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Chlorine in PDB 2qvx: 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate

Enzymatic activity of 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate

All present enzymatic activity of 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate:
6.2.1.33;

Protein crystallography data

The structure of 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate, PDB code: 2qvx was solved by R.Wu, A.S.Reger, J.Cao, A.M.Gulick, D.Dunaway-Mariano, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.00 / 2.70
Space group P 32 2 1
Cell size a, b, c (Å), α, β, γ (°) 127.993, 127.993, 71.461, 90.00, 90.00, 120.00
R / Rfree (%) 18.8 / 27.1

Chlorine Binding Sites:

The binding sites of Chlorine atom in the 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate (pdb code 2qvx). 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 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate, PDB code: 2qvx:

Chlorine binding site 1 out of 1 in 2qvx

Go back to Chlorine Binding Sites List in 2qvx
Chlorine binding site 1 out of 1 in the 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of 4-Chlorobenzoyl-Coa Ligase/Synthetase, I303G Mutation, Bound to 3- Chlorobenzoate within 5.0Å range:
probe atom residue distance (Å) B Occ
X:Cl505

b:57.8
occ:1.00
CL3 X:3BZ505 0.0 57.8 1.0
C3 X:3BZ505 1.8 56.8 1.0
C4 X:3BZ505 2.8 54.5 1.0
C2 X:3BZ505 2.8 55.4 1.0
OD1 X:ASN311 3.3 53.2 1.0
C X:GLY303 3.8 51.7 1.0
C X:TYR304 3.9 49.9 1.0
N X:TYR304 3.9 53.1 1.0
N X:GLY305 4.0 47.8 1.0
CA X:GLY303 4.0 45.6 1.0
O X:TYR304 4.0 49.1 1.0
CG X:ASN311 4.1 46.8 1.0
C5 X:3BZ505 4.1 57.1 1.0
C1 X:3BZ505 4.1 54.8 1.0
CA X:GLY305 4.2 42.4 1.0
O X:GLY303 4.2 47.4 1.0
CE1 X:PHE184 4.2 37.3 1.0
CB X:ASN311 4.3 42.2 1.0
CZ X:PHE249 4.4 40.6 1.0
CA X:TYR304 4.4 44.2 1.0
CZ X:PHE184 4.4 39.9 1.0
CA X:ASN311 4.5 42.6 1.0
C6 X:3BZ505 4.6 54.2 1.0
CE2 X:PHE249 4.9 42.6 1.0
CG2 X:VAL209 5.0 39.2 1.0

Reference:

R.Wu, A.S.Reger, J.Cao, A.M.Gulick, D.Dunaway-Mariano. Rational Redesign of the 4-Chlorobenzoate Binding Site of 4-Chlorobenzoate: Coenzyme A Ligase For Expanded Substrate Range. Biochemistry V. 46 14487 2007.
ISSN: ISSN 0006-2960
PubMed: 18027984
DOI: 10.1021/BI701609W
Page generated: Sat Jul 20 10:58:04 2024

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