Fluorine in PDB 5mrs: Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf
Protein crystallography data
The structure of Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf, PDB code: 5mrs
was solved by
A.Gabdulkhakov,
S.Tishchenko,
A.Lisov,
A.Leontievsky,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
48.21 /
1.90
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
41.855,
122.553,
78.988,
90.00,
98.64,
90.00
|
R / Rfree (%)
|
20.1 /
24.2
|
Other elements in 5mrs:
The structure of Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf
(pdb code 5mrs). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the
Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf, PDB code: 5mrs:
Jump to Fluorine binding site number:
1;
2;
3;
Fluorine binding site 1 out
of 3 in 5mrs
Go back to
Fluorine Binding Sites List in 5mrs
Fluorine binding site 1 out
of 3 in the Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F202
b:38.8
occ:1.00
|
F
|
B:AES202
|
0.0
|
38.8
|
1.0
|
S
|
B:AES202
|
1.6
|
57.7
|
1.0
|
OG
|
B:SER144
|
2.1
|
43.8
|
1.0
|
O1S
|
B:AES202
|
2.4
|
50.6
|
1.0
|
O2S
|
B:AES202
|
2.5
|
42.8
|
1.0
|
C1
|
B:AES202
|
2.7
|
44.1
|
1.0
|
N
|
B:SER144
|
2.8
|
18.5
|
1.0
|
N
|
B:GLY142
|
3.0
|
17.2
|
1.0
|
CB
|
B:SER144
|
3.0
|
28.9
|
1.0
|
C2
|
B:AES202
|
3.1
|
37.4
|
1.0
|
CA
|
B:SER144
|
3.3
|
24.3
|
1.0
|
CA
|
B:ARG141
|
3.4
|
20.2
|
1.0
|
O
|
B:GLY140
|
3.5
|
17.4
|
1.0
|
N
|
B:ASP143
|
3.5
|
23.7
|
1.0
|
C
|
B:ARG141
|
3.6
|
21.0
|
1.0
|
O
|
B:HOH317
|
3.8
|
32.8
|
1.0
|
C
|
B:ASP143
|
3.9
|
22.6
|
1.0
|
C6
|
B:AES202
|
3.9
|
35.4
|
1.0
|
CA
|
B:GLY142
|
3.9
|
15.8
|
1.0
|
C
|
B:GLY142
|
3.9
|
21.9
|
1.0
|
N
|
B:ARG141
|
4.1
|
22.2
|
1.0
|
C
|
B:GLY140
|
4.1
|
21.7
|
1.0
|
CA
|
B:ASP143
|
4.2
|
20.9
|
1.0
|
C3
|
B:AES202
|
4.4
|
31.7
|
1.0
|
CB
|
B:ARG141
|
4.5
|
24.9
|
1.0
|
CB
|
B:ASP143
|
4.6
|
23.7
|
1.0
|
C
|
B:SER144
|
4.8
|
22.5
|
1.0
|
O
|
B:ARG141
|
4.8
|
22.2
|
1.0
|
O
|
B:GLY142
|
4.9
|
22.2
|
1.0
|
O
|
B:ASP143
|
4.9
|
23.5
|
1.0
|
NE2
|
B:HIS36
|
5.0
|
22.6
|
1.0
|
|
Fluorine binding site 2 out
of 3 in 5mrs
Go back to
Fluorine Binding Sites List in 5mrs
Fluorine binding site 2 out
of 3 in the Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:F202
b:50.5
occ:1.00
|
F
|
C:AES202
|
0.0
|
50.5
|
1.0
|
S
|
C:AES202
|
1.6
|
67.0
|
1.0
|
OG
|
C:SER144
|
2.1
|
49.6
|
1.0
|
O1S
|
C:AES202
|
2.4
|
51.9
|
1.0
|
O2S
|
C:AES202
|
2.5
|
43.2
|
1.0
|
C1
|
C:AES202
|
2.6
|
54.3
|
1.0
|
C6
|
C:AES202
|
2.8
|
47.3
|
1.0
|
CB
|
C:SER144
|
3.0
|
37.7
|
1.0
|
N
|
C:GLY142
|
3.0
|
22.9
|
1.0
|
N
|
C:SER144
|
3.2
|
21.6
|
1.0
|
O
|
C:HOH318
|
3.3
|
31.1
|
1.0
|
CA
|
C:SER144
|
3.5
|
27.7
|
1.0
|
CA
|
C:ARG141
|
3.6
|
27.8
|
1.0
|
C
|
C:ARG141
|
3.8
|
30.8
|
1.0
|
C2
|
C:AES202
|
3.9
|
48.2
|
1.0
|
CA
|
C:GLY142
|
4.0
|
24.8
|
1.0
|
N
|
C:ASP143
|
4.0
|
21.6
|
1.0
|
O
|
C:GLY140
|
4.1
|
23.3
|
1.0
|
C
|
C:GLY142
|
4.2
|
26.0
|
1.0
|
C5
|
C:AES202
|
4.2
|
44.5
|
1.0
|
C
|
C:ASP143
|
4.4
|
22.4
|
1.0
|
CB
|
C:ARG141
|
4.5
|
21.3
|
1.0
|
NE2
|
C:HIS36
|
4.5
|
34.9
|
1.0
|
N
|
C:ARG141
|
4.5
|
24.4
|
1.0
|
C
|
C:GLY140
|
4.6
|
32.0
|
1.0
|
CA
|
C:ASP143
|
4.7
|
22.7
|
1.0
|
CG
|
C:ARG141
|
4.8
|
29.4
|
1.0
|
C
|
C:SER144
|
5.0
|
24.6
|
1.0
|
C3
|
C:AES202
|
5.0
|
39.1
|
1.0
|
|
Fluorine binding site 3 out
of 3 in 5mrs
Go back to
Fluorine Binding Sites List in 5mrs
Fluorine binding site 3 out
of 3 in the Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:F203
b:38.5
occ:1.00
|
F
|
D:AES203
|
0.0
|
38.5
|
1.0
|
S
|
D:AES203
|
1.6
|
46.3
|
1.0
|
O1S
|
D:AES203
|
2.4
|
37.2
|
1.0
|
O2S
|
D:AES203
|
2.5
|
41.6
|
1.0
|
OG
|
D:SER144
|
2.5
|
46.5
|
1.0
|
C1
|
D:AES203
|
2.6
|
41.3
|
1.0
|
N
|
D:SER144
|
2.9
|
28.0
|
1.0
|
N
|
D:GLY142
|
3.0
|
22.8
|
1.0
|
C2
|
D:AES203
|
3.1
|
32.9
|
1.0
|
CB
|
D:SER144
|
3.2
|
32.7
|
1.0
|
O
|
D:GLY140
|
3.4
|
21.0
|
1.0
|
N
|
D:ASP143
|
3.4
|
19.2
|
1.0
|
CA
|
D:SER144
|
3.5
|
25.1
|
1.0
|
CA
|
D:ARG141
|
3.5
|
27.9
|
1.0
|
C
|
D:ARG141
|
3.7
|
26.4
|
1.0
|
C6
|
D:AES203
|
3.8
|
41.2
|
1.0
|
C
|
D:ASP143
|
3.9
|
22.6
|
1.0
|
C
|
D:GLY142
|
3.9
|
22.6
|
1.0
|
O
|
D:HOH333
|
3.9
|
27.0
|
1.0
|
CA
|
D:GLY142
|
3.9
|
19.1
|
1.0
|
C
|
D:GLY140
|
4.1
|
24.8
|
1.0
|
N
|
D:ARG141
|
4.1
|
24.6
|
1.0
|
CA
|
D:ASP143
|
4.1
|
22.4
|
1.0
|
C3
|
D:AES203
|
4.4
|
35.1
|
1.0
|
CB
|
D:ASP143
|
4.6
|
17.2
|
1.0
|
CB
|
D:ARG141
|
4.7
|
23.6
|
1.0
|
O
|
D:GLY142
|
4.8
|
21.0
|
1.0
|
O
|
D:ARG141
|
4.9
|
27.8
|
1.0
|
C
|
D:SER144
|
4.9
|
25.7
|
1.0
|
C5
|
D:AES203
|
5.0
|
43.9
|
1.0
|
O
|
D:ASP143
|
5.0
|
21.2
|
1.0
|
|
Reference:
A.Gabdulkhakov,
S.Tishchenko,
A.Lisov,
A.Leontievsky.
Crystal Structure of L1 Protease Lysobacter Sp. XL1 in Complex with Aebsf To Be Published.
Page generated: Thu Aug 1 11:45:43 2024
|