Sodium in PDB 5m99: Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Enzymatic activity of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
All present enzymatic activity of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization:
3.2.1.1;
Protein crystallography data
The structure of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization, PDB code: 5m99
was solved by
U.Hameed,
I.Price,
O.A.Mirza,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
50.16 /
1.96
|
Space group
|
P 65
|
Cell size a, b, c (Å), α, β, γ (°)
|
153.237,
153.237,
143.056,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
15.2 /
18.4
|
Other elements in 5m99:
The structure of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
(pdb code 5m99). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 8 binding sites of Sodium where determined in the
Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization, PDB code: 5m99:
Jump to Sodium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Sodium binding site 1 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 1 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 1 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na601
b:38.3
occ:1.00
|
O
|
A:GLY401
|
2.3
|
44.2
|
1.0
|
O
|
A:ASP411
|
2.4
|
36.1
|
1.0
|
O
|
A:CYS408
|
2.4
|
31.8
|
1.0
|
OD2
|
A:ASP406
|
2.5
|
46.6
|
1.0
|
OD1
|
A:ASP406
|
2.7
|
46.8
|
1.0
|
CG
|
A:ASP406
|
2.9
|
53.6
|
1.0
|
OD1
|
A:ASP412
|
3.0
|
50.4
|
1.0
|
C
|
A:ASP411
|
3.5
|
35.4
|
1.0
|
C
|
A:GLY401
|
3.5
|
44.5
|
1.0
|
C
|
A:CYS408
|
3.6
|
34.3
|
1.0
|
O
|
A:HOH890
|
4.1
|
42.6
|
1.0
|
CG
|
A:ASP412
|
4.2
|
46.0
|
1.0
|
CB
|
A:CYS408
|
4.2
|
33.4
|
1.0
|
CA
|
A:ASP412
|
4.2
|
33.5
|
1.0
|
C
|
A:ASN402
|
4.3
|
46.0
|
1.0
|
N
|
A:ASP412
|
4.3
|
33.7
|
1.0
|
CA
|
A:CYS408
|
4.3
|
31.1
|
1.0
|
O
|
A:ASN402
|
4.3
|
47.4
|
1.0
|
CA
|
A:GLY401
|
4.4
|
42.2
|
1.0
|
N
|
A:ASP411
|
4.4
|
34.0
|
1.0
|
CB
|
A:ASP406
|
4.4
|
52.8
|
1.0
|
O
|
A:HOH813
|
4.4
|
48.2
|
1.0
|
N
|
A:CYS408
|
4.5
|
30.5
|
1.0
|
N
|
A:ASN402
|
4.5
|
41.0
|
1.0
|
CB
|
A:ASN402
|
4.5
|
46.6
|
1.0
|
O
|
A:HOH968
|
4.5
|
50.6
|
1.0
|
N
|
A:ALA403
|
4.5
|
42.4
|
1.0
|
CA
|
A:ASP411
|
4.5
|
35.3
|
1.0
|
O
|
A:ILE409
|
4.6
|
25.0
|
1.0
|
C
|
A:ILE409
|
4.6
|
30.4
|
1.0
|
CA
|
A:ASN402
|
4.6
|
41.5
|
1.0
|
N
|
A:ILE409
|
4.6
|
28.8
|
1.0
|
CA
|
A:ALA403
|
4.7
|
41.0
|
1.0
|
CB
|
A:ASP412
|
4.8
|
36.5
|
1.0
|
CA
|
A:ILE409
|
4.8
|
26.7
|
1.0
|
|
Sodium binding site 2 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 2 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 2 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na602
b:34.5
occ:1.00
|
O
|
A:VAL48
|
2.3
|
28.6
|
1.0
|
OD1
|
A:ASP46
|
2.3
|
35.7
|
1.0
|
OD1
|
A:ASP42
|
2.4
|
33.2
|
1.0
|
OD2
|
A:ASP50
|
2.4
|
33.5
|
1.0
|
O
|
A:HOH867
|
2.4
|
34.8
|
1.0
|
OD1
|
A:ASP44
|
2.5
|
40.0
|
1.0
|
CG
|
A:ASP46
|
3.2
|
39.0
|
1.0
|
CG
|
A:ASP42
|
3.3
|
29.2
|
1.0
|
C
|
A:VAL48
|
3.5
|
30.3
|
1.0
|
CG
|
A:ASP50
|
3.5
|
32.3
|
1.0
|
OD2
|
A:ASP46
|
3.5
|
35.7
|
1.0
|
CG
|
A:ASP44
|
3.5
|
43.8
|
1.0
|
N
|
A:VAL48
|
3.9
|
29.1
|
1.0
|
CB
|
A:ASP50
|
4.0
|
30.1
|
1.0
|
CB
|
A:ASP42
|
4.0
|
29.1
|
1.0
|
CA
|
A:ASP42
|
4.0
|
30.8
|
1.0
|
OD2
|
A:ASP44
|
4.0
|
47.1
|
1.0
|
O
|
A:HOH897
|
4.1
|
41.1
|
1.0
|
CA
|
A:VAL48
|
4.1
|
24.4
|
1.0
|
N
|
A:ASP44
|
4.1
|
38.6
|
1.0
|
N
|
A:SER43
|
4.1
|
33.0
|
1.0
|
CB
|
A:VAL48
|
4.2
|
30.2
|
1.0
|
OD2
|
A:ASP42
|
4.2
|
33.8
|
1.0
|
N
|
A:ASP46
|
4.3
|
39.8
|
1.0
|
C
|
A:ASP42
|
4.4
|
33.1
|
1.0
|
N
|
A:GLY45
|
4.5
|
35.1
|
1.0
|
CB
|
A:ASP46
|
4.5
|
38.1
|
1.0
|
N
|
A:GLY49
|
4.6
|
25.4
|
1.0
|
N
|
A:ASP50
|
4.6
|
25.3
|
1.0
|
C
|
A:GLY49
|
4.6
|
26.3
|
1.0
|
OD1
|
A:ASP50
|
4.6
|
35.0
|
1.0
|
CB
|
A:ASP44
|
4.6
|
38.1
|
1.0
|
N
|
A:GLY47
|
4.7
|
34.5
|
1.0
|
CA
|
A:ASP44
|
4.7
|
41.5
|
1.0
|
CA
|
A:GLY49
|
4.8
|
20.3
|
1.0
|
C
|
A:ASP44
|
4.8
|
40.4
|
1.0
|
CA
|
A:ASP46
|
4.8
|
36.5
|
1.0
|
CA
|
A:ASP50
|
4.9
|
28.8
|
1.0
|
CG1
|
A:VAL48
|
4.9
|
25.6
|
1.0
|
O
|
A:GLY49
|
4.9
|
28.9
|
1.0
|
O
|
A:HOH866
|
5.0
|
46.3
|
1.0
|
O
|
A:ASP94
|
5.0
|
29.5
|
1.0
|
|
Sodium binding site 3 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 3 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 3 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na603
b:26.8
occ:1.00
|
O
|
A:HOH778
|
2.3
|
23.2
|
1.0
|
O
|
A:HIS217
|
2.3
|
23.1
|
1.0
|
O
|
A:HOH701
|
2.4
|
34.4
|
1.0
|
OD1
|
A:ASN122
|
2.4
|
24.6
|
1.0
|
O
|
A:HOH729
|
2.6
|
34.0
|
1.0
|
O
|
A:ILE218
|
2.8
|
24.8
|
1.0
|
C
|
A:ILE218
|
3.3
|
22.3
|
1.0
|
C
|
A:HIS217
|
3.4
|
23.9
|
1.0
|
CG
|
A:ASN122
|
3.5
|
25.9
|
1.0
|
OD2
|
A:ASP183
|
3.5
|
43.5
|
1.0
|
CA
|
A:ILE218
|
3.6
|
24.9
|
1.0
|
O
|
A:HOH801
|
3.7
|
20.6
|
1.0
|
ND2
|
A:ASN122
|
3.9
|
25.2
|
1.0
|
N
|
A:ILE218
|
3.9
|
20.4
|
1.0
|
CG
|
A:ASP183
|
4.0
|
33.4
|
1.0
|
O
|
A:ASN122
|
4.1
|
21.8
|
1.0
|
O
|
A:HOH955
|
4.1
|
28.9
|
1.0
|
N
|
A:TYR219
|
4.2
|
20.6
|
1.0
|
CB
|
A:ASP183
|
4.3
|
25.2
|
1.0
|
O
|
A:LEU184
|
4.6
|
21.0
|
1.0
|
CA
|
A:HIS217
|
4.6
|
23.7
|
1.0
|
CB
|
A:HIS217
|
4.6
|
23.0
|
1.0
|
CA
|
A:TYR219
|
4.6
|
23.7
|
1.0
|
O2
|
A:EDO612
|
4.6
|
35.2
|
1.0
|
OD1
|
A:ASP183
|
4.7
|
39.6
|
1.0
|
CB
|
A:ASN122
|
4.7
|
20.0
|
1.0
|
C
|
A:ASN122
|
4.9
|
21.8
|
1.0
|
CA
|
A:ASN122
|
4.9
|
21.1
|
1.0
|
C
|
A:TYR219
|
4.9
|
26.2
|
1.0
|
|
Sodium binding site 4 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 4 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 4 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na604
b:31.9
occ:1.00
|
O
|
A:ASP225
|
2.3
|
35.4
|
1.0
|
O
|
A:HOH787
|
2.3
|
32.7
|
1.0
|
O
|
A:LYS216
|
2.4
|
22.7
|
1.0
|
O
|
A:TYR219
|
2.4
|
22.2
|
1.0
|
O
|
A:HOH826
|
2.5
|
24.1
|
1.0
|
C
|
A:ASP225
|
3.5
|
38.0
|
1.0
|
C
|
A:LYS216
|
3.5
|
29.1
|
1.0
|
CA
|
A:HIS217
|
3.5
|
23.7
|
1.0
|
C
|
A:TYR219
|
3.6
|
26.2
|
1.0
|
C
|
A:GLY226
|
3.7
|
35.9
|
1.0
|
O
|
A:GLY226
|
3.8
|
28.5
|
1.0
|
OG
|
A:SER230
|
3.9
|
22.8
|
1.0
|
N
|
A:ILE227
|
3.9
|
29.2
|
1.0
|
N
|
A:HIS217
|
4.0
|
21.6
|
1.0
|
CA
|
A:GLY220
|
4.0
|
29.3
|
1.0
|
CA
|
A:GLY226
|
4.0
|
31.2
|
1.0
|
ND1
|
A:HIS217
|
4.1
|
24.5
|
1.0
|
O
|
A:HOH801
|
4.1
|
20.6
|
1.0
|
N
|
A:GLY226
|
4.2
|
29.5
|
1.0
|
C
|
A:HIS217
|
4.2
|
23.9
|
1.0
|
O
|
A:TRP223
|
4.3
|
30.9
|
1.0
|
N
|
A:GLY220
|
4.3
|
26.3
|
1.0
|
N
|
A:ASP225
|
4.4
|
31.4
|
1.0
|
CA
|
A:ILE227
|
4.5
|
28.8
|
1.0
|
O
|
A:SER222
|
4.5
|
28.2
|
1.0
|
CB
|
A:HIS217
|
4.5
|
23.0
|
1.0
|
CA
|
A:ASP225
|
4.5
|
33.5
|
1.0
|
CG
|
A:LYS216
|
4.6
|
32.8
|
1.0
|
O
|
A:HIS217
|
4.6
|
23.1
|
1.0
|
CG
|
A:HIS217
|
4.7
|
24.3
|
1.0
|
CA
|
A:LYS216
|
4.7
|
21.8
|
1.0
|
N
|
A:TYR219
|
4.8
|
20.6
|
1.0
|
CA
|
A:TYR219
|
4.8
|
23.7
|
1.0
|
N
|
A:ILE218
|
4.9
|
20.4
|
1.0
|
CB
|
A:SER230
|
5.0
|
21.1
|
1.0
|
CE1
|
A:HIS217
|
5.0
|
26.2
|
1.0
|
|
Sodium binding site 5 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 5 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 5 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na601
b:34.7
occ:1.00
|
O
|
B:GLY401
|
2.3
|
35.8
|
1.0
|
O
|
B:ASP411
|
2.3
|
30.8
|
1.0
|
O
|
B:CYS408
|
2.4
|
26.6
|
1.0
|
OD2
|
B:ASP406
|
2.5
|
42.7
|
1.0
|
OD1
|
B:ASP406
|
2.6
|
39.7
|
1.0
|
OD1
|
B:ASP412
|
2.9
|
40.3
|
1.0
|
CG
|
B:ASP406
|
3.0
|
47.2
|
1.0
|
C
|
B:ASP411
|
3.4
|
32.0
|
1.0
|
C
|
B:GLY401
|
3.5
|
39.5
|
1.0
|
C
|
B:CYS408
|
3.6
|
28.9
|
1.0
|
O
|
B:HOH938
|
3.6
|
38.3
|
1.0
|
CG
|
B:ASP412
|
4.1
|
37.1
|
1.0
|
CA
|
B:ASP412
|
4.2
|
28.6
|
1.0
|
N
|
B:ASP412
|
4.2
|
29.3
|
1.0
|
N
|
B:ASP411
|
4.2
|
25.1
|
1.0
|
CB
|
B:CYS408
|
4.3
|
29.4
|
1.0
|
CA
|
B:GLY401
|
4.3
|
37.0
|
1.0
|
C
|
B:ASN402
|
4.3
|
41.4
|
1.0
|
CA
|
B:CYS408
|
4.3
|
29.0
|
1.0
|
O
|
B:ASN402
|
4.4
|
41.1
|
1.0
|
N
|
B:CYS408
|
4.4
|
28.8
|
1.0
|
CA
|
B:ASP411
|
4.4
|
29.2
|
1.0
|
O
|
B:HOH1027
|
4.4
|
40.7
|
1.0
|
O
|
B:ILE409
|
4.4
|
24.4
|
1.0
|
N
|
B:ASN402
|
4.5
|
37.9
|
1.0
|
N
|
B:ALA403
|
4.5
|
37.4
|
1.0
|
CB
|
B:ASN402
|
4.5
|
44.4
|
1.0
|
CB
|
B:ASP406
|
4.5
|
47.1
|
1.0
|
C
|
B:ILE409
|
4.5
|
28.3
|
1.0
|
N
|
B:ILE409
|
4.6
|
25.7
|
1.0
|
CA
|
B:ASN402
|
4.6
|
38.4
|
1.0
|
CA
|
B:ALA403
|
4.7
|
34.3
|
1.0
|
CA
|
B:ILE409
|
4.7
|
27.4
|
1.0
|
CB
|
B:ASP412
|
4.7
|
25.8
|
1.0
|
O
|
B:HOH803
|
4.8
|
42.5
|
1.0
|
OD2
|
B:ASP412
|
5.0
|
44.4
|
1.0
|
N
|
B:TYR410
|
5.0
|
25.3
|
1.0
|
|
Sodium binding site 6 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 6 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 6 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na602
b:26.2
occ:1.00
|
OD1
|
B:ASP42
|
2.3
|
27.6
|
1.0
|
O
|
B:VAL48
|
2.4
|
25.6
|
1.0
|
OD2
|
B:ASP50
|
2.4
|
24.4
|
1.0
|
OD1
|
B:ASP46
|
2.4
|
31.2
|
1.0
|
OD1
|
B:ASP44
|
2.4
|
34.9
|
1.0
|
O
|
B:HOH809
|
2.5
|
28.4
|
1.0
|
CG
|
B:ASP46
|
3.3
|
31.7
|
1.0
|
CG
|
B:ASP42
|
3.3
|
30.0
|
1.0
|
CG
|
B:ASP50
|
3.5
|
24.0
|
1.0
|
CG
|
B:ASP44
|
3.5
|
40.0
|
1.0
|
C
|
B:VAL48
|
3.5
|
25.4
|
1.0
|
OD2
|
B:ASP46
|
3.7
|
30.0
|
1.0
|
CB
|
B:ASP50
|
3.9
|
26.1
|
1.0
|
CB
|
B:ASP42
|
4.0
|
23.5
|
1.0
|
N
|
B:VAL48
|
4.0
|
27.0
|
1.0
|
N
|
B:ASP44
|
4.0
|
30.9
|
1.0
|
CA
|
B:ASP42
|
4.0
|
23.6
|
1.0
|
O
|
B:HOH977
|
4.1
|
36.9
|
1.0
|
OD2
|
B:ASP44
|
4.1
|
42.0
|
1.0
|
CA
|
B:VAL48
|
4.1
|
25.2
|
1.0
|
N
|
B:SER43
|
4.1
|
24.2
|
1.0
|
CB
|
B:VAL48
|
4.2
|
24.4
|
1.0
|
OD2
|
B:ASP42
|
4.2
|
27.4
|
1.0
|
N
|
B:ASP46
|
4.3
|
28.1
|
1.0
|
C
|
B:ASP42
|
4.4
|
28.3
|
1.0
|
N
|
B:GLY45
|
4.4
|
31.0
|
1.0
|
CB
|
B:ASP44
|
4.6
|
30.2
|
1.0
|
OD1
|
B:ASP50
|
4.6
|
28.6
|
1.0
|
N
|
B:ASP50
|
4.6
|
24.0
|
1.0
|
N
|
B:GLY49
|
4.6
|
22.2
|
1.0
|
CB
|
B:ASP46
|
4.6
|
30.1
|
1.0
|
C
|
B:GLY49
|
4.6
|
21.4
|
1.0
|
CA
|
B:ASP44
|
4.6
|
33.4
|
1.0
|
C
|
B:ASP44
|
4.8
|
38.4
|
1.0
|
O
|
B:HOH787
|
4.8
|
42.4
|
1.0
|
N
|
B:GLY47
|
4.8
|
28.6
|
1.0
|
CA
|
B:GLY49
|
4.8
|
19.4
|
1.0
|
CA
|
B:ASP50
|
4.9
|
24.9
|
1.0
|
CA
|
B:ASP46
|
4.9
|
27.5
|
1.0
|
CG1
|
B:VAL48
|
4.9
|
27.5
|
1.0
|
O
|
B:GLY49
|
4.9
|
20.9
|
1.0
|
O
|
B:HOH1158
|
4.9
|
40.5
|
1.0
|
O
|
B:ASP94
|
5.0
|
29.3
|
1.0
|
|
Sodium binding site 7 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 7 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 7 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na603
b:29.7
occ:1.00
|
O
|
B:HIS217
|
2.3
|
23.3
|
1.0
|
O
|
B:HOH757
|
2.3
|
24.1
|
1.0
|
OD1
|
B:ASN122
|
2.4
|
28.4
|
1.0
|
O
|
B:HOH710
|
2.5
|
34.5
|
1.0
|
O
|
B:HOH712
|
2.6
|
36.3
|
1.0
|
O
|
B:ILE218
|
2.8
|
26.0
|
1.0
|
C
|
B:ILE218
|
3.3
|
29.7
|
1.0
|
C
|
B:HIS217
|
3.3
|
25.0
|
1.0
|
CG
|
B:ASN122
|
3.4
|
27.1
|
1.0
|
CA
|
B:ILE218
|
3.6
|
27.2
|
1.0
|
O
|
B:HOH813
|
3.6
|
24.9
|
1.0
|
OD2
|
B:ASP183
|
3.6
|
47.2
|
1.0
|
ND2
|
B:ASN122
|
3.8
|
24.4
|
1.0
|
N
|
B:ILE218
|
3.9
|
25.7
|
1.0
|
O
|
B:ASN122
|
4.1
|
23.7
|
1.0
|
CG
|
B:ASP183
|
4.1
|
30.6
|
1.0
|
O
|
B:HOH1000
|
4.2
|
27.0
|
1.0
|
N
|
B:TYR219
|
4.3
|
24.3
|
1.0
|
CB
|
B:ASP183
|
4.4
|
26.1
|
1.0
|
CA
|
B:HIS217
|
4.5
|
21.9
|
1.0
|
CB
|
B:HIS217
|
4.6
|
19.6
|
1.0
|
O
|
B:LEU184
|
4.6
|
24.6
|
1.0
|
CB
|
B:ASN122
|
4.6
|
25.4
|
1.0
|
CA
|
B:TYR219
|
4.7
|
26.5
|
1.0
|
CA
|
B:ASN122
|
4.9
|
22.2
|
1.0
|
C
|
B:ASN122
|
4.9
|
23.6
|
1.0
|
O1
|
B:EDO610
|
4.9
|
47.0
|
1.0
|
OD1
|
B:ASP183
|
4.9
|
42.6
|
1.0
|
C
|
B:TYR219
|
4.9
|
32.4
|
1.0
|
|
Sodium binding site 8 out
of 8 in 5m99
Go back to
Sodium Binding Sites List in 5m99
Sodium binding site 8 out
of 8 in the Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 8 of Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Archaic Form of Dimerization within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na604
b:34.2
occ:1.00
|
O
|
B:ASP225
|
2.3
|
34.4
|
1.0
|
O
|
B:HOH879
|
2.4
|
33.7
|
1.0
|
O
|
B:HOH877
|
2.4
|
26.7
|
1.0
|
O
|
B:LYS216
|
2.4
|
25.3
|
1.0
|
O
|
B:TYR219
|
2.5
|
24.9
|
1.0
|
C
|
B:ASP225
|
3.5
|
35.3
|
1.0
|
C
|
B:LYS216
|
3.5
|
24.8
|
1.0
|
CA
|
B:HIS217
|
3.6
|
21.9
|
1.0
|
C
|
B:TYR219
|
3.7
|
32.4
|
1.0
|
C
|
B:GLY226
|
3.7
|
35.2
|
1.0
|
O
|
B:GLY226
|
3.7
|
32.6
|
1.0
|
OG
|
B:SER230
|
4.0
|
24.4
|
1.0
|
CA
|
B:GLY220
|
4.0
|
30.7
|
1.0
|
N
|
B:HIS217
|
4.0
|
21.0
|
1.0
|
CA
|
B:GLY226
|
4.1
|
32.1
|
1.0
|
N
|
B:ILE227
|
4.1
|
27.9
|
1.0
|
ND1
|
B:HIS217
|
4.1
|
26.4
|
1.0
|
O
|
B:TRP223
|
4.2
|
31.8
|
1.0
|
N
|
B:GLY226
|
4.2
|
33.3
|
1.0
|
O
|
B:HOH813
|
4.3
|
24.9
|
1.0
|
C
|
B:HIS217
|
4.3
|
25.0
|
1.0
|
N
|
B:GLY220
|
4.3
|
29.9
|
1.0
|
O
|
B:SER222
|
4.4
|
32.6
|
1.0
|
N
|
B:ASP225
|
4.5
|
29.8
|
1.0
|
CA
|
B:ASP225
|
4.6
|
32.0
|
1.0
|
CA
|
B:ILE227
|
4.6
|
29.1
|
1.0
|
CB
|
B:HIS217
|
4.6
|
19.6
|
1.0
|
CG
|
B:LYS216
|
4.6
|
31.8
|
1.0
|
O
|
B:HIS217
|
4.7
|
23.3
|
1.0
|
CG
|
B:HIS217
|
4.7
|
29.4
|
1.0
|
CA
|
B:LYS216
|
4.8
|
24.9
|
1.0
|
N
|
B:TYR219
|
4.8
|
24.3
|
1.0
|
CA
|
B:TYR219
|
4.8
|
26.5
|
1.0
|
CB
|
B:SER230
|
4.9
|
22.6
|
1.0
|
C
|
B:TRP223
|
4.9
|
30.4
|
1.0
|
C
|
B:ASP224
|
5.0
|
29.9
|
1.0
|
N
|
B:ILE218
|
5.0
|
25.7
|
1.0
|
CE1
|
B:HIS217
|
5.0
|
28.6
|
1.0
|
|
Reference:
U.Hameed,
I.Price,
A.Ke,
D.B.Wilson,
O.Mirza.
Functional Characterization and Crystal Structure of Thermostable Amylase From Thermotoga Petrophila, Reveals High Thermostability and An Unusual Form of Dimerization. Biochim. Biophys. Acta V.1865 1237 2017.
ISSN: ISSN 0006-3002
PubMed: 28648523
DOI: 10.1016/J.BBAPAP.2017.06.015
Page generated: Mon Oct 7 22:31:18 2024
|