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Chlorine in PDB 3vkq: Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose

Enzymatic activity of Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose

All present enzymatic activity of Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose:
1.7.7.1;

Protein crystallography data

The structure of Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose, PDB code: 3vkq was solved by S.Nakano, M.Takahashi, A.Sakamoto, H.Morikawa, K.Katayanagi, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 37.27 / 1.60
Space group P 4 21 2
Cell size a, b, c (Å), α, β, γ (°) 134.150, 134.150, 77.994, 90.00, 90.00, 90.00
R / Rfree (%) 15.2 / 16.8

Other elements in 3vkq:

The structure of Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose also contains other interesting chemical elements:

Potassium (K) 1 atom
Iron (Fe) 5 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose (pdb code 3vkq). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose, PDB code: 3vkq:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 3vkq

Go back to Chlorine Binding Sites List in 3vkq
Chlorine binding site 1 out of 2 in the Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl604

b:17.2
occ:1.00
O A:HOH1285 2.9 16.5 1.0
N A:MET175 3.0 7.0 1.0
O A:HOH1065 3.1 12.5 1.0
NH1 A:ARG179 3.6 8.3 1.0
CA A:MET175 3.7 7.5 1.0
CE2 A:PHE96 3.8 6.9 1.0
O A:HOH1054 3.9 16.9 1.0
CMA A:SRM601 4.0 7.7 1.0
C A:GLY174 4.0 7.4 1.0
CG A:MET175 4.1 9.4 1.0
CD A:LYS91 4.1 9.4 1.0
CA A:GLY174 4.1 7.2 1.0
SD A:MET175 4.1 11.9 1.0
CB A:MET175 4.5 7.5 1.0
O A:HOH1908 4.5 20.2 1.0
CZ A:ARG179 4.6 6.6 1.0
O3D A:SRM601 4.6 12.0 1.0
CD2 A:PHE96 4.6 7.5 1.0
CZ A:PHE96 4.7 6.7 1.0
CE A:LYS91 4.9 11.9 1.0
NZ A:LYS91 4.9 12.4 1.0
NH2 A:ARG179 4.9 7.1 1.0
O A:HOH1221 4.9 22.8 1.0
CHA A:SRM601 4.9 6.4 1.0
C A:MET175 4.9 7.1 1.0
CG A:LYS91 4.9 8.3 1.0
O1 A:NO2606 5.0 17.8 1.0

Chlorine binding site 2 out of 2 in 3vkq

Go back to Chlorine Binding Sites List in 3vkq
Chlorine binding site 2 out of 2 in the Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Assimilatory Nitrite Reductase (NII3) - NO2 Complex From Tobbaco Leaf Analysed with Middle X-Ray Dose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl605

b:17.9
occ:1.00
O A:HOH1940 2.8 42.3 1.0
O A:HOH1133 3.0 15.6 1.0
O A:HOH1018 3.2 10.2 1.0
O A:HOH1864 3.3 36.9 1.0
N A:LYS100 3.3 11.3 1.0
O A:HOH1417 3.4 34.6 1.0
N A:ARG99 3.5 9.4 1.0
CB A:LYS100 3.8 12.2 1.0
CA A:GLY447 3.8 9.3 1.0
CB A:ARG99 4.1 9.9 1.0
CA A:ARG99 4.1 10.1 1.0
C A:ARG98 4.2 8.8 1.0
CA A:LYS100 4.2 11.6 1.0
N A:GLY447 4.2 8.9 1.0
C A:ARG99 4.2 10.7 1.0
O A:HIS97 4.3 8.9 1.0
O A:HOH1588 4.5 31.8 1.0
CA A:ARG98 4.5 8.4 1.0
O A:HOH1958 4.8 28.9 1.0
O A:HOH2052 4.9 19.0 1.0
C A:GLY447 4.9 9.7 1.0
O A:HOH1938 4.9 43.9 1.0
N A:ASN101 4.9 11.0 1.0
O A:ARG98 4.9 9.1 1.0
O A:HOH2028 5.0 40.0 1.0

Reference:

S.Nakano, M.Takahashi, A.Sakamoto, H.Morikawa, K.Katayanagi. The Reductive Reaction Mechanism of Tobacco Nitrite Reductase Derived From A Combination of Crystal Structures and Ultraviolet-Visible Microspectroscopy Proteins V. 80 2035 2012.
ISSN: ISSN 0887-3585
PubMed: 22499059
DOI: 10.1002/PROT.24094
Page generated: Fri Jul 11 11:44:11 2025

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