Nickel in PDB 3m1v: Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues

All present enzymatic activity of Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues:
2.8.4.1;

The structure of Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues, PDB code: 3m1v was solved by P.E.Cedervall, M.Dey, S.W.Ragsdale, C.M.Wilmot, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	20.15 / 1.45
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	82.016, 118.260, 122.387, 90.00, 91.84, 90.00
R / Rfree (%)	13.5 / 16.2

The structure of Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues also contains other interesting chemical elements:

Magnesium	(Mg)	9 atoms
Zinc	(Zn)	1 atom

The binding sites of Nickel atom in the Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues (pdb code 3m1v). This binding sites where shown within 5.0 Angstroms radius around Nickel atom.
In total 2 binding sites of Nickel where determined in the Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues, PDB code: 3m1v:
Jump to Nickel binding site number: 1; 2;

Nickel binding site 1 out of 2 in the Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues


Mono view


Stereo pair view

A full contact list of Nickel with other atoms in the Ni binding site number 1 of Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues within 5.0Å range: probe atom residue distance (Å) B Occ A:Ni1 b:6.7 occ:1.00 NI A:F431 0.0 6.7 1.0 NC A:F431 2.1 5.8 1.0 ND A:F431 2.1 6.5 1.0 NB A:F431 2.1 6.0 1.0 NA A:F431 2.1 5.1 1.0 OE1 A:GLN147 2.3 9.3 1.0 S1 D:COM554 2.4 7.8 1.0 C4B A:F431 3.0 6.6 1.0 C1A A:F431 3.0 4.5 1.0 C1C A:F431 3.0 7.3 1.0 C1D A:F431 3.1 6.2 1.0 C4D A:F431 3.1 7.2 1.0 C4C A:F431 3.1 7.0 1.0 C1B A:F431 3.2 6.1 1.0 C1 D:COM554 3.3 9.2 1.0 C4A A:F431 3.3 5.6 1.0 CHC A:F431 3.3 5.1 1.0 CD A:GLN147 3.4 8.2 1.0 CHA A:F431 3.4 6.3 1.0 CHB A:F431 3.5 5.3 1.0 CHD A:F431 3.5 6.3 1.0 NE2 A:GLN147 3.8 9.2 1.0 N5B A:F431 3.9 6.5 1.0 C2 D:COM554 4.1 7.1 1.0 OH E:TYR367 4.1 7.7 0.8 C3A A:F431 4.3 6.3 1.0 OH D:TYR333 4.4 7.7 1.0 C2A A:F431 4.4 5.4 1.0 C3B A:F431 4.4 5.9 1.0 C3D A:F431 4.4 5.9 1.0 C2D A:F431 4.4 6.8 1.0 C2C A:F431 4.4 6.7 1.0 C3C A:F431 4.4 7.6 1.0 C2B A:F431 4.5 6.8 1.0 CAA A:F431 4.7 7.2 1.0 CG A:GLN147 4.7 7.0 1.0 CAB A:F431 4.9 7.5 1.0 C7D A:F431 5.0 8.6 1.0

Nickel binding site 2 out of 2 in the Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues


Mono view


Stereo pair view

A full contact list of Nickel with other atoms in the Ni binding site number 2 of Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues within 5.0Å range: probe atom residue distance (Å) B Occ D:Ni552 b:7.1 occ:1.00 NI D:F43552 0.0 7.1 1.0 ND D:F43552 2.0 6.8 1.0 NC D:F43552 2.1 6.5 1.0 NA D:F43552 2.1 5.9 1.0 NB D:F43552 2.1 7.4 1.0 OE1 D:GLN147 2.3 9.9 1.0 S1 A:COM554 2.4 8.7 1.0 C4B D:F43552 3.0 6.9 1.0 C1A D:F43552 3.0 5.3 1.0 C1C D:F43552 3.1 6.3 1.0 C1D D:F43552 3.1 5.0 1.0 C4D D:F43552 3.1 6.6 1.0 C4C D:F43552 3.1 5.5 1.0 C1B D:F43552 3.2 5.8 1.0 C4A D:F43552 3.3 6.7 1.0 C1 A:COM554 3.3 9.7 1.0 CHC D:F43552 3.3 7.0 1.0 CHA D:F43552 3.4 5.8 1.0 CD D:GLN147 3.4 7.4 1.0 CHB D:F43552 3.4 6.6 1.0 CHD D:F43552 3.6 6.5 1.0 NE2 D:GLN147 3.8 11.0 1.0 N5B D:F43552 3.9 6.3 1.0 C2 A:COM554 4.1 8.8 1.0 OH B:TYR367 4.1 9.7 1.0 C3B D:F43552 4.3 6.8 1.0 C3A D:F43552 4.3 6.8 1.0 C2A D:F43552 4.4 4.6 1.0 OH A:TYR333 4.4 7.8 1.0 C3D D:F43552 4.4 5.0 1.0 C2D D:F43552 4.4 5.2 1.0 C2C D:F43552 4.4 6.2 1.0 C3C D:F43552 4.5 8.4 1.0 C2B D:F43552 4.5 6.6 1.0 CAA D:F43552 4.7 8.2 1.0 CG D:GLN147 4.7 7.8 1.0 CAB D:F43552 5.0 6.1 1.0

P.E.Cedervall, M.Dey, A.R.Pearson, S.W.Ragsdale, C.M.Wilmot. Structural Insight Into Methyl-Coenzyme M Reductase Chemistry Using Coenzyme B Analogues. Biochemistry V. 49 7683 2010.
ISSN: ISSN 0006-2960
PubMed: 20707311
DOI: 10.1021/BI100458D