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Zinc in PDB 9jyw: Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus

Protein crystallography data

The structure of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus, PDB code: 9jyw was solved by S.H.Choi, M.S.Jin, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.36 / 1.70
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 118.911, 110.672, 98.578, 90, 118.8, 90
R / Rfree (%) 21.3 / 24.5

Zinc Binding Sites:

Pages:

>>> Page 1 <<< Page 2, Binding sites: 11 - 12;

Binding sites:

The binding sites of Zinc atom in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus (pdb code 9jyw). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 12 binding sites of Zinc where determined in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus, PDB code: 9jyw:
Jump to Zinc binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Zinc binding site 1 out of 12 in 9jyw

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Zinc binding site 1 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


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Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn201

b:10.3
occ:1.00
NE2 A:HIS87 2.1 11.8 1.0
NE2 C:HIS82 2.1 11.1 1.0
ND1 A:HIS65 2.1 8.3 1.0
O C:HOH364 2.3 2.9 1.0
CD2 A:HIS87 2.9 11.7 1.0
CE1 C:HIS82 3.0 10.9 1.0
CE1 A:HIS65 3.0 11.2 1.0
CG A:HIS65 3.1 11.3 1.0
CE1 A:HIS87 3.1 14.3 1.0
CD2 C:HIS82 3.1 12.1 1.0
CB A:HIS65 3.3 10.9 1.0
OH C:TYR159 4.0 16.8 1.0
O A:GLN66 4.1 10.5 1.0
O C:HOH333 4.1 24.1 1.0
ND1 C:HIS82 4.1 9.5 1.0
CG A:HIS87 4.1 12.0 1.0
NE2 A:HIS65 4.2 10.3 1.0
ND1 A:HIS87 4.2 11.9 1.0
CD2 A:HIS65 4.2 10.7 1.0
OE1 C:GLN59 4.2 12.7 1.0
CG C:HIS82 4.2 9.7 1.0
O A:HOH325 4.3 15.9 1.0
N A:GLN66 4.5 10.8 1.0
CA A:HIS65 4.6 10.2 1.0
CE C:MET99 4.8 19.9 1.0
C A:GLN66 4.8 12.0 1.0
C A:HIS65 4.8 10.2 1.0

Zinc binding site 2 out of 12 in 9jyw

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Zinc binding site 2 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn202

b:31.6
occ:1.00
O B:HOH400 2.1 19.9 1.0
O C:HOH368 2.1 23.3 1.0
O A:HOH390 2.1 31.0 1.0
O C:HOH319 2.2 30.7 1.0
O A:HOH359 2.2 25.1 1.0
O B:HOH350 2.3 29.1 1.0
O A:HOH312 3.9 21.8 1.0
O C:HOH313 4.0 30.8 1.0
O B:HOH313 4.0 23.1 1.0
O B:HOH415 4.1 28.0 1.0
O B:HOH327 4.2 18.3 1.0
O A:HOH302 4.2 19.6 1.0
OE1 C:GLN83 4.3 14.5 1.0
O C:HOH315 4.3 21.2 1.0
OE1 B:GLN83 4.3 14.3 1.0
OE1 A:GLN83 4.4 14.7 1.0
O B:HOH346 4.4 27.0 1.0
O C:HOH336 4.4 26.9 1.0
O B:GLN83 4.5 17.2 1.0
O A:HOH355 4.5 28.8 1.0
O C:GLN83 4.5 18.0 1.0
O A:GLN83 4.6 15.8 1.0
CB B:GLN83 4.7 12.1 1.0
CB C:GLN83 4.7 11.7 1.0
CB A:GLN83 4.8 12.8 1.0
CD B:GLN83 4.8 15.0 1.0
CD C:GLN83 4.8 12.8 1.0
CD A:GLN83 4.9 15.0 1.0

Zinc binding site 3 out of 12 in 9jyw

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Zinc binding site 3 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 3 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn201

b:11.7
occ:1.00
ND1 B:HIS65 2.1 12.4 1.0
NE2 B:HIS87 2.2 13.6 1.0
NE2 A:HIS82 2.2 12.1 1.0
O A:HOH377 2.3 8.9 1.0
CD2 B:HIS87 3.0 13.1 1.0
CE1 B:HIS65 3.0 12.2 1.0
CE1 A:HIS82 3.0 11.4 1.0
CG B:HIS65 3.1 13.4 1.0
CD2 A:HIS82 3.1 12.5 1.0
CE1 B:HIS87 3.2 15.7 1.0
CB B:HIS65 3.4 13.6 1.0
O B:GLN66 4.1 13.6 1.0
NE2 B:HIS65 4.1 11.4 1.0
CG B:HIS87 4.2 12.2 1.0
ND1 A:HIS82 4.2 11.3 1.0
CD2 B:HIS65 4.2 12.4 1.0
ND1 B:HIS87 4.2 12.6 1.0
OH A:TYR159 4.2 19.2 1.0
OE1 A:GLN59 4.2 15.4 1.0
CG A:HIS82 4.2 10.5 1.0
O A:HOH351 4.3 28.2 1.0
O B:HOH344 4.3 28.6 1.0
N B:GLN66 4.6 13.8 1.0
CE A:MET99 4.7 19.7 1.0
CA B:HIS65 4.7 12.3 1.0
C B:GLN66 4.8 15.9 1.0
C B:HIS65 4.9 13.6 1.0

Zinc binding site 4 out of 12 in 9jyw

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Zinc binding site 4 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 4 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn202

b:14.6
occ:1.00
OE1 B:GLN164 2.2 19.2 1.0
OE2 D:GLU153 2.3 11.8 1.0
OE1 B:GLU161 2.3 15.5 1.0
O B:HOH394 2.3 14.1 1.0
OE1 D:GLU153 2.3 10.6 1.0
OE2 B:GLU161 2.5 12.4 1.0
CD D:GLU153 2.5 10.1 1.0
CD B:GLU161 2.6 12.4 1.0
CD B:GLN164 3.1 17.6 1.0
NE2 B:GLN164 3.4 18.3 1.0
CG D:GLU153 4.1 12.4 1.0
O D:HOH341 4.1 19.0 1.0
CG B:GLU161 4.1 12.9 1.0
O B:HOH322 4.1 21.7 1.0
O B:HOH398 4.2 24.6 1.0
CD2 D:LEU149 4.4 22.2 1.0
CG D:LEU149 4.4 21.5 1.0
O B:HOH328 4.4 34.9 1.0
CG B:GLN164 4.5 16.7 1.0
CA B:GLU161 4.6 13.0 1.0
CG D:GLN150 4.7 24.7 1.0
CB B:GLN164 4.7 16.0 1.0
CB B:GLU161 4.8 12.9 1.0
NH2 D:ARG157 4.8 18.4 1.0
CB D:GLU153 4.9 13.1 1.0

Zinc binding site 5 out of 12 in 9jyw

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Zinc binding site 5 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 5 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn203

b:24.8
occ:1.00
O D:HOH309 2.1 9.8 1.0
O B:HOH365 2.1 16.5 1.0
OE1 B:GLU34 2.1 17.2 1.0
OD2 D:ASP77 2.1 16.3 1.0
OE2 B:GLU34 2.2 22.3 1.0
O B:HOH389 2.3 26.9 1.0
CD B:GLU34 2.4 17.8 1.0
CG D:ASP77 3.1 15.2 1.0
CB D:ASP77 3.5 12.8 1.0
O B:HOH354 3.9 16.5 1.0
CG B:GLU34 4.0 15.7 1.0
O B:HOH388 4.0 28.3 1.0
OD1 D:ASP77 4.2 15.8 1.0
O B:HOH391 4.5 31.1 1.0
O1 D:SO4204 4.5 30.5 1.0
O D:HOH353 4.6 19.4 1.0
O2 D:SO4204 4.6 33.4 1.0
O D:HOH365 4.8 23.9 1.0
CB B:GLU34 4.9 14.5 1.0
O D:HOH363 5.0 15.4 1.0
NH2 D:ARG156 5.0 21.7 1.0

Zinc binding site 6 out of 12 in 9jyw

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Zinc binding site 6 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 6 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn204

b:27.9
occ:1.00
OD2 B:ASP77 2.0 18.4 1.0
OE1 D:GLU34 2.0 15.6 1.0
O B:HOH302 2.1 10.1 1.0
O D:HOH351 2.2 18.1 1.0
OE2 D:GLU34 2.3 25.9 1.0
CD D:GLU34 2.5 18.4 1.0
CG B:ASP77 3.0 16.4 1.0
CB B:ASP77 3.4 14.7 1.0
O D:HOH342 3.7 16.6 1.0
CG D:GLU34 4.0 15.3 1.0
OD1 B:ASP77 4.1 15.2 1.0
O1 B:SO4205 4.1 26.9 1.0
O D:HOH322 4.6 18.3 1.0
O B:HOH345 4.8 14.0 1.0
O D:HOH366 4.8 29.8 1.0
CD D:ARG55 4.9 15.3 1.0
CB D:GLU34 4.9 14.4 1.0
CA B:ASP77 4.9 12.3 1.0

Zinc binding site 7 out of 12 in 9jyw

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Zinc binding site 7 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 7 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Zn201

b:11.3
occ:1.00
ND1 C:HIS65 2.1 13.9 1.0
NE2 C:HIS87 2.2 15.3 1.0
NE2 B:HIS82 2.2 8.8 1.0
O B:HOH393 2.3 4.4 1.0
CE1 C:HIS65 3.0 12.8 1.0
CD2 C:HIS87 3.0 12.7 1.0
CE1 B:HIS82 3.0 9.9 1.0
CG C:HIS65 3.1 14.2 1.0
CD2 B:HIS82 3.2 11.4 1.0
CE1 C:HIS87 3.2 15.2 1.0
CB C:HIS65 3.4 13.8 1.0
OH B:TYR159 4.1 13.8 1.0
O B:HOH348 4.1 29.0 1.0
O C:GLN66 4.1 12.2 1.0
NE2 C:HIS65 4.1 12.7 1.0
CD2 C:HIS65 4.2 12.8 1.0
ND1 B:HIS82 4.2 10.0 1.0
CG C:HIS87 4.2 13.3 1.0
ND1 C:HIS87 4.2 12.7 1.0
OE1 B:GLN59 4.2 11.3 1.0
CG B:HIS82 4.3 8.7 1.0
O C:HOH343 4.3 22.8 1.0
N C:GLN66 4.6 13.3 1.0
CE B:MET99 4.6 17.8 1.0
CA C:HIS65 4.7 12.5 1.0
C C:GLN66 4.9 13.0 1.0
C C:HIS65 4.9 12.6 1.0

Zinc binding site 8 out of 12 in 9jyw

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Zinc binding site 8 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 8 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Zn201

b:12.8
occ:1.00
ND1 D:HIS65 2.1 13.8 1.0
NE2 E:HIS82 2.1 11.1 1.0
NE2 D:HIS87 2.2 11.2 1.0
O E:HOH363 2.3 6.2 1.0
CD2 D:HIS87 3.0 12.4 1.0
CE1 E:HIS82 3.0 12.6 1.0
CE1 D:HIS65 3.0 15.5 1.0
CG D:HIS65 3.1 15.4 1.0
CD2 E:HIS82 3.1 11.7 1.0
CE1 D:HIS87 3.1 12.4 1.0
CB D:HIS65 3.4 14.0 1.0
O E:HOH337 4.0 26.2 1.0
OH E:TYR159 4.1 17.8 1.0
NE2 D:HIS65 4.2 14.2 1.0
O D:GLN66 4.2 15.1 1.0
ND1 E:HIS82 4.2 12.9 1.0
CG D:HIS87 4.2 11.8 1.0
CD2 D:HIS65 4.2 14.6 1.0
ND1 D:HIS87 4.2 11.0 1.0
OE1 E:GLN59 4.2 18.1 1.0
CG E:HIS82 4.2 11.4 1.0
N D:GLN66 4.6 13.4 1.0
CA D:HIS65 4.7 13.8 1.0
CE E:MET99 4.8 18.9 1.0
C D:GLN66 4.9 14.6 1.0
C D:HIS65 4.9 14.4 1.0

Zinc binding site 9 out of 12 in 9jyw

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Zinc binding site 9 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 9 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Zn202

b:17.6
occ:1.00
OE1 D:GLU161 2.0 17.5 1.0
O D:HOH383 2.1 13.1 1.0
OE1 D:GLN164 2.1 17.6 1.0
OE2 B:GLU153 2.2 17.1 1.0
OE1 B:GLU153 2.3 15.1 1.0
CD B:GLU153 2.5 15.9 1.0
OE2 D:GLU161 2.6 19.8 1.0
CD D:GLU161 2.6 17.0 1.0
CD D:GLN164 3.1 17.2 1.0
NE2 D:GLN164 3.4 18.3 1.0
CG B:GLU153 4.0 15.2 1.0
O B:HOH317 4.0 20.9 1.0
O D:HOH392 4.1 25.3 1.0
CG D:GLU161 4.1 15.7 1.0
O D:HOH313 4.3 29.6 1.0
CG B:LEU149 4.4 26.1 1.0
CD2 B:LEU149 4.4 25.7 1.0
CG D:GLN164 4.5 17.6 1.0
CA D:GLU161 4.6 15.1 1.0
CG B:GLN150 4.7 25.1 1.0
CB D:GLN164 4.7 16.3 1.0
CB D:GLU161 4.8 15.6 1.0
NH2 B:ARG157 4.8 18.7 1.0
O B:HOH370 4.9 38.9 1.0
CB B:GLU153 4.9 15.0 1.0

Zinc binding site 10 out of 12 in 9jyw

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Zinc binding site 10 out of 12 in the Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 10 of Crystal Structure of the Gamma-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Zn203

b:30.2
occ:1.00
O E:HOH373 2.1 30.9 1.0
O D:HOH397 2.1 19.5 1.0
O E:HOH350 2.2 22.4 1.0
O D:HOH358 2.2 27.4 1.0
O F:HOH406 2.2 31.7 1.0
O F:HOH446 2.2 21.5 1.0
O D:HOH308 3.8 25.6 1.0
O F:HOH412 3.9 23.0 1.0
O E:HOH305 3.9 21.6 1.0
O F:HOH453 4.2 31.7 1.0
O E:HOH308 4.2 24.1 1.0
O F:HOH425 4.2 24.2 1.0
O D:HOH321 4.2 17.7 1.0
OE1 F:GLN83 4.3 16.7 1.0
OE1 D:GLN83 4.3 17.4 1.0
O F:HOH405 4.3 20.5 1.0
OE1 E:GLN83 4.4 17.9 1.0
O E:HOH340 4.4 27.4 1.0
O D:GLN83 4.5 16.3 1.0
O D:HOH340 4.5 23.7 1.0
O E:GLN83 4.5 17.5 1.0
O F:GLN83 4.6 19.9 1.0
CB D:GLN83 4.7 12.6 1.0
CB E:GLN83 4.8 13.1 1.0
CD D:GLN83 4.8 15.3 1.0
CD F:GLN83 4.8 16.6 1.0
CB F:GLN83 4.8 14.6 1.0
CD E:GLN83 4.8 13.6 1.0

Reference:

S.H.Choi, M.S.Jin. Crystal Structure of the R-Carbonic Anhydrase From the Polyextremophilic Bacterium Aeribacillus Pallidus To Be Published.
Page generated: Sun Dec 15 12:18:47 2024

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