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Chlorine in PDB 1ndt: Nitrite Reductase From Alcaligenes Xylosoxidans

Enzymatic activity of Nitrite Reductase From Alcaligenes Xylosoxidans

All present enzymatic activity of Nitrite Reductase From Alcaligenes Xylosoxidans:
1.7.99.3;

Protein crystallography data

The structure of Nitrite Reductase From Alcaligenes Xylosoxidans, PDB code: 1ndt was solved by F.E.Dodd, J.Vanbeeumen, 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) 20.00 / 2.10
Space group P 63
Cell size a, b, c (Å), α, β, γ (°) 81.236, 81.236, 100.034, 90.00, 90.00, 120.00
R / Rfree (%) 16.7 / 20.8

Other elements in 1ndt:

The structure of Nitrite Reductase From Alcaligenes Xylosoxidans also contains other interesting chemical elements:

Copper (Cu) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Nitrite Reductase From Alcaligenes Xylosoxidans (pdb code 1ndt). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Nitrite Reductase From Alcaligenes Xylosoxidans, PDB code: 1ndt:

Chlorine binding site 1 out of 1 in 1ndt

Go back to Chlorine Binding Sites List in 1ndt
Chlorine binding site 1 out of 1 in the Nitrite Reductase From Alcaligenes Xylosoxidans


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Nitrite Reductase From Alcaligenes Xylosoxidans within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl503

b:21.9
occ:1.00
CU A:CU502 2.2 14.8 1.0
NE2 A:HIS129 3.3 14.6 1.0
CE1 A:HIS129 3.5 13.7 1.0
OD2 A:ASP92 4.0 19.4 1.0
NE2 A:HIS94 4.1 8.6 1.0
CD2 A:HIS129 4.7 11.8 1.0
ND1 A:HIS129 4.8 14.1 1.0
CD2 A:HIS94 4.9 8.7 1.0
CE1 A:HIS94 5.0 9.4 1.0

Reference:

F.E.Dodd, J.Van Beeumen, R.R.Eady, S.S.Hasnain. X-Ray Structure of A Blue-Copper Nitrite Reductase in Two Crystal Forms. the Nature of the Copper Sites, Mode of Substrate Binding and Recognition By Redox Partner. J.Mol.Biol. V. 282 369 1998.
ISSN: ISSN 0022-2836
PubMed: 9735294
DOI: 10.1006/JMBI.1998.2007
Page generated: Sat Jul 20 00:29:23 2024

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