Chlorine in PDB 6c89: Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics

Protein crystallography data

The structure of Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics, PDB code: 6c89 was solved by T.Palzkill, Z.Sun, B.Sankaran, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 37.24 / 1.75
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 46.167, 68.861, 68.441, 92.23, 77.03, 91.84
R / Rfree (%) 15.6 / 20

Other elements in 6c89:

The structure of Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics also contains other interesting chemical elements:

Zinc (Zn) 8 atoms
Sodium (Na) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics (pdb code 6c89). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics, PDB code: 6c89:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 6c89

Go back to Chlorine Binding Sites List in 6c89
Chlorine binding site 1 out of 2 in the Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl403

b:39.5
occ:1.00
NH2 B:ARG247 2.3 14.9 0.5
NA B:NA404 2.5 33.3 1.0
O B:HOH570 2.6 20.4 1.0
O C:HOH603 3.1 31.9 1.0
CZ B:ARG247 3.3 14.0 0.5
NH2 C:ARG247 3.4 17.9 0.5
NH1 B:ARG247 3.4 19.1 0.5
CZ C:ARG247 3.5 17.6 0.5
N B:ALA244 3.7 13.3 1.0
NH1 C:ARG247 3.9 14.1 0.5
CB B:ALA244 3.9 15.7 1.0
NE C:ARG247 3.9 20.7 0.5
CB B:ALA243 3.9 17.1 1.0
O A:HOH612 3.9 32.7 1.0
OD1 B:ASP309 4.0 29.1 1.0
CA B:ALA244 4.1 16.7 1.0
NH1 C:ARG247 4.3 14.9 0.5
NH1 B:ARG312 4.3 37.1 1.0
C B:ALA243 4.4 13.8 1.0
OD2 C:ASP309 4.4 25.6 1.0
CD B:ARG312 4.4 33.7 1.0
NH1 B:ARG247 4.5 17.2 0.5
NE B:ARG247 4.5 18.6 0.5
CZ B:ARG312 4.6 35.5 1.0
NE B:ARG312 4.7 37.5 1.0
CA B:ALA243 4.7 16.1 1.0
CD C:ARG247 4.7 15.4 0.5
CZ C:ARG247 4.7 14.2 0.5
CD C:ARG247 4.8 14.9 0.5
NE C:ARG247 5.0 16.1 0.5

Chlorine binding site 2 out of 2 in 6c89

Go back to Chlorine Binding Sites List in 6c89
Chlorine binding site 2 out of 2 in the Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Ndm-1 Beta-Lactamase Exhibits Differential Active Site Sequence Requirements For the Hydrolysis of Penicillin Versus Carbapenem Antibiotics within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Cl404

b:42.2
occ:1.00
N D:GLN119 2.8 13.9 1.0
CA D:HIS118 3.4 10.0 1.0
C D:HIS118 3.6 12.9 1.0
CB D:GLN119 3.6 16.5 1.0
CA D:GLN119 3.7 14.7 1.0
CB D:HIS118 3.7 13.8 1.0
CD2 D:HIS118 3.9 16.9 1.0
CG D:HIS118 4.0 15.9 1.0
OE1 D:GLU149 4.1 30.6 1.0
O D:ALA117 4.7 20.2 1.0
N D:HIS118 4.7 12.3 1.0
O D:HIS118 4.8 11.5 1.0
C D:GLN119 5.0 13.5 1.0
NE2 D:HIS118 5.0 18.2 1.0

Reference:

Z.Sun, L.Hu, B.Sankaran, B.V.V.Prasad, T.Palzkill. Differential Active Site Requirements For Ndm-1 Beta-Lactamase Hydrolysis of Carbapenem Versus Penicillin and Cephalosporin Antibiotics. Nat Commun V. 9 4524 2018.
ISSN: ESSN 2041-1723
PubMed: 30375382
DOI: 10.1038/S41467-018-06839-1
Page generated: Sat Dec 12 12:48:47 2020

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