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Zinc in PDB 3szy: Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form

Enzymatic activity of Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form

All present enzymatic activity of Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form:
3.6.1.9;

Protein crystallography data

The structure of Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form, PDB code: 3szy was solved by V.Agarwal, S.K.Nair, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 25.00 / 1.35
Space group P 43 21 2
Cell size a, b, c (Å), α, β, γ (°) 111.768, 111.768, 72.824, 90.00, 90.00, 90.00
R / Rfree (%) 19.7 / 20.9

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form (pdb code 3szy). 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 Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form, PDB code: 3szy:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 3szy

Go back to Zinc Binding Sites List in 3szy
Zinc binding site 1 out of 2 in the Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form


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 Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn501

b:23.5
occ:1.00
OD1 A:ASP29 1.9 10.3 0.5
NE2 A:HIS251 2.0 9.5 1.0
OG1 A:THR68 2.1 9.9 1.0
OD2 A:ASP250 2.4 11.5 1.0
CG A:ASP29 2.7 9.5 0.5
CE1 A:HIS251 2.9 9.5 1.0
OD2 A:ASP29 2.9 11.2 0.5
CD2 A:HIS251 3.0 9.0 1.0
CB A:THR68 3.1 8.8 1.0
CG A:ASP250 3.2 8.3 1.0
OD1 A:ASP250 3.4 8.2 1.0
OD2 A:ASP211 3.5 12.8 1.0
CG2 A:THR68 3.6 8.9 1.0
CA A:THR68 3.6 8.7 1.0
OD2 A:ASP29 3.6 9.9 0.5
O A:HOH655 3.8 19.9 1.0
CG A:ASP211 3.9 10.8 1.0
ND1 A:HIS251 3.9 9.3 1.0
CG A:HIS251 4.0 8.3 1.0
N A:THR68 4.1 8.4 1.0
CB A:ASP29 4.1 8.7 0.5
CB A:ASP29 4.1 8.8 0.5
CB A:ASP211 4.2 10.7 1.0
CG A:ASP29 4.2 9.1 0.5
N A:GLY30 4.2 8.6 1.0
CE1 A:HIS377 4.4 8.3 1.0
CB A:ASP250 4.5 7.6 1.0
CA A:ASP29 4.5 8.6 0.5
CA A:ASP29 4.5 8.6 0.5
OD1 A:ASP211 4.5 12.9 1.0
ZN A:ZN502 4.6 15.1 1.0
NE2 A:HIS377 4.6 9.1 1.0
C A:ASP29 4.7 8.6 1.0
C A:PHE67 4.9 8.6 1.0
C A:THR68 4.9 8.8 1.0
CA A:GLY30 5.0 8.7 1.0

Zinc binding site 2 out of 2 in 3szy

Go back to Zinc Binding Sites List in 3szy
Zinc binding site 2 out of 2 in the Crystal Structure of Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form


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 Phosphonoacetate Hydrolase From Sinorhizobium Meliloti 1021 in Apo Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn502

b:15.1
occ:1.00
OD2 A:ASP211 1.9 12.8 1.0
NE2 A:HIS377 2.1 9.1 1.0
NE2 A:HIS215 2.1 10.4 1.0
CG A:ASP211 3.0 10.8 1.0
CE1 A:HIS377 3.0 8.3 1.0
CE1 A:HIS215 3.1 9.8 1.0
CD2 A:HIS215 3.1 10.2 1.0
CD2 A:HIS377 3.2 8.8 1.0
OD1 A:ASP211 3.3 12.9 1.0
ND1 A:HIS377 4.2 9.1 1.0
ND1 A:HIS215 4.2 10.0 1.0
CG A:HIS215 4.3 10.3 1.0
CG A:HIS377 4.3 9.0 1.0
CB A:ASP211 4.3 10.7 1.0
OG1 A:THR68 4.3 9.9 1.0
CE1 A:HIS251 4.5 9.5 1.0
ZN A:ZN501 4.6 23.5 1.0
NE2 A:HIS251 4.6 9.5 1.0
O A:HOH615 4.8 15.6 1.0
CE A:MET253 4.9 10.6 1.0
CD1 A:ILE287 4.9 15.2 1.0
O A:HOH655 4.9 19.9 1.0

Reference:

V.Agarwal, S.A.Borisova, W.W.Metcalf, W.A.Van Der Donk, S.K.Nair. Structural and Mechanistic Insights Into C-P Bond Hydrolysis By Phosphonoacetate Hydrolase. Chem.Biol. V. 18 1230 2011.
ISSN: ISSN 1074-5521
PubMed: 22035792
DOI: 10.1016/J.CHEMBIOL.2011.07.019
Page generated: Sat Oct 26 16:13:15 2024

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