Zinc in PDB 7f2l: Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A

Enzymatic activity of Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A

All present enzymatic activity of Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A:
3.1.4.53;

Protein crystallography data

The structure of Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A, PDB code: 7f2l was solved by Y.-Y.Huang, X.He, H.-B.Luo, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 23.52 / 2.10
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 57.962, 80.559, 163.544, 90, 90, 90
R / Rfree (%) 20.8 / 25.1

Other elements in 7f2l:

The structure of Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A also contains other interesting chemical elements:

Fluorine (F) 2 atoms
Magnesium (Mg) 2 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A (pdb code 7f2l). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A, PDB code: 7f2l:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 7f2l

Go back to Zinc Binding Sites List in 7f2l
Zinc binding site 1 out of 2 in the Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn601

b:15.1
occ:1.00
O A:HOH788 2.1 12.9 1.0
O37 A:1AS603 2.1 14.9 1.0
OD2 A:ASP201 2.1 7.6 1.0
OD1 A:ASP318 2.2 14.6 1.0
NE2 A:HIS164 2.3 9.5 1.0
NE2 A:HIS200 2.4 7.2 1.0
C35 A:1AS603 2.9 10.7 1.0
CG A:ASP318 3.1 12.5 1.0
CD2 A:HIS200 3.1 8.4 1.0
CG A:ASP201 3.1 11.9 1.0
CD2 A:HIS164 3.2 9.8 1.0
O36 A:1AS603 3.2 34.2 1.0
OD2 A:ASP318 3.2 10.5 1.0
CE1 A:HIS164 3.3 10.8 1.0
CE1 A:HIS200 3.5 11.5 1.0
MG A:MG602 3.6 3.0 1.0
OD1 A:ASP201 3.6 8.8 1.0
O A:HOH701 4.1 7.1 1.0
C34 A:1AS603 4.2 21.4 1.0
CD2 A:HIS160 4.3 8.9 1.0
CG A:HIS200 4.3 9.3 1.0
CB A:ASP201 4.4 8.4 1.0
CG A:HIS164 4.4 10.9 1.0
ND1 A:HIS164 4.4 9.8 1.0
CB A:ASP318 4.5 8.4 1.0
ND1 A:HIS200 4.5 10.9 1.0
NE2 A:HIS160 4.7 9.8 1.0
O A:HOH739 4.8 10.7 1.0
C33 A:1AS603 4.8 13.6 1.0
CG2 A:VAL168 5.0 6.7 1.0

Zinc binding site 2 out of 2 in 7f2l

Go back to Zinc Binding Sites List in 7f2l
Zinc binding site 2 out of 2 in the Crystal Structure of PDE4D Catalytic Domain Complexed with Compound 18A


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 PDE4D Catalytic Domain Complexed with Compound 18A within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn601

b:19.1
occ:1.00
O B:HOH775 2.0 18.0 1.0
OD2 B:ASP201 2.2 8.9 1.0
OD1 B:ASP318 2.2 14.7 1.0
NE2 B:HIS164 2.3 15.3 1.0
NE2 B:HIS200 2.4 13.0 1.0
O37 B:1AS603 2.4 18.9 1.0
C35 B:1AS603 3.0 13.8 1.0
CG B:ASP201 3.1 11.5 1.0
O36 B:1AS603 3.1 28.9 1.0
CG B:ASP318 3.1 15.8 1.0
CD2 B:HIS200 3.1 16.0 1.0
CD2 B:HIS164 3.2 15.7 1.0
CE1 B:HIS164 3.3 12.4 1.0
OD2 B:ASP318 3.3 16.8 1.0
CE1 B:HIS200 3.4 14.4 1.0
OD1 B:ASP201 3.4 11.8 1.0
MG B:MG602 3.5 7.6 1.0
O B:HOH705 3.9 7.7 1.0
CD2 B:HIS160 4.2 12.4 1.0
CB B:ASP201 4.3 9.7 1.0
CG B:HIS200 4.3 15.4 1.0
C34 B:1AS603 4.4 21.7 1.0
CG B:HIS164 4.4 13.1 1.0
ND1 B:HIS164 4.4 15.8 1.0
ND1 B:HIS200 4.4 12.7 1.0
CB B:ASP318 4.5 15.0 1.0
NE2 B:HIS160 4.7 14.6 1.0
O B:HOH743 4.9 12.0 1.0
CG2 B:VAL168 4.9 14.6 1.0
C33 B:1AS603 5.0 17.1 1.0

Reference:

Y.Y.Huang, J.Deng, Y.J.Tian, J.Liang, X.Xie, Y.Huang, J.Zhu, Z.Zhu, Q.Zhou, X.He, H.B.Luo. Mangostanin Derivatives As Novel and Orally Active Phosphodiesterase 4 Inhibitors For the Treatment of Idiopathic Pulmonary Fibrosis with Improved Safety. J.Med.Chem. V. 64 13736 2021.
ISSN: ISSN 0022-2623
PubMed: 34520193
DOI: 10.1021/ACS.JMEDCHEM.1C01085
Page generated: Fri Nov 5 16:51:30 2021

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