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Zinc in PDB 5jn9: Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide

Enzymatic activity of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide

All present enzymatic activity of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide:
4.2.1.1;

Protein crystallography data

The structure of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide, PDB code: 5jn9 was solved by Z.Chen, A.Waheed, E.Di Cera, W.S.Sly, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.00 / 2.10
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 64.784, 123.980, 151.336, 90.00, 90.00, 90.00
R / Rfree (%) 17 / 22

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide (pdb code 5jn9). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide, PDB code: 5jn9:
Jump to Zinc binding site number: 1; 2; 3; 4;

Zinc binding site 1 out of 4 in 5jn9

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Zinc binding site 1 out of 4 in the Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn301

b:18.6
occ:1.00
N1 A:EZL302 2.1 22.2 1.0
NE2 A:HIS96 2.1 17.6 1.0
ND1 A:HIS119 2.2 19.3 1.0
NE2 A:HIS94 2.2 22.9 1.0
CD2 A:HIS94 3.0 22.4 1.0
CE1 A:HIS119 3.0 19.2 1.0
S1 A:EZL302 3.0 22.5 1.0
O1 A:EZL302 3.0 21.7 1.0
CD2 A:HIS96 3.0 17.1 1.0
CE1 A:HIS96 3.2 18.2 1.0
CG A:HIS119 3.3 20.0 1.0
CE1 A:HIS94 3.3 21.7 1.0
CB A:HIS119 3.7 19.1 1.0
OG1 A:THR199 3.8 18.4 1.0
OE1 A:GLU106 3.9 18.2 1.0
O2 A:EZL302 4.0 21.2 1.0
O A:HOH583 4.1 22.8 1.0
C1 A:EZL302 4.2 24.0 1.0
NE2 A:HIS119 4.2 20.5 1.0
CG A:HIS94 4.2 22.4 1.0
CG A:HIS96 4.2 17.5 1.0
ND1 A:HIS96 4.2 18.3 1.0
ND1 A:HIS94 4.3 22.9 1.0
CD2 A:HIS119 4.3 19.1 1.0
O A:HOH729 4.5 24.6 1.0
CD A:GLU106 4.9 17.9 1.0
N2 A:EZL302 4.9 23.8 1.0

Zinc binding site 2 out of 4 in 5jn9

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Zinc binding site 2 out of 4 in the Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn301

b:19.2
occ:1.00
N1 B:EZL302 2.1 22.6 1.0
NE2 B:HIS94 2.1 20.4 1.0
NE2 B:HIS96 2.2 23.6 1.0
ND1 B:HIS119 2.3 20.2 1.0
O1 B:EZL302 3.0 22.2 1.0
CD2 B:HIS96 3.0 22.5 1.0
CD2 B:HIS94 3.0 21.6 1.0
S1 B:EZL302 3.0 22.9 1.0
CE1 B:HIS94 3.1 21.5 1.0
CE1 B:HIS119 3.1 19.1 1.0
CE1 B:HIS96 3.2 23.2 1.0
CG B:HIS119 3.3 21.3 1.0
CB B:HIS119 3.7 20.9 1.0
OG1 B:THR199 3.8 18.6 1.0
OE1 B:GLU106 4.0 20.1 1.0
O2 B:EZL302 4.1 21.5 1.0
C1 B:EZL302 4.1 25.9 1.0
CG B:HIS94 4.2 21.2 1.0
CG B:HIS96 4.2 20.9 1.0
ND1 B:HIS94 4.2 21.7 1.0
ND1 B:HIS96 4.3 23.1 1.0
NE2 B:HIS119 4.3 18.9 1.0
CD2 B:HIS119 4.4 20.6 1.0
O B:HOH592 4.9 48.4 1.0
CD B:GLU106 4.9 20.7 1.0
S2 B:EZL302 4.9 31.6 1.0
N2 B:EZL302 5.0 25.9 1.0

Zinc binding site 3 out of 4 in 5jn9

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Zinc binding site 3 out of 4 in the Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 3 of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Zn301

b:19.9
occ:1.00
NE2 C:HIS94 2.1 21.4 1.0
ND1 C:HIS119 2.1 16.8 1.0
N1 C:EZL302 2.1 21.0 1.0
NE2 C:HIS96 2.1 20.7 1.0
CE1 C:HIS119 2.9 16.7 1.0
O1 C:EZL302 2.9 20.9 1.0
CD2 C:HIS94 3.0 21.3 1.0
S1 C:EZL302 3.0 21.2 1.0
CD2 C:HIS96 3.0 18.9 1.0
CE1 C:HIS94 3.1 21.6 1.0
CE1 C:HIS96 3.2 20.0 1.0
CG C:HIS119 3.2 17.7 1.0
CB C:HIS119 3.6 18.6 1.0
OG1 C:THR199 3.8 17.5 1.0
O C:HOH437 4.0 32.0 1.0
O2 C:EZL302 4.0 21.9 1.0
OE1 C:GLU106 4.1 19.0 1.0
NE2 C:HIS119 4.1 15.2 1.0
ND1 C:HIS94 4.1 21.9 1.0
CG C:HIS94 4.2 21.3 1.0
C1 C:EZL302 4.2 23.9 1.0
CG C:HIS96 4.2 18.5 1.0
ND1 C:HIS96 4.3 19.6 1.0
CD2 C:HIS119 4.3 16.6 1.0
O C:HOH592 4.4 24.9 1.0
CD C:GLU106 5.0 21.0 1.0
N2 C:EZL302 5.0 24.7 1.0
S2 C:EZL302 5.0 25.9 1.0

Zinc binding site 4 out of 4 in 5jn9

Go back to Zinc Binding Sites List in 5jn9
Zinc binding site 4 out of 4 in the Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 4 of Crystal Structure For the Complex of Human Carbonic Anhydrase IV and Ethoxyzolamide within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Zn301

b:20.6
occ:1.00
N1 D:EZL302 2.1 24.4 1.0
NE2 D:HIS94 2.1 19.3 1.0
ND1 D:HIS119 2.2 18.4 1.0
NE2 D:HIS96 2.2 18.1 1.0
O1 D:EZL302 3.0 22.7 1.0
CE1 D:HIS119 3.0 17.9 1.0
CD2 D:HIS94 3.0 19.2 1.0
S1 D:EZL302 3.1 24.3 1.0
CD2 D:HIS96 3.1 17.9 1.0
CE1 D:HIS94 3.2 21.3 1.0
CE1 D:HIS96 3.2 19.0 1.0
CG D:HIS119 3.3 17.4 1.0
O D:HOH698 3.6 37.5 1.0
CB D:HIS119 3.7 16.4 1.0
OG1 D:THR199 3.9 18.6 1.0
O2 D:EZL302 4.0 23.3 1.0
OE1 D:GLU106 4.1 21.1 1.0
C1 D:EZL302 4.2 25.6 1.0
NE2 D:HIS119 4.2 17.5 1.0
CG D:HIS94 4.2 19.9 1.0
ND1 D:HIS94 4.2 20.5 1.0
CG D:HIS96 4.3 18.7 1.0
ND1 D:HIS96 4.3 19.1 1.0
CD2 D:HIS119 4.3 17.5 1.0
O D:HOH813 4.8 39.1 1.0
CD D:GLU106 4.9 22.6 1.0
N2 D:EZL302 4.9 25.4 1.0

Reference:

A.Mickeviciute, D.D.Timm, M.Gedgaudas, V.Linkuviene, Z.Chen, A.Waheed, V.Michailoviene, A.Zubriene, A.Smirnov, E.Capkauskaite, L.Baranauskiene, J.Jachno, J.Revuckiene, E.Manakova, S.Grazulis, J.Matuliene, E.Di Cera, W.S.Sly, D.Matulis. Intrinsic Thermodynamics of High Affinity Inhibitor Binding to Recombinant Human Carbonic Anhydrase IV. Eur. Biophys. J. V. 47 271 2018.
ISSN: ISSN 1432-1017
PubMed: 28975383
DOI: 10.1007/S00249-017-1256-0
Page generated: Wed Dec 16 06:25:34 2020

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