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Copper in PDB 8rg8: High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy]

Protein crystallography data

The structure of High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy], PDB code: 8rg8 was solved by S.L.Rose, F.M.Ferroni, S.V.Antonyuk, R.R.Eady, S.S.Hasnain, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.00 / 1.21
Space group P 21 3
Cell size a, b, c (Å), α, β, γ (°) 106.99, 106.99, 106.99, 90, 90, 90
R / Rfree (%) 11.5 / 13.9

Copper Binding Sites:

The binding sites of Copper atom in the High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy] (pdb code 8rg8). This binding sites where shown within 5.0 Angstroms radius around Copper atom.
In total 2 binding sites of Copper where determined in the High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy], PDB code: 8rg8:
Jump to Copper binding site number: 1; 2;

Copper binding site 1 out of 2 in 8rg8

Go back to Copper Binding Sites List in 8rg8
Copper binding site 1 out of 2 in the High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy]


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 1 of High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy] within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cu501

b:13.1
occ:1.00
ND1 A:HIS140 2.0 11.7 1.0
ND1 A:HIS89 2.0 12.4 1.0
SG A:CYS130 2.2 12.8 1.0
SD A:MET145 2.5 14.0 1.0
CE1 A:HIS89 2.9 12.7 1.0
CE1 A:HIS140 3.0 11.7 1.0
CG A:HIS140 3.0 12.2 1.0
CG A:HIS89 3.1 12.3 1.0
CB A:CYS130 3.2 12.3 1.0
CE A:MET145 3.3 14.0 1.0
CB A:HIS140 3.5 11.5 1.0
CB A:HIS89 3.5 12.4 1.0
CA A:HIS89 3.8 12.7 1.0
CG A:MET145 4.0 14.3 1.0
NE2 A:HIS140 4.1 13.3 1.0
O A:PRO88 4.1 14.0 1.0
NE2 A:HIS89 4.1 12.8 1.0
CD2 A:HIS140 4.1 13.6 1.0
CG A:PRO132 4.2 14.1 1.0
CD2 A:HIS89 4.2 12.0 1.0
CB A:MET145 4.4 12.7 1.0
SD A:MET56 4.6 14.8 0.4
N A:ASN90 4.6 12.6 1.0
CD A:PRO132 4.6 12.5 1.0
CA A:CYS130 4.6 10.7 1.0
CA A:HIS140 4.7 10.8 1.0
N A:HIS89 4.8 13.2 1.0
C A:HIS89 4.8 12.6 1.0
C A:PRO88 4.9 13.3 1.0
CE A:MET56 4.9 14.2 0.6

Copper binding site 2 out of 2 in 8rg8

Go back to Copper Binding Sites List in 8rg8
Copper binding site 2 out of 2 in the High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy]


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 2 of High pH (8.0) Nitrite-Bound Msox Movie Series Dataset 1 of the Copper Nitrite Reductase From Bradyrhizobium Sp. ORS375 (Two-Domain)[1.12 Mgy] within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cu502

b:12.3
occ:0.95
O1 A:NO2503 2.0 21.0 0.7
NE2 A:HIS94 2.0 10.7 1.0
N A:NO2503 2.0 22.4 0.7
NE2 A:HIS129 2.1 10.6 1.0
O2 A:NO2503 2.1 18.6 0.7
CE1 A:HIS94 3.0 11.0 1.0
CD2 A:HIS129 3.0 11.1 1.0
CD2 A:HIS94 3.1 10.4 1.0
CE1 A:HIS129 3.1 11.5 1.0
OD2 A:ASP92 3.2 16.7 0.3
OD2 A:ASP92 3.8 19.0 0.5
ND1 A:HIS94 4.1 10.5 1.0
CG A:ASP92 4.2 16.1 0.3
O A:HOH942 4.2 31.7 0.5
CG A:HIS129 4.2 10.7 1.0
CG A:HIS94 4.2 10.1 1.0
O A:HOH916 4.2 13.1 0.2
ND1 A:HIS129 4.2 11.1 1.0
O A:HOH786 4.2 27.4 0.5
CG A:ASP92 4.3 17.0 0.5
OD1 A:ASP92 4.5 16.7 0.5
OD1 A:ASP92 4.7 16.5 0.3
OD2 A:ASP92 4.7 12.7 0.2
O A:HOH884 4.9 18.0 1.0

Reference:

S.L.Rose, F.Martin Ferroni, S.Horrell, C.Dante Brondino, R.R.Eady, S.Jaho, M.A.Hough, R.L.Owen, S.V.Antonyuk, S.Samar Hasnain. Spectroscopically Validated pH-Dependent Msox Movies Provide Detailed Mechanism of Copper Nitrite Reductases. J.Mol.Biol. 68706 2024.
ISSN: ESSN 1089-8638
PubMed: 39002715
DOI: 10.1016/J.JMB.2024.168706
Page generated: Mon Jul 14 09:23:06 2025

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