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Vanadium in PDB 7q0x: Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic

Enzymatic activity of Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic

All present enzymatic activity of Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic:
3.4.21.4;

Protein crystallography data

The structure of Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic, PDB code: 7q0x was solved by M.F.A.Santos, A.C.P.Fernandes, I.Correia, G.Sciortino, E.Garribba, T.Santos-Silva, J.C.Pessoa, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 41.22 / 1.09
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 54.522, 54.522, 108.199, 90, 90, 120
R / Rfree (%) 11.1 / 13.6

Other elements in 7q0x:

The structure of Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic also contains other interesting chemical elements:

Calcium (Ca) 1 atom

Vanadium Binding Sites:

The binding sites of Vanadium atom in the Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic (pdb code 7q0x). This binding sites where shown within 5.0 Angstroms radius around Vanadium atom.
In total only one binding site of Vanadium was determined in the Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic, PDB code: 7q0x:

Vanadium binding site 1 out of 1 in 7q0x

Go back to Vanadium Binding Sites List in 7q0x
Vanadium binding site 1 out of 1 in the Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic


Mono view


Stereo pair view

A full contact list of Vanadium with other atoms in the V binding site number 1 of Bovine Trypsin Co-Crystallized with V(IV)OSO4 and Pic within 5.0Å range:
probe atom residue distance (Å) B Occ
A:V301

b:10.1
occ:0.80
O A:O302 1.7 11.4 0.8
OG A:SER195 2.0 10.5 1.0
O1 A:6PC304 2.0 11.9 0.8
N2 A:6PC304 2.1 11.2 0.8
O2 A:6PC303 2.1 9.6 0.8
N2 A:6PC303 2.1 10.7 0.8
C2 A:6PC304 2.8 12.9 0.8
C2 A:6PC303 2.9 10.5 0.8
C1 A:6PC304 2.9 11.6 0.8
C1 A:6PC303 2.9 10.8 0.8
CB A:SER195 3.0 9.8 1.0
C3 A:6PC303 3.1 11.6 0.8
C3 A:6PC304 3.1 12.2 0.8
CA A:SER195 3.9 9.0 1.0
N A:SER195 3.9 9.2 1.0
NE2 A:HIS57 4.0 10.8 1.0
O2 A:6PC304 4.0 16.3 0.8
O1 A:6PC303 4.1 12.5 0.8
N A:GLY193 4.2 11.6 1.0
C6 A:6PC304 4.3 14.5 0.8
C6 A:6PC303 4.3 11.9 0.8
O A:HOH456 4.3 14.1 1.0
O A:HOH600 4.4 48.1 1.0
C4 A:6PC304 4.4 14.0 0.8
C4 A:6PC303 4.4 12.8 0.8
CA A:GLN192 4.5 14.2 1.0
O A:CYS191 4.7 14.1 1.0
CD2 A:HIS57 4.7 10.2 1.0
C5 A:6PC304 4.8 15.0 0.8
C5 A:6PC303 4.9 13.0 0.8
C A:GLN192 4.9 12.6 1.0
N A:ASP194 5.0 9.8 1.0

Reference:

M.F.A.Santos, G.Sciortino, I.Correia, A.C.P.Fernandes, T.Santos-Silva, F.Pisanu, E.Garribba, J.Costa Pessoa. Binding of V IV O 2+ , V IV Ol, V IV Ol 2 and V V O 2 L Moieties to Proteins: X-Ray/Theoretical Characterization and Biological Implications. Chemistry V. 28 00105 2022.
ISSN: ISSN 0947-6539
PubMed: 35486702
DOI: 10.1002/CHEM.202200105
Page generated: Fri Oct 11 20:41:16 2024

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