Calcium in PDB 1rgi: Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin
Protein crystallography data
The structure of Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin, PDB code: 1rgi
was solved by
L.D.Burtnick,
D.Urosev,
E.Irobi,
K.Narayan,
R.C.Robinson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
19.96 /
3.00
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
145.245,
145.245,
129.948,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
22.4 /
25.8
|
Calcium Binding Sites:
The binding sites of Calcium atom in the Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin
(pdb code 1rgi). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 4 binding sites of Calcium where determined in the
Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin, PDB code: 1rgi:
Jump to Calcium binding site number:
1;
2;
3;
4;
Calcium binding site 1 out
of 4 in 1rgi
Go back to
Calcium Binding Sites List in 1rgi
Calcium binding site 1 out
of 4 in the Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 1 of Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Ca403
b:25.9
occ:1.00
|
O
|
G:GLY65
|
2.2
|
23.6
|
1.0
|
O
|
G:VAL145
|
2.3
|
27.6
|
1.0
|
OE1
|
G:GLU97
|
2.4
|
29.7
|
1.0
|
OD2
|
G:ASP66
|
2.4
|
24.2
|
1.0
|
OE2
|
G:GLU97
|
2.9
|
32.2
|
1.0
|
CD
|
G:GLU97
|
3.0
|
29.3
|
1.0
|
C
|
G:GLY65
|
3.3
|
23.5
|
1.0
|
C
|
G:VAL145
|
3.4
|
27.3
|
1.0
|
CG
|
G:ASP66
|
3.6
|
25.0
|
1.0
|
N
|
G:VAL145
|
3.9
|
26.5
|
1.0
|
C
|
G:GLY144
|
4.1
|
25.6
|
1.0
|
CA
|
G:GLY65
|
4.2
|
22.9
|
1.0
|
N
|
G:ASP66
|
4.2
|
23.6
|
1.0
|
CA
|
G:ASP66
|
4.3
|
23.5
|
1.0
|
N
|
G:ALA146
|
4.3
|
27.8
|
1.0
|
CA
|
G:GLY144
|
4.3
|
24.9
|
1.0
|
CA
|
G:VAL145
|
4.3
|
27.2
|
1.0
|
CA
|
G:ALA146
|
4.4
|
28.1
|
1.0
|
CG
|
G:GLU97
|
4.4
|
26.8
|
1.0
|
OD1
|
G:ASP66
|
4.4
|
23.6
|
1.0
|
C
|
G:ALA146
|
4.5
|
28.5
|
1.0
|
N
|
G:SER147
|
4.5
|
28.7
|
1.0
|
CB
|
G:ASP66
|
4.6
|
23.9
|
1.0
|
O
|
G:GLY144
|
4.6
|
25.9
|
1.0
|
CG1
|
G:VAL145
|
4.7
|
28.0
|
1.0
|
N
|
G:SER94
|
4.8
|
28.7
|
1.0
|
OG
|
G:SER94
|
4.9
|
27.5
|
1.0
|
CA
|
G:CYS93
|
4.9
|
30.1
|
1.0
|
O
|
G:ALA146
|
5.0
|
29.1
|
1.0
|
|
Calcium binding site 2 out
of 4 in 1rgi
Go back to
Calcium Binding Sites List in 1rgi
Calcium binding site 2 out
of 4 in the Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 2 of Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Ca404
b:36.3
occ:1.00
|
OE1
|
A:GLU167
|
2.3
|
31.3
|
1.0
|
O
|
G:GLY114
|
2.4
|
32.8
|
1.0
|
OD2
|
G:ASP109
|
2.6
|
33.0
|
1.0
|
O
|
A:HOH402
|
2.6
|
27.3
|
1.0
|
O
|
G:ALA116
|
3.0
|
29.9
|
1.0
|
C
|
G:GLY114
|
3.3
|
33.0
|
1.0
|
CG
|
G:ASP109
|
3.4
|
32.0
|
1.0
|
OD1
|
G:ASP109
|
3.4
|
33.6
|
1.0
|
CD
|
A:GLU167
|
3.5
|
30.0
|
1.0
|
CA
|
G:GLY114
|
3.8
|
33.2
|
1.0
|
C
|
G:ALA116
|
4.0
|
29.7
|
1.0
|
OE2
|
A:GLU167
|
4.1
|
31.6
|
1.0
|
N
|
G:ALA116
|
4.2
|
31.0
|
1.0
|
N
|
G:ARG115
|
4.5
|
32.9
|
1.0
|
CG
|
A:GLU167
|
4.6
|
28.3
|
1.0
|
CB
|
A:GLU167
|
4.6
|
27.4
|
1.0
|
CA
|
G:ALA116
|
4.7
|
30.3
|
1.0
|
NE2
|
G:GLN118
|
4.8
|
21.3
|
1.0
|
CB
|
G:ASP109
|
4.8
|
30.8
|
1.0
|
C
|
G:ARG115
|
5.0
|
32.2
|
1.0
|
CA
|
G:ARG115
|
5.0
|
33.1
|
1.0
|
N
|
G:VAL117
|
5.0
|
28.8
|
1.0
|
|
Calcium binding site 3 out
of 4 in 1rgi
Go back to
Calcium Binding Sites List in 1rgi
Calcium binding site 3 out
of 4 in the Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 3 of Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Ca406
b:47.9
occ:1.00
|
O
|
G:GLU302
|
2.6
|
31.9
|
1.0
|
OE2
|
G:GLU327
|
2.7
|
33.0
|
1.0
|
OE1
|
G:GLU327
|
2.8
|
31.7
|
1.0
|
OD1
|
G:ASP303
|
3.0
|
31.1
|
1.0
|
CD
|
G:GLU327
|
3.1
|
31.4
|
1.0
|
C
|
G:GLU302
|
3.7
|
31.7
|
1.0
|
OD1
|
G:ASN278
|
3.9
|
22.3
|
1.0
|
ND2
|
G:ASN324
|
4.1
|
29.7
|
1.0
|
CG
|
G:ASP303
|
4.2
|
32.4
|
1.0
|
OG
|
G:SER277
|
4.2
|
27.3
|
1.0
|
CB
|
G:GLU302
|
4.3
|
32.8
|
1.0
|
CA
|
G:GLU302
|
4.4
|
32.4
|
1.0
|
CA
|
G:GLY279
|
4.5
|
23.5
|
1.0
|
CG
|
G:GLU327
|
4.5
|
30.8
|
1.0
|
N
|
G:ASP303
|
4.6
|
31.1
|
1.0
|
CA
|
G:ASP303
|
4.6
|
31.1
|
1.0
|
N
|
G:GLY279
|
4.6
|
23.6
|
1.0
|
CB
|
G:ASP303
|
4.9
|
31.2
|
1.0
|
CA
|
G:ALA323
|
5.0
|
27.3
|
1.0
|
N
|
G:ASN324
|
5.0
|
27.6
|
1.0
|
N
|
G:ASN278
|
5.0
|
24.3
|
1.0
|
|
Calcium binding site 4 out
of 4 in 1rgi
Go back to
Calcium Binding Sites List in 1rgi
Calcium binding site 4 out
of 4 in the Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 4 of Crystal Structure of Gelsolin Domains G1-G3 Bound to Actin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca401
b:31.1
occ:1.00
|
O3G
|
A:ATP380
|
2.5
|
26.8
|
1.0
|
O2B
|
A:ATP380
|
2.5
|
21.9
|
1.0
|
OE1
|
A:GLN137
|
3.7
|
27.9
|
1.0
|
PG
|
A:ATP380
|
3.8
|
26.2
|
1.0
|
PB
|
A:ATP380
|
4.0
|
19.9
|
1.0
|
O1G
|
A:ATP380
|
4.0
|
23.9
|
1.0
|
OD2
|
A:ASP154
|
4.3
|
40.3
|
1.0
|
OD1
|
A:ASP154
|
4.3
|
40.2
|
1.0
|
O3B
|
A:ATP380
|
4.4
|
23.2
|
1.0
|
CD
|
A:GLN137
|
4.4
|
28.0
|
1.0
|
O1A
|
A:ATP380
|
4.4
|
22.0
|
1.0
|
CG
|
A:ASP154
|
4.6
|
37.4
|
1.0
|
OD2
|
A:ASP11
|
4.6
|
38.0
|
1.0
|
CA
|
A:GLY13
|
4.6
|
28.2
|
1.0
|
O3A
|
A:ATP380
|
4.7
|
21.8
|
1.0
|
O1B
|
A:ATP380
|
4.9
|
17.4
|
1.0
|
O2G
|
A:ATP380
|
4.9
|
22.4
|
1.0
|
NE2
|
A:GLN137
|
4.9
|
26.5
|
1.0
|
OD1
|
A:ASP11
|
5.0
|
36.1
|
1.0
|
|
Reference:
L.D.Burtnick,
D.Urosev,
E.Irobi,
K.Narayan,
R.C.Robinson.
Structure of the N-Terminal Half of Gelsolin Bound to Actin: Roles in Severing, Apoptosis and Faf Embo J. V. 23 2713 2004.
ISSN: ISSN 0261-4189
PubMed: 15215896
DOI: 10.1038/SJ.EMBOJ.7600280
Page generated: Thu Jul 11 22:10:42 2024
|