Sodium in PDB 3qs4: Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan
Protein crystallography data
The structure of Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan, PDB code: 3qs4
was solved by
C.L.Piscitelli,
E.Gouaux,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
45.02 /
2.63
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
90.219,
86.595,
82.058,
90.00,
93.63,
90.00
|
R / Rfree (%)
|
21.4 /
22.8
|
Sodium Binding Sites:
The binding sites of Sodium atom in the Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan
(pdb code 3qs4). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the
Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan, PDB code: 3qs4:
Jump to Sodium binding site number:
1;
2;
Sodium binding site 1 out
of 2 in 3qs4
Go back to
Sodium Binding Sites List in 3qs4
Sodium binding site 1 out
of 2 in the Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan
 Mono view
 Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 1 of Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na751
b:51.6
occ:1.00
|
OG1
|
A:THR354
|
2.1
|
52.5
|
1.0
|
O
|
A:VAL23
|
2.2
|
59.4
|
1.0
|
O
|
A:ALA351
|
2.2
|
53.2
|
1.0
|
O
|
A:GLY20
|
2.2
|
54.4
|
1.0
|
OG
|
A:SER355
|
2.6
|
55.9
|
1.0
|
CB
|
A:THR354
|
3.2
|
52.7
|
1.0
|
C
|
A:ALA351
|
3.3
|
55.4
|
1.0
|
N
|
A:SER355
|
3.4
|
50.1
|
1.0
|
C
|
A:VAL23
|
3.4
|
53.9
|
1.0
|
C
|
A:GLY20
|
3.4
|
59.2
|
1.0
|
C
|
A:THR354
|
3.5
|
49.2
|
1.0
|
CB
|
A:SER355
|
3.7
|
49.5
|
1.0
|
CA
|
A:THR354
|
3.7
|
52.6
|
1.0
|
CA
|
A:ALA351
|
3.8
|
56.0
|
1.0
|
CA
|
A:SER355
|
3.9
|
51.8
|
1.0
|
N
|
A:THR354
|
4.0
|
55.4
|
1.0
|
O
|
A:THR354
|
4.0
|
54.2
|
1.0
|
O
|
A:PHE350
|
4.1
|
54.2
|
1.0
|
CA
|
A:GLY20
|
4.2
|
49.8
|
1.0
|
N
|
A:GLY24
|
4.3
|
52.0
|
1.0
|
CA
|
A:GLY24
|
4.3
|
54.6
|
1.0
|
CA
|
A:VAL23
|
4.3
|
57.4
|
1.0
|
N
|
A:GLY352
|
4.4
|
46.5
|
1.0
|
N
|
A:ASN21
|
4.4
|
55.8
|
1.0
|
CG2
|
A:THR354
|
4.4
|
55.3
|
1.0
|
N
|
A:VAL23
|
4.5
|
53.3
|
1.0
|
O
|
A:ASN21
|
4.5
|
60.1
|
1.0
|
O
|
A:GLY352
|
4.5
|
49.6
|
1.0
|
CB
|
A:VAL23
|
4.5
|
65.5
|
1.0
|
C
|
A:ASN21
|
4.6
|
58.5
|
1.0
|
CA
|
A:ASN21
|
4.6
|
56.8
|
1.0
|
C
|
A:GLY352
|
4.6
|
57.5
|
1.0
|
CA
|
A:GLY352
|
4.8
|
52.9
|
1.0
|
CB
|
A:ALA351
|
4.8
|
48.2
|
1.0
|
CG1
|
A:VAL23
|
4.9
|
58.1
|
1.0
|
N
|
A:ALA351
|
4.9
|
54.3
|
1.0
|
C
|
A:PHE350
|
5.0
|
53.7
|
1.0
|
|
Sodium binding site 2 out
of 2 in 3qs4
Go back to
Sodium Binding Sites List in 3qs4
Sodium binding site 2 out
of 2 in the Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan
 Mono view
 Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 2 of Crystal Structure of Leut Mutant F259V Bound to Sodium and L- Tryptophan within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na752
b:65.9
occ:1.00
|
OD1
|
A:ASN27
|
2.1
|
64.7
|
1.0
|
O
|
A:ALA22
|
2.2
|
49.5
|
1.0
|
OG1
|
A:THR254
|
2.4
|
58.3
|
1.0
|
OXT
|
A:TRP601
|
2.4
|
55.1
|
1.0
|
OD1
|
A:ASN286
|
2.4
|
54.2
|
1.0
|
O
|
A:THR254
|
2.8
|
56.5
|
1.0
|
CG
|
A:ASN27
|
2.9
|
59.6
|
1.0
|
ND2
|
A:ASN27
|
3.0
|
55.6
|
1.0
|
CG
|
A:ASN286
|
3.2
|
56.7
|
1.0
|
C
|
A:ALA22
|
3.2
|
57.0
|
1.0
|
CB
|
A:THR254
|
3.4
|
60.5
|
1.0
|
CA
|
A:THR254
|
3.4
|
60.7
|
1.0
|
ND2
|
A:ASN286
|
3.4
|
51.3
|
1.0
|
C
|
A:THR254
|
3.4
|
60.2
|
1.0
|
C
|
A:TRP601
|
3.6
|
53.8
|
1.0
|
O
|
A:HOH826
|
3.6
|
62.0
|
1.0
|
CA
|
A:VAL23
|
3.8
|
57.4
|
1.0
|
OE1
|
A:GLU290
|
3.8
|
69.8
|
1.0
|
N
|
A:VAL23
|
3.9
|
53.3
|
1.0
|
N
|
A:TRP601
|
4.0
|
54.8
|
1.0
|
N
|
A:GLY24
|
4.0
|
52.0
|
1.0
|
CB
|
A:ASN27
|
4.3
|
58.2
|
1.0
|
CA
|
A:ALA22
|
4.3
|
56.3
|
1.0
|
O
|
A:TRP601
|
4.4
|
55.0
|
1.0
|
C
|
A:VAL23
|
4.4
|
53.9
|
1.0
|
CA
|
A:TRP601
|
4.4
|
54.5
|
1.0
|
CB
|
A:ALA22
|
4.6
|
53.8
|
1.0
|
CG2
|
A:THR254
|
4.6
|
56.4
|
1.0
|
N
|
A:ASN27
|
4.7
|
59.4
|
1.0
|
CB
|
A:ASN286
|
4.7
|
56.8
|
1.0
|
N
|
A:LEU255
|
4.7
|
56.2
|
1.0
|
CA
|
A:ASN27
|
4.8
|
59.5
|
1.0
|
N
|
A:THR254
|
4.8
|
59.1
|
1.0
|
CD
|
A:GLU290
|
4.9
|
70.9
|
1.0
|
|
Reference:
C.L.Piscitelli,
E.Gouaux.
Insights Into Transport Mechanism From Leut Engineered to Transport Tryptophan. Embo J. V. 31 228 2012.
ISSN: ISSN 0261-4189
PubMed: 21952050
DOI: 10.1038/EMBOJ.2011.353
Page generated: Mon Oct 7 12:41:25 2024
|