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Potassium in PDB 6ev8: Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form

Enzymatic activity of Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form

All present enzymatic activity of Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form:
4.1.1.102;

Protein crystallography data

The structure of Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form, PDB code: 6ev8 was solved by S.S.Bailey, L.David, K.A.P.Payne, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 42.08 / 1.03
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 95.910, 63.810, 87.750, 90.00, 90.00, 90.00
R / Rfree (%) 14.6 / 16.5

Other elements in 6ev8:

The structure of Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form also contains other interesting chemical elements:

Manganese (Mn) 1 atom

Potassium Binding Sites:

The binding sites of Potassium atom in the Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form (pdb code 6ev8). This binding sites where shown within 5.0 Angstroms radius around Potassium atom.
In total 2 binding sites of Potassium where determined in the Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form, PDB code: 6ev8:
Jump to Potassium binding site number: 1; 2;

Potassium binding site 1 out of 2 in 6ev8

Go back to Potassium Binding Sites List in 6ev8
Potassium binding site 1 out of 2 in the Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form


Mono view


Stereo pair view

A full contact list of Potassium with other atoms in the K binding site number 1 of Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:K602

b:8.5
occ:1.00
O A:HOH710 2.6 48.2 1.0
OE2 A:GLU233 2.8 7.7 1.0
O A:MET225 2.8 8.3 1.0
O A:ALA222 2.8 8.3 1.0
O8 A:BYN604 2.9 7.2 1.0
O7 A:BYN604 3.0 7.6 1.0
O A:TRP169 3.1 7.7 1.0
O A:SER223 3.1 9.1 1.0
O A:HOH770 3.3 7.8 1.0
P1 A:BYN604 3.4 7.3 1.0
C A:SER223 3.5 7.7 1.0
CD A:GLU233 3.6 7.2 1.0
O9 A:BYN604 3.6 8.3 1.0
MN A:MN601 3.7 7.9 1.0
CA A:SER223 3.7 7.6 1.0
CG A:GLU233 3.8 8.0 1.0
C A:ALA222 3.9 7.2 1.0
C A:MET225 3.9 7.9 1.0
N A:MET225 4.0 7.8 1.0
C22 A:BYN604 4.2 7.7 1.0
N A:SER223 4.2 7.5 1.0
C A:TRP169 4.3 7.3 1.0
O6 A:BYN604 4.3 8.7 1.0
C21 A:BYN604 4.3 7.4 1.0
N A:SER224 4.3 7.2 0.5
N A:SER224 4.4 7.5 0.5
CB A:SER170 4.4 8.1 1.0
CA A:SER170 4.4 7.3 1.0
CA A:MET225 4.6 8.2 1.0
OE1 A:GLU233 4.7 8.0 1.0
C A:SER224 4.8 8.2 0.5
C A:SER224 4.8 8.4 0.5
ND2 A:ASN168 4.8 8.2 1.0
O10 A:BYN604 4.9 8.1 1.0
N A:SER170 4.9 7.0 1.0
CG1 A:ILE227 4.9 9.7 1.0
N A:ILE227 4.9 8.0 1.0
N A:PRO226 4.9 7.5 1.0
CA A:SER224 5.0 6.8 0.5
CB A:SER223 5.0 7.6 1.0
CA A:SER224 5.0 7.3 0.5

Potassium binding site 2 out of 2 in 6ev8

Go back to Potassium Binding Sites List in 6ev8
Potassium binding site 2 out of 2 in the Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form


Mono view


Stereo pair view

A full contact list of Potassium with other atoms in the K binding site number 2 of Structure of E277Q A. Niger FDC1 with Prfmn in the Hydroxylated Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:K603

b:8.8
occ:1.00
O A:ARG421 2.7 9.0 1.0
O A:LEU461 2.7 10.3 1.0
O A:ASP459 2.7 8.8 1.0
O A:HOH1013 2.8 14.3 1.0
O A:HOH1283 2.8 11.6 1.0
OD2 A:ASP427 2.8 9.3 1.0
O A:HOH914 2.9 27.8 1.0
CG A:ASP427 3.4 9.8 1.0
O A:HOH1083 3.5 15.4 1.0
C A:ASP459 3.7 7.9 1.0
C A:LEU461 3.8 8.6 1.0
C A:ARG421 3.8 7.7 1.0
CB A:ASP427 3.9 9.1 1.0
OD1 A:ASP427 4.1 10.7 1.0
CA A:CYS422 4.1 8.0 1.0
N A:LEU461 4.2 8.6 1.0
O A:HOH841 4.3 10.3 1.0
CA A:ALA460 4.3 8.0 1.0
C A:ALA460 4.4 7.5 1.0
N A:ALA460 4.4 7.6 1.0
N A:CYS422 4.4 7.8 1.0
CG A:ASP459 4.5 10.7 1.0
CB A:ASP459 4.5 9.0 1.0
N A:MET462 4.6 9.3 1.0
CA A:LEU461 4.6 8.0 1.0
CA A:MET462 4.7 9.3 1.0
O A:HOH773 4.7 51.3 1.0
N A:ARG423 4.7 7.8 1.0
OD1 A:ASP459 4.8 11.0 1.0
CA A:ASP459 4.8 8.4 1.0
OD2 A:ASP459 4.8 14.8 1.0
CA A:ARG421 4.9 8.3 1.0

Reference:

S.S.Bailey, K.A.P.Payne, K.Fisher, S.A.Marshall, M.J.Cliff, R.Spiess, D.A.Parker, S.E.J.Rigby, D.Leys. The Role of Conserved Residues in Fdc Decarboxylase in Prenylated Flavin Mononucleotide Oxidative Maturation, Cofactor Isomerization, and Catalysis. J. Biol. Chem. V. 293 2272 2018.
ISSN: ESSN 1083-351X
PubMed: 29259125
DOI: 10.1074/JBC.RA117.000881
Page generated: Mon Dec 14 00:36:44 2020

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