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Chlorine in PDB 4qop: Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.

Enzymatic activity of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.

All present enzymatic activity of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.:
1.11.1.6;

Protein crystallography data

The structure of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound., PDB code: 4qop was solved by P.C.Loewen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 104.13 / 1.90
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 92.279, 109.455, 104.199, 90.00, 92.05, 90.00
R / Rfree (%) 23 / 26.1

Other elements in 4qop:

The structure of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. also contains other interesting chemical elements:

Iron (Fe) 8 atoms
Sodium (Na) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. (pdb code 4qop). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 6 binding sites of Chlorine where determined in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound., PDB code: 4qop:
Jump to Chlorine binding site number: 1; 2; 3; 4; 5; 6;

Chlorine binding site 1 out of 6 in 4qop

Go back to Chlorine Binding Sites List in 4qop
Chlorine binding site 1 out of 6 in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl504

b:32.4
occ:1.00
 NH2 A:ARG48 3.2 20.8 1.0
NH2 B:ARG48 3.2 19.7 1.0
NE A:ARG48 3.4 20.2 1.0
O C:HOH924 3.4 30.2 1.0
NE B:ARG48 3.5 18.0 1.0
O D:HOH794 3.5 27.4 1.0
CZ A:ARG48 3.7 19.6 1.0
CZ B:ARG48 3.8 18.5 1.0
CB D:HIS346 4.0 24.2 1.0
CB C:HIS346 4.1 23.7 1.0
CA D:HIS346 4.2 21.9 1.0
CA C:HIS346 4.2 21.6 1.0
N D:HIS346 4.2 20.6 1.0
N C:HIS346 4.3 22.0 1.0
C D:ARG345 4.6 20.4 1.0
C C:ARG345 4.6 20.8 1.0
CD A:ARG48 4.6 19.1 1.0
O D:ARG345 4.7 21.9 1.0
CD B:ARG48 4.7 18.4 1.0
O C:ARG345 4.7 23.4 1.0
CB D:ARG345 4.8 18.7 1.0
CB C:ARG345 4.8 17.8 1.0

Chlorine binding site 2 out of 6 in 4qop

Go back to Chlorine Binding Sites List in 4qop
Chlorine binding site 2 out of 6 in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl505

b:22.1
occ:1.00
 O B:HOH637 2.9 20.7 1.0
O A:HOH735 3.0 30.8 1.0
N A:ASN367 3.3 19.9 1.0
O A:HOH612 3.3 20.1 1.0
CB A:ASN366 3.7 20.8 1.0
CB A:ASN367 3.8 20.2 1.0
CE C:LYS42 3.8 19.8 1.0
CA A:ASN367 3.9 20.4 1.0
CD C:LYS42 4.2 18.8 1.0
CG C:LYS42 4.2 18.4 1.0
N A:GLN368 4.2 19.1 1.0
CD1 C:LEU9 4.2 33.1 0.5
C A:ASN367 4.2 20.3 1.0
C A:ASN366 4.3 22.1 1.0
NZ C:LYS42 4.4 20.8 1.0
CG A:ASN366 4.4 21.9 1.0
CA A:ASN366 4.5 21.3 1.0
CG A:GLN368 4.5 21.7 1.0
CD1 C:LEU9 4.5 32.6 0.5
CD2 C:LEU9 4.5 34.4 0.5
CE1 C:HIS38 4.6 25.3 1.0
O B:HOH615 4.6 24.3 1.0
OD1 A:ASN366 4.6 22.6 1.0
OD1 A:ASN367 4.6 22.8 1.0
CG A:ASN367 4.7 20.2 1.0
OD1 C:ASN20 4.7 20.4 1.0
CG C:LEU9 4.8 33.5 0.5
CG C:LEU9 4.9 31.8 0.5
OD1 B:ASP145 4.9 22.2 1.0
O A:ASN367 5.0 19.7 1.0

Chlorine binding site 3 out of 6 in 4qop

Go back to Chlorine Binding Sites List in 4qop
Chlorine binding site 3 out of 6 in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl504

b:24.7
occ:1.00
 O B:HOH841 2.8 37.6 1.0
O A:HOH605 3.2 18.1 1.0
O D:HOH678 3.2 21.5 1.0
N B:ASN367 3.3 22.6 1.0
CB B:ASN366 3.7 23.3 1.0
CB B:ASN367 3.8 22.5 1.0
CE D:LYS42 3.8 24.4 1.0
CA B:ASN367 3.9 21.7 1.0
N B:GLN368 4.1 21.6 1.0
C B:ASN367 4.1 22.5 1.0
CG D:LYS42 4.2 22.7 1.0
CD D:LYS42 4.2 23.5 1.0
CG B:GLN368 4.3 20.8 1.0
CG B:ASN366 4.3 23.5 1.0
C B:ASN366 4.4 22.6 1.0
NZ D:LYS42 4.4 23.4 1.0
O A:HOH640 4.4 27.1 1.0
CA B:ASN366 4.5 23.0 1.0
OD1 B:ASN366 4.6 20.7 1.0
CD1 D:LEU9 4.6 35.8 1.0
CE1 D:HIS38 4.6 26.3 1.0
CG B:ASN367 4.7 22.6 1.0
OD1 B:ASN367 4.7 23.5 1.0
OD1 D:ASN20 4.8 19.6 1.0
O B:ASN367 4.9 21.6 1.0
CG D:LEU9 5.0 35.9 1.0

Chlorine binding site 4 out of 6 in 4qop

Go back to Chlorine Binding Sites List in 4qop
Chlorine binding site 4 out of 6 in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl504

b:27.7
occ:1.00
 NH2 C:ARG48 3.1 21.0 1.0
NH2 D:ARG48 3.2 20.1 1.0
NE C:ARG48 3.3 18.4 1.0
NE D:ARG48 3.5 19.8 1.0
CZ C:ARG48 3.7 19.5 1.0
O B:HOH814 3.7 41.1 1.0
O A:HOH874 3.9 41.9 1.0
CZ D:ARG48 3.9 19.3 1.0
N A:HIS346 4.1 20.5 1.0
CB A:HIS346 4.1 25.1 1.0
CA A:HIS346 4.1 22.1 1.0
CB B:HIS346 4.1 22.6 1.0
CA B:HIS346 4.2 21.2 1.0
N B:HIS346 4.3 20.4 1.0
C A:ARG345 4.4 19.8 1.0
O A:ARG345 4.6 21.7 1.0
CD C:ARG48 4.6 17.8 1.0
C B:ARG345 4.7 21.0 1.0
CB A:ARG345 4.7 20.3 1.0
CD D:ARG48 4.8 19.4 1.0
O B:ARG345 4.8 20.9 1.0
NH1 C:ARG48 5.0 20.0 1.0
CB B:ARG345 5.0 20.9 1.0

Chlorine binding site 5 out of 6 in 4qop

Go back to Chlorine Binding Sites List in 4qop
Chlorine binding site 5 out of 6 in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 5 of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl505

b:28.2
occ:1.00
 O C:HOH984 3.0 33.5 1.0
O D:HOH681 3.2 31.5 1.0
O A:HOH679 3.3 29.8 1.0
O C:HOH623 3.3 18.9 1.0
N C:ASN367 3.3 22.2 1.0
CB C:ASN366 3.7 23.7 1.0
CB C:ASN367 3.8 24.5 1.0
CE A:LYS42 3.8 21.9 1.0
CA C:ASN367 3.9 23.6 1.0
CD A:LYS42 4.1 21.7 1.0
N C:GLN368 4.2 22.0 1.0
CG A:LYS42 4.2 22.0 1.0
C C:ASN367 4.2 24.4 1.0
C C:ASN366 4.3 23.8 1.0
CG C:ASN366 4.4 23.3 1.0
NZ A:LYS42 4.4 22.3 1.0
CG C:GLN368 4.4 21.3 1.0
CA C:ASN366 4.4 24.5 1.0
CE1 A:HIS38 4.6 26.3 1.0
O D:HOH624 4.6 22.9 1.0
CD1 A:LEU9 4.6 35.6 1.0
OD1 C:ASN366 4.6 24.4 1.0
CG C:ASN367 4.7 25.4 1.0
OD1 C:ASN367 4.7 29.4 1.0
OD1 A:ASN20 4.7 22.7 1.0
O C:ASN367 5.0 26.0 1.0
CG A:LEU9 5.0 36.2 1.0

Chlorine binding site 6 out of 6 in 4qop

Go back to Chlorine Binding Sites List in 4qop
Chlorine binding site 6 out of 6 in the Structure of Bacillus Pumilus Catalase with Hydroquinone Bound.


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 6 of Structure of Bacillus Pumilus Catalase with Hydroquinone Bound. within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Cl504

b:25.3
occ:1.00
 O C:HOH606 3.1 27.4 1.0
N D:ASN367 3.2 23.1 1.0
O D:HOH677 3.3 17.8 1.0
O B:HOH641 3.5 31.3 1.0
CB D:ASN367 3.7 21.8 1.0
CB D:ASN366 3.7 23.7 1.0
CA D:ASN367 3.8 22.9 1.0
CE B:LYS42 3.9 19.1 1.0
C D:ASN367 4.1 22.1 1.0
N D:GLN368 4.1 20.7 1.0
CD B:LYS42 4.2 20.0 1.0
CG B:LYS42 4.2 19.9 1.0
C D:ASN366 4.3 25.7 1.0
CG D:ASN366 4.4 23.3 1.0
CG D:GLN368 4.4 20.4 1.0
O C:HOH641 4.4 23.0 1.0
CA D:ASN366 4.4 24.0 1.0
NZ B:LYS42 4.4 19.2 1.0
OD1 D:ASN366 4.6 20.6 1.0
CG D:ASN367 4.6 22.0 1.0
CD1 B:LEU9 4.6 38.5 1.0
OD1 D:ASN367 4.6 23.9 1.0
CE1 B:HIS38 4.6 25.4 1.0
OD1 B:ASN20 4.7 23.2 1.0
O D:ASN367 4.9 23.5 1.0
NE2 D:GLN368 5.0 25.4 1.0
CG B:LEU9 5.0 38.6 1.0

Reference:

P.C.Loewen, J.Villanueva, J.Switala, L.J.Donald, A.Ivancich. Unprecedented Access of Phenolic Substrates to the Heme Active Site of A Catalase: Substrate Binding and Peroxidase-Like Reactivity of Bacillus Pumilus Catalase Monitored By X-Ray Crystallography and Epr Spectroscopy. Proteins 2015.
ISSN: ESSN 1097-0134
PubMed: 25663126
DOI: 10.1002/PROT.24777
Page generated: Sat Dec 12 11:06:11 2020

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