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Tungsten in PDB 8bqh: W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min

Protein crystallography data

The structure of W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min, PDB code: 8bqh was solved by G.Vilela-Alves, C.Mota, A.R.Oliveira, R.R.Manuel, I.C.Pereira, M.J.Romao, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 90.65 / 1.61
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 64.361, 127.456, 128.952, 90, 90, 90
R / Rfree (%) 15.1 / 17.5

Other elements in 8bqh:

The structure of W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min also contains other interesting chemical elements:

Iron (Fe) 16 atoms
Chlorine (Cl) 5 atoms

Tungsten Binding Sites:

The binding sites of Tungsten atom in the W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min (pdb code 8bqh). This binding sites where shown within 5.0 Angstroms radius around Tungsten atom.
In total only one binding site of Tungsten was determined in the W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min, PDB code: 8bqh:

Tungsten binding site 1 out of 1 in 8bqh

Go back to Tungsten Binding Sites List in 8bqh
Tungsten binding site 1 out of 1 in the W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min


Mono view


Stereo pair view

A full contact list of Tungsten with other atoms in the W binding site number 1 of W-Formate Dehydrogenase From Desulfovibrio Vulgaris - Soaking with Formate 1.5 Min within 5.0Å range:
probe atom residue distance (Å) B Occ
A:W1105

b:12.2
occ:1.00
S13 A:MGD1101 2.3 14.8 1.0
S13 A:MGD1102 2.4 12.4 1.0
S A:H2S1104 2.4 17.4 1.0
S12 A:MGD1102 2.4 12.3 1.0
S12 A:MGD1101 2.4 11.0 1.0
SE A:SEC192 2.5 18.1 1.0
C13 A:MGD1102 3.4 13.8 1.0
C13 A:MGD1101 3.4 9.7 1.0
C12 A:MGD1102 3.4 12.5 1.0
C12 A:MGD1101 3.4 10.9 1.0
CB A:SEC192 3.7 21.1 1.0
CA A:GLY442 4.3 12.4 1.0
NH2 A:ARG884 4.4 16.2 1.0
NE2 A:GLN890 4.5 20.7 1.0
NE2 A:HIS193 4.7 17.7 1.0
C14 A:MGD1102 4.8 12.4 1.0
C14 A:MGD1101 4.8 10.6 1.0
N A:GLU443 4.8 15.9 1.0
C11 A:MGD1102 4.8 11.6 1.0
CB A:GLN188 4.9 14.5 1.0
C11 A:MGD1101 4.9 12.1 1.0
O A:GLN188 4.9 16.4 1.0
OE1 A:GLN890 4.9 21.2 1.0
CA A:SEC192 5.0 21.0 1.0

Reference:

G.Vilela-Alves, R.R.Manuel, A.R.Oliveira, I.C.Pereira, M.J.Romao, C.Mota. Tracking W-Formate Dehydrogenase Structural Changes During Catalysis and Enzyme Reoxidation. Int J Mol Sci V. 24 2022.
ISSN: ESSN 1422-0067
PubMed: 36613918
DOI: 10.3390/IJMS24010476
Page generated: Sat Oct 12 15:43:47 2024

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