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Zinc in PDB 3frg: Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor

Enzymatic activity of Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor

All present enzymatic activity of Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor:
3.1.4.17;

Protein crystallography data

The structure of Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor, PDB code: 3frg was solved by D.O.Somers, M.Neu, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 1.70
Space group I 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 88.485, 94.831, 105.320, 90.00, 90.00, 90.00
R / Rfree (%) 20.9 / 24.2

Other elements in 3frg:

The structure of Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor also contains other interesting chemical elements:

Magnesium (Mg) 1 atom
Arsenic (As) 4 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor (pdb code 3frg). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor, PDB code: 3frg:

Zinc binding site 1 out of 1 in 3frg

Go back to Zinc Binding Sites List in 3frg
Zinc binding site 1 out of 1 in the Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Catalytic Domain of Human Phosphodiesterase 4B2B in Complex with A Quinoline Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn504

b:21.8
occ:1.00
 OD2 A:ASP275 2.1 16.7 1.0
NE2 A:HIS238 2.1 20.8 1.0
NE2 A:HIS274 2.2 19.7 1.0
OD1 A:ASP392 2.3 18.6 1.0
O A:HOH581 2.3 21.8 1.0
O A:HOH668 2.3 22.7 1.0
CD2 A:HIS274 3.0 17.0 1.0
CD2 A:HIS238 3.1 16.2 1.0
CG A:ASP275 3.1 16.4 1.0
CG A:ASP392 3.1 20.9 1.0
CE1 A:HIS238 3.2 17.2 1.0
CE1 A:HIS274 3.2 22.0 1.0
OD2 A:ASP392 3.3 24.4 1.0
OD1 A:ASP275 3.6 17.8 1.0
MG A:MG505 3.8 22.6 1.0
O A:HOH585 4.1 18.9 1.0
CG A:HIS274 4.2 19.2 1.0
O A:HOH667 4.2 20.8 1.0
CD2 A:HIS234 4.2 20.2 1.0
CG A:HIS238 4.2 16.5 1.0
ND1 A:HIS238 4.3 21.0 1.0
ND1 A:HIS274 4.3 19.7 1.0
CB A:ASP275 4.3 14.8 1.0
CB A:ASP392 4.5 18.3 1.0
NE2 A:HIS234 4.5 19.7 1.0
O A:HOH582 4.7 21.2 1.0
CG2 A:VAL242 4.8 19.9 1.0
C26 A:SK41 4.9 22.2 1.0
CA A:ASP392 5.0 20.1 1.0

Reference:

C.J.Lunniss, A.W.Cooper, C.D.Eldred, M.Kranz, M.Lindvall, F.S.Lucas, M.Neu, A.G.Preston, L.E.Ranshaw, A.J.Redgrave, J.Ed Robinson, T.J.Shipley, Y.E.Solanke, D.O.Somers, J.O.Wiseman. Quinolines As A Novel Structural Class of Potent and Selective PDE4 Inhibitors: Optimisation For Oral Administration. Bioorg.Med.Chem.Lett. V. 19 1380 2009.
ISSN: ISSN 0960-894X
PubMed: 19195882
DOI: 10.1016/J.BMCL.2009.01.045
Page generated: Wed Dec 16 04:19:01 2020

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