Magnesium in PDB 1f1z: Tnsa, A Catalytic Component of the TN7 Transposition System
Protein crystallography data
The structure of Tnsa, A Catalytic Component of the TN7 Transposition System, PDB code: 1f1z
was solved by
A.B.Hickman,
Y.Li,
S.V.Mathew,
E.W.May,
N.L.Craig,
F.Dyda,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.00 /
2.40
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
38.350,
83.680,
97.940,
90.00,
94.07,
90.00
|
R / Rfree (%)
|
20.2 /
25.4
|
Other elements in 1f1z:
The structure of Tnsa, A Catalytic Component of the TN7 Transposition System also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Tnsa, A Catalytic Component of the TN7 Transposition System
(pdb code 1f1z). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Tnsa, A Catalytic Component of the TN7 Transposition System, PDB code: 1f1z:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 1f1z
Go back to
Magnesium Binding Sites List in 1f1z
Magnesium binding site 1 out
of 4 in the Tnsa, A Catalytic Component of the TN7 Transposition System
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Tnsa, A Catalytic Component of the TN7 Transposition System within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg2001
b:38.7
occ:1.00
|
O
|
A:HOH1005
|
2.0
|
23.9
|
1.0
|
O
|
A:HOH1010
|
2.0
|
51.0
|
1.0
|
O
|
A:HOH1004
|
2.1
|
39.5
|
1.0
|
O
|
A:HOH1006
|
2.1
|
33.6
|
1.0
|
OD1
|
A:ASP114
|
2.3
|
34.7
|
1.0
|
O
|
A:HOH1007
|
2.6
|
13.8
|
1.0
|
CG
|
A:ASP114
|
3.5
|
35.5
|
1.0
|
MG
|
A:MG2002
|
3.9
|
35.5
|
1.0
|
O
|
A:HOH1003
|
3.9
|
56.9
|
1.0
|
OE1
|
A:GLN82
|
4.0
|
35.4
|
1.0
|
OD2
|
A:ASP114
|
4.0
|
31.2
|
1.0
|
O
|
A:SER112
|
4.1
|
34.4
|
1.0
|
OE1
|
A:GLN130
|
4.2
|
30.1
|
1.0
|
OG
|
A:SER112
|
4.3
|
34.0
|
1.0
|
O
|
A:HOH1009
|
4.3
|
44.2
|
1.0
|
NE2
|
A:GLN130
|
4.4
|
23.5
|
1.0
|
OE2
|
A:GLU63
|
4.6
|
41.6
|
1.0
|
CD1
|
A:LEU33
|
4.7
|
52.2
|
1.0
|
CB
|
A:ASP114
|
4.7
|
33.8
|
1.0
|
CD
|
A:GLN130
|
4.7
|
25.6
|
1.0
|
N
|
A:ASP114
|
4.8
|
37.0
|
1.0
|
CA
|
A:ASP114
|
4.8
|
35.3
|
1.0
|
C
|
A:SER112
|
5.0
|
35.5
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 1f1z
Go back to
Magnesium Binding Sites List in 1f1z
Magnesium binding site 2 out
of 4 in the Tnsa, A Catalytic Component of the TN7 Transposition System
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Tnsa, A Catalytic Component of the TN7 Transposition System within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg2002
b:35.5
occ:1.00
|
O
|
A:HOH1009
|
2.0
|
44.2
|
1.0
|
O
|
A:HOH1007
|
2.1
|
13.8
|
1.0
|
O
|
A:HOH1008
|
2.1
|
37.5
|
1.0
|
O
|
A:VAL131
|
2.1
|
35.4
|
1.0
|
OE1
|
A:GLN130
|
2.2
|
30.1
|
1.0
|
OD2
|
A:ASP114
|
2.7
|
31.2
|
1.0
|
C
|
A:VAL131
|
3.4
|
34.3
|
1.0
|
CD
|
A:GLN130
|
3.4
|
25.6
|
1.0
|
CG
|
A:LYS132
|
3.5
|
40.1
|
1.0
|
CG
|
A:ASP114
|
3.5
|
35.5
|
1.0
|
OD1
|
A:ASP114
|
3.6
|
34.7
|
1.0
|
NZ
|
A:LYS132
|
3.9
|
56.0
|
1.0
|
MG
|
A:MG2001
|
3.9
|
38.7
|
1.0
|
CE
|
A:LYS132
|
4.1
|
54.6
|
1.0
|
O
|
A:HOH1006
|
4.2
|
33.6
|
1.0
|
N
|
A:VAL131
|
4.2
|
31.9
|
1.0
|
NE2
|
A:GLN130
|
4.2
|
23.5
|
1.0
|
O
|
A:HOH1004
|
4.3
|
39.5
|
1.0
|
CA
|
A:VAL131
|
4.3
|
33.8
|
1.0
|
N
|
A:LYS132
|
4.3
|
31.7
|
1.0
|
CD
|
A:LYS132
|
4.4
|
45.4
|
1.0
|
OE2
|
A:GLU63
|
4.4
|
41.6
|
1.0
|
CA
|
A:LYS132
|
4.4
|
31.7
|
1.0
|
CG
|
A:GLN130
|
4.4
|
27.6
|
1.0
|
CB
|
A:LYS132
|
4.5
|
32.4
|
1.0
|
CL
|
A:CL2003
|
4.6
|
50.4
|
1.0
|
CB
|
A:VAL131
|
4.7
|
33.1
|
1.0
|
O
|
A:HOH1003
|
4.8
|
56.9
|
1.0
|
O
|
A:HOH1010
|
4.9
|
51.0
|
1.0
|
CB
|
A:ASP114
|
5.0
|
33.8
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 1f1z
Go back to
Magnesium Binding Sites List in 1f1z
Magnesium binding site 3 out
of 4 in the Tnsa, A Catalytic Component of the TN7 Transposition System
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Tnsa, A Catalytic Component of the TN7 Transposition System within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg2004
b:36.3
occ:1.00
|
O
|
B:HOH1176
|
2.0
|
65.8
|
1.0
|
O
|
B:HOH1177
|
2.0
|
33.5
|
1.0
|
O
|
B:HOH1181
|
2.0
|
51.4
|
1.0
|
O
|
B:HOH1178
|
2.1
|
56.6
|
1.0
|
OD1
|
B:ASP114
|
2.3
|
40.0
|
1.0
|
O
|
B:HOH1103
|
2.8
|
21.3
|
1.0
|
CG
|
B:ASP114
|
3.5
|
40.1
|
1.0
|
MG
|
B:MG2005
|
3.9
|
44.0
|
1.0
|
OD2
|
B:ASP114
|
4.0
|
37.0
|
1.0
|
OE1
|
B:GLN82
|
4.0
|
42.7
|
1.0
|
OE1
|
B:GLN130
|
4.1
|
28.2
|
1.0
|
O
|
B:SER112
|
4.2
|
39.5
|
1.0
|
O
|
B:HOH1175
|
4.3
|
44.0
|
1.0
|
OE2
|
B:GLU63
|
4.4
|
45.7
|
1.0
|
OG
|
B:SER112
|
4.4
|
38.5
|
1.0
|
O
|
B:HOH1180
|
4.4
|
39.9
|
1.0
|
NE2
|
B:GLN130
|
4.5
|
25.8
|
1.0
|
CB
|
B:ASP114
|
4.7
|
35.8
|
1.0
|
CD
|
B:GLN130
|
4.8
|
28.3
|
1.0
|
N
|
B:ASP114
|
4.8
|
35.1
|
1.0
|
CD1
|
B:LEU33
|
4.8
|
47.8
|
1.0
|
CA
|
B:ASP114
|
4.8
|
36.3
|
1.0
|
O
|
B:HOH1179
|
4.9
|
45.5
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 1f1z
Go back to
Magnesium Binding Sites List in 1f1z
Magnesium binding site 4 out
of 4 in the Tnsa, A Catalytic Component of the TN7 Transposition System
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Tnsa, A Catalytic Component of the TN7 Transposition System within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg2005
b:44.0
occ:1.00
|
O
|
B:VAL131
|
2.1
|
31.9
|
1.0
|
O
|
B:HOH1180
|
2.1
|
39.9
|
1.0
|
OE1
|
B:GLN130
|
2.3
|
28.2
|
1.0
|
O
|
B:HOH1103
|
2.3
|
21.3
|
1.0
|
O
|
B:HOH1104
|
2.4
|
44.7
|
1.0
|
OD2
|
B:ASP114
|
2.7
|
37.0
|
1.0
|
C
|
B:VAL131
|
3.3
|
34.4
|
1.0
|
CG
|
B:LYS132
|
3.4
|
46.8
|
1.0
|
CD
|
B:GLN130
|
3.5
|
28.3
|
1.0
|
CG
|
B:ASP114
|
3.6
|
40.1
|
1.0
|
OD1
|
B:ASP114
|
3.7
|
40.0
|
1.0
|
NZ
|
B:LYS132
|
3.9
|
35.1
|
1.0
|
MG
|
B:MG2004
|
3.9
|
36.3
|
1.0
|
CE
|
B:LYS132
|
4.0
|
39.2
|
1.0
|
O
|
B:HOH1181
|
4.1
|
51.4
|
1.0
|
N
|
B:VAL131
|
4.2
|
36.0
|
1.0
|
N
|
B:LYS132
|
4.2
|
36.8
|
1.0
|
CA
|
B:VAL131
|
4.3
|
33.5
|
1.0
|
CD
|
B:LYS132
|
4.3
|
42.9
|
1.0
|
OE2
|
B:GLU63
|
4.3
|
45.7
|
1.0
|
CA
|
B:LYS132
|
4.4
|
40.1
|
1.0
|
NE2
|
B:GLN130
|
4.4
|
25.8
|
1.0
|
CB
|
B:LYS132
|
4.5
|
39.2
|
1.0
|
CG
|
B:GLN130
|
4.5
|
24.0
|
1.0
|
CL
|
B:CL2006
|
4.6
|
52.2
|
1.0
|
O
|
B:HOH1178
|
4.6
|
56.6
|
1.0
|
O
|
B:HOH1105
|
4.6
|
58.0
|
1.0
|
CB
|
B:VAL131
|
4.7
|
31.2
|
1.0
|
O
|
B:HOH1179
|
4.8
|
45.5
|
1.0
|
|
Reference:
A.B.Hickman,
Y.Li,
S.V.Mathew,
E.W.May,
N.L.Craig,
F.Dyda.
Unexpected Structural Diversity in Dna Recombination: the Restriction Endonuclease Connection. Mol.Cell V. 5 1025 2000.
ISSN: ISSN 1097-2765
PubMed: 10911996
DOI: 10.1016/S1097-2765(00)80267-1
Page generated: Tue Aug 13 03:05:36 2024
|