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Chlorine in PDB 4oc4: X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine

Enzymatic activity of X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine

All present enzymatic activity of X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine:
3.4.17.21;

Protein crystallography data

The structure of X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine, PDB code: 4oc4 was solved by J.Pavlicek, J.Ptacek, J.Cerny, Y.Byun, L.Skultetyova, M.Pomper, J.Lubkowski, C.Barinka, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.99 / 1.66
Space group I 2 2 2
Cell size a, b, c (Å), α, β, γ (°) 101.441, 130.459, 159.063, 90.00, 90.00, 90.00
R / Rfree (%) 15.9 / 19.1

Other elements in 4oc4:

The structure of X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine also contains other interesting chemical elements:

Iodine (I) 1 atom
Calcium (Ca) 1 atom
Zinc (Zn) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine (pdb code 4oc4). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine, PDB code: 4oc4:

Chlorine binding site 1 out of 1 in 4oc4

Go back to Chlorine Binding Sites List in 4oc4
Chlorine binding site 1 out of 1 in the X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of X-Ray Structure of of Human Glutamate Carboxypeptidase II (Gcpii) in A Complex with Cpibzl, A Urea-Based Inhibitor N~2~-{[(1S)-1-Carboxy-2- (Pyridin-4-Yl)Ethyl]Carbamoyl}-N~6~-(4-Iodobenzoyl)-L-Lysine within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl817

b:24.4
occ:1.00
O A:HOH920 3.2 27.8 1.0
ND2 A:ASN451 3.3 21.8 1.0
NH1 A:ARG534 3.4 23.5 1.0
N A:ASP453 3.4 21.4 1.0
NH2 A:ARG536 3.4 25.7 1.0
NE A:ARG534 3.5 22.0 1.0
CD A:ARG536 3.5 24.3 0.1
CB A:ASP453 3.7 20.9 1.0
CZ A:ARG534 3.9 22.4 1.0
CA A:ASP453 3.9 21.6 1.0
NH2 A:ARG580 4.0 23.2 1.0
CB A:ARG534 4.1 20.7 1.0
C A:ASP453 4.2 22.6 1.0
CG A:ASN451 4.2 20.9 1.0
CB A:ASN451 4.2 20.2 1.0
CZ A:ARG536 4.3 25.0 1.0
N A:ALA452 4.3 22.0 1.0
NE A:ARG536 4.4 21.3 0.5
NE A:ARG536 4.4 24.8 0.1
O A:ASP453 4.4 23.7 1.0
C A:ALA452 4.4 22.5 1.0
C A:ASN451 4.5 21.4 1.0
CA A:ALA452 4.5 21.8 1.0
O A:SER454 4.6 22.3 0.8
CG A:ARG536 4.6 24.0 0.1
O A:ASN451 4.6 23.4 1.0
CD A:ARG534 4.6 20.8 1.0
N A:SER454 4.7 23.1 0.2
ND2 A:ASN519 4.7 19.8 1.0
N A:SER454 4.8 22.1 0.8
CG A:ARG534 4.8 22.0 1.0
CZ A:ARG580 4.8 24.3 1.0
CG A:ASN519 4.9 20.3 1.0

Reference:

J.Pavlicek, J.Ptacek, J.Cerny, Y.Byun, L.Skultetyova, M.G.Pomper, J.Lubkowski, C.Barinka. Structural Characterization of P1'-Diversified Urea-Based Inhibitors of Glutamate Carboxypeptidase II. Bioorg.Med.Chem.Lett. V. 24 2340 2014.
ISSN: ISSN 0960-894X
PubMed: 24731280
DOI: 10.1016/J.BMCL.2014.03.066
Page generated: Fri Jul 11 19:59:41 2025

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