Atomistry » Cobalt » PDB 1vz0-1zft » 1yvm
Atomistry »
  Cobalt »
    PDB 1vz0-1zft »
      1yvm »

Cobalt in PDB 1yvm: E. Coli Methionine Aminopeptidase in Complex with Thiabendazole

Enzymatic activity of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole

All present enzymatic activity of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole:
3.4.11.18;

Protein crystallography data

The structure of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole, PDB code: 1yvm was solved by R.Schiffmann, A.Heine, G.Klebe, C.D.Klein, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.00 / 1.60
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 38.910, 66.130, 48.530, 90.00, 111.25, 90.00
R / Rfree (%) 17 / 23.3

Other elements in 1yvm:

The structure of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole also contains other interesting chemical elements:

Sodium (Na) 1 atom

Cobalt Binding Sites:

The binding sites of Cobalt atom in the E. Coli Methionine Aminopeptidase in Complex with Thiabendazole (pdb code 1yvm). This binding sites where shown within 5.0 Angstroms radius around Cobalt atom.
In total 4 binding sites of Cobalt where determined in the E. Coli Methionine Aminopeptidase in Complex with Thiabendazole, PDB code: 1yvm:
Jump to Cobalt binding site number: 1; 2; 3; 4;

Cobalt binding site 1 out of 4 in 1yvm

Go back to Cobalt Binding Sites List in 1yvm
Cobalt binding site 1 out of 4 in the E. Coli Methionine Aminopeptidase in Complex with Thiabendazole


Mono view


Stereo pair view

A full contact list of Cobalt with other atoms in the Co binding site number 1 of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Co401

b:25.1
occ:1.00
O A:HOH3071 2.0 19.0 1.0
N7 A:TMG501 2.1 20.3 1.0
N11 A:TMG501 2.2 27.2 1.0
NE2 A:HIS79 2.3 25.2 1.0
O A:HOH3196 2.3 26.4 1.0
O A:HOH3149 2.3 21.8 1.0
C9 A:TMG501 2.9 27.9 1.0
C10 A:TMG501 2.9 28.6 1.0
CD2 A:HIS79 3.1 16.9 1.0
C2 A:TMG501 3.2 30.9 1.0
C12 A:TMG501 3.3 32.8 1.0
CE1 A:HIS79 3.3 28.7 1.0
C1 A:TMG501 3.8 27.2 1.0
O A:HOH3158 4.1 17.5 1.0
N8 A:TMG501 4.1 28.7 1.0
NE2 A:HIS178 4.2 20.8 1.0
C14 A:TMG501 4.2 30.1 1.0
C6 A:TMG501 4.2 26.1 1.0
O A:HOH3053 4.2 17.6 1.0
CG A:HIS79 4.3 19.7 1.0
O A:HOH3165 4.4 14.9 1.0
ND1 A:HIS79 4.4 24.1 1.0
OD2 A:ASP97 4.6 18.8 1.0
O A:HOH3107 4.7 32.9 1.0
S13 A:TMG501 4.7 40.2 1.0
CE1 A:HIS178 4.9 20.4 1.0

Cobalt binding site 2 out of 4 in 1yvm

Go back to Cobalt Binding Sites List in 1yvm
Cobalt binding site 2 out of 4 in the E. Coli Methionine Aminopeptidase in Complex with Thiabendazole


Mono view


Stereo pair view

A full contact list of Cobalt with other atoms in the Co binding site number 2 of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Co402

b:16.7
occ:1.00
OD1 A:ASP108 1.9 16.4 1.0
O A:HOH3158 2.1 17.5 1.0
OD1 A:ASP97 2.1 15.9 1.0
O A:HOH3165 2.2 14.9 1.0
OE1 A:GLU235 2.2 12.9 1.0
OD2 A:ASP97 2.5 18.8 1.0
CG A:ASP97 2.5 12.5 1.0
CG A:ASP108 2.9 20.8 1.0
CD A:GLU235 3.0 17.7 1.0
CO A:CO403 3.1 18.0 1.0
OD2 A:ASP108 3.1 16.2 1.0
OE2 A:GLU235 3.3 15.6 1.0
O A:HOH3149 3.8 21.8 1.0
O A:HOH3194 3.9 16.4 1.0
OG1 A:THR99 4.0 16.9 1.0
CB A:ASP97 4.1 14.1 1.0
OE1 A:GLU204 4.2 20.3 1.0
O A:HOH3071 4.3 19.0 1.0
O A:HOH3033 4.3 27.6 1.0
CB A:ASP108 4.3 18.9 1.0
CG A:GLU235 4.4 14.3 1.0
N A:THR109 4.5 13.5 1.0
O A:VAL98 4.6 15.7 1.0
OE2 A:GLU204 4.6 15.6 1.0
O A:HOH3053 4.7 17.6 1.0
CD A:GLU204 4.7 17.3 1.0
C A:ASP108 4.7 15.4 1.0
O A:THR109 4.8 15.6 1.0
CA A:ASP108 4.8 17.6 1.0
CA A:ASP97 4.8 13.7 1.0
CB A:GLU235 4.9 13.5 1.0
C A:THR109 4.9 14.1 1.0
N A:VAL98 4.9 14.8 1.0
C A:ASP97 5.0 18.4 1.0

Cobalt binding site 3 out of 4 in 1yvm

Go back to Cobalt Binding Sites List in 1yvm
Cobalt binding site 3 out of 4 in the E. Coli Methionine Aminopeptidase in Complex with Thiabendazole


Mono view


Stereo pair view

A full contact list of Cobalt with other atoms in the Co binding site number 3 of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Co403

b:18.0
occ:1.00
O A:HOH3158 1.9 17.5 1.0
OD2 A:ASP108 2.1 16.2 1.0
OE2 A:GLU235 2.1 15.6 1.0
NE2 A:HIS171 2.1 14.4 1.0
OE2 A:GLU204 2.2 15.6 1.0
CD A:GLU235 3.0 17.7 1.0
CG A:ASP108 3.0 20.8 1.0
CD2 A:HIS171 3.0 16.7 1.0
CE1 A:HIS171 3.0 14.6 1.0
CD A:GLU204 3.1 17.3 1.0
CO A:CO402 3.1 16.7 1.0
OE1 A:GLU235 3.3 12.9 1.0
OD1 A:ASP108 3.3 16.4 1.0
OE1 A:GLU204 3.4 20.3 1.0
OG1 A:THR202 3.6 15.2 1.0
O A:HOH3149 3.7 21.8 1.0
CG2 A:THR202 3.9 21.1 1.0
CB A:THR202 4.0 15.1 1.0
ND1 A:HIS171 4.2 17.7 1.0
CG A:HIS171 4.2 15.2 1.0
CB A:ASP108 4.2 18.9 1.0
O A:HOH3165 4.3 14.9 1.0
CG A:GLU235 4.3 14.3 1.0
CG A:GLU204 4.4 16.7 1.0
CB A:GLU204 4.9 15.6 1.0
CE1 A:PHE177 5.0 22.9 1.0

Cobalt binding site 4 out of 4 in 1yvm

Go back to Cobalt Binding Sites List in 1yvm
Cobalt binding site 4 out of 4 in the E. Coli Methionine Aminopeptidase in Complex with Thiabendazole


Mono view


Stereo pair view

A full contact list of Cobalt with other atoms in the Co binding site number 4 of E. Coli Methionine Aminopeptidase in Complex with Thiabendazole within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Co404

b:54.9
occ:1.00
O A:HOH3213 2.0 42.8 1.0
O A:HOH3222 2.2 45.6 1.0
O A:HOH3093 2.3 42.4 1.0
OE2 A:GLU123 2.5 43.3 1.0
O A:HOH3269 2.8 63.2 1.0
CD A:GLU123 3.4 46.4 1.0
OE1 A:GLU123 3.8 42.8 1.0
O A:HOH3264 4.4 43.6 1.0
O A:HOH3129 4.5 35.1 1.0
CG A:GLU123 4.7 36.3 1.0
CD1 A:ILE120 4.9 34.0 1.0

Reference:

R.Schiffmann, A.Heine, G.Klebe, C.D.Klein. Metal Ions As Cofactors For the Binding of Inhibitors to Methionine Aminopeptidase: A Critical View of the Relevance of in Vitro Metalloenzyme Assays. Angew.Chem.Int.Ed.Engl. V. 44 3620 2005.
ISSN: ISSN 1433-7851
PubMed: 15880695
DOI: 10.1002/ANIE.200500592
Page generated: Sun Jul 13 18:00:14 2025

Last articles

Fe in 2YXO
Fe in 2YRS
Fe in 2YXC
Fe in 2YNM
Fe in 2YVJ
Fe in 2YP1
Fe in 2YU2
Fe in 2YU1
Fe in 2YQB
Fe in 2YOO
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy