Calcium in PDB 1fzc: Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands
Protein crystallography data
The structure of Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands, PDB code: 1fzc
was solved by
S.J.Everse,
G.Spraggon,
L.Veerapandian,
M.Riley,
R.F.Doolittle,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
2.30
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
83.443,
95.600,
113.641,
90.00,
90.19,
90.00
|
R / Rfree (%)
|
22 /
29
|
Calcium Binding Sites:
The binding sites of Calcium atom in the Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands
(pdb code 1fzc). 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 Fragment Double-D From Human Fibrin with Two Different Bound Ligands, PDB code: 1fzc:
Jump to Calcium binding site number:
1;
2;
3;
4;
Calcium binding site 1 out
of 4 in 1fzc
Go back to
Calcium Binding Sites List in 1fzc
Calcium binding site 1 out
of 4 in the Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands
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 Fragment Double-D From Human Fibrin with Two Different Bound Ligands within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ca2
b:4.6
occ:1.00
|
O
|
B:HOH595
|
2.3
|
44.0
|
1.0
|
O
|
B:TRP385
|
2.3
|
28.3
|
1.0
|
OD2
|
B:ASP381
|
2.4
|
37.0
|
1.0
|
OD1
|
B:ASP383
|
2.6
|
20.7
|
1.0
|
O
|
B:HOH570
|
2.6
|
47.3
|
1.0
|
OD1
|
B:ASP381
|
2.8
|
37.5
|
1.0
|
CG
|
B:ASP381
|
3.1
|
36.1
|
1.0
|
CG
|
B:ASP383
|
3.3
|
20.4
|
1.0
|
C
|
B:TRP385
|
3.5
|
31.9
|
1.0
|
OD2
|
B:ASP383
|
3.6
|
25.1
|
1.0
|
N
|
B:TRP385
|
4.2
|
26.4
|
1.0
|
CA
|
B:TRP385
|
4.3
|
27.9
|
1.0
|
CB
|
B:TRP385
|
4.4
|
22.9
|
1.0
|
N
|
B:ASP383
|
4.4
|
21.5
|
1.0
|
CB
|
B:ASP383
|
4.4
|
19.6
|
1.0
|
C
|
B:ASP383
|
4.4
|
23.2
|
1.0
|
O
|
B:ASP383
|
4.5
|
21.0
|
1.0
|
N
|
B:LEU386
|
4.5
|
37.9
|
1.0
|
CB
|
B:ASP381
|
4.5
|
31.5
|
1.0
|
CA
|
B:ASP383
|
4.6
|
21.8
|
1.0
|
CA
|
B:LEU386
|
4.7
|
43.2
|
1.0
|
N
|
B:THR387
|
4.8
|
51.0
|
1.0
|
O
|
B:LYS392
|
4.9
|
38.1
|
1.0
|
|
Calcium binding site 2 out
of 4 in 1fzc
Go back to
Calcium Binding Sites List in 1fzc
Calcium binding site 2 out
of 4 in the Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands
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 Fragment Double-D From Human Fibrin with Two Different Bound Ligands within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Ca1
b:3.3
occ:1.00
|
OD1
|
C:ASP320
|
2.3
|
24.7
|
1.0
|
OD2
|
C:ASP318
|
2.4
|
38.8
|
1.0
|
O
|
C:GLY324
|
2.4
|
41.2
|
1.0
|
OD1
|
C:ASP318
|
2.6
|
39.9
|
1.0
|
O
|
C:PHE322
|
2.6
|
48.1
|
1.0
|
CG
|
C:ASP318
|
2.8
|
40.7
|
1.0
|
CG
|
C:ASP320
|
3.3
|
30.8
|
1.0
|
C
|
C:GLY324
|
3.6
|
40.9
|
1.0
|
OD2
|
C:ASP320
|
3.6
|
33.0
|
1.0
|
C
|
C:PHE322
|
3.7
|
46.3
|
1.0
|
O
|
C:ASP320
|
4.1
|
34.8
|
1.0
|
N
|
C:PHE322
|
4.3
|
44.3
|
1.0
|
CB
|
C:ASP318
|
4.3
|
38.5
|
1.0
|
O
|
C:GLU323
|
4.3
|
38.5
|
1.0
|
C
|
C:GLU323
|
4.3
|
44.2
|
1.0
|
CA
|
C:PHE322
|
4.4
|
44.5
|
1.0
|
N
|
C:ASN325
|
4.4
|
39.2
|
1.0
|
CA
|
C:ASN325
|
4.4
|
37.7
|
1.0
|
N
|
C:ASP320
|
4.4
|
32.7
|
1.0
|
N
|
C:GLY324
|
4.5
|
41.7
|
1.0
|
C
|
C:ASP320
|
4.6
|
35.2
|
1.0
|
N
|
C:GLU323
|
4.6
|
46.8
|
1.0
|
CB
|
C:ASP320
|
4.6
|
30.6
|
1.0
|
CA
|
C:GLY324
|
4.6
|
39.9
|
1.0
|
CB
|
C:PHE322
|
4.7
|
44.7
|
1.0
|
CA
|
C:ASP320
|
4.8
|
34.7
|
1.0
|
CA
|
C:GLU323
|
4.8
|
47.2
|
1.0
|
|
Calcium binding site 3 out
of 4 in 1fzc
Go back to
Calcium Binding Sites List in 1fzc
Calcium binding site 3 out
of 4 in the Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands
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 Fragment Double-D From Human Fibrin with Two Different Bound Ligands within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Ca2
b:3.0
occ:1.00
|
OD2
|
E:ASP381
|
2.5
|
27.5
|
1.0
|
O
|
E:TRP385
|
2.5
|
27.7
|
1.0
|
O
|
E:HOH475
|
2.6
|
18.5
|
1.0
|
OD1
|
E:ASP383
|
2.7
|
22.5
|
1.0
|
O
|
E:HOH517
|
3.1
|
40.9
|
1.0
|
CG
|
E:ASP381
|
3.1
|
29.6
|
1.0
|
OD1
|
E:ASP381
|
3.1
|
26.4
|
1.0
|
CG
|
E:ASP383
|
3.5
|
19.8
|
1.0
|
OD2
|
E:ASP383
|
3.5
|
18.9
|
1.0
|
C
|
E:TRP385
|
3.7
|
28.8
|
1.0
|
N
|
E:TRP385
|
4.3
|
24.8
|
1.0
|
CA
|
E:TRP385
|
4.4
|
27.0
|
1.0
|
O
|
E:ASP383
|
4.4
|
20.9
|
1.0
|
CB
|
E:TRP385
|
4.6
|
23.3
|
1.0
|
N
|
E:LEU386
|
4.6
|
31.9
|
1.0
|
CB
|
E:ASP381
|
4.6
|
24.9
|
1.0
|
N
|
E:ASP383
|
4.7
|
22.5
|
1.0
|
CA
|
E:LEU386
|
4.7
|
34.9
|
1.0
|
C
|
E:ASP383
|
4.7
|
24.4
|
1.0
|
CB
|
E:ASP383
|
4.7
|
18.7
|
1.0
|
N
|
E:THR387
|
4.8
|
39.6
|
1.0
|
CA
|
E:ASP383
|
4.9
|
23.1
|
1.0
|
O
|
E:ASP381
|
5.0
|
26.2
|
1.0
|
|
Calcium binding site 4 out
of 4 in 1fzc
Go back to
Calcium Binding Sites List in 1fzc
Calcium binding site 4 out
of 4 in the Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands
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 Fragment Double-D From Human Fibrin with Two Different Bound Ligands within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
F:Ca1
b:3.6
occ:1.00
|
O
|
F:GLY324
|
2.2
|
26.1
|
1.0
|
OD2
|
F:ASP318
|
2.4
|
32.2
|
1.0
|
OD1
|
F:ASP320
|
2.5
|
21.9
|
1.0
|
O
|
F:PHE322
|
2.7
|
39.6
|
1.0
|
O
|
F:HOH475
|
2.7
|
49.2
|
1.0
|
OD1
|
F:ASP318
|
2.9
|
31.3
|
1.0
|
CG
|
F:ASP318
|
3.0
|
31.6
|
1.0
|
CG
|
F:ASP320
|
3.3
|
25.6
|
1.0
|
OD2
|
F:ASP320
|
3.4
|
25.4
|
1.0
|
C
|
F:GLY324
|
3.5
|
30.1
|
1.0
|
C
|
F:PHE322
|
3.5
|
37.9
|
1.0
|
C
|
F:GLU323
|
4.2
|
37.0
|
1.0
|
CB
|
F:PHE322
|
4.2
|
34.8
|
1.0
|
CA
|
F:ASN325
|
4.2
|
31.8
|
1.0
|
N
|
F:GLY324
|
4.2
|
34.4
|
1.0
|
CA
|
F:PHE322
|
4.2
|
36.5
|
1.0
|
N
|
F:PHE322
|
4.3
|
33.8
|
1.0
|
N
|
F:ASN325
|
4.4
|
29.1
|
1.0
|
O
|
F:ASP320
|
4.4
|
27.0
|
1.0
|
N
|
F:GLU323
|
4.4
|
39.2
|
1.0
|
O
|
F:HOH428
|
4.4
|
37.7
|
1.0
|
O
|
F:GLU323
|
4.5
|
35.5
|
1.0
|
N
|
F:ASP320
|
4.5
|
26.8
|
1.0
|
CA
|
F:GLY324
|
4.5
|
31.9
|
1.0
|
CB
|
F:ASP320
|
4.5
|
25.9
|
1.0
|
CB
|
F:ASP318
|
4.5
|
32.5
|
1.0
|
C
|
F:ASP320
|
4.6
|
29.1
|
1.0
|
CA
|
F:GLU323
|
4.6
|
40.1
|
1.0
|
CA
|
F:ASP320
|
4.7
|
29.7
|
1.0
|
O
|
F:HOH476
|
4.8
|
47.9
|
1.0
|
N
|
F:CYS326
|
5.0
|
30.6
|
1.0
|
CG
|
F:PHE322
|
5.0
|
35.4
|
1.0
|
|
Reference:
S.J.Everse,
G.Spraggon,
L.Veerapandian,
M.Riley,
R.F.Doolittle.
Crystal Structure of Fragment Double-D From Human Fibrin with Two Different Bound Ligands. Biochemistry V. 37 8637 1998.
ISSN: ISSN 0006-2960
PubMed: 9628725
DOI: 10.1021/BI9804129
Page generated: Thu Jul 11 08:22:19 2024
|