Sodium in PDB 2wft: Crystal Structure of the Human Hip Ectodomain
Protein crystallography data
The structure of Crystal Structure of the Human Hip Ectodomain, PDB code: 2wft
was solved by
B.Bishop,
A.R.Aricescu,
K.Harlos,
C.A.O'callaghan,
E.Y.Jones,
C.Siebold,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
19.89 /
2.80
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
100.976,
100.976,
305.916,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
19.9 /
23.8
|
Other elements in 2wft:
The structure of Crystal Structure of the Human Hip Ectodomain also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the Crystal Structure of the Human Hip Ectodomain
(pdb code 2wft). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 3 binding sites of Sodium where determined in the
Crystal Structure of the Human Hip Ectodomain, PDB code: 2wft:
Jump to Sodium binding site number:
1;
2;
3;
Sodium binding site 1 out
of 3 in 2wft
Go back to
Sodium Binding Sites List in 2wft
Sodium binding site 1 out
of 3 in the Crystal Structure of the Human Hip Ectodomain
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 1 of Crystal Structure of the Human Hip Ectodomain within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na1672
b:83.5
occ:1.00
|
O
|
A:ARG241
|
3.0
|
52.9
|
1.0
|
OE1
|
A:GLU558
|
3.1
|
77.3
|
1.0
|
OG
|
A:SER235
|
3.1
|
51.0
|
1.0
|
OG
|
A:SER239
|
3.2
|
45.9
|
1.0
|
N
|
A:ARG241
|
3.2
|
29.0
|
1.0
|
N
|
A:SER235
|
3.3
|
56.7
|
1.0
|
OD1
|
A:ASP237
|
3.4
|
55.8
|
1.0
|
N
|
A:GLN240
|
3.6
|
38.5
|
1.0
|
CB
|
A:ARG241
|
3.6
|
42.8
|
1.0
|
CA
|
A:ARG241
|
3.7
|
42.2
|
1.0
|
C
|
A:ARG241
|
3.7
|
43.3
|
1.0
|
CB
|
A:HIS234
|
3.8
|
47.9
|
1.0
|
CB
|
A:SER235
|
3.9
|
59.9
|
1.0
|
C
|
A:GLN240
|
4.0
|
42.8
|
1.0
|
CA
|
A:GLN240
|
4.0
|
44.7
|
1.0
|
CA
|
A:SER235
|
4.1
|
57.2
|
1.0
|
CA
|
A:HIS234
|
4.1
|
51.4
|
1.0
|
CD
|
A:GLU558
|
4.1
|
80.1
|
1.0
|
CE1
|
A:PHE243
|
4.2
|
44.4
|
1.0
|
C
|
A:SER239
|
4.2
|
66.6
|
1.0
|
C
|
A:HIS234
|
4.2
|
59.4
|
1.0
|
CG
|
A:ASP237
|
4.3
|
64.8
|
1.0
|
N
|
A:GLY236
|
4.3
|
60.0
|
1.0
|
N
|
A:SER239
|
4.3
|
46.4
|
1.0
|
CB
|
A:SER239
|
4.4
|
45.6
|
1.0
|
C
|
A:SER235
|
4.4
|
54.1
|
1.0
|
NE
|
A:ARG241
|
4.5
|
64.5
|
1.0
|
CA
|
A:SER239
|
4.5
|
51.8
|
1.0
|
N
|
A:ASP237
|
4.6
|
45.5
|
1.0
|
CG
|
A:ARG241
|
4.6
|
46.0
|
1.0
|
OD2
|
A:ASP237
|
4.7
|
74.8
|
1.0
|
O
|
A:HOH2004
|
4.8
|
54.4
|
1.0
|
CG
|
A:HIS234
|
4.9
|
67.0
|
1.0
|
OE2
|
A:GLU558
|
4.9
|
81.4
|
1.0
|
CD1
|
A:PHE243
|
4.9
|
38.5
|
1.0
|
ND1
|
A:HIS234
|
4.9
|
51.4
|
1.0
|
CG
|
A:GLU558
|
4.9
|
67.2
|
1.0
|
CB
|
A:GLU558
|
5.0
|
43.9
|
1.0
|
N
|
A:LEU242
|
5.0
|
45.9
|
1.0
|
O
|
A:GLN240
|
5.0
|
56.1
|
1.0
|
|
Sodium binding site 2 out
of 3 in 2wft
Go back to
Sodium Binding Sites List in 2wft
Sodium binding site 2 out
of 3 in the Crystal Structure of the Human Hip Ectodomain
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 2 of Crystal Structure of the Human Hip Ectodomain within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na1673
b:0.2
occ:1.00
|
O
|
A:ASP443
|
3.4
|
0.3
|
1.0
|
O
|
A:HIS440
|
3.6
|
0.1
|
1.0
|
O
|
A:ILE446
|
3.8
|
99.8
|
1.0
|
OD1
|
A:ASN447
|
3.9
|
0.4
|
1.0
|
CA
|
A:ILE444
|
4.2
|
0.5
|
1.0
|
O
|
A:ILE444
|
4.4
|
97.5
|
1.0
|
C
|
A:ASP443
|
4.4
|
0.2
|
1.0
|
C
|
A:ILE444
|
4.6
|
0.8
|
1.0
|
CA
|
A:ASN447
|
4.7
|
98.5
|
1.0
|
N
|
A:ILE444
|
4.8
|
0.1
|
1.0
|
C
|
A:HIS440
|
4.8
|
0.4
|
1.0
|
C
|
A:ILE446
|
4.8
|
0.5
|
1.0
|
CG
|
A:ASN447
|
4.9
|
0.5
|
1.0
|
O
|
A:ASN447
|
5.0
|
87.2
|
1.0
|
|
Sodium binding site 3 out
of 3 in 2wft
Go back to
Sodium Binding Sites List in 2wft
Sodium binding site 3 out
of 3 in the Crystal Structure of the Human Hip Ectodomain
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 3 of Crystal Structure of the Human Hip Ectodomain within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na1671
b:75.3
occ:1.00
|
OE1
|
B:GLU558
|
3.0
|
59.4
|
1.0
|
OG
|
B:SER235
|
3.1
|
46.3
|
1.0
|
O
|
B:ARG241
|
3.1
|
36.5
|
1.0
|
N
|
B:SER235
|
3.2
|
46.3
|
1.0
|
N
|
B:ARG241
|
3.3
|
34.2
|
1.0
|
OD1
|
B:ASP237
|
3.5
|
36.1
|
1.0
|
OG
|
B:SER239
|
3.5
|
40.8
|
1.0
|
N
|
B:GLN240
|
3.5
|
39.5
|
1.0
|
CB
|
B:HIS234
|
3.6
|
35.3
|
1.0
|
C
|
B:ARG241
|
3.9
|
35.1
|
1.0
|
CA
|
B:ARG241
|
3.9
|
35.1
|
1.0
|
CD
|
B:GLU558
|
3.9
|
79.2
|
1.0
|
CB
|
B:SER235
|
3.9
|
56.9
|
1.0
|
CA
|
B:GLN240
|
4.0
|
42.4
|
1.0
|
CB
|
B:ARG241
|
4.0
|
30.1
|
1.0
|
CA
|
B:SER235
|
4.0
|
55.6
|
1.0
|
C
|
B:GLN240
|
4.0
|
38.9
|
1.0
|
CA
|
B:HIS234
|
4.0
|
47.2
|
1.0
|
C
|
B:HIS234
|
4.1
|
56.5
|
1.0
|
N
|
B:GLY236
|
4.1
|
52.4
|
1.0
|
C
|
B:SER239
|
4.3
|
58.8
|
1.0
|
C
|
B:SER235
|
4.3
|
50.2
|
1.0
|
CE1
|
B:PHE243
|
4.3
|
42.3
|
1.0
|
N
|
B:SER239
|
4.3
|
37.1
|
1.0
|
CG
|
B:ASP237
|
4.4
|
68.0
|
1.0
|
N
|
B:ASP237
|
4.4
|
47.3
|
1.0
|
CB
|
B:SER239
|
4.5
|
37.3
|
1.0
|
CA
|
B:SER239
|
4.6
|
43.9
|
1.0
|
CG
|
B:HIS234
|
4.6
|
64.8
|
1.0
|
O
|
B:HOH2016
|
4.6
|
56.4
|
1.0
|
OE2
|
B:GLU558
|
4.7
|
79.0
|
1.0
|
CG
|
B:GLU558
|
4.7
|
74.2
|
1.0
|
ND1
|
B:HIS234
|
4.7
|
54.4
|
1.0
|
CB
|
B:GLU558
|
4.7
|
48.7
|
1.0
|
NE
|
B:ARG241
|
4.8
|
58.7
|
1.0
|
OD2
|
B:ASP237
|
4.8
|
71.2
|
1.0
|
CG
|
B:ARG241
|
4.9
|
42.1
|
1.0
|
CD1
|
B:PHE243
|
5.0
|
34.6
|
1.0
|
CA
|
B:GLY236
|
5.0
|
45.9
|
1.0
|
|
Reference:
B.Bishop,
A.R.Aricescu,
K.Harlos,
C.A.O'callaghan,
E.Y.Jones,
C.Siebold.
Structural Insights Into Hedgehog Ligand Sequestration By the Human Hedgehog-Interacting Protein Hip Nat.Struct.Mol.Biol. V. 16 698 2009.
ISSN: ISSN 1545-9993
PubMed: 19561611
DOI: 10.1038/NSMB.1607
Page generated: Mon Oct 7 04:38:05 2024
|