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Nickel in PDB 6rp1: 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5

Enzymatic activity of 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5

All present enzymatic activity of 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5:
3.5.1.5;

Protein crystallography data

The structure of 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5, PDB code: 6rp1 was solved by L.Mazzei, M.Cianci, S.Benini, S.Ciurli, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 114.15 / 1.49
Space group P 63 2 2
Cell size a, b, c (Å), α, β, γ (°) 131.813, 131.813, 189.028, 90.00, 90.00, 120.00
R / Rfree (%) 13.6 / 15.3

Nickel Binding Sites:

The binding sites of Nickel atom in the 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5 (pdb code 6rp1). This binding sites where shown within 5.0 Angstroms radius around Nickel atom.
In total 2 binding sites of Nickel where determined in the 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5, PDB code: 6rp1:
Jump to Nickel binding site number: 1; 2;

Nickel binding site 1 out of 2 in 6rp1

Go back to Nickel Binding Sites List in 6rp1
Nickel binding site 1 out of 2 in the 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5


Mono view


Stereo pair view

A full contact list of Nickel with other atoms in the Ni binding site number 1 of 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5 within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Ni601

b:16.0
occ:1.00
OQ1 C:KCX220 2.0 14.7 1.0
ND1 C:HIS249 2.0 14.3 1.0
NE2 C:HIS275 2.0 16.1 1.0
O1 C:2PA619 2.1 14.7 1.0
O3 C:2PA619 2.2 15.5 1.0
P2 C:2PA619 2.6 18.4 1.0
CE1 C:HIS249 2.9 15.0 1.0
CD2 C:HIS275 3.0 15.6 1.0
CE1 C:HIS275 3.0 16.7 1.0
CX C:KCX220 3.0 14.8 1.0
CG C:HIS249 3.1 14.9 1.0
O C:GLY280 3.1 18.5 1.0
OQ2 C:KCX220 3.4 14.2 1.0
CB C:HIS249 3.5 14.2 1.0
NE2 C:HIS222 3.6 14.6 1.0
NI C:NI602 3.8 14.6 1.0
N4 C:2PA619 3.8 16.7 1.0
N5 C:2PA619 4.0 15.3 1.0
CD2 C:HIS222 4.0 13.5 1.0
NE2 C:HIS249 4.1 15.2 1.0
CE1 C:HIS137 4.1 13.8 1.0
ND1 C:HIS275 4.1 15.8 1.0
CG C:HIS275 4.1 15.0 1.0
C C:GLY280 4.2 17.4 1.0
CD2 C:HIS249 4.2 15.0 1.0
NZ C:KCX220 4.2 13.9 1.0
NE2 C:HIS137 4.3 13.9 1.0
OD2 C:ASP363 4.6 17.8 1.0
CE1 C:HIS222 4.6 14.9 1.0
CE C:KCX220 4.7 13.6 1.0
O4 C:SO4618 4.7 51.7 0.5
CA C:HIS249 4.8 14.0 1.0
CA C:GLY281 4.8 17.0 1.0
N C:GLY281 4.9 16.4 1.0

Nickel binding site 2 out of 2 in 6rp1

Go back to Nickel Binding Sites List in 6rp1
Nickel binding site 2 out of 2 in the 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5


Mono view


Stereo pair view

A full contact list of Nickel with other atoms in the Ni binding site number 2 of 1.49 A Resolution of Sporosarcina Pasteurii Urease Inhibited in the Presence of Nbpto at pH 6.5 within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Ni602

b:14.6
occ:1.00
OQ2 C:KCX220 2.1 14.2 1.0
NE2 C:HIS137 2.1 13.9 1.0
NE2 C:HIS139 2.1 13.0 1.0
OD1 C:ASP363 2.1 14.7 1.0
O3 C:2PA619 2.2 15.5 1.0
N5 C:2PA619 2.3 15.3 1.0
P2 C:2PA619 2.8 18.4 1.0
CE1 C:HIS139 2.9 13.3 1.0
CD2 C:HIS137 3.1 13.8 1.0
CG C:ASP363 3.1 16.9 1.0
CE1 C:HIS137 3.1 13.8 1.0
CX C:KCX220 3.1 14.8 1.0
CD2 C:HIS139 3.2 13.3 1.0
OD2 C:ASP363 3.3 17.8 1.0
OQ1 C:KCX220 3.4 14.7 1.0
O1 C:2PA619 3.7 14.7 1.0
NI C:NI601 3.8 16.0 1.0
O C:ALA366 4.0 20.6 1.0
CG2 C:THR172 4.1 13.8 1.0
N4 C:2PA619 4.1 16.7 1.0
ND1 C:HIS139 4.1 13.0 1.0
NZ C:KCX220 4.2 13.9 1.0
ND1 C:HIS137 4.2 13.9 1.0
CG C:HIS137 4.2 13.4 1.0
CG C:HIS139 4.3 12.7 1.0
O C:ALA170 4.3 13.2 1.0
CB C:ASP363 4.4 15.1 1.0
CB C:ALA366 4.4 16.3 1.0
CA C:ASP363 4.7 14.5 1.0
CD2 C:HIS275 4.9 15.6 1.0
NE2 C:HIS275 4.9 16.1 1.0
N C:THR172 4.9 12.8 1.0

Reference:

L.Mazzei, M.Cianci, S.Benini, S.Ciurli. The Impact of pH on Catalytically Critical Protein Conformational Changes: the Case of the Urease, A Nickel Enzyme. Chemistry V. 25 12145 2019.
ISSN: ISSN 0947-6539
PubMed: 31271481
DOI: 10.1002/CHEM.201902320
Page generated: Wed Dec 16 01:53:22 2020

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