Calcium in PDB 1n73: Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide
Protein crystallography data
The structure of Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide, PDB code: 1n73
was solved by
Z.Yang,
L.Pandi,
R.F.Doolittle,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
2.90
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
49.732,
99.302,
120.732,
99.58,
101.46,
92.36
|
R / Rfree (%)
|
25.8 /
28.9
|
Calcium Binding Sites:
The binding sites of Calcium atom in the Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide
(pdb code 1n73). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 4 binding sites of Calcium where determined in the
Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide, PDB code: 1n73:
Jump to Calcium binding site number:
1;
2;
3;
4;
Calcium binding site 1 out
of 4 in 1n73
Go back to
Calcium Binding Sites List in 1n73
Calcium binding site 1 out
of 4 in the Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 1 of Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Ca1
b:50.1
occ:1.00
|
O
|
C:TYR320
|
2.3
|
52.1
|
1.0
|
O
|
C:GLY322
|
2.4
|
46.2
|
1.0
|
OD1
|
C:ASP318
|
2.4
|
50.6
|
1.0
|
OD2
|
C:ASP316
|
2.5
|
43.0
|
1.0
|
OD1
|
C:ASP316
|
2.9
|
45.1
|
1.0
|
CG
|
C:ASP316
|
3.0
|
43.2
|
1.0
|
CG
|
C:ASP318
|
3.4
|
48.9
|
1.0
|
C
|
C:TYR320
|
3.4
|
50.0
|
1.0
|
C
|
C:GLY322
|
3.5
|
47.2
|
1.0
|
OD2
|
C:ASP318
|
3.6
|
51.4
|
1.0
|
C
|
C:GLU321
|
3.9
|
48.8
|
1.0
|
N
|
C:GLY322
|
4.0
|
48.0
|
1.0
|
O
|
C:GLU321
|
4.1
|
47.4
|
1.0
|
N
|
C:TYR320
|
4.2
|
47.9
|
1.0
|
CA
|
C:TYR320
|
4.2
|
48.3
|
1.0
|
CA
|
C:GLY322
|
4.3
|
47.9
|
1.0
|
N
|
C:GLU321
|
4.3
|
50.9
|
1.0
|
CB
|
C:ASP316
|
4.4
|
42.8
|
1.0
|
CB
|
C:TYR320
|
4.4
|
48.9
|
1.0
|
CA
|
C:GLU321
|
4.4
|
50.0
|
1.0
|
N
|
C:SER323
|
4.5
|
47.4
|
1.0
|
CA
|
C:SER323
|
4.6
|
47.5
|
1.0
|
CB
|
C:ASP318
|
4.7
|
46.4
|
1.0
|
O
|
C:ASP318
|
4.7
|
46.7
|
1.0
|
C
|
C:ASP318
|
4.8
|
45.6
|
1.0
|
N
|
C:ASP318
|
4.9
|
44.1
|
1.0
|
|
Calcium binding site 2 out
of 4 in 1n73
Go back to
Calcium Binding Sites List in 1n73
Calcium binding site 2 out
of 4 in the Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 2 of Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
F:Ca2
b:62.3
occ:1.00
|
OD1
|
F:ASP318
|
2.3
|
52.6
|
1.0
|
O
|
F:TYR320
|
2.3
|
49.0
|
1.0
|
O
|
F:GLY322
|
2.3
|
44.7
|
1.0
|
OD2
|
F:ASP316
|
2.4
|
43.4
|
1.0
|
OD1
|
F:ASP316
|
2.8
|
41.1
|
1.0
|
CG
|
F:ASP316
|
2.9
|
42.5
|
1.0
|
CG
|
F:ASP318
|
3.2
|
50.8
|
1.0
|
C
|
F:TYR320
|
3.4
|
48.9
|
1.0
|
OD2
|
F:ASP318
|
3.5
|
52.8
|
1.0
|
C
|
F:GLY322
|
3.5
|
48.2
|
1.0
|
C
|
F:GLU321
|
4.0
|
52.0
|
1.0
|
N
|
F:GLY322
|
4.1
|
51.9
|
1.0
|
N
|
F:TYR320
|
4.1
|
46.4
|
1.0
|
CA
|
F:TYR320
|
4.2
|
47.7
|
1.0
|
O
|
F:GLU321
|
4.2
|
51.9
|
1.0
|
CB
|
F:ASP316
|
4.3
|
41.7
|
1.0
|
CB
|
F:TYR320
|
4.3
|
47.5
|
1.0
|
CA
|
F:GLY322
|
4.3
|
49.2
|
1.0
|
N
|
F:GLU321
|
4.4
|
50.2
|
1.0
|
N
|
F:SER323
|
4.4
|
49.6
|
1.0
|
CA
|
F:GLU321
|
4.5
|
51.4
|
1.0
|
CA
|
F:SER323
|
4.5
|
50.2
|
1.0
|
CB
|
F:ASP318
|
4.6
|
46.9
|
1.0
|
O
|
F:ASP318
|
4.7
|
46.6
|
1.0
|
C
|
F:ASP318
|
4.7
|
45.0
|
1.0
|
N
|
F:ASP318
|
4.8
|
41.5
|
1.0
|
CA
|
F:ASP318
|
4.9
|
44.1
|
1.0
|
|
Calcium binding site 3 out
of 4 in 1n73
Go back to
Calcium Binding Sites List in 1n73
Calcium binding site 3 out
of 4 in the Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 3 of Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ca3
b:52.0
occ:1.00
|
OD2
|
B:ASP401
|
2.0
|
49.9
|
1.0
|
OD1
|
B:ASP403
|
2.4
|
58.2
|
1.0
|
O
|
B:TRP405
|
2.5
|
62.7
|
1.0
|
O
|
B:LYS412
|
2.5
|
57.6
|
1.0
|
CG
|
B:ASP401
|
2.9
|
47.9
|
1.0
|
OD1
|
B:ASP401
|
3.0
|
51.5
|
1.0
|
O
|
B:ASN406
|
3.2
|
64.6
|
1.0
|
CG
|
B:ASP403
|
3.4
|
57.4
|
1.0
|
C
|
B:TRP405
|
3.5
|
61.4
|
1.0
|
OD2
|
B:ASP403
|
3.7
|
57.5
|
1.0
|
C
|
B:LYS412
|
3.7
|
57.8
|
1.0
|
C
|
B:ASN406
|
3.8
|
63.9
|
1.0
|
CB
|
B:LYS412
|
4.2
|
57.8
|
1.0
|
CA
|
B:TRP405
|
4.2
|
60.0
|
1.0
|
O
|
B:ASP409
|
4.2
|
58.8
|
1.0
|
N
|
B:TRP405
|
4.2
|
59.0
|
1.0
|
CB
|
B:TRP405
|
4.2
|
59.5
|
1.0
|
CB
|
B:ASP401
|
4.3
|
48.3
|
1.0
|
N
|
B:PRO407
|
4.3
|
63.6
|
1.0
|
O
|
B:PRO407
|
4.4
|
64.6
|
1.0
|
N
|
B:ASN406
|
4.4
|
62.2
|
1.0
|
CA
|
B:PRO407
|
4.4
|
64.7
|
1.0
|
CA
|
B:LYS412
|
4.5
|
58.0
|
1.0
|
CA
|
B:ASN406
|
4.6
|
62.9
|
1.0
|
O
|
B:ASP403
|
4.7
|
56.8
|
1.0
|
N
|
B:HIS413
|
4.7
|
56.0
|
1.0
|
C
|
B:PRO407
|
4.7
|
64.7
|
1.0
|
CB
|
B:ASP403
|
4.7
|
57.2
|
1.0
|
CA
|
B:HIS413
|
4.8
|
57.0
|
1.0
|
C
|
B:ASP403
|
4.9
|
55.6
|
1.0
|
N
|
B:ASP403
|
4.9
|
53.1
|
1.0
|
|
Calcium binding site 4 out
of 4 in 1n73
Go back to
Calcium Binding Sites List in 1n73
Calcium binding site 4 out
of 4 in the Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 4 of Fibrin D-Dimer, Lamprey Complexed with the Peptide Ligand: Gly-His- Arg-Pro-Amide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Ca4
b:75.4
occ:1.00
|
O
|
E:TRP405
|
2.2
|
63.9
|
1.0
|
OD2
|
E:ASP401
|
2.3
|
51.9
|
1.0
|
OD1
|
E:ASP403
|
2.3
|
58.9
|
1.0
|
O
|
E:LYS412
|
2.4
|
60.3
|
1.0
|
CG
|
E:ASP401
|
3.1
|
49.6
|
1.0
|
O
|
E:ASN406
|
3.2
|
66.5
|
1.0
|
C
|
E:TRP405
|
3.2
|
63.2
|
1.0
|
OD1
|
E:ASP401
|
3.2
|
50.2
|
1.0
|
CG
|
E:ASP403
|
3.3
|
59.9
|
1.0
|
C
|
E:LYS412
|
3.6
|
61.0
|
1.0
|
OD2
|
E:ASP403
|
3.6
|
62.1
|
1.0
|
C
|
E:ASN406
|
3.7
|
64.8
|
1.0
|
CA
|
E:TRP405
|
3.9
|
63.3
|
1.0
|
CB
|
E:TRP405
|
4.0
|
63.3
|
1.0
|
CB
|
E:LYS412
|
4.0
|
59.6
|
1.0
|
N
|
E:TRP405
|
4.0
|
62.9
|
1.0
|
N
|
E:ASN406
|
4.2
|
63.4
|
1.0
|
O
|
E:ASP409
|
4.3
|
59.0
|
1.0
|
N
|
E:PRO407
|
4.3
|
65.4
|
1.0
|
CA
|
E:LYS412
|
4.4
|
60.6
|
1.0
|
CA
|
E:PRO407
|
4.5
|
65.7
|
1.0
|
CA
|
E:ASN406
|
4.5
|
64.2
|
1.0
|
CB
|
E:ASP401
|
4.5
|
49.7
|
1.0
|
O
|
E:PRO407
|
4.6
|
65.8
|
1.0
|
N
|
E:HIS413
|
4.6
|
61.0
|
1.0
|
O
|
E:ASP403
|
4.7
|
57.7
|
1.0
|
CB
|
E:ASP403
|
4.7
|
58.6
|
1.0
|
CG
|
E:TRP405
|
4.7
|
63.7
|
1.0
|
CA
|
E:HIS413
|
4.8
|
61.0
|
1.0
|
C
|
E:ASP403
|
4.8
|
57.7
|
1.0
|
C
|
E:PRO407
|
4.9
|
65.7
|
1.0
|
N
|
E:ASP403
|
4.9
|
54.0
|
1.0
|
|
Reference:
Z.Yang,
L.Pandi,
R.F.Doolittle.
The Crystal Structure of Fragment Double-D From Cross-Linked Lamprey Fibrin Reveals Isopeptide Linkages Across An Unexpected D-D Interface Biochemistry V. 41 15610 2002.
ISSN: ISSN 0006-2960
PubMed: 12501189
DOI: 10.1021/BI026666I
Page generated: Thu Jul 11 12:45:17 2024
|