Potassium in PDB 4qrh: Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp
Enzymatic activity of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp
All present enzymatic activity of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp:
2.7.4.8;
Protein crystallography data
The structure of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp, PDB code: 4qrh
was solved by
K.Liu,
K.Krasny,
A.R.Myers,
K.A.Satyshur,
J.L.Keck,
J.D.Wnag,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
39.26 /
1.65
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
69.486,
93.961,
85.259,
90.00,
111.09,
90.00
|
R / Rfree (%)
|
20.1 /
22.7
|
Other elements in 4qrh:
The structure of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp also contains other interesting chemical elements:
Potassium Binding Sites:
The binding sites of Potassium atom in the Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp
(pdb code 4qrh). This binding sites where shown within
5.0 Angstroms radius around Potassium atom.
In total 3 binding sites of Potassium where determined in the
Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp, PDB code: 4qrh:
Jump to Potassium binding site number:
1;
2;
3;
Potassium binding site 1 out
of 3 in 4qrh
Go back to
Potassium Binding Sites List in 4qrh
Potassium binding site 1 out
of 3 in the Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp
 Mono view
 Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 1 of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K302
b:14.8
occ:1.00
|
O
|
B:GLU103
|
2.7
|
13.2
|
1.0
|
O
|
B:HOH411
|
2.8
|
19.6
|
1.0
|
O
|
B:HOH410
|
2.8
|
12.7
|
1.0
|
OH
|
B:TYR36
|
2.9
|
19.2
|
1.0
|
OG
|
B:SER39
|
2.9
|
15.1
|
1.0
|
N7
|
B:0O2303
|
3.0
|
14.2
|
1.0
|
O
|
B:HOH412
|
3.0
|
24.0
|
1.0
|
C8
|
B:0O2303
|
3.5
|
15.2
|
1.0
|
CB
|
B:SER39
|
3.8
|
15.2
|
1.0
|
C5
|
B:0O2303
|
3.8
|
14.3
|
1.0
|
C
|
B:GLU103
|
3.9
|
13.8
|
1.0
|
CZ
|
B:TYR36
|
3.9
|
17.9
|
1.0
|
OE1
|
B:GLU103
|
4.1
|
19.6
|
1.0
|
O
|
B:HOH409
|
4.3
|
12.6
|
1.0
|
O6
|
B:0O2303
|
4.3
|
14.2
|
1.0
|
O
|
B:SER37
|
4.4
|
14.8
|
1.0
|
CE1
|
B:TYR36
|
4.4
|
17.0
|
1.0
|
N
|
B:GLU103
|
4.4
|
13.2
|
1.0
|
O
|
B:HOH413
|
4.4
|
27.1
|
1.0
|
CB
|
B:GLU103
|
4.4
|
15.2
|
1.0
|
C6
|
B:0O2303
|
4.5
|
13.9
|
1.0
|
CA
|
B:GLU103
|
4.5
|
14.0
|
1.0
|
CE1
|
B:TYR55
|
4.5
|
19.1
|
1.0
|
CD
|
B:GLU103
|
4.5
|
18.1
|
1.0
|
N9
|
B:0O2303
|
4.5
|
15.7
|
1.0
|
N
|
B:SER39
|
4.6
|
15.3
|
1.0
|
C4
|
B:0O2303
|
4.7
|
14.3
|
1.0
|
CG2
|
B:ILE104
|
4.8
|
14.2
|
1.0
|
CA
|
B:SER39
|
4.8
|
15.3
|
1.0
|
OH
|
B:TYR55
|
4.8
|
19.1
|
1.0
|
CE2
|
B:TYR36
|
4.9
|
17.4
|
1.0
|
N
|
B:ILE104
|
5.0
|
13.8
|
1.0
|
CZ
|
B:TYR55
|
5.0
|
19.3
|
1.0
|
|
Potassium binding site 2 out
of 3 in 4qrh
Go back to
Potassium Binding Sites List in 4qrh
Potassium binding site 2 out
of 3 in the Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp
 Mono view
 Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 2 of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:K302
b:15.6
occ:1.00
|
O
|
C:GLU103
|
2.7
|
14.4
|
1.0
|
O
|
C:HOH423
|
2.8
|
20.4
|
1.0
|
OG
|
C:SER39
|
2.8
|
15.6
|
1.0
|
OH
|
C:TYR36
|
2.8
|
19.6
|
1.0
|
O
|
C:HOH422
|
2.9
|
15.2
|
1.0
|
N7
|
C:0O2304
|
3.0
|
14.5
|
1.0
|
O
|
C:HOH424
|
3.2
|
22.6
|
1.0
|
C8
|
C:0O2304
|
3.6
|
14.8
|
1.0
|
CB
|
C:SER39
|
3.7
|
15.9
|
1.0
|
C
|
C:GLU103
|
3.8
|
14.6
|
1.0
|
C5
|
C:0O2304
|
3.8
|
14.4
|
1.0
|
CZ
|
C:TYR36
|
3.9
|
18.1
|
1.0
|
OE1
|
C:GLU103
|
4.0
|
18.9
|
1.0
|
O
|
C:SER37
|
4.3
|
16.1
|
1.0
|
O6
|
C:0O2304
|
4.3
|
15.2
|
1.0
|
O
|
C:HOH421
|
4.3
|
15.3
|
1.0
|
N
|
C:GLU103
|
4.3
|
14.8
|
1.0
|
CB
|
C:GLU103
|
4.4
|
15.7
|
1.0
|
CD
|
C:GLU103
|
4.4
|
17.6
|
1.0
|
O
|
C:HOH468
|
4.4
|
35.1
|
1.0
|
CA
|
C:GLU103
|
4.4
|
14.9
|
1.0
|
CE1
|
C:TYR36
|
4.4
|
18.0
|
1.0
|
C6
|
C:0O2304
|
4.5
|
14.2
|
1.0
|
N
|
C:SER39
|
4.5
|
16.0
|
1.0
|
CE1
|
C:TYR55
|
4.5
|
18.5
|
1.0
|
N9
|
C:0O2304
|
4.6
|
15.2
|
1.0
|
CG2
|
C:ILE104
|
4.7
|
14.9
|
1.0
|
CA
|
C:SER39
|
4.7
|
15.9
|
1.0
|
C4
|
C:0O2304
|
4.7
|
14.0
|
1.0
|
OE2
|
C:GLU103
|
4.8
|
20.0
|
1.0
|
OH
|
C:TYR55
|
4.9
|
20.3
|
1.0
|
CE2
|
C:TYR36
|
4.9
|
17.9
|
1.0
|
N
|
C:ILE104
|
4.9
|
14.4
|
1.0
|
CG
|
C:GLU103
|
4.9
|
16.3
|
1.0
|
|
Potassium binding site 3 out
of 3 in 4qrh
Go back to
Potassium Binding Sites List in 4qrh
Potassium binding site 3 out
of 3 in the Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp
 Mono view
 Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 3 of Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:K302
b:15.2
occ:1.00
|
O
|
D:GLU103
|
2.7
|
13.9
|
1.0
|
O
|
D:HOH424
|
2.7
|
18.9
|
1.0
|
OH
|
D:TYR36
|
2.8
|
17.8
|
1.0
|
OG
|
D:SER39
|
2.8
|
14.0
|
1.0
|
O
|
D:HOH419
|
2.8
|
15.8
|
1.0
|
N7
|
D:0O2306
|
3.0
|
14.5
|
1.0
|
O
|
D:HOH429
|
3.1
|
21.9
|
1.0
|
C8
|
D:0O2306
|
3.5
|
14.7
|
1.0
|
CB
|
D:SER39
|
3.7
|
14.3
|
1.0
|
C
|
D:GLU103
|
3.8
|
13.9
|
1.0
|
C5
|
D:0O2306
|
3.8
|
13.3
|
1.0
|
CZ
|
D:TYR36
|
3.9
|
17.2
|
1.0
|
OE1
|
D:GLU103
|
3.9
|
17.4
|
1.0
|
CD
|
D:GLU103
|
4.3
|
16.7
|
1.0
|
CB
|
D:GLU103
|
4.3
|
14.8
|
1.0
|
N
|
D:GLU103
|
4.3
|
13.5
|
1.0
|
O
|
D:HOH511
|
4.3
|
31.6
|
1.0
|
O
|
D:SER37
|
4.3
|
15.6
|
1.0
|
O6
|
D:0O2306
|
4.3
|
12.8
|
1.0
|
CE1
|
D:TYR36
|
4.4
|
16.9
|
1.0
|
O
|
D:HOH420
|
4.4
|
14.6
|
1.0
|
CA
|
D:GLU103
|
4.4
|
14.2
|
1.0
|
C6
|
D:0O2306
|
4.5
|
13.5
|
1.0
|
CE1
|
D:TYR55
|
4.5
|
16.9
|
1.0
|
N
|
D:SER39
|
4.5
|
15.3
|
1.0
|
N9
|
D:0O2306
|
4.6
|
14.2
|
1.0
|
C4
|
D:0O2306
|
4.7
|
14.1
|
1.0
|
CA
|
D:SER39
|
4.7
|
14.8
|
1.0
|
CG2
|
D:ILE104
|
4.7
|
13.8
|
1.0
|
OE2
|
D:GLU103
|
4.8
|
18.3
|
1.0
|
OH
|
D:TYR55
|
4.9
|
17.0
|
1.0
|
CG
|
D:GLU103
|
4.9
|
15.1
|
1.0
|
CE2
|
D:TYR36
|
4.9
|
17.2
|
1.0
|
N
|
D:ILE104
|
4.9
|
13.8
|
1.0
|
|
Reference:
K.Liu,
A.R.Myers,
T.Pisithkul,
K.R.Claas,
K.A.Satyshur,
D.Amador-Noguez,
J.L.Keck,
J.D.Wang.
Molecular Mechanism and Evolution of Guanylate Kinase Regulation By (P)Ppgpp. Mol.Cell V. 57 735 2015.
ISSN: ISSN 1097-2765
PubMed: 25661490
DOI: 10.1016/J.MOLCEL.2014.12.037
Page generated: Mon Aug 12 11:54:44 2024
|