Iron in PDB 4ue6: Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Enzymatic activity of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
All present enzymatic activity of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase:
1.12.2.1;
Protein crystallography data
The structure of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase, PDB code: 4ue6
was solved by
A.Volbeda,
L.Martin,
P.-P.Liebgott,
J.C.Fontecilla-Camps,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
23.90 /
2.30
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
65.280,
99.550,
184.020,
90.00,
91.16,
90.00
|
R / Rfree (%)
|
15.066 /
18.141
|
Other elements in 4ue6:
The structure of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase also contains other interesting chemical elements:
Iron Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
20;
Page 3, Binding sites: 21 -
30;
Page 4, Binding sites: 31 -
36;
Binding sites:
The binding sites of Iron atom in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
(pdb code 4ue6). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 36 binding sites of Iron where determined in the
Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase, PDB code: 4ue6:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Iron binding site 1 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 1 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1265
b:26.1
occ:1.00
|
FE1
|
A:SF41265
|
0.0
|
26.1
|
1.0
|
SG
|
A:CYS218
|
2.2
|
25.2
|
1.0
|
S2
|
A:SF41265
|
2.3
|
23.9
|
1.0
|
S4
|
A:SF41265
|
2.3
|
26.4
|
1.0
|
S3
|
A:SF41265
|
2.3
|
24.7
|
1.0
|
FE3
|
A:SF41265
|
2.7
|
27.4
|
1.0
|
FE4
|
A:SF41265
|
2.7
|
25.3
|
1.0
|
FE2
|
A:SF41265
|
2.8
|
25.2
|
1.0
|
CB
|
A:CYS218
|
3.2
|
21.0
|
1.0
|
S1
|
A:SF41265
|
3.9
|
27.6
|
1.0
|
CG2
|
A:VAL239
|
4.4
|
19.1
|
1.0
|
CD
|
A:PRO221
|
4.5
|
19.7
|
1.0
|
N
|
A:GLY220
|
4.5
|
18.6
|
1.0
|
CA
|
A:CYS218
|
4.5
|
20.3
|
1.0
|
CA
|
A:GLY220
|
4.6
|
18.3
|
1.0
|
ND1
|
A:HIS184
|
4.6
|
26.9
|
1.0
|
SG
|
A:CYS212
|
4.7
|
23.1
|
1.0
|
N
|
A:TYR214
|
4.7
|
22.6
|
1.0
|
SG
|
A:CYS187
|
4.7
|
23.1
|
1.0
|
N
|
A:LEU213
|
4.8
|
21.9
|
1.0
|
C
|
A:CYS218
|
4.8
|
19.9
|
1.0
|
CB
|
A:LEU213
|
4.9
|
20.5
|
1.0
|
|
Iron binding site 2 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 2 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1265
b:25.2
occ:1.00
|
FE2
|
A:SF41265
|
0.0
|
25.2
|
1.0
|
S1
|
A:SF41265
|
2.3
|
27.6
|
1.0
|
SG
|
A:CYS212
|
2.3
|
23.1
|
1.0
|
S3
|
A:SF41265
|
2.3
|
24.7
|
1.0
|
S4
|
A:SF41265
|
2.3
|
26.4
|
1.0
|
FE3
|
A:SF41265
|
2.7
|
27.4
|
1.0
|
FE4
|
A:SF41265
|
2.7
|
25.3
|
1.0
|
FE1
|
A:SF41265
|
2.8
|
26.1
|
1.0
|
CB
|
A:CYS212
|
3.4
|
22.8
|
1.0
|
N
|
A:LEU213
|
3.7
|
21.9
|
1.0
|
CA
|
A:CYS212
|
3.8
|
23.0
|
1.0
|
S2
|
A:SF41265
|
3.9
|
23.9
|
1.0
|
N
|
A:TYR214
|
4.1
|
22.6
|
1.0
|
C
|
A:CYS212
|
4.2
|
23.0
|
1.0
|
CB
|
A:PHE193
|
4.3
|
21.3
|
1.0
|
CD2
|
A:PHE193
|
4.3
|
20.5
|
1.0
|
ND1
|
A:HIS184
|
4.5
|
26.9
|
1.0
|
CB
|
A:ARG189
|
4.5
|
23.2
|
1.0
|
CE1
|
A:HIS184
|
4.6
|
28.3
|
1.0
|
CB
|
A:TYR214
|
4.7
|
21.7
|
1.0
|
CG
|
A:PHE193
|
4.7
|
21.4
|
1.0
|
CA
|
A:LEU213
|
4.7
|
21.0
|
1.0
|
O
|
A:ARG189
|
4.8
|
27.5
|
1.0
|
SG
|
A:CYS218
|
4.8
|
25.2
|
1.0
|
C
|
A:LEU213
|
4.8
|
21.6
|
1.0
|
CA
|
A:TYR214
|
4.8
|
21.6
|
1.0
|
SG
|
A:CYS187
|
4.9
|
23.1
|
1.0
|
C
|
A:ARG189
|
4.9
|
26.9
|
1.0
|
CB
|
A:CYS218
|
5.0
|
21.0
|
1.0
|
|
Iron binding site 3 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 3 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1265
b:27.4
occ:1.00
|
FE3
|
A:SF41265
|
0.0
|
27.4
|
1.0
|
S4
|
A:SF41265
|
2.3
|
26.4
|
1.0
|
S2
|
A:SF41265
|
2.3
|
23.9
|
1.0
|
SG
|
A:CYS187
|
2.3
|
23.1
|
1.0
|
S1
|
A:SF41265
|
2.3
|
27.6
|
1.0
|
FE1
|
A:SF41265
|
2.7
|
26.1
|
1.0
|
FE4
|
A:SF41265
|
2.7
|
25.3
|
1.0
|
FE2
|
A:SF41265
|
2.7
|
25.2
|
1.0
|
CB
|
A:CYS187
|
3.1
|
21.4
|
1.0
|
S3
|
A:SF41265
|
3.9
|
24.7
|
1.0
|
CB
|
A:ARG189
|
3.9
|
23.2
|
1.0
|
CG1
|
A:VAL239
|
4.3
|
19.5
|
1.0
|
ND1
|
A:HIS184
|
4.4
|
26.9
|
1.0
|
CA
|
A:ARG189
|
4.6
|
25.1
|
1.0
|
CA
|
A:CYS187
|
4.6
|
21.2
|
1.0
|
C
|
A:ARG189
|
4.6
|
26.9
|
1.0
|
N
|
A:ARG189
|
4.6
|
23.9
|
1.0
|
CG2
|
A:VAL239
|
4.7
|
19.1
|
1.0
|
CG
|
A:ARG189
|
4.7
|
22.0
|
1.0
|
N
|
A:LEU190
|
4.7
|
26.7
|
1.0
|
SG
|
A:CYS218
|
4.7
|
25.2
|
1.0
|
SG
|
A:CYS212
|
4.9
|
23.1
|
1.0
|
C
|
A:CYS187
|
5.0
|
20.9
|
1.0
|
|
Iron binding site 4 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 4 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1265
b:25.3
occ:1.00
|
FE4
|
A:SF41265
|
0.0
|
25.3
|
1.0
|
ND1
|
A:HIS184
|
2.0
|
26.9
|
1.0
|
S2
|
A:SF41265
|
2.3
|
23.9
|
1.0
|
S3
|
A:SF41265
|
2.3
|
24.7
|
1.0
|
S1
|
A:SF41265
|
2.3
|
27.6
|
1.0
|
FE3
|
A:SF41265
|
2.7
|
27.4
|
1.0
|
FE1
|
A:SF41265
|
2.7
|
26.1
|
1.0
|
FE2
|
A:SF41265
|
2.7
|
25.2
|
1.0
|
CE1
|
A:HIS184
|
2.8
|
28.3
|
1.0
|
CG
|
A:HIS184
|
3.2
|
24.6
|
1.0
|
CB
|
A:HIS184
|
3.7
|
22.4
|
1.0
|
S4
|
A:SF41265
|
3.9
|
26.4
|
1.0
|
CA
|
A:HIS184
|
3.9
|
22.2
|
1.0
|
NE2
|
A:HIS184
|
4.0
|
26.5
|
1.0
|
CG
|
A:PRO221
|
4.2
|
20.6
|
1.0
|
CD2
|
A:HIS184
|
4.2
|
26.7
|
1.0
|
CD
|
A:PRO221
|
4.2
|
19.7
|
1.0
|
CB
|
A:CYS187
|
4.5
|
21.4
|
1.0
|
O
|
A:HIS184
|
4.5
|
25.7
|
1.0
|
CD2
|
A:PHE193
|
4.6
|
20.5
|
1.0
|
SG
|
A:CYS187
|
4.6
|
23.1
|
1.0
|
SG
|
A:CYS212
|
4.7
|
23.1
|
1.0
|
SG
|
A:CYS218
|
4.7
|
25.2
|
1.0
|
N
|
A:PRO221
|
4.7
|
20.2
|
1.0
|
C
|
A:HIS184
|
4.7
|
24.3
|
1.0
|
CA
|
A:GLY220
|
4.9
|
18.3
|
1.0
|
CG
|
A:PHE193
|
4.9
|
21.4
|
1.0
|
CB
|
A:PHE193
|
5.0
|
21.3
|
1.0
|
C
|
A:GLY220
|
5.0
|
20.0
|
1.0
|
|
Iron binding site 5 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 5 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 5 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1266
b:25.3
occ:1.00
|
FE1
|
A:F3S1266
|
0.0
|
25.3
|
1.0
|
S2
|
A:F3S1266
|
2.2
|
28.1
|
1.0
|
S1
|
A:F3S1266
|
2.2
|
24.5
|
1.0
|
S3
|
A:F3S1266
|
2.2
|
25.4
|
1.0
|
SG
|
A:CYS248
|
2.3
|
22.1
|
1.0
|
FE3
|
A:F3S1266
|
2.7
|
25.8
|
1.0
|
FE4
|
A:F3S1266
|
2.7
|
27.1
|
1.0
|
CB
|
A:CYS248
|
3.4
|
19.2
|
1.0
|
O
|
A:HOH2171
|
3.6
|
20.3
|
1.0
|
S4
|
A:F3S1266
|
3.8
|
27.2
|
1.0
|
N
|
A:CYS248
|
3.8
|
19.5
|
1.0
|
CA
|
A:CYS248
|
4.1
|
19.6
|
1.0
|
O
|
A:HOH2106
|
4.1
|
20.6
|
1.0
|
ND2
|
A:ASN225
|
4.6
|
18.7
|
1.0
|
C
|
A:CYS248
|
4.6
|
21.1
|
1.0
|
N
|
A:SER249
|
4.6
|
20.8
|
1.0
|
SG
|
A:CYS245
|
4.7
|
20.7
|
1.0
|
SG
|
A:CYS227
|
4.8
|
22.3
|
1.0
|
O
|
A:HOH2105
|
4.9
|
24.6
|
1.0
|
CE
|
Q:LYS225
|
5.0
|
19.8
|
1.0
|
C
|
A:GLY247
|
5.0
|
19.3
|
1.0
|
|
Iron binding site 6 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 6 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 6 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1266
b:25.8
occ:1.00
|
FE3
|
A:F3S1266
|
0.0
|
25.8
|
1.0
|
S4
|
A:F3S1266
|
2.2
|
27.2
|
1.0
|
S1
|
A:F3S1266
|
2.2
|
24.5
|
1.0
|
S3
|
A:F3S1266
|
2.3
|
25.4
|
1.0
|
SG
|
A:CYS245
|
2.3
|
20.7
|
1.0
|
FE1
|
A:F3S1266
|
2.7
|
25.3
|
1.0
|
FE4
|
A:F3S1266
|
2.8
|
27.1
|
1.0
|
CB
|
A:CYS245
|
3.2
|
19.6
|
1.0
|
CA
|
A:CYS245
|
3.7
|
19.3
|
1.0
|
S2
|
A:F3S1266
|
3.9
|
28.1
|
1.0
|
N
|
A:LEU246
|
3.9
|
19.3
|
1.0
|
N
|
A:GLY247
|
4.1
|
18.6
|
1.0
|
C
|
A:CYS245
|
4.2
|
19.5
|
1.0
|
N
|
A:CYS248
|
4.5
|
19.5
|
1.0
|
CG2
|
A:THR223
|
4.6
|
18.4
|
1.0
|
CA
|
A:GLY247
|
4.7
|
18.7
|
1.0
|
CG2
|
A:VAL183
|
4.8
|
20.0
|
1.0
|
SG
|
A:CYS248
|
4.8
|
22.1
|
1.0
|
SG
|
A:CYS227
|
4.8
|
22.3
|
1.0
|
NE2
|
Q:GLN230
|
4.9
|
19.9
|
1.0
|
|
Iron binding site 7 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 7 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 7 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1266
b:27.1
occ:1.00
|
FE4
|
A:F3S1266
|
0.0
|
27.1
|
1.0
|
S2
|
A:F3S1266
|
2.2
|
28.1
|
1.0
|
S3
|
A:F3S1266
|
2.2
|
25.4
|
1.0
|
S4
|
A:F3S1266
|
2.2
|
27.2
|
1.0
|
SG
|
A:CYS227
|
2.3
|
22.3
|
1.0
|
FE1
|
A:F3S1266
|
2.7
|
25.3
|
1.0
|
FE3
|
A:F3S1266
|
2.8
|
25.8
|
1.0
|
CB
|
A:CYS227
|
3.4
|
20.0
|
1.0
|
S1
|
A:F3S1266
|
3.9
|
24.5
|
1.0
|
ND2
|
A:ASN225
|
4.0
|
18.7
|
1.0
|
CE2
|
A:PHE232
|
4.3
|
17.8
|
1.0
|
O
|
A:HOH2106
|
4.3
|
20.6
|
1.0
|
CZ
|
A:PHE232
|
4.5
|
17.9
|
1.0
|
CG
|
A:ASN225
|
4.5
|
19.7
|
1.0
|
CB
|
A:ASN225
|
4.6
|
19.5
|
1.0
|
CG2
|
A:VAL183
|
4.6
|
20.0
|
1.0
|
CA
|
A:CYS227
|
4.8
|
22.4
|
1.0
|
SG
|
A:CYS248
|
4.8
|
22.1
|
1.0
|
SG
|
A:CYS245
|
4.8
|
20.7
|
1.0
|
CD
|
A:PRO238
|
5.0
|
20.1
|
1.0
|
|
Iron binding site 8 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 8 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 8 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1267
b:24.1
occ:1.00
|
FE1
|
A:SF41267
|
0.0
|
24.1
|
1.0
|
S3
|
A:SF41267
|
2.3
|
24.0
|
1.0
|
SG
|
A:CYS17
|
2.3
|
19.1
|
1.0
|
S2
|
A:SF41267
|
2.3
|
23.7
|
1.0
|
S4
|
A:SF41267
|
2.3
|
25.1
|
1.0
|
FE2
|
A:SF41267
|
2.7
|
23.1
|
1.0
|
FE4
|
A:SF41267
|
2.7
|
25.9
|
1.0
|
FE3
|
A:SF41267
|
2.8
|
23.4
|
1.0
|
CB
|
A:CYS17
|
3.3
|
18.6
|
1.0
|
N
|
A:CYS17
|
3.7
|
20.1
|
1.0
|
S1
|
A:SF41267
|
3.9
|
24.5
|
1.0
|
CA
|
A:CYS17
|
3.9
|
20.6
|
1.0
|
N
|
A:GLY19
|
4.0
|
19.2
|
1.0
|
NE2
|
Q:HIS228
|
4.2
|
17.7
|
1.0
|
CA
|
A:GLY19
|
4.3
|
18.3
|
1.0
|
N
|
A:THR18
|
4.4
|
20.2
|
1.0
|
C
|
A:CYS17
|
4.4
|
20.7
|
1.0
|
N
|
A:CYS20
|
4.6
|
17.2
|
1.0
|
O
|
A:HOH2013
|
4.6
|
22.3
|
1.0
|
SG
|
A:CYS147
|
4.7
|
18.7
|
1.0
|
SG
|
A:CYS114
|
4.8
|
22.8
|
1.0
|
C
|
A:GLU16
|
4.8
|
21.2
|
1.0
|
C
|
A:GLY19
|
4.9
|
19.0
|
1.0
|
CG
|
Q:ARG70
|
4.9
|
18.3
|
1.0
|
CD2
|
Q:HIS228
|
4.9
|
18.6
|
1.0
|
SG
|
A:CYS20
|
4.9
|
22.2
|
1.0
|
|
Iron binding site 9 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 9 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 9 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1267
b:23.1
occ:1.00
|
FE2
|
A:SF41267
|
0.0
|
23.1
|
1.0
|
SG
|
A:CYS147
|
2.2
|
18.7
|
1.0
|
S4
|
A:SF41267
|
2.3
|
25.1
|
1.0
|
S1
|
A:SF41267
|
2.3
|
24.5
|
1.0
|
S3
|
A:SF41267
|
2.3
|
24.0
|
1.0
|
FE4
|
A:SF41267
|
2.7
|
25.9
|
1.0
|
FE1
|
A:SF41267
|
2.7
|
24.1
|
1.0
|
FE3
|
A:SF41267
|
2.8
|
23.4
|
1.0
|
CB
|
A:CYS147
|
3.4
|
16.1
|
1.0
|
CA
|
A:CYS147
|
3.4
|
17.4
|
1.0
|
O
|
A:HOH2087
|
3.8
|
19.3
|
1.0
|
S2
|
A:SF41267
|
3.9
|
23.7
|
1.0
|
C
|
A:CYS147
|
3.9
|
17.7
|
1.0
|
O
|
A:CYS147
|
4.3
|
16.4
|
1.0
|
CG
|
Q:ARG70
|
4.3
|
18.3
|
1.0
|
N
|
A:PRO148
|
4.4
|
18.8
|
1.0
|
SG
|
A:CYS114
|
4.4
|
22.8
|
1.0
|
CD2
|
Q:HIS228
|
4.6
|
18.6
|
1.0
|
NE2
|
Q:HIS228
|
4.6
|
17.7
|
1.0
|
SG
|
A:CYS17
|
4.6
|
19.1
|
1.0
|
O
|
A:GLY146
|
4.6
|
20.4
|
1.0
|
CA
|
A:PRO148
|
4.6
|
17.8
|
1.0
|
NE
|
Q:ARG70
|
4.7
|
19.5
|
1.0
|
N
|
A:CYS147
|
4.8
|
18.5
|
1.0
|
SG
|
A:CYS20
|
4.9
|
22.2
|
1.0
|
|
Iron binding site 10 out
of 36 in 4ue6
Go back to
Iron Binding Sites List in 4ue6
Iron binding site 10 out
of 36 in the Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 10 of Structure of Methylene Blue-Treated Anaerobically Purified D. Fructosovorans Nife-Hydrogenase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1267
b:23.4
occ:1.00
|
FE3
|
A:SF41267
|
0.0
|
23.4
|
1.0
|
S4
|
A:SF41267
|
2.3
|
25.1
|
1.0
|
S1
|
A:SF41267
|
2.3
|
24.5
|
1.0
|
SG
|
A:CYS20
|
2.3
|
22.2
|
1.0
|
S2
|
A:SF41267
|
2.3
|
23.7
|
1.0
|
FE1
|
A:SF41267
|
2.8
|
24.1
|
1.0
|
FE4
|
A:SF41267
|
2.8
|
25.9
|
1.0
|
FE2
|
A:SF41267
|
2.8
|
23.1
|
1.0
|
CB
|
A:CYS20
|
3.5
|
19.9
|
1.0
|
N
|
A:CYS20
|
3.6
|
17.2
|
1.0
|
O
|
A:HOH2063
|
3.8
|
15.7
|
1.0
|
CA
|
A:CYS20
|
4.0
|
18.2
|
1.0
|
S3
|
A:SF41267
|
4.0
|
24.0
|
1.0
|
CB
|
A:PRO148
|
4.2
|
17.4
|
1.0
|
CA
|
A:PRO148
|
4.4
|
17.8
|
1.0
|
C
|
A:GLY19
|
4.4
|
19.0
|
1.0
|
CA
|
A:GLY112
|
4.4
|
18.4
|
1.0
|
CA
|
A:GLY19
|
4.7
|
18.3
|
1.0
|
O
|
A:GLY146
|
4.8
|
20.4
|
1.0
|
SG
|
A:CYS17
|
4.8
|
19.1
|
1.0
|
N
|
A:GLY19
|
4.8
|
19.2
|
1.0
|
CA
|
A:CYS147
|
4.8
|
17.4
|
1.0
|
N
|
A:PRO148
|
4.9
|
18.8
|
1.0
|
SG
|
A:CYS147
|
4.9
|
18.7
|
1.0
|
SG
|
A:CYS114
|
5.0
|
22.8
|
1.0
|
|
Reference:
A.Volbeda,
L.Martin,
P.-P.Liebgott,
A.L.De Lacey,
J.C.Fontecilla-Camps.
[Nife]-Hydrogenases Revisited: Nickel-Carboxamido Bond Formation in A Variant with Accrued O2-Tolerance and A Tentative Re-Interpretation of Ni-Si States. Metallomics 2015.
ISSN: ESSN 1756-591X
PubMed: 25780984
DOI: 10.1039/C4MT00309H
Page generated: Mon Aug 5 12:37:03 2024
|