Magnesium in PDB 3hke: Tubulin-T138067: RB3 Stathmin-Like Domain Complex
Protein crystallography data
The structure of Tubulin-T138067: RB3 Stathmin-Like Domain Complex, PDB code: 3hke
was solved by
A.Dorleans,
B.Gigant,
R.B.G.Ravelli,
P.Mailliet,
V.Mikol,
M.Knossow,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
3.60
|
Space group
|
P 65
|
Cell size a, b, c (Å), α, β, γ (°)
|
326.710,
326.710,
54.120,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
20.7 /
25.3
|
Other elements in 3hke:
The structure of Tubulin-T138067: RB3 Stathmin-Like Domain Complex also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Tubulin-T138067: RB3 Stathmin-Like Domain Complex
(pdb code 3hke). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 3 binding sites of Magnesium where determined in the
Tubulin-T138067: RB3 Stathmin-Like Domain Complex, PDB code: 3hke:
Jump to Magnesium binding site number:
1;
2;
3;
Magnesium binding site 1 out
of 3 in 3hke
Go back to
Magnesium Binding Sites List in 3hke
Magnesium binding site 1 out
of 3 in the Tubulin-T138067: RB3 Stathmin-Like Domain Complex
 Mono view
 Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Tubulin-T138067: RB3 Stathmin-Like Domain Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg601
b:30.2
occ:1.00
|
O2B
|
A:GTP600
|
1.8
|
64.6
|
1.0
|
O3G
|
A:GTP600
|
2.1
|
65.8
|
1.0
|
N
|
A:GLY144
|
3.0
|
65.8
|
1.0
|
PB
|
A:GTP600
|
3.1
|
66.0
|
1.0
|
PG
|
A:GTP600
|
3.2
|
66.5
|
1.0
|
N
|
A:THR145
|
3.2
|
65.7
|
1.0
|
CG2
|
A:THR145
|
3.3
|
65.1
|
1.0
|
CA
|
A:GLY144
|
3.3
|
65.7
|
1.0
|
CB
|
A:ALA99
|
3.3
|
65.6
|
1.0
|
O2G
|
A:GTP600
|
3.4
|
66.5
|
1.0
|
N
|
A:ASN101
|
3.6
|
65.1
|
1.0
|
O3B
|
A:GTP600
|
3.6
|
65.5
|
1.0
|
O3A
|
A:GTP600
|
3.7
|
66.0
|
1.0
|
C
|
A:GLY144
|
3.7
|
65.6
|
1.0
|
OD1
|
A:ASP98
|
3.9
|
68.8
|
1.0
|
N
|
A:ALA100
|
4.0
|
65.3
|
1.0
|
CA
|
A:ALA99
|
4.1
|
65.4
|
1.0
|
C
|
A:ALA99
|
4.1
|
65.3
|
1.0
|
CA
|
A:ASN101
|
4.2
|
64.8
|
1.0
|
C
|
A:GLY143
|
4.2
|
65.9
|
1.0
|
N
|
A:ALA99
|
4.2
|
65.6
|
1.0
|
O1B
|
A:GTP600
|
4.3
|
65.8
|
1.0
|
CA
|
A:THR145
|
4.3
|
65.8
|
1.0
|
CB
|
A:THR145
|
4.3
|
65.8
|
1.0
|
OD1
|
A:ASN101
|
4.5
|
65.2
|
1.0
|
O1G
|
A:GTP600
|
4.5
|
66.6
|
1.0
|
C
|
A:ALA100
|
4.6
|
65.3
|
1.0
|
CA
|
A:ALA100
|
4.7
|
65.5
|
1.0
|
CA
|
A:GLY143
|
4.8
|
66.0
|
1.0
|
O
|
A:ALA99
|
4.8
|
65.0
|
1.0
|
OG1
|
A:THR145
|
4.9
|
66.9
|
1.0
|
O
|
A:GLY144
|
5.0
|
65.4
|
1.0
|
|
Magnesium binding site 2 out
of 3 in 3hke
Go back to
Magnesium Binding Sites List in 3hke
Magnesium binding site 2 out
of 3 in the Tubulin-T138067: RB3 Stathmin-Like Domain Complex
 Mono view
 Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Tubulin-T138067: RB3 Stathmin-Like Domain Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg601
b:53.5
occ:1.00
|
O2A
|
B:GDP600
|
3.5
|
66.4
|
1.0
|
ND2
|
B:ASN101
|
3.5
|
66.4
|
1.0
|
OE1
|
C:GLU254
|
3.9
|
68.5
|
1.0
|
OE1
|
B:GLN11
|
4.1
|
67.6
|
1.0
|
O2B
|
B:GDP600
|
4.3
|
66.3
|
1.0
|
CG
|
B:ASN101
|
4.5
|
66.0
|
1.0
|
O3B
|
B:GDP600
|
4.6
|
65.7
|
1.0
|
CB
|
B:GLN11
|
4.6
|
66.5
|
1.0
|
PA
|
B:GDP600
|
4.7
|
67.3
|
1.0
|
O3A
|
B:GDP600
|
4.7
|
67.2
|
1.0
|
CG
|
B:GLN11
|
4.7
|
67.0
|
1.0
|
PB
|
B:GDP600
|
4.8
|
67.0
|
1.0
|
CD
|
B:GLN11
|
4.9
|
67.3
|
1.0
|
CD
|
C:GLU254
|
4.9
|
68.2
|
1.0
|
OD1
|
B:ASN101
|
4.9
|
66.0
|
1.0
|
OD2
|
B:ASP179
|
5.0
|
67.5
|
1.0
|
|
Magnesium binding site 3 out
of 3 in 3hke
Go back to
Magnesium Binding Sites List in 3hke
Magnesium binding site 3 out
of 3 in the Tubulin-T138067: RB3 Stathmin-Like Domain Complex
 Mono view
 Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Tubulin-T138067: RB3 Stathmin-Like Domain Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg601
b:30.2
occ:1.00
|
O2B
|
C:GTP600
|
1.9
|
64.7
|
1.0
|
O3G
|
C:GTP600
|
2.0
|
65.9
|
1.0
|
PG
|
C:GTP600
|
3.0
|
66.5
|
1.0
|
PB
|
C:GTP600
|
3.1
|
65.1
|
1.0
|
N
|
C:GLY144
|
3.2
|
65.8
|
1.0
|
CG2
|
C:THR145
|
3.2
|
65.4
|
1.0
|
CB
|
C:ALA99
|
3.3
|
65.5
|
1.0
|
N
|
C:THR145
|
3.3
|
65.8
|
1.0
|
O2G
|
C:GTP600
|
3.3
|
66.2
|
1.0
|
CA
|
C:GLY144
|
3.4
|
65.8
|
1.0
|
O3B
|
C:GTP600
|
3.6
|
65.2
|
1.0
|
N
|
C:ASN101
|
3.6
|
65.0
|
1.0
|
OD1
|
C:ASP98
|
3.7
|
68.6
|
1.0
|
O3A
|
C:GTP600
|
3.8
|
65.8
|
1.0
|
C
|
C:GLY144
|
3.9
|
65.8
|
1.0
|
N
|
C:ALA100
|
4.0
|
65.3
|
1.0
|
CA
|
C:ALA99
|
4.1
|
65.4
|
1.0
|
N
|
C:ALA99
|
4.1
|
65.7
|
1.0
|
C
|
C:ALA99
|
4.1
|
65.2
|
1.0
|
CA
|
C:ASN101
|
4.2
|
64.7
|
1.0
|
C
|
C:GLY143
|
4.3
|
65.8
|
1.0
|
O1G
|
C:GTP600
|
4.3
|
66.7
|
1.0
|
O1B
|
C:GTP600
|
4.3
|
65.3
|
1.0
|
CB
|
C:THR145
|
4.4
|
65.9
|
1.0
|
OD1
|
C:ASN101
|
4.4
|
65.1
|
1.0
|
CA
|
C:THR145
|
4.4
|
65.8
|
1.0
|
NZ
|
D:LYS254
|
4.5
|
67.7
|
1.0
|
C
|
C:ALA100
|
4.6
|
65.3
|
1.0
|
CA
|
C:ALA100
|
4.7
|
65.4
|
1.0
|
O
|
C:ALA99
|
4.8
|
64.9
|
1.0
|
CA
|
C:GLY143
|
4.8
|
66.0
|
1.0
|
CG
|
C:ASP98
|
4.9
|
67.4
|
1.0
|
OG1
|
C:THR145
|
4.9
|
66.7
|
1.0
|
|
Reference:
A.Dorleans,
B.Gigant,
R.B.G.Ravelli,
P.Mailliet,
V.Mikol,
M.Knossow.
Variations in the Colchicine-Binding Domain Provide Insight Into the Structural Switch of Tubulin Proc.Natl.Acad.Sci.Usa V. 106 13775 2009.
ISSN: ISSN 0027-8424
PubMed: 19666559
DOI: 10.1073/PNAS.0904223106
Page generated: Wed Aug 14 15:10:53 2024
|