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Sodium in PDB 3q9c: Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine

Protein crystallography data

The structure of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine, PDB code: 3q9c was solved by P.M.Lombardi, D.W.Christianson, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.00 / 2.30
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 117.461, 120.154, 118.448, 98.47, 94.41, 115.89
R / Rfree (%) 18.6 / 22.7

Other elements in 3q9c:

The structure of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine also contains other interesting chemical elements:

Potassium (K) 12 atoms
Zinc (Zn) 12 atoms

Sodium Binding Sites:

Pages:

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

Binding sites:

The binding sites of Sodium atom in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine (pdb code 3q9c). This binding sites where shown within 5.0 Angstroms radius around Sodium atom.
In total 12 binding sites of Sodium where determined in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine, PDB code: 3q9c:
Jump to Sodium binding site number: 1; 2; 3; 4; 5; 6; 7; 8; 9; 10;

Sodium binding site 1 out of 12 in 3q9c

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Sodium binding site 1 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Na344

b:19.0
occ:1.00
O A:HOH353 2.2 16.9 1.0
O A:ARG209 2.3 21.5 1.0
OG1 A:THR243 2.4 23.5 1.0
O A:PHE206 2.4 15.5 1.0
O A:VAL212 2.5 17.4 1.0
O A:HOH358 3.2 27.1 1.0
CB A:THR243 3.2 21.5 1.0
C A:ARG209 3.4 20.3 1.0
C A:PHE206 3.5 14.6 1.0
C A:VAL212 3.7 18.9 1.0
CB A:PHE206 3.8 14.8 1.0
O A:THR243 3.9 21.0 1.0
N A:ARG209 4.0 19.8 1.0
CA A:ARG209 4.1 20.6 1.0
CG2 A:THR243 4.1 19.7 1.0
CA A:PHE206 4.2 14.6 1.0
CB A:ARG209 4.2 20.4 1.0
O A:GLY240 4.3 18.2 1.0
C A:THR243 4.3 19.8 1.0
CA A:THR243 4.4 19.8 1.0
N A:GLY210 4.5 20.1 1.0
O A:HOH360 4.5 9.8 1.0
O A:TYR207 4.5 19.1 1.0
N A:TYR207 4.5 13.8 1.0
C A:TYR207 4.5 17.2 1.0
CA A:VAL212 4.6 19.6 1.0
CA A:GLY240 4.6 19.0 1.0
N A:PHE213 4.6 17.1 1.0
N A:VAL212 4.6 20.6 1.0
CA A:TYR207 4.7 16.4 1.0
CA A:PHE213 4.7 16.6 1.0
CB A:VAL212 4.7 19.5 1.0
CA A:GLY210 4.7 20.5 1.0
OG1 A:THR244 4.9 23.2 1.0
C A:GLY240 4.9 18.1 1.0
N A:GLU208 5.0 18.3 1.0

Sodium binding site 2 out of 12 in 3q9c

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Sodium binding site 2 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 2 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Na344

b:24.7
occ:1.00
O B:HOH352 2.1 19.9 1.0
O B:ARG209 2.3 23.7 1.0
O B:VAL212 2.3 19.4 1.0
OG1 B:THR243 2.4 23.7 1.0
O B:PHE206 2.4 16.2 1.0
CB B:THR243 3.2 24.0 1.0
C B:ARG209 3.5 24.4 1.0
C B:VAL212 3.5 18.9 1.0
C B:PHE206 3.5 16.2 1.0
O B:HOH690 3.5 24.9 1.0
CB B:PHE206 3.8 13.8 1.0
O B:THR243 3.9 22.1 1.0
N B:ARG209 4.1 24.6 1.0
CG2 B:THR243 4.1 23.1 1.0
CA B:ARG209 4.2 24.4 1.0
CA B:PHE206 4.2 15.8 1.0
C B:THR243 4.3 22.6 1.0
O B:HOH361 4.4 22.6 1.0
CA B:VAL212 4.4 18.5 1.0
CA B:THR243 4.4 23.2 1.0
CB B:ARG209 4.4 25.1 1.0
N B:VAL212 4.4 20.9 1.0
N B:PHE213 4.4 18.4 1.0
O B:GLY240 4.5 21.7 1.0
CB B:VAL212 4.5 19.5 1.0
CA B:PHE213 4.5 17.7 1.0
N B:TYR207 4.5 15.9 1.0
N B:GLY210 4.5 23.4 1.0
C B:TYR207 4.6 18.8 1.0
O B:TYR207 4.6 19.5 1.0
CA B:TYR207 4.7 17.1 1.0
CA B:GLY240 4.7 20.6 1.0
CA B:GLY210 4.8 23.2 1.0
OG1 B:THR244 5.0 23.5 1.0
CG B:PHE206 5.0 16.9 1.0

Sodium binding site 3 out of 12 in 3q9c

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Sodium binding site 3 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 3 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Na344

b:19.4
occ:1.00
O C:HOH351 2.2 19.7 1.0
O C:ARG209 2.2 25.2 1.0
OG1 C:THR243 2.2 20.2 1.0
O C:VAL212 2.3 17.2 1.0
O C:PHE206 2.6 18.7 1.0
CB C:THR243 3.0 21.7 1.0
C C:ARG209 3.4 23.4 1.0
O C:HOH353 3.4 23.7 1.0
C C:VAL212 3.5 17.9 1.0
C C:PHE206 3.7 18.6 1.0
O C:THR243 3.8 18.5 1.0
CG2 C:THR243 3.9 20.4 1.0
CB C:PHE206 4.0 16.6 1.0
N C:ARG209 4.0 23.5 1.0
CA C:ARG209 4.0 23.4 1.0
CB C:ARG209 4.1 22.4 1.0
C C:THR243 4.2 19.6 1.0
CA C:THR243 4.2 20.0 1.0
CA C:VAL212 4.4 17.7 1.0
CA C:PHE206 4.4 17.5 1.0
N C:VAL212 4.4 18.9 1.0
O C:GLY240 4.4 21.4 1.0
N C:GLY210 4.5 22.9 1.0
N C:PHE213 4.5 17.3 1.0
O C:TYR207 4.5 18.4 1.0
CA C:PHE213 4.5 16.0 1.0
CA C:GLY240 4.5 21.7 1.0
CB C:VAL212 4.5 19.2 1.0
O C:HOH371 4.6 13.4 1.0
C C:TYR207 4.7 19.4 1.0
CA C:GLY210 4.7 21.6 1.0
N C:TYR207 4.7 16.6 1.0
CA C:TYR207 4.8 18.4 1.0
OG1 C:THR244 4.9 23.9 1.0
C C:GLY240 5.0 21.3 1.0

Sodium binding site 4 out of 12 in 3q9c

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Sodium binding site 4 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 4 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Na344

b:19.5
occ:1.00
O D:HOH351 2.1 18.1 1.0
O D:VAL212 2.2 20.3 1.0
OG1 D:THR243 2.3 19.8 1.0
O D:ARG209 2.3 23.1 1.0
O D:PHE206 2.5 16.8 1.0
CB D:THR243 3.1 21.4 1.0
C D:VAL212 3.4 20.1 1.0
C D:ARG209 3.5 23.9 1.0
C D:PHE206 3.6 17.2 1.0
O D:HOH353 3.7 23.9 1.0
CB D:PHE206 3.8 17.2 1.0
O D:THR243 3.9 20.3 1.0
CG2 D:THR243 3.9 20.2 1.0
N D:ARG209 4.2 23.2 1.0
CA D:ARG209 4.2 23.8 1.0
CA D:VAL212 4.3 20.9 1.0
CA D:PHE206 4.3 17.4 1.0
C D:THR243 4.3 19.3 1.0
CB D:ARG209 4.3 24.7 1.0
CA D:THR243 4.3 20.4 1.0
N D:VAL212 4.4 22.4 1.0
N D:PHE213 4.4 19.2 1.0
O D:GLY240 4.4 18.6 1.0
CB D:VAL212 4.4 22.3 1.0
O D:HOH365 4.4 15.4 1.0
CA D:PHE213 4.5 18.1 1.0
CA D:GLY240 4.6 18.2 1.0
N D:GLY210 4.6 22.5 1.0
N D:TYR207 4.6 17.2 1.0
CG1 D:VAL212 4.8 21.0 1.0
C D:TYR207 4.8 19.4 1.0
CA D:GLY210 4.8 23.0 1.0
CA D:TYR207 4.8 17.9 1.0
O D:TYR207 4.9 19.7 1.0
N D:PHE214 4.9 15.8 1.0
C D:GLY240 5.0 18.0 1.0
CG D:PHE206 5.0 20.1 1.0

Sodium binding site 5 out of 12 in 3q9c

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Sodium binding site 5 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 5 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Na344

b:17.9
occ:1.00
O E:HOH348 2.2 13.0 1.0
O E:VAL212 2.2 23.3 1.0
O E:ARG209 2.3 22.0 1.0
OG1 E:THR243 2.3 19.0 1.0
O E:PHE206 2.6 17.0 1.0
CB E:THR243 3.0 20.2 1.0
C E:VAL212 3.4 22.1 1.0
C E:ARG209 3.4 22.2 1.0
C E:PHE206 3.7 18.8 1.0
O E:HOH345 3.7 13.2 1.0
O E:THR243 3.8 18.0 1.0
CG2 E:THR243 3.9 20.4 1.0
CB E:PHE206 3.9 17.6 1.0
N E:ARG209 4.1 22.2 1.0
CA E:ARG209 4.1 21.9 1.0
CB E:ARG209 4.1 23.0 1.0
CA E:VAL212 4.2 22.5 1.0
CA E:THR243 4.3 19.5 1.0
N E:VAL212 4.3 22.9 1.0
C E:THR243 4.3 18.7 1.0
CA E:PHE206 4.3 17.8 1.0
CB E:VAL212 4.4 22.3 1.0
N E:PHE213 4.4 20.8 1.0
O E:GLY240 4.4 21.5 1.0
N E:GLY210 4.5 21.5 1.0
CA E:PHE213 4.5 20.3 1.0
O E:HOH368 4.6 25.0 1.0
CA E:GLY240 4.7 20.1 1.0
CA E:GLY210 4.7 21.7 1.0
O E:TYR207 4.7 21.1 1.0
N E:TYR207 4.7 17.7 1.0
C E:TYR207 4.7 21.1 1.0
CG1 E:VAL212 4.8 21.9 1.0
C E:GLY210 4.9 21.9 1.0
CA E:TYR207 4.9 19.4 1.0

Sodium binding site 6 out of 12 in 3q9c

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Sodium binding site 6 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 6 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Na344

b:27.7
occ:1.00
O F:HOH1031 2.2 22.0 1.0
O F:ARG209 2.3 18.5 1.0
O F:PHE206 2.3 18.1 1.0
O F:VAL212 2.4 22.7 1.0
OG1 F:THR243 2.5 21.2 1.0
CB F:THR243 3.3 20.1 1.0
C F:ARG209 3.4 18.5 1.0
C F:PHE206 3.4 17.6 1.0
C F:VAL212 3.6 21.3 1.0
CB F:PHE206 3.6 17.0 1.0
O F:HOH346 3.8 14.0 1.0
N F:ARG209 3.9 20.6 1.0
CA F:ARG209 4.0 19.2 1.0
CA F:PHE206 4.1 16.6 1.0
CG2 F:THR243 4.1 18.5 1.0
CB F:ARG209 4.2 21.5 1.0
O F:THR243 4.2 23.3 1.0
CA F:VAL212 4.4 20.2 1.0
N F:VAL212 4.4 21.4 1.0
O F:HOH352 4.4 13.5 1.0
CB F:VAL212 4.5 20.1 1.0
N F:TYR207 4.5 17.6 1.0
N F:GLY210 4.5 18.9 1.0
O F:GLY240 4.5 18.8 1.0
CA F:THR243 4.5 21.1 1.0
N F:PHE213 4.5 21.7 1.0
O F:TYR207 4.6 15.6 1.0
C F:TYR207 4.6 18.2 1.0
C F:THR243 4.6 22.4 1.0
CA F:PHE213 4.7 20.4 1.0
CA F:TYR207 4.7 17.8 1.0
CA F:GLY240 4.8 19.4 1.0
CA F:GLY210 4.8 20.1 1.0
CG F:PHE206 4.8 17.6 1.0
CG1 F:VAL212 4.9 20.1 1.0

Sodium binding site 7 out of 12 in 3q9c

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Sodium binding site 7 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 7 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
G:Na344

b:18.1
occ:1.00
O G:HOH347 2.2 13.6 1.0
OG1 G:THR243 2.2 19.0 1.0
O G:VAL212 2.2 17.6 1.0
O G:ARG209 2.3 20.7 1.0
O G:PHE206 2.5 15.5 1.0
CB G:THR243 2.8 20.9 1.0
C G:VAL212 3.4 18.1 1.0
C G:ARG209 3.5 20.3 1.0
O G:THR243 3.6 18.5 1.0
C G:PHE206 3.7 15.9 1.0
CG2 G:THR243 3.7 21.7 1.0
O G:HOH346 3.8 24.0 1.0
CB G:PHE206 3.9 13.4 1.0
CA G:THR243 4.0 19.6 1.0
C G:THR243 4.1 19.2 1.0
N G:ARG209 4.3 20.7 1.0
CA G:VAL212 4.3 19.1 1.0
CA G:ARG209 4.3 20.4 1.0
O G:HOH362 4.3 17.0 1.0
N G:PHE213 4.3 16.8 1.0
CA G:PHE206 4.4 14.4 1.0
CB G:ARG209 4.4 19.1 1.0
N G:VAL212 4.4 20.6 1.0
CA G:PHE213 4.4 15.0 1.0
CB G:VAL212 4.5 18.9 1.0
O G:GLY240 4.5 18.2 1.0
N G:GLY210 4.5 21.1 1.0
CA G:GLY210 4.7 21.0 1.0
N G:TYR207 4.7 15.7 1.0
C G:TYR207 4.8 17.1 1.0
O G:TYR207 4.8 17.2 1.0
CA G:GLY240 4.8 15.8 1.0
CA G:TYR207 4.9 16.4 1.0
N G:PHE214 4.9 14.3 1.0
OG1 G:THR244 4.9 22.4 1.0
CG1 G:VAL212 4.9 19.9 1.0
C G:PHE213 5.0 14.6 1.0
N G:THR243 5.0 20.1 1.0

Sodium binding site 8 out of 12 in 3q9c

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Sodium binding site 8 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 8 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
H:Na344

b:27.7
occ:1.00
OG1 H:THR243 2.1 20.9 1.0
O H:HOH381 2.2 19.8 1.0
O H:ARG209 2.3 28.9 1.0
O H:VAL212 2.3 26.0 1.0
O H:PHE206 2.4 20.0 1.0
CB H:THR243 2.9 21.7 1.0
C H:ARG209 3.5 26.9 1.0
C H:VAL212 3.6 25.5 1.0
C H:PHE206 3.6 18.6 1.0
O H:HOH359 3.6 19.4 1.0
CG2 H:THR243 3.7 19.6 1.0
O H:THR243 3.8 20.4 1.0
CB H:PHE206 4.0 17.5 1.0
CA H:THR243 4.1 21.7 1.0
N H:ARG209 4.1 26.1 1.0
C H:THR243 4.2 21.0 1.0
CA H:ARG209 4.2 26.8 1.0
CB H:ARG209 4.2 26.7 1.0
CA H:PHE206 4.3 17.2 1.0
O H:HOH358 4.4 14.8 1.0
N H:VAL212 4.4 27.6 1.0
O H:GLY240 4.4 26.9 1.0
CA H:VAL212 4.4 25.9 1.0
N H:PHE213 4.5 24.3 1.0
N H:GLY210 4.5 26.3 1.0
N H:TYR207 4.5 20.0 1.0
O H:TYR207 4.6 19.7 1.0
CA H:PHE213 4.6 22.4 1.0
C H:TYR207 4.6 20.5 1.0
CB H:VAL212 4.6 28.2 1.0
CA H:TYR207 4.7 20.9 1.0
CA H:GLY240 4.7 26.5 1.0
CA H:GLY210 4.7 27.6 1.0
N H:THR243 5.0 22.4 1.0
C H:GLY210 5.0 28.7 1.0

Sodium binding site 9 out of 12 in 3q9c

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Sodium binding site 9 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 9 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
I:Na344

b:22.3
occ:1.00
O I:HOH402 2.2 11.6 1.0
O I:VAL212 2.4 19.1 1.0
O I:ARG209 2.4 22.6 1.0
OG1 I:THR243 2.4 19.9 1.0
O I:PHE206 2.5 13.1 1.0
CB I:THR243 3.2 19.4 1.0
O I:HOH352 3.5 20.5 1.0
C I:VAL212 3.5 19.2 1.0
C I:PHE206 3.5 15.7 1.0
C I:ARG209 3.6 22.1 1.0
CB I:PHE206 3.8 16.1 1.0
O I:THR243 4.0 21.0 1.0
CG2 I:THR243 4.1 17.7 1.0
N I:ARG209 4.1 23.4 1.0
CA I:PHE206 4.2 15.1 1.0
CA I:ARG209 4.3 22.6 1.0
CA I:VAL212 4.3 18.7 1.0
O I:HOH1020 4.4 17.1 1.0
C I:THR243 4.4 20.0 1.0
CA I:THR243 4.4 19.4 1.0
N I:VAL212 4.4 20.0 1.0
N I:PHE213 4.4 19.4 1.0
CB I:VAL212 4.5 18.9 1.0
CB I:ARG209 4.5 20.8 1.0
O I:GLY240 4.5 22.7 1.0
CA I:PHE213 4.5 18.9 1.0
N I:TYR207 4.5 17.4 1.0
O I:TYR207 4.6 18.9 1.0
C I:TYR207 4.6 19.8 1.0
N I:GLY210 4.6 22.2 1.0
CA I:TYR207 4.8 19.2 1.0
CA I:GLY240 4.8 21.1 1.0
CG1 I:VAL212 4.8 15.5 1.0
CA I:GLY210 4.8 22.3 1.0
OG1 I:THR244 4.9 17.8 1.0

Sodium binding site 10 out of 12 in 3q9c

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Sodium binding site 10 out of 12 in the Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 10 of Crystal Structure of H159A Apah Complexed with N8-Acetylspermidine within 5.0Å range:
probe atom residue distance (Å) B Occ
J:Na344

b:14.8
occ:1.00
OG1 J:THR243 2.2 18.6 1.0
O J:ARG209 2.2 24.0 1.0
O J:HOH363 2.3 22.1 1.0
O J:VAL212 2.4 26.0 1.0
O J:PHE206 2.4 16.5 1.0
CB J:THR243 3.0 20.3 1.0
C J:ARG209 3.3 23.9 1.0
C J:PHE206 3.5 18.4 1.0
C J:VAL212 3.6 25.2 1.0
O J:HOH347 3.6 18.1 1.0
CG2 J:THR243 3.8 18.4 1.0
N J:ARG209 3.8 23.4 1.0
CB J:PHE206 3.8 17.9 1.0
O J:THR243 4.0 19.5 1.0
CA J:ARG209 4.0 23.3 1.0
CA J:THR243 4.2 19.2 1.0
CB J:ARG209 4.3 21.6 1.0
CA J:PHE206 4.3 16.6 1.0
C J:THR243 4.3 19.7 1.0
O J:GLY240 4.3 23.6 1.0
N J:VAL212 4.4 26.3 1.0
CA J:VAL212 4.4 25.6 1.0
N J:GLY210 4.4 24.5 1.0
O J:TYR207 4.5 17.1 1.0
C J:TYR207 4.5 20.6 1.0
N J:TYR207 4.6 17.8 1.0
CA J:GLY240 4.6 22.5 1.0
N J:PHE213 4.6 24.1 1.0
CB J:VAL212 4.6 25.0 1.0
O J:HOH350 4.6 18.4 1.0
CA J:GLY210 4.7 26.5 1.0
CA J:PHE213 4.7 21.8 1.0
CA J:TYR207 4.7 19.2 1.0
N J:GLU208 4.9 21.9 1.0
C J:GLY240 4.9 22.2 1.0
C J:GLU208 5.0 23.7 1.0

Reference:

P.M.Lombardi, H.D.Angell, D.A.Whittington, E.F.Flynn, K.R.Rajashankar, D.W.Christianson. Structure of Prokaryotic Polyamine Deacetylase Reveals Evolutionary Functional Relationships with Eukaryotic Histone Deacetylases . Biochemistry V. 50 1808 2011.
ISSN: ISSN 0006-2960
PubMed: 21268586
DOI: 10.1021/BI101859K
Page generated: Mon Oct 7 12:26:49 2024

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Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
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