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Chlorine in PDB 3c45: Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor

Enzymatic activity of Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor

All present enzymatic activity of Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor:
3.4.14.5;

Protein crystallography data

The structure of Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor, PDB code: 3c45 was solved by G.Scapin, S.D.Edmondson, A.E.Weber, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.00 / 2.05
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 117.888, 125.909, 136.750, 90.00, 90.00, 90.00
R / Rfree (%) n/a / n/a

Other elements in 3c45:

The structure of Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor also contains other interesting chemical elements:

Fluorine (F) 2 atoms
Sodium (Na) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor (pdb code 3c45). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor, PDB code: 3c45:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 3c45

Go back to Chlorine Binding Sites List in 3c45
Chlorine binding site 1 out of 2 in the Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1521

b:35.2
occ:1.00
CL47 A:3171521 0.0 35.2 1.0
C36 A:3171521 1.7 33.4 1.0
C35 A:3171521 2.7 33.3 1.0
C31 A:3171521 2.8 32.8 1.0
N29 A:3171521 3.1 35.3 1.0
C28 A:3171521 3.4 32.8 1.0
CZ A:PHE357 3.4 22.6 1.0
O A:HOH1722 3.6 27.1 1.0
CA A:SER552 3.7 20.9 1.0
O A:PRO550 3.7 18.6 1.0
O A:CYS551 3.9 22.3 1.0
CB A:SER552 3.9 21.8 1.0
N A:SER552 3.9 20.5 1.0
C34 A:3171521 4.0 32.9 1.0
C A:CYS551 4.0 21.0 1.0
CE1 A:PHE357 4.1 23.4 1.0
C32 A:3171521 4.1 32.2 1.0
CE1 A:TYR547 4.2 19.2 1.0
O A:HOH1601 4.3 28.9 1.0
CE2 A:PHE357 4.4 23.7 1.0
O30 A:3171521 4.5 31.1 1.0
C33 A:3171521 4.6 32.9 1.0
N27 A:3171521 4.7 31.1 1.0
C A:PRO550 4.7 19.0 1.0
CD1 A:TYR547 4.8 18.8 1.0
CA A:CYS551 5.0 20.3 1.0
CB A:CYS551 5.0 20.9 1.0

Chlorine binding site 2 out of 2 in 3c45

Go back to Chlorine Binding Sites List in 3c45
Chlorine binding site 2 out of 2 in the Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Human Dipeptidyl Peptidase IV/CD26 in Complex with A Fluoroolefin Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl2

b:41.0
occ:1.00
CL47 B:3172 0.0 41.0 1.0
C36 B:3172 1.7 38.9 1.0
C35 B:3172 2.6 38.1 1.0
C31 B:3172 2.8 36.9 1.0
N29 B:3172 3.2 37.9 1.0
CZ B:PHE357 3.4 21.8 1.0
C28 B:3172 3.4 36.1 1.0
O B:HOH2612 3.5 29.5 1.0
O B:HOH2606 3.6 35.9 1.0
CA B:SER552 3.7 22.0 1.0
O B:PRO550 3.7 21.8 1.0
O B:CYS551 3.9 25.1 1.0
N B:SER552 3.9 22.6 1.0
CB B:SER552 4.0 22.9 1.0
C34 B:3172 4.0 37.2 1.0
C B:CYS551 4.0 23.3 1.0
CE1 B:PHE357 4.1 22.3 1.0
C32 B:3172 4.1 36.8 1.0
O B:HOH2508 4.2 27.6 1.0
CE1 B:TYR547 4.2 23.6 1.0
CE2 B:PHE357 4.4 22.7 1.0
O30 B:3172 4.5 32.8 1.0
C33 B:3172 4.6 37.0 1.0
N27 B:3172 4.7 33.1 1.0
C B:PRO550 4.7 22.0 1.0
CD1 B:TYR547 4.9 22.6 1.0
CB B:CYS551 4.9 24.0 1.0
CA B:CYS551 4.9 23.4 1.0
O B:GLY549 5.0 21.0 1.0

Reference:

S.D.Edmondson, L.Wei, J.Xu, J.Shang, S.Xu, J.Pang, A.Chaudhary, D.C.Dean, H.He, B.Leiting, K.A.Lyons, R.A.Patel, S.B.Patel, G.Scapin, J.K.Wu, M.G.Beconi, N.A.Thornberry, A.E.Weber. Fluoroolefins As Amide Bond Mimics in Dipeptidyl Peptidase IV Inhibitors Bioorg.Med.Chem.Lett. V. 18 2409 2008.
ISSN: ISSN 0960-894X
PubMed: 18331795
DOI: 10.1016/J.BMCL.2008.02.050
Page generated: Sat Dec 12 09:34:15 2020

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