Zinc in PDB 8q0f: Inward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm.

All present enzymatic activity of Inward-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 Inward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm. also contains other interesting chemical elements:

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

The binding sites of Zinc atom in the Inward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm. (pdb code 8q0f). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Inward-Facing, OPEN2 Proteoliposome Complex I at 3.1 A. Initially Purified in Ddm., PDB code: 8q0f:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in the Inward-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 Inward-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:92.7 occ:1.00 NE2 M:HIS82 2.3 48.3 1.0 NE2 M:HIS338 2.3 54.8 1.0 O M:GLU335 3.1 49.6 1.0 CD2 M:HIS82 3.2 48.3 1.0 CD2 M:HIS338 3.2 54.8 1.0 CE1 M:HIS338 3.3 54.8 1.0 CE1 M:HIS82 3.4 48.3 1.0 CA M:GLU335 3.7 49.6 1.0 C M:GLU335 3.9 49.6 1.0 CB M:GLU335 4.0 49.6 1.0 OD1 g:ASP34 4.0 70.2 1.0 OD2 g:ASP34 4.3 70.2 1.0 CG M:GLU335 4.3 49.6 1.0 CG M:HIS82 4.4 48.3 1.0 CG g:ASP34 4.4 70.2 1.0 ND1 M:HIS338 4.4 54.8 1.0 CG M:HIS338 4.4 54.8 1.0 ND1 M:HIS82 4.4 48.3 1.0

Zinc binding site 2 out of 2 in the Inward-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 Inward-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:48.3 occ:1.00 NE2 R:HIS68 2.1 25.2 1.0 SG R:CYS87 2.2 28.9 1.0 SG R:CYS84 2.2 31.2 1.0 SG R:CYS59 2.4 30.1 1.0 CE1 R:HIS68 2.8 25.2 1.0 CD2 R:HIS68 3.2 25.2 1.0 CB R:CYS84 3.3 31.2 1.0 CB R:CYS87 3.3 28.9 1.0 CB R:CYS59 3.5 30.1 1.0 N R:GLY61 3.6 27.1 1.0 N R:CYS87 3.7 28.9 1.0 ND1 R:HIS68 4.0 25.2 1.0 CA R:GLY61 4.0 27.1 1.0 CA R:CYS87 4.1 28.9 1.0 CG R:HIS68 4.2 25.2 1.0 C R:CYS59 4.4 30.1 1.0 N R:ASP60 4.4 27.2 1.0 C R:ASP60 4.5 27.2 1.0 CA R:CYS59 4.5 30.1 1.0 CB R:TYR86 4.6 24.4 1.0 CA R:CYS84 4.7 31.2 1.0 CA R:ASP60 4.7 27.2 1.0 O R:CYS59 4.8 30.1 1.0 C R:TYR86 4.8 24.4 1.0 C R:CYS87 4.9 28.9 1.0 N R:TYR86 5.0 24.4 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