Zinc in PDB 8q0o: Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm.

All present enzymatic activity of Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm.:
1.6.5.3; 1.6.99.3; 7.1.1.2;

The structure of Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm. also contains other interesting chemical elements:

Iron	(Fe)	28 atoms
Potassium	(K)	1 atom
Magnesium	(Mg)	1 atom

The binding sites of Zinc atom in the Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm. (pdb code 8q0o). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm., PDB code: 8q0o:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in the Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm.


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm. within 5.0Å range: probe atom residue distance (Å) B Occ M:Zn601 b:92.1 occ:1.00 NE2 M:HIS338 2.3 48.9 1.0 NE2 M:HIS82 2.3 43.3 1.0 CD2 M:HIS82 2.9 43.3 1.0 CD2 M:HIS338 3.1 48.9 1.0 CE1 M:HIS338 3.2 48.9 1.0 CE1 M:HIS82 3.5 43.3 1.0 OD2 g:ASP34 3.5 70.3 1.0 O M:GLU335 3.8 46.2 1.0 CA M:GLU335 4.0 46.2 1.0 CG M:HIS338 4.2 48.9 1.0 CG M:HIS82 4.2 43.3 1.0 ND1 M:HIS338 4.2 48.9 1.0 C M:GLU335 4.3 46.2 1.0 CG g:ASP34 4.4 70.3 1.0 ND1 M:HIS82 4.4 43.3 1.0 CG M:GLU335 4.4 46.2 1.0 CB M:GLU335 4.5 46.2 1.0 OD1 g:ASP34 4.7 70.3 1.0 CE2 M:TYR334 4.8 42.0 1.0 O M:TYR334 4.9 42.0 1.0

Zinc binding site 2 out of 2 in the Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm.


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Outward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm. within 5.0Å range: probe atom residue distance (Å) B Occ R:Zn201 b:39.7 occ:1.00 NE2 R:HIS68 2.0 20.1 1.0 SG R:CYS87 2.2 22.7 1.0 SG R:CYS84 2.2 25.9 1.0 SG R:CYS59 2.3 24.3 1.0 CE1 R:HIS68 2.8 20.1 1.0 CD2 R:HIS68 3.2 20.1 1.0 CB R:CYS84 3.3 25.9 1.0 CB R:CYS87 3.3 22.7 1.0 CB R:CYS59 3.4 24.3 1.0 N R:GLY61 3.8 21.5 1.0 N R:CYS87 3.8 22.7 1.0 ND1 R:HIS68 3.9 20.1 1.0 CA R:CYS87 4.1 22.7 1.0 CG R:HIS68 4.2 20.1 1.0 CA R:GLY61 4.2 21.5 1.0 C R:CYS59 4.4 24.3 1.0 N R:ASP60 4.5 21.5 1.0 CA R:CYS59 4.5 24.3 1.0 CA R:CYS84 4.7 25.9 1.0 C R:ASP60 4.7 21.5 1.0 CB R:TYR86 4.8 18.1 1.0 O R:CYS59 4.8 24.3 1.0 C R:CYS87 4.9 22.7 1.0 C R:TYR86 4.9 18.1 1.0 CA R:ASP60 4.9 21.5 1.0 N R:GLY88 5.0 26.9 1.0

D.N.Grba, J.J.Wright, W.Fisher, Z.Yin, J.Hirst. Molecular Mechanism of the Ischemia-Induced Regulatory Switch in Mammalian Complex I Science 2024.
ISSN: ESSN 1095-9203
DOI: 10.1126/SCIENCE.ADO2075