Atomistry » Iron » PDB 8py6-8qbq » 8q25
Atomistry »
  Iron »
    PDB 8py6-8qbq »
      8q25 »

Iron in PDB 8q25: Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.

Enzymatic activity of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.

All present enzymatic activity of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.:
1.6.5.3; 1.6.99.3; 7.1.1.2;

Other elements in 8q25:

The structure of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. also contains other interesting chemical elements:

Potassium (K) 1 atom
Zinc (Zn) 2 atoms
Magnesium (Mg) 1 atom

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 Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. (pdb code 8q25). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 28 binding sites of Iron where determined in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng., PDB code: 8q25:
Jump to Iron binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Iron binding site 1 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 1 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe201

b:23.0
occ:1.00
FE1 B:SF4201 0.0 23.0 1.0
SG B:CYS119 2.2 21.7 1.0
S3 B:SF4201 2.3 23.0 1.0
S4 B:SF4201 2.3 23.0 1.0
S2 B:SF4201 2.3 23.0 1.0
FE3 B:SF4201 2.7 23.0 1.0
FE2 B:SF4201 2.7 23.0 1.0
FE4 B:SF4201 2.7 23.0 1.0
CB B:CYS119 3.2 21.7 1.0
S1 B:SF4201 3.9 23.0 1.0
N B:CYS119 4.0 21.7 1.0
OG1 B:THR91 4.1 24.7 1.0
CA B:CYS119 4.2 21.7 1.0
SG B:CYS149 4.5 20.2 1.0
CQ2 D:2MR85 4.6 25.2 1.0
SG B:CYS54 4.8 24.6 1.0
SG B:CYS55 4.8 24.8 1.0
CE2 B:TYR126 4.8 24.4 1.0
N B:THR91 5.0 24.7 1.0

Iron binding site 2 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 2 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe201

b:23.0
occ:1.00
FE2 B:SF4201 0.0 23.0 1.0
SG B:CYS149 2.3 20.2 1.0
S1 B:SF4201 2.3 23.0 1.0
S4 B:SF4201 2.3 23.0 1.0
S3 B:SF4201 2.3 23.0 1.0
FE4 B:SF4201 2.7 23.0 1.0
FE1 B:SF4201 2.7 23.0 1.0
FE3 B:SF4201 2.7 23.0 1.0
CB B:CYS149 3.5 20.2 1.0
CA B:CYS149 3.6 20.2 1.0
C B:CYS149 3.8 20.2 1.0
S2 B:SF4201 3.9 23.0 1.0
O B:CYS149 4.1 20.2 1.0
NE D:ARG105 4.2 21.6 1.0
N B:PRO150 4.2 21.2 1.0
CD2 D:HIS190 4.5 21.5 1.0
NE2 D:HIS190 4.6 21.5 1.0
NH2 D:ARG105 4.6 21.6 1.0
CA B:PRO150 4.6 21.2 1.0
SG B:CYS55 4.7 24.8 1.0
SG B:CYS119 4.7 21.7 1.0
SG B:CYS54 4.8 24.6 1.0
CZ D:ARG105 4.8 21.6 1.0
CD B:PRO150 4.9 21.2 1.0
N B:CYS149 4.9 20.2 1.0

Iron binding site 3 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 3 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe201

b:23.0
occ:1.00
FE3 B:SF4201 0.0 23.0 1.0
SG B:CYS54 2.3 24.6 1.0
S1 B:SF4201 2.3 23.0 1.0
S4 B:SF4201 2.3 23.0 1.0
S2 B:SF4201 2.3 23.0 1.0
FE1 B:SF4201 2.7 23.0 1.0
FE4 B:SF4201 2.7 23.0 1.0
FE2 B:SF4201 2.7 23.0 1.0
CB B:CYS54 3.2 24.6 1.0
CQ2 D:2MR85 3.8 25.2 1.0
N B:CYS54 3.9 24.6 1.0
S3 B:SF4201 3.9 23.0 1.0
NE2 D:HIS190 4.0 21.5 1.0
CA B:CYS54 4.0 24.6 1.0
N B:CYS55 4.1 24.8 1.0
C B:CYS54 4.4 24.6 1.0
CG D:ARG105 4.4 21.6 1.0
CD2 D:HIS190 4.7 21.5 1.0
CB B:ALA53 4.7 26.6 1.0
SG B:CYS119 4.8 21.7 1.0
SG B:CYS55 4.8 24.8 1.0
NE D:ARG105 4.9 21.6 1.0
SG B:CYS149 4.9 20.2 1.0
NH2 D:2MR85 4.9 25.2 1.0
C B:ALA53 4.9 26.6 1.0
CD D:ARG105 5.0 21.6 1.0
CE1 D:HIS190 5.0 21.5 1.0

Iron binding site 4 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 4 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe201

b:23.0
occ:1.00
FE4 B:SF4201 0.0 23.0 1.0
SG B:CYS55 2.3 24.8 1.0
S2 B:SF4201 2.3 23.0 1.0
S3 B:SF4201 2.3 23.0 1.0
S1 B:SF4201 2.3 23.0 1.0
FE2 B:SF4201 2.7 23.0 1.0
FE3 B:SF4201 2.7 23.0 1.0
FE1 B:SF4201 2.7 23.0 1.0
CB B:CYS55 3.3 24.8 1.0
N B:CYS55 3.6 24.8 1.0
CA B:CYS55 3.8 24.8 1.0
S4 B:SF4201 3.9 23.0 1.0
CB B:PRO150 4.4 21.2 1.0
CA B:PRO150 4.5 21.2 1.0
C B:CYS54 4.5 24.6 1.0
SG B:CYS54 4.7 24.6 1.0
SG B:CYS149 4.8 20.2 1.0
CB B:CYS54 4.8 24.6 1.0
CA B:GLY117 4.8 21.4 1.0
SG B:CYS119 4.8 21.7 1.0
CA B:CYS149 4.8 20.2 1.0
N B:PRO150 4.8 21.2 1.0
CB B:CYS119 4.9 21.7 1.0
N B:CYS54 4.9 24.6 1.0
CA B:CYS54 5.0 24.6 1.0

Iron binding site 5 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 5 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 5 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Fe301

b:51.8
occ:1.00
FE1 E:FES301 0.0 51.8 1.0
S2 E:FES301 2.2 51.8 1.0
S1 E:FES301 2.2 51.8 1.0
SG E:CYS108 2.3 49.1 1.0
SG E:CYS103 2.3 50.5 1.0
FE2 E:FES301 2.7 51.8 1.0
CB E:CYS108 3.3 49.1 1.0
CB E:CYS103 3.3 50.5 1.0
N E:CYS108 4.2 49.1 1.0
CA E:CYS144 4.2 48.0 1.0
CA E:CYS108 4.3 49.1 1.0
N E:LEU145 4.4 50.9 1.0
SG E:CYS144 4.6 48.0 1.0
CA E:CYS103 4.7 50.5 1.0
CB E:CYS144 4.7 48.0 1.0
SG E:CYS148 4.8 50.8 1.0
CB E:THR105 4.8 45.5 1.0
OG1 E:THR105 4.8 45.5 1.0
CA E:CYS148 4.9 50.8 1.0
N E:THR105 4.9 45.5 1.0
CG E:MET153 4.9 54.9 1.0
C E:CYS103 4.9 50.5 1.0
C E:CYS144 4.9 48.0 1.0

Iron binding site 6 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 6 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 6 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Fe301

b:51.8
occ:1.00
FE2 E:FES301 0.0 51.8 1.0
S2 E:FES301 2.2 51.8 1.0
S1 E:FES301 2.2 51.8 1.0
SG E:CYS148 2.3 50.8 1.0
SG E:CYS144 2.3 48.0 1.0
FE1 E:FES301 2.7 51.8 1.0
CB E:CYS144 3.3 48.0 1.0
CB E:CYS148 3.3 50.8 1.0
CA E:CYS148 3.6 50.8 1.0
CA E:CYS144 3.7 48.0 1.0
N E:CYS148 3.7 50.8 1.0
N E:LEU145 4.0 50.9 1.0
C E:CYS144 4.3 48.0 1.0
N E:ALA147 4.3 52.1 1.0
N E:GLY146 4.3 49.8 1.0
SG E:CYS103 4.3 50.5 1.0
C E:ALA147 4.4 52.1 1.0
SG E:CYS108 4.5 49.1 1.0
N F:GLY103 4.6 47.9 1.0
O E:ALA147 4.9 52.1 1.0
CA E:GLY146 4.9 49.8 1.0
CB E:PRO107 5.0 47.3 1.0
CA E:ALA147 5.0 52.1 1.0
N E:CYS144 5.0 48.0 1.0

Iron binding site 7 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 7 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 7 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Fe501

b:31.2
occ:1.00
FE1 F:SF4501 0.0 31.2 1.0
SG F:CYS359 2.3 33.1 1.0
S3 F:SF4501 2.3 31.2 1.0
S2 F:SF4501 2.3 31.2 1.0
S4 F:SF4501 2.3 31.2 1.0
FE2 F:SF4501 2.7 31.2 1.0
FE4 F:SF4501 2.7 31.2 1.0
FE3 F:SF4501 2.7 31.2 1.0
CB F:CYS359 3.3 33.1 1.0
N F:CYS359 3.8 33.1 1.0
S1 F:SF4501 3.9 31.2 1.0
CA F:CYS359 3.9 33.1 1.0
N F:GLN361 3.9 30.7 1.0
CB F:GLN361 4.0 30.7 1.0
N F:GLY360 4.1 31.0 1.0
C F:CYS359 4.2 33.1 1.0
CD F:PRO203 4.3 35.8 1.0
CA F:GLN361 4.5 30.7 1.0
N F:CYS362 4.6 28.9 1.0
NE2 F:GLN361 4.6 30.7 1.0
SG F:CYS365 4.8 29.9 1.0
CG F:PRO203 4.8 35.8 1.0
SG F:CYS405 4.8 32.7 1.0
OG F:SER358 4.9 33.5 1.0
SG F:CYS362 4.9 28.9 1.0
C F:GLY360 5.0 31.0 1.0
O F:CYS359 5.0 33.1 1.0

Iron binding site 8 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 8 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 8 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Fe501

b:31.2
occ:1.00
FE2 F:SF4501 0.0 31.2 1.0
SG F:CYS365 2.2 29.9 1.0
S1 F:SF4501 2.3 31.2 1.0
S3 F:SF4501 2.3 31.2 1.0
S4 F:SF4501 2.3 31.2 1.0
FE4 F:SF4501 2.7 31.2 1.0
FE1 F:SF4501 2.7 31.2 1.0
FE3 F:SF4501 2.7 31.2 1.0
CB F:CYS365 3.0 29.9 1.0
OG F:SER358 3.4 33.5 1.0
S2 F:SF4501 3.9 31.2 1.0
N F:CYS359 4.3 33.1 1.0
CA F:CYS365 4.3 29.9 1.0
CB F:SER358 4.5 33.5 1.0
SG F:CYS362 4.5 28.9 1.0
C F:CYS365 4.6 29.9 1.0
CD2 F:LEU407 4.6 36.4 1.0
CA F:SER358 4.7 33.5 1.0
SG F:CYS405 4.7 32.7 1.0
SG F:CYS359 4.8 33.1 1.0
CB F:LEU407 4.9 36.4 1.0
N F:ARG366 4.9 28.4 1.0
N F:GLY360 4.9 31.0 1.0
N F:GLY408 4.9 35.3 1.0
C F:SER358 5.0 33.5 1.0

Iron binding site 9 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 9 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 9 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Fe501

b:31.2
occ:1.00
FE3 F:SF4501 0.0 31.2 1.0
S1 F:SF4501 2.3 31.2 1.0
S4 F:SF4501 2.3 31.2 1.0
S2 F:SF4501 2.3 31.2 1.0
SG F:CYS405 2.3 32.7 1.0
FE2 F:SF4501 2.7 31.2 1.0
FE1 F:SF4501 2.7 31.2 1.0
FE4 F:SF4501 2.7 31.2 1.0
CB F:CYS405 3.4 32.7 1.0
S3 F:SF4501 3.9 31.2 1.0
N F:CYS405 4.0 32.7 1.0
CA F:CYS405 4.1 32.7 1.0
CB F:LEU407 4.2 36.4 1.0
CG F:PRO203 4.3 35.8 1.0
C F:CYS405 4.4 32.7 1.0
O F:CYS405 4.5 32.7 1.0
CD1 F:ILE185 4.5 38.0 1.0
CD F:PRO203 4.7 35.8 1.0
N F:LEU407 4.8 36.4 1.0
SG F:CYS365 4.8 29.9 1.0
SG F:CYS359 4.8 33.1 1.0
SG F:CYS362 4.8 28.9 1.0
N F:GLY408 4.9 35.3 1.0

Iron binding site 10 out of 28 in 8q25

Go back to Iron Binding Sites List in 8q25
Iron binding site 10 out of 28 in the Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 10 of Outward-Facing, OPEN1 Proteoliposome Complex I at 2.8 A, After Deactivation Treatment. Initially Purified in Lmng. within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Fe501

b:31.2
occ:1.00
FE4 F:SF4501 0.0 31.2 1.0
S3 F:SF4501 2.3 31.2 1.0
S1 F:SF4501 2.3 31.2 1.0
S2 F:SF4501 2.3 31.2 1.0
SG F:CYS362 2.3 28.9 1.0
FE2 F:SF4501 2.7 31.2 1.0
FE1 F:SF4501 2.7 31.2 1.0
FE3 F:SF4501 2.7 31.2 1.0
CB F:CYS362 3.4 28.9 1.0
N F:CYS362 3.7 28.9 1.0
S4 F:SF4501 3.9 31.2 1.0
CA F:CYS362 4.0 28.9 1.0
O F:CYS362 4.2 28.9 1.0
CB F:CYS365 4.3 29.9 1.0
N F:ILE404 4.3 30.4 1.0
CB F:ILE404 4.4 30.4 1.0
C F:CYS362 4.5 28.9 1.0
SG F:CYS365 4.6 29.9 1.0
CG1 F:ILE404 4.6 30.4 1.0
CB F:GLN361 4.7 30.7 1.0
CB F:THR403 4.7 30.3 1.0
N F:CYS405 4.7 32.7 1.0
SG F:CYS359 4.8 33.1 1.0
C F:GLN361 4.8 30.7 1.0
SG F:CYS405 4.9 32.7 1.0
CD1 F:ILE404 4.9 30.4 1.0
N F:GLN361 4.9 30.7 1.0
CA F:ILE404 4.9 30.4 1.0

Reference:

D.N.Grba, J.J.Wright, W.Fisher, Z.Yin, J.Hirst. Structure of Complex I Embedded in Liposomes Reveals Mechanism of Active/Deactive Transition Science 2024.
ISSN: ESSN 1095-9203
DOI: 10.1126/SCIENCE.ADO2075
Page generated: Thu Aug 7 20:39:24 2025

Last articles

Mg in 9MO5
Mg in 9MO4
Mg in 9MMI
Mg in 9MM6
Mg in 9MM2
Mg in 9MHS
Mg in 9MJ5
Mg in 9MHG
Mg in 9MHH
Mg in 9MHF
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy