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Chlorine in PDB 4q89: Crystal Structure of the Cota Native Enzyme

Protein crystallography data

The structure of Crystal Structure of the Cota Native Enzyme, PDB code: 4q89 was solved by T.Xie, Z.C.Liu, G.G.Wang, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.62 / 2.31
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 53.013, 119.864, 84.136, 90.00, 93.99, 90.00
R / Rfree (%) 15 / 21.5

Other elements in 4q89:

The structure of Crystal Structure of the Cota Native Enzyme also contains other interesting chemical elements:

Copper (Cu) 8 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of the Cota Native Enzyme (pdb code 4q89). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of the Cota Native Enzyme, PDB code: 4q89:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 4q89

Go back to Chlorine Binding Sites List in 4q89
Chlorine binding site 1 out of 2 in the Crystal Structure of the Cota Native Enzyme


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of the Cota Native Enzyme within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl605

b:31.0
occ:1.00
ND2 A:ASN264 3.0 24.7 1.0
OG A:SER293 3.2 24.5 1.0
O A:HOH1010 3.2 36.9 1.0
CB A:SER293 3.7 21.2 1.0
CB A:ASN264 3.8 26.1 1.0
CG A:ASN264 3.9 25.5 1.0
CG2 A:THR262 3.9 18.8 1.0
CB A:ALA320 4.2 27.5 1.0
O A:TYR263 4.2 26.2 1.0
CA A:SER293 4.4 22.4 1.0
CA A:ASN264 4.7 25.2 1.0
C A:TYR263 4.8 24.3 1.0
O A:HOH804 4.9 33.3 1.0
O A:HOH872 4.9 39.4 1.0
N A:ASN264 5.0 24.8 1.0

Chlorine binding site 2 out of 2 in 4q89

Go back to Chlorine Binding Sites List in 4q89
Chlorine binding site 2 out of 2 in the Crystal Structure of the Cota Native Enzyme


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Crystal Structure of the Cota Native Enzyme within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl606

b:50.5
occ:1.00
N A:SER186 3.2 34.6 1.0
NH2 A:ARG248 3.4 37.3 1.0
O A:HOH953 3.5 36.7 1.0
CA A:PRO185 3.6 34.9 1.0
CB A:SER349 3.7 48.4 1.0
O A:SER186 3.8 37.2 1.0
C A:PRO185 3.9 33.4 1.0
CD2 A:TYR189 4.0 33.8 1.0
CA A:SER186 4.1 32.6 1.0
NH1 A:ARG248 4.2 39.6 1.0
CZ A:ARG248 4.3 40.4 1.0
C A:SER186 4.4 35.5 1.0
CB A:SER186 4.4 34.8 1.0
OG A:SER186 4.4 36.6 1.0
CB A:PRO185 4.4 35.1 1.0
O A:LEU184 4.5 33.5 1.0
CB A:TYR189 4.5 31.4 1.0
CA A:SER349 4.6 46.4 1.0
CG A:TYR189 4.7 32.9 1.0
OG A:SER349 4.7 43.6 1.0
N A:PRO185 4.7 33.3 1.0
N A:SER349 4.8 52.8 1.0
CE2 A:TYR189 4.8 33.9 1.0

Reference:

T.Xie, Z.C.Liu, G.G.Wang. The Crystal Structure of Cota Laccase Complexed with Sinapic Acid To Be Published.
Page generated: Fri Jul 11 20:42:54 2025

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