Fluorine in PDB 7ky5: Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
Enzymatic activity of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
All present enzymatic activity of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State:
7.6.2.1;
Other elements in 7ky5:
The structure of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
(pdb code 7ky5). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 4 binding sites of Fluorine where determined in the
Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State, PDB code: 7ky5:
Jump to Fluorine binding site number:
1;
2;
3;
4;
Fluorine binding site 1 out
of 4 in 7ky5
Go back to
Fluorine Binding Sites List in 7ky5
Fluorine binding site 1 out
of 4 in the Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F1703
b:193.6
occ:1.00
|
F1
|
A:ALF1703
|
0.0
|
193.6
|
1.0
|
AL
|
A:ALF1703
|
1.8
|
193.6
|
1.0
|
F4
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
F3
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
OD1
|
A:ASP712
|
2.9
|
144.4
|
1.0
|
C
|
A:THR1032
|
3.1
|
162.8
|
1.0
|
O
|
A:THR1032
|
3.3
|
162.8
|
1.0
|
N
|
A:GLY1033
|
3.3
|
172.2
|
1.0
|
O
|
A:LEU1031
|
3.5
|
152.8
|
1.0
|
CG
|
A:ASP712
|
3.6
|
144.4
|
1.0
|
F2
|
A:ALF1703
|
3.6
|
193.6
|
1.0
|
CA
|
A:THR1032
|
3.6
|
162.8
|
1.0
|
CA
|
A:GLY1033
|
3.7
|
172.2
|
1.0
|
OD2
|
A:ASP712
|
3.7
|
144.4
|
1.0
|
N
|
A:THR1032
|
3.9
|
162.8
|
1.0
|
C
|
A:LEU1031
|
3.9
|
152.8
|
1.0
|
CG1
|
A:VAL1148
|
4.3
|
166.8
|
1.0
|
NZ
|
A:LYS1153
|
4.6
|
162.9
|
1.0
|
ND2
|
A:ASN1176
|
4.7
|
167.8
|
1.0
|
OD1
|
A:ASP484
|
4.8
|
192.2
|
1.0
|
CB
|
A:ASP712
|
4.8
|
144.4
|
1.0
|
CB
|
A:LEU1031
|
4.9
|
152.8
|
1.0
|
N
|
A:LYS713
|
5.0
|
147.6
|
1.0
|
O
|
A:VAL1148
|
5.0
|
166.8
|
1.0
|
|
Fluorine binding site 2 out
of 4 in 7ky5
Go back to
Fluorine Binding Sites List in 7ky5
Fluorine binding site 2 out
of 4 in the Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F1703
b:193.6
occ:1.00
|
F2
|
A:ALF1703
|
0.0
|
193.6
|
1.0
|
AL
|
A:ALF1703
|
1.8
|
193.6
|
1.0
|
F3
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
F4
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
OD1
|
A:ASP484
|
2.8
|
192.2
|
1.0
|
CG
|
A:ASP484
|
3.0
|
192.2
|
1.0
|
O
|
A:LEU483
|
3.2
|
176.5
|
1.0
|
CA
|
A:ASP484
|
3.3
|
192.2
|
1.0
|
CB
|
A:ASP484
|
3.3
|
192.2
|
1.0
|
ND2
|
A:ASN1176
|
3.3
|
167.8
|
1.0
|
F1
|
A:ALF1703
|
3.6
|
193.6
|
1.0
|
OD2
|
A:ASP484
|
3.7
|
192.2
|
1.0
|
CA
|
A:GLY1033
|
3.9
|
172.2
|
1.0
|
C
|
A:LEU483
|
4.1
|
176.5
|
1.0
|
N
|
A:ASP484
|
4.2
|
192.2
|
1.0
|
O
|
A:VAL1148
|
4.3
|
166.8
|
1.0
|
N
|
A:GLY485
|
4.3
|
195.1
|
1.0
|
C
|
A:ASP484
|
4.4
|
192.2
|
1.0
|
NZ
|
A:LYS1153
|
4.4
|
162.9
|
1.0
|
CG
|
A:ASN1176
|
4.4
|
167.8
|
1.0
|
N
|
A:GLY1033
|
4.8
|
172.2
|
1.0
|
CB
|
A:ASN1176
|
4.8
|
167.8
|
1.0
|
C
|
A:GLY1033
|
4.8
|
172.2
|
1.0
|
|
Fluorine binding site 3 out
of 4 in 7ky5
Go back to
Fluorine Binding Sites List in 7ky5
Fluorine binding site 3 out
of 4 in the Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F1703
b:193.6
occ:1.00
|
F3
|
A:ALF1703
|
0.0
|
193.6
|
1.0
|
AL
|
A:ALF1703
|
1.8
|
193.6
|
1.0
|
F2
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
F1
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
O
|
A:VAL1148
|
2.6
|
166.8
|
1.0
|
CG1
|
A:VAL1148
|
3.3
|
166.8
|
1.0
|
O
|
A:THR1032
|
3.4
|
162.8
|
1.0
|
NZ
|
A:LYS1153
|
3.5
|
162.9
|
1.0
|
CA
|
A:GLY1033
|
3.5
|
172.2
|
1.0
|
F4
|
A:ALF1703
|
3.6
|
193.6
|
1.0
|
C
|
A:VAL1148
|
3.7
|
166.8
|
1.0
|
C
|
A:THR1032
|
3.9
|
162.8
|
1.0
|
N
|
A:VAL1148
|
4.0
|
166.8
|
1.0
|
N
|
A:GLY1033
|
4.0
|
172.2
|
1.0
|
CA
|
A:VAL1148
|
4.2
|
166.8
|
1.0
|
CB
|
A:VAL1148
|
4.4
|
166.8
|
1.0
|
OD1
|
A:ASP484
|
4.5
|
192.2
|
1.0
|
CE
|
A:LYS1153
|
4.6
|
162.9
|
1.0
|
C
|
A:GLY1033
|
4.8
|
172.2
|
1.0
|
N
|
A:SER1149
|
4.9
|
168.7
|
1.0
|
CD
|
A:LYS1153
|
4.9
|
162.9
|
1.0
|
ND2
|
A:ASN1176
|
4.9
|
167.8
|
1.0
|
C
|
A:ARG1147
|
5.0
|
167.6
|
1.0
|
CG
|
A:ASP484
|
5.0
|
192.2
|
1.0
|
|
Fluorine binding site 4 out
of 4 in 7ky5
Go back to
Fluorine Binding Sites List in 7ky5
Fluorine binding site 4 out
of 4 in the Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 4 of Structure of the S. Cerevisiae Phosphatidylcholine Flippase DNF2-LEM3 Complex in the E2P Transition State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F1703
b:193.6
occ:1.00
|
F4
|
A:ALF1703
|
0.0
|
193.6
|
1.0
|
AL
|
A:ALF1703
|
1.8
|
193.6
|
1.0
|
F1
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
F2
|
A:ALF1703
|
2.5
|
193.6
|
1.0
|
OD1
|
A:ASP712
|
3.0
|
144.4
|
1.0
|
ND2
|
A:ASN1176
|
3.0
|
167.8
|
1.0
|
OD1
|
A:ASP484
|
3.2
|
192.2
|
1.0
|
OD2
|
A:ASP712
|
3.3
|
144.4
|
1.0
|
N
|
A:GLY485
|
3.4
|
195.1
|
1.0
|
CG
|
A:ASP712
|
3.5
|
144.4
|
1.0
|
F3
|
A:ALF1703
|
3.6
|
193.6
|
1.0
|
CG2
|
A:THR714
|
3.7
|
150.2
|
1.0
|
CA
|
A:ASP484
|
3.7
|
192.2
|
1.0
|
C
|
A:ASP484
|
3.9
|
192.2
|
1.0
|
CA
|
A:GLY1033
|
4.0
|
172.2
|
1.0
|
CG
|
A:ASP484
|
4.1
|
192.2
|
1.0
|
CG
|
A:ASN1176
|
4.1
|
167.8
|
1.0
|
N
|
A:GLY1033
|
4.2
|
172.2
|
1.0
|
CA
|
A:GLY485
|
4.4
|
195.1
|
1.0
|
CB
|
A:ASP484
|
4.4
|
192.2
|
1.0
|
O
|
A:LEU483
|
4.5
|
176.5
|
1.0
|
OD1
|
A:ASN1176
|
4.5
|
167.8
|
1.0
|
N
|
A:ASP484
|
4.7
|
192.2
|
1.0
|
C
|
A:THR1032
|
4.7
|
162.8
|
1.0
|
N
|
A:LYS713
|
4.9
|
147.6
|
1.0
|
N
|
A:THR714
|
4.9
|
150.2
|
1.0
|
C
|
A:LEU483
|
5.0
|
176.5
|
1.0
|
|
Reference:
L.Bai,
Q.You,
B.K.Jain,
H.D.Duan,
A.Kovach,
T.R.Graham,
H.Li.
Transport Mechanism of P4 Atpase Phosphatidylcholine Flippases. Elife V. 9 2020.
ISSN: ESSN 2050-084X
PubMed: 33320091
DOI: 10.7554/ELIFE.62163
Page generated: Fri Aug 2 08:34:08 2024
|