Binding sites: 11 - 20; Page 3, Binding sites: 21 - 28;

Binding sites:

The binding sites of Iron atom in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii (pdb code 9f47). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 28 binding sites of Iron where determined in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii, PDB code: 9f47:
Jump to Iron binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Iron binding site 1 out of 28 in 9f47

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Iron binding site 1 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe701

b:80.6
occ:1.00
FE1 A:402701 0.0 80.6 1.0
C4 A:402701 1.8 76.7 1.0
C3 A:402701 1.8 72.9 1.0
C5 A:402701 1.9 94.0 1.0
SG A:CYS571 2.3 83.2 1.0
S1 A:402701 2.3 83.9 1.0
S2 A:402701 2.3 80.8 1.0
FE2 A:402701 2.5 76.6 1.0
O3 A:402701 2.9 77.1 1.0
N4 A:402701 3.0 85.4 1.0
O5 A:402701 3.0 104.0 1.0
HB3 A:CYS571 3.0 98.7 1.0
CB A:CYS571 3.1 82.2 1.0
HB2 A:CYS571 3.2 98.7 1.0
C2 A:402701 3.5 72.2 1.0
C1 A:402701 3.5 86.6 1.0
C6 A:402701 3.8 84.8 1.0
N1 A:402701 3.8 76.2 1.0
C7 A:402701 3.8 88.4 1.0
FE4 A:SF4702 3.9 78.6 1.0
HB1 A:ALA292 4.0 85.0 1.0
HD2 A:PRO293 4.0 96.1 1.0
HE3 A:LYS426 4.0 61.6 1.0
HA2 A:GLY486 4.1 83.0 1.0
HE3 A:MET421 4.3 79.7 1.0
HE1 A:MET421 4.4 79.7 1.0
HG3 A:PRO422 4.5 67.7 1.0
CA A:CYS571 4.6 71.2 1.0
S2 A:SF4702 4.6 66.3 1.0
HB2 A:CYS367 4.6 83.2 1.0
HG2 A:PRO422 4.6 67.7 1.0
HD2 A:PRO422 4.7 83.4 1.0
HE2 A:LYS426 4.7 61.6 1.0
N6 A:402701 4.7 76.1 1.0
HA A:CYS571 4.8 85.4 1.0
H A:CYS571 4.8 87.4 1.0
CE A:MET421 4.8 66.4 1.0
O7 A:402701 4.8 68.8 1.0
CE A:LYS426 4.8 51.3 1.0
HD3 A:PRO422 4.8 83.4 1.0
CB A:ALA292 4.8 70.8 1.0
CG A:PRO422 4.9 56.4 1.0
HB2 A:ALA292 4.9 85.0 1.0
CD A:PRO293 5.0 80.1 1.0

Iron binding site 2 out of 28 in 9f47

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Iron binding site 2 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe701

b:76.6
occ:1.00
FE2 A:402701 0.0 76.6 1.0
C6 A:402701 1.7 84.8 1.0
C7 A:402701 1.8 88.4 1.0
C5 A:402701 1.9 94.0 1.0
S1 A:402701 2.3 83.9 1.0
S2 A:402701 2.3 80.8 1.0
FE1 A:402701 2.5 80.6 1.0
O5 A:402701 2.7 104.0 1.0
HB2 A:CYS367 2.8 83.2 1.0
O7 A:402701 2.9 68.8 1.0
N6 A:402701 2.9 76.1 1.0
SG A:CYS367 3.2 73.1 1.0
N1 A:402701 3.3 76.2 1.0
CB A:CYS367 3.4 69.3 1.0
C1 A:402701 3.4 86.6 1.0
C2 A:402701 3.5 72.2 1.0
C4 A:402701 3.6 76.7 1.0
HG2 A:PRO392 3.7 70.2 1.0
C3 A:402701 3.7 72.9 1.0
HB3 A:CYS367 3.8 83.2 1.0
HD2 A:PRO392 3.9 81.4 1.0
HD2 A:PHE485 3.9 88.5 1.0
HE3 A:LYS426 3.9 61.6 1.0
HZ1 A:LYS426 4.1 68.8 1.0
HB3 A:PHE485 4.1 95.1 1.0
HD2 A:PRO293 4.2 96.1 1.0
SG A:CYS571 4.3 83.2 1.0
HE1 A:MET421 4.4 79.7 1.0
CG A:PRO392 4.5 58.5 1.0
N4 A:402701 4.5 85.4 1.0
HB2 A:PRO392 4.6 86.4 1.0
NZ A:LYS426 4.6 57.4 1.0
HZ2 A:LYS426 4.6 68.8 1.0
CD A:PRO392 4.6 67.8 1.0
CE A:LYS426 4.6 51.3 1.0
O3 A:402701 4.7 77.1 1.0
CA A:CYS367 4.8 70.9 1.0
HG2 A:PRO293 4.8 78.2 1.0
CD2 A:PHE485 4.8 73.8 1.0
HE2 A:LYS426 4.8 61.6 1.0
H A:CYS367 4.9 74.0 1.0
HG21 A:THR330 5.0 70.6 1.0
O A:CYS367 5.0 77.3 1.0
CD A:PRO293 5.0 80.1 1.0
C A:CYS367 5.0 67.3 1.0
HD3 A:PRO293 5.0 96.1 1.0
HB1 A:ALA292 5.0 85.0 1.0

Iron binding site 3 out of 28 in 9f47

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Iron binding site 3 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:83.5
occ:1.00
FE1 A:SF4702 0.0 83.5 1.0
S2 A:SF4702 2.1 66.3 1.0
S3 A:SF4702 2.1 60.2 1.0
S4 A:SF4702 2.1 71.3 1.0
SG A:CYS423 2.2 86.4 1.0
HB3 A:CYS423 2.7 69.8 1.0
CB A:CYS423 2.8 58.2 1.0
HB2 A:CYS423 3.0 69.8 1.0
FE4 A:SF4702 3.0 78.6 1.0
FE3 A:SF4702 3.0 77.1 1.0
FE2 A:SF4702 3.0 91.3 1.0
HB3 A:ALA425 3.6 103.8 1.0
S1 A:SF4702 3.7 63.5 1.0
HG2 A:LYS426 4.1 75.9 1.0
HG2 A:PRO422 4.2 67.7 1.0
O3 A:402701 4.3 77.1 1.0
CA A:CYS423 4.3 70.2 1.0
HD2 A:PRO369 4.3 70.6 1.0
CB A:ALA425 4.4 86.5 1.0
H A:ALA425 4.5 94.0 1.0
HE2 A:LYS426 4.5 61.6 1.0
HB2 A:ALA425 4.5 103.8 1.0
HD3 A:PRO369 4.7 70.6 1.0
HA A:CYS571 4.7 85.4 1.0
H A:LYS426 4.7 79.8 1.0
N A:CYS423 4.8 77.0 1.0
C3 A:402701 4.8 72.9 1.0
HD2 A:PRO422 4.8 83.4 1.0
HA A:CYS423 4.9 84.3 1.0
SG A:CYS368 4.9 62.0 1.0
HA3 A:GLY574 4.9 76.8 1.0
SG A:CYS567 4.9 94.9 1.0
CG A:LYS426 4.9 63.2 1.0
HA A:CYS368 4.9 88.4 1.0
CD A:PRO369 5.0 58.8 1.0
HA2 A:GLY574 5.0 76.8 1.0
SG A:CYS571 5.0 83.2 1.0
HG3 A:LYS426 5.0 75.9 1.0

Iron binding site 4 out of 28 in 9f47

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Iron binding site 4 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:91.3
occ:1.00
FE2 A:SF4702 0.0 91.3 1.0
S1 A:SF4702 2.1 63.5 1.0
S3 A:SF4702 2.1 60.2 1.0
S4 A:SF4702 2.1 71.3 1.0
SG A:CYS567 2.3 94.9 1.0
HB2 A:CYS567 2.6 78.9 1.0
CB A:CYS567 3.0 65.8 1.0
FE3 A:SF4702 3.0 77.1 1.0
FE4 A:SF4702 3.0 78.6 1.0
FE1 A:SF4702 3.0 83.5 1.0
HA2 A:GLY574 3.2 76.8 1.0
HA A:CYS571 3.5 85.4 1.0
H A:CYS567 3.5 92.1 1.0
HB3 A:CYS567 3.6 78.9 1.0
S2 A:SF4702 3.7 66.3 1.0
HA3 A:GLY574 3.9 76.8 1.0
HB3 A:CYS423 3.9 69.8 1.0
CA A:GLY574 3.9 64.0 1.0
N A:CYS567 4.0 76.8 1.0
CA A:CYS567 4.1 70.4 1.0
HB3 A:ALA566 4.2 111.0 1.0
CA A:CYS571 4.4 71.2 1.0
N A:GLY574 4.4 66.9 1.0
O A:GLY570 4.4 59.0 1.0
HA A:CYS567 4.6 84.5 1.0
CB A:CYS423 4.6 58.2 1.0
H A:GLY575 4.7 97.1 1.0
H A:GLY574 4.7 80.3 1.0
HB2 A:CYS423 4.7 69.8 1.0
C A:GLY570 4.7 70.1 1.0
HG3 A:MET565 4.7 99.2 1.0
N A:CYS571 4.8 72.8 1.0
H A:ALA566 4.8 101.3 1.0
C A:GLY573 4.9 74.6 1.0
SG A:CYS423 4.9 86.4 1.0
HG A:CYS368 5.0 74.4 1.0

Iron binding site 5 out of 28 in 9f47

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Iron binding site 5 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 5 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:77.1
occ:1.00
FE3 A:SF4702 0.0 77.1 1.0
S1 A:SF4702 2.1 63.5 1.0
S4 A:SF4702 2.1 71.3 1.0
S2 A:SF4702 2.1 66.3 1.0
SG A:CYS368 2.3 62.0 1.0
HG A:CYS368 2.4 74.4 1.0
FE2 A:SF4702 3.0 91.3 1.0
FE1 A:SF4702 3.0 83.5 1.0
FE4 A:SF4702 3.0 78.6 1.0
HB3 A:ALA566 3.2 111.0 1.0
HB2 A:CYS368 3.2 76.3 1.0
H A:ALA566 3.3 101.3 1.0
CB A:CYS368 3.3 63.6 1.0
HA A:CYS368 3.7 88.4 1.0
S3 A:SF4702 3.7 60.2 1.0
HG3 A:MET565 3.8 99.2 1.0
H A:CYS567 3.9 92.1 1.0
HD2 A:PRO369 4.0 70.6 1.0
CB A:ALA566 4.1 92.5 1.0
CA A:CYS368 4.1 73.6 1.0
N A:ALA566 4.1 84.5 1.0
HB3 A:CYS368 4.1 76.3 1.0
HB2 A:ALA566 4.2 111.0 1.0
HB2 A:SER370 4.4 72.3 1.0
H A:SER370 4.4 75.2 1.0
HD3 A:PRO369 4.5 70.6 1.0
OG A:SER370 4.6 67.6 1.0
SG A:CYS567 4.6 94.9 1.0
HA A:MET565 4.6 78.3 1.0
N A:CYS567 4.6 76.8 1.0
CD A:PRO369 4.6 58.8 1.0
CA A:ALA566 4.6 85.9 1.0
HB2 A:CYS567 4.7 78.9 1.0
CG A:MET565 4.7 82.7 1.0
HB1 A:ALA566 4.8 111.0 1.0
HB3 A:ALA425 4.8 103.8 1.0
C2 A:402701 4.8 72.2 1.0
C A:CYS368 4.9 69.1 1.0
CB A:SER370 5.0 60.3 1.0
SG A:CYS571 5.0 83.2 1.0

Iron binding site 6 out of 28 in 9f47

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Iron binding site 6 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 6 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:78.6
occ:1.00
FE4 A:SF4702 0.0 78.6 1.0
S2 A:SF4702 2.1 66.3 1.0
S1 A:SF4702 2.1 63.5 1.0
S3 A:SF4702 2.1 60.2 1.0
SG A:CYS571 2.3 83.2 1.0
HA A:CYS571 2.5 85.4 1.0
FE1 A:SF4702 3.0 83.5 1.0
CB A:CYS571 3.0 82.2 1.0
FE2 A:SF4702 3.0 91.3 1.0
FE3 A:SF4702 3.0 77.1 1.0
CA A:CYS571 3.1 71.2 1.0
HB3 A:CYS571 3.1 98.7 1.0
N A:CYS571 3.6 72.8 1.0
S4 A:SF4702 3.7 71.3 1.0
H A:CYS571 3.8 87.4 1.0
C3 A:402701 3.8 72.9 1.0
FE1 A:402701 3.9 80.6 1.0
C2 A:402701 3.9 72.2 1.0
HB2 A:CYS571 3.9 98.7 1.0
S2 A:402701 4.0 80.8 1.0
HG2 A:PRO422 4.0 67.7 1.0
O3 A:402701 4.1 77.1 1.0
HG3 A:MET565 4.1 99.2 1.0
C A:GLY570 4.4 70.1 1.0
C A:CYS571 4.5 69.3 1.0
HB2 A:CYS368 4.5 76.3 1.0
SG A:CYS423 4.6 86.4 1.0
HB2 A:CYS567 4.6 78.9 1.0
HG2 A:MET565 4.7 99.2 1.0
O A:CYS571 4.8 80.7 1.0
CG A:MET565 4.8 82.7 1.0
O A:GLY570 4.8 59.0 1.0
HA A:CYS368 4.8 88.4 1.0
HB3 A:CYS423 4.8 69.8 1.0
HA2 A:GLY570 4.9 78.7 1.0
CG A:PRO422 4.9 56.4 1.0
C1 A:402701 4.9 86.6 1.0
N1 A:402701 4.9 76.2 1.0
HG3 A:PRO422 4.9 67.7 1.0
C4 A:402701 4.9 76.7 1.0
SG A:CYS368 4.9 62.0 1.0

Iron binding site 7 out of 28 in 9f47

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Iron binding site 7 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 7 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe703

b:107.7
occ:1.00
FE1 A:SF4703 0.0 107.7 1.0
S4 A:SF4703 2.1 109.9 1.0
S3 A:SF4703 2.1 94.8 1.0
S2 A:SF4703 2.1 149.8 1.0
SG A:CYS228 2.3 106.8 1.0
HB3 A:CYS228 2.8 133.6 1.0
H A:CYS228 2.9 125.4 1.0
FE4 A:SF4703 3.0 144.1 1.0
FE3 A:SF4703 3.0 104.4 1.0
FE2 A:SF4703 3.0 157.1 1.0
CB A:CYS228 3.1 111.3 1.0
N A:CYS228 3.7 104.5 1.0
S1 A:SF4703 3.7 95.3 1.0
H A:GLY226 3.8 159.0 1.0
HB2 A:CYS228 3.8 133.6 1.0
HD11 A:ILE267 3.8 101.9 1.0
CA A:CYS228 4.0 106.5 1.0
HD13 A:ILE218 4.1 105.2 1.0
HB2 A:HIS245 4.3 133.6 1.0
H A:LYS229 4.3 127.9 1.0
H A:ALA227 4.3 137.6 1.0
HD1 A:HIS245 4.4 129.6 1.0
N A:GLY226 4.5 132.5 1.0
N A:ALA227 4.5 114.7 1.0
HA2 A:GLY226 4.5 140.1 1.0
ND1 A:HIS245 4.6 108.0 1.0
CD1 A:ILE267 4.7 84.9 1.0
HA A:CYS228 4.7 127.7 1.0
HD12 A:ILE267 4.7 101.9 1.0
C A:GLY226 4.7 114.0 1.0
H A:CYS225 4.8 162.5 1.0
HB3 A:ALA227 4.8 123.7 1.0
CA A:GLY226 4.8 116.8 1.0
HB2 A:CYS262 4.8 140.2 1.0
SG A:CYS225 4.8 157.2 1.0
N A:LYS229 4.8 106.6 1.0
CG A:HIS245 4.8 108.9 1.0
C A:ALA227 4.9 109.9 1.0
HA A:CYS262 4.9 124.0 1.0
C A:CYS228 4.9 105.8 1.0
HG23 A:ILE218 4.9 107.1 1.0
SG A:CYS222 4.9 108.5 1.0
HD13 A:ILE237 4.9 96.0 1.0
SG A:CYS262 5.0 86.6 1.0
CB A:HIS245 5.0 111.3 1.0

Iron binding site 8 out of 28 in 9f47

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Iron binding site 8 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 8 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe703

b:157.1
occ:1.00
FE2 A:SF4703 0.0 157.1 1.0
S3 A:SF4703 2.1 94.8 1.0
S4 A:SF4703 2.1 109.9 1.0
S1 A:SF4703 2.1 95.3 1.0
SG A:CYS225 2.4 157.2 1.0
HB3 A:CYS225 2.5 162.0 1.0
H A:GLY226 2.5 159.0 1.0
H A:CYS225 2.7 162.5 1.0
CB A:CYS225 2.8 135.0 1.0
FE3 A:SF4703 3.0 104.4 1.0
FE4 A:SF4703 3.0 144.1 1.0
FE1 A:SF4703 3.0 107.7 1.0
N A:GLY226 3.3 132.5 1.0
N A:CYS225 3.4 135.4 1.0
H A:ALA227 3.4 137.6 1.0
CA A:CYS225 3.5 127.5 1.0
HB2 A:CYS225 3.7 162.0 1.0
S2 A:SF4703 3.7 149.8 1.0
HG13 A:ILE223 3.7 139.8 1.0
C A:CYS225 3.9 128.3 1.0
HD2 A:PRO263 4.1 125.1 1.0
N A:ALA227 4.1 114.7 1.0
H A:CYS228 4.2 125.4 1.0
HG2 A:PRO263 4.3 113.5 1.0
HB3 A:ALA227 4.3 123.7 1.0
CA A:GLY226 4.4 116.8 1.0
HA A:CYS225 4.4 153.0 1.0
H A:GLY224 4.5 144.7 1.0
CG1 A:ILE223 4.5 116.5 1.0
H A:ILE223 4.5 125.5 1.0
HG12 A:ILE223 4.5 139.8 1.0
C A:GLY224 4.6 125.6 1.0
HA2 A:GLY226 4.6 140.1 1.0
C A:GLY226 4.7 114.0 1.0
HA A:CYS262 4.7 124.0 1.0
HD13 A:ILE223 4.7 139.8 1.0
HD12 A:ILE223 4.8 139.8 1.0
N A:GLY224 4.8 120.6 1.0
CD A:PRO263 4.9 104.2 1.0
SG A:CYS262 4.9 86.6 1.0
CG A:PRO263 4.9 94.6 1.0
CD1 A:ILE223 4.9 116.5 1.0
HA2 A:GLY224 4.9 151.3 1.0

Iron binding site 9 out of 28 in 9f47

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Iron binding site 9 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 9 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe703

b:104.4
occ:1.00
FE3 A:SF4703 0.0 104.4 1.0
S1 A:SF4703 2.1 95.3 1.0
S4 A:SF4703 2.1 109.9 1.0
S2 A:SF4703 2.1 149.8 1.0
SG A:CYS262 2.3 86.6 1.0
HB3 A:ALA266 3.0 121.5 1.0
FE2 A:SF4703 3.0 157.1 1.0
FE1 A:SF4703 3.0 107.7 1.0
FE4 A:SF4703 3.0 144.1 1.0
HB2 A:CYS262 3.4 140.2 1.0
CB A:CYS262 3.4 116.8 1.0
HA A:CYS262 3.5 124.0 1.0
S3 A:SF4703 3.7 94.8 1.0
CB A:ALA266 3.8 101.2 1.0
HB2 A:ALA266 3.9 121.5 1.0
HG23 A:VAL264 3.9 118.2 1.0
HD12 A:ILE267 3.9 101.9 1.0
HB1 A:ALA266 4.0 121.5 1.0
CA A:CYS262 4.0 103.4 1.0
HD2 A:PRO263 4.0 125.1 1.0
HD11 A:ILE267 4.1 101.9 1.0
HB3 A:CYS262 4.2 140.2 1.0
H A:VAL264 4.3 134.5 1.0
CD1 A:ILE267 4.5 84.9 1.0
HA A:CYS222 4.6 132.6 1.0
HG13 A:ILE267 4.6 113.6 1.0
HB3 A:CYS228 4.6 133.6 1.0
HB2 A:CYS222 4.6 138.9 1.0
HG2 A:PRO263 4.6 113.5 1.0
H A:ALA266 4.7 132.9 1.0
CD A:PRO263 4.8 104.2 1.0
C A:CYS262 4.8 108.8 1.0
H A:ILE223 4.8 125.5 1.0
N A:PRO263 4.8 105.5 1.0
CG2 A:VAL264 4.8 98.5 1.0
HG23 A:ILE218 4.9 107.1 1.0
H A:CYS228 5.0 125.4 1.0
SG A:CYS222 5.0 108.5 1.0

Iron binding site 10 out of 28 in 9f47

Go back to Iron Binding Sites List in 9f47
Iron binding site 10 out of 28 in the Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 10 of Crystal Structure of [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe703

b:144.1
occ:1.00
FE4 A:SF4703 0.0 144.1 1.0
S2 A:SF4703 2.1 149.8 1.0
S3 A:SF4703 2.1 94.8 1.0
S1 A:SF4703 2.1 95.3 1.0
SG A:CYS222 2.3 108.5 1.0
H A:GLY224 2.9 144.7 1.0
FE1 A:SF4703 3.0 107.7 1.0
FE2 A:SF4703 3.0 157.1 1.0
FE3 A:SF4703 3.0 104.4 1.0
H A:ILE223 3.2 125.5 1.0
HB2 A:CYS222 3.2 138.9 1.0
CB A:CYS222 3.3 115.7 1.0
H A:CYS225 3.4 162.5 1.0
HD1 A:HIS245 3.4 129.6 1.0
HA A:CYS222 3.6 132.6 1.0
N A:GLY224 3.7 120.6 1.0
S4 A:SF4703 3.7 109.9 1.0
N A:ILE223 3.8 104.6 1.0
HA2 A:GLY224 3.8 151.3 1.0
CA A:CYS222 3.9 110.5 1.0
HG13 A:ILE223 4.0 139.8 1.0
ND1 A:HIS245 4.0 108.0 1.0
HB3 A:CYS222 4.1 138.9 1.0
N A:CYS225 4.1 135.4 1.0
C A:CYS222 4.2 114.8 1.0
CA A:GLY224 4.2 126.0 1.0
HG21 A:ILE218 4.3 107.1 1.0
HB2 A:HIS245 4.3 133.6 1.0
HB1 A:ALA266 4.3 121.5 1.0
HG23 A:ILE218 4.4 107.1 1.0
H A:HIS245 4.4 117.2 1.0
H A:GLY226 4.4 159.0 1.0
HB3 A:ALA266 4.5 121.5 1.0
HB3 A:CYS225 4.5 162.0 1.0
C A:ILE223 4.6 113.3 1.0
C A:GLY224 4.7 125.6 1.0
CG2 A:ILE218 4.7 89.3 1.0
CB A:ALA266 4.7 101.2 1.0
HB2 A:ALA266 4.7 121.5 1.0
HE1 A:HIS245 4.7 127.4 1.0
CE1 A:HIS245 4.8 106.2 1.0
CA A:ILE223 4.8 105.3 1.0
SG A:CYS228 4.9 106.8 1.0
HD13 A:ILE218 4.9 105.2 1.0
CG1 A:ILE223 4.9 116.5 1.0
CG A:HIS245 4.9 108.9 1.0
HG22 A:ILE218 4.9 107.1 1.0

Reference:

J.Duan, A.Rutz, A.Kawamoto, S.Naskar, K.Edenharter, S.Leimkuehler, E.Hofmann, T.Happe, G.Kurisu. A Zinc Binding Four-Helix Domain Stabilizes the Dimeric Structure of O2-Stable [Fefe]-Hydrogenase CBA5H From Clostridium Beijerinckii To Be Published.
Page generated: Sat Feb 8 19:40:33 2025

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