Iron in PDB 3icf: Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
Enzymatic activity of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
All present enzymatic activity of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5:
3.1.3.16;
Protein crystallography data
The structure of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5, PDB code: 3icf
was solved by
A.U.Singer,
X.Xu,
C.Chang,
H.Cui,
O.Kagan,
A.M.Edwards,
A.Joachimiak,
A.F.Yakunin,
A.Savchenko,
Midwest Center For Structural Genomics(Mcsg),
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
40.29 /
2.30
|
Space group
|
P 32
|
Cell size a, b, c (Å), α, β, γ (°)
|
47.194,
47.194,
237.096,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
19 /
24
|
Other elements in 3icf:
The structure of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5 also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
(pdb code 3icf). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the
Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5, PDB code: 3icf:
Jump to Iron binding site number:
1;
2;
3;
4;
Iron binding site 1 out
of 4 in 3icf
Go back to
Iron Binding Sites List in 3icf
Iron binding site 1 out
of 4 in the Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe601
b:50.6
occ:1.00
|
NE2
|
A:HIS359
|
1.9
|
47.1
|
1.0
|
ND1
|
A:HIS434
|
1.9
|
51.0
|
1.0
|
O4
|
A:PO41
|
2.0
|
46.4
|
1.0
|
OD2
|
A:ASP278
|
2.1
|
53.0
|
1.0
|
OD1
|
A:ASN310
|
2.1
|
50.4
|
1.0
|
CE1
|
A:HIS434
|
2.6
|
50.1
|
1.0
|
CE1
|
A:HIS359
|
2.8
|
46.0
|
1.0
|
CD2
|
A:HIS359
|
3.0
|
46.9
|
1.0
|
CG
|
A:ASP278
|
3.0
|
50.0
|
1.0
|
CG
|
A:HIS434
|
3.1
|
50.2
|
1.0
|
CG
|
A:ASN310
|
3.2
|
50.3
|
1.0
|
P
|
A:PO41
|
3.2
|
47.8
|
1.0
|
FE
|
A:FE602
|
3.3
|
52.2
|
1.0
|
OD1
|
A:ASP278
|
3.4
|
52.3
|
1.0
|
O1
|
A:PO41
|
3.6
|
49.5
|
1.0
|
CA
|
A:HIS434
|
3.6
|
48.6
|
1.0
|
CB
|
A:HIS434
|
3.7
|
48.5
|
1.0
|
ND2
|
A:ASN310
|
3.7
|
47.4
|
1.0
|
O2
|
A:PO41
|
3.7
|
51.2
|
1.0
|
NE2
|
A:HIS434
|
3.8
|
49.5
|
1.0
|
ND1
|
A:HIS359
|
3.9
|
42.5
|
1.0
|
OD2
|
A:ASP249
|
4.0
|
52.8
|
1.0
|
CD2
|
A:HIS434
|
4.0
|
50.5
|
1.0
|
CG
|
A:HIS359
|
4.1
|
47.3
|
1.0
|
O
|
A:HIS434
|
4.1
|
50.3
|
1.0
|
CB
|
A:ASP278
|
4.3
|
48.9
|
1.0
|
C
|
A:HIS434
|
4.4
|
49.0
|
1.0
|
CB
|
A:ASN310
|
4.5
|
51.8
|
1.0
|
O3
|
A:PO41
|
4.5
|
49.2
|
1.0
|
N
|
A:ASN310
|
4.6
|
51.9
|
1.0
|
O
|
A:LEU392
|
4.6
|
50.4
|
1.0
|
N
|
A:HIS434
|
4.7
|
48.2
|
1.0
|
CD2
|
A:HIS311
|
4.7
|
50.1
|
1.0
|
NE2
|
A:HIS251
|
4.9
|
52.9
|
1.0
|
NH1
|
A:ARG407
|
5.0
|
53.8
|
1.0
|
O
|
A:HOH517
|
5.0
|
36.4
|
1.0
|
CG
|
A:ASP249
|
5.0
|
50.5
|
1.0
|
|
Iron binding site 2 out
of 4 in 3icf
Go back to
Iron Binding Sites List in 3icf
Iron binding site 2 out
of 4 in the Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe602
b:52.2
occ:1.00
|
NE2
|
A:HIS251
|
2.0
|
52.9
|
1.0
|
O1
|
A:PO41
|
2.0
|
49.5
|
1.0
|
OD2
|
A:ASP249
|
2.1
|
52.8
|
1.0
|
OD2
|
A:ASP278
|
2.1
|
53.0
|
1.0
|
CE1
|
A:HIS251
|
2.8
|
52.1
|
1.0
|
O
|
A:HOH517
|
2.9
|
36.4
|
1.0
|
CG
|
A:ASP278
|
3.1
|
50.0
|
1.0
|
P
|
A:PO41
|
3.1
|
47.8
|
1.0
|
CD2
|
A:HIS251
|
3.1
|
52.5
|
1.0
|
FE
|
A:FE601
|
3.3
|
50.6
|
1.0
|
CG
|
A:ASP249
|
3.3
|
50.5
|
1.0
|
O4
|
A:PO41
|
3.4
|
46.4
|
1.0
|
CB
|
A:ASP278
|
3.5
|
48.9
|
1.0
|
O2
|
A:PO41
|
3.7
|
51.2
|
1.0
|
ND1
|
A:HIS251
|
4.0
|
50.6
|
1.0
|
CE1
|
A:HIS359
|
4.1
|
46.0
|
1.0
|
CB
|
A:ASP249
|
4.1
|
51.1
|
1.0
|
NH2
|
A:ARG282
|
4.1
|
48.1
|
1.0
|
CD2
|
A:HIS311
|
4.2
|
50.1
|
1.0
|
OD1
|
A:ASP249
|
4.2
|
51.3
|
1.0
|
CG
|
A:HIS251
|
4.2
|
51.3
|
1.0
|
OD1
|
A:ASP278
|
4.2
|
52.3
|
1.0
|
NE2
|
A:HIS359
|
4.2
|
47.1
|
1.0
|
O3
|
A:PO41
|
4.3
|
49.2
|
1.0
|
O
|
A:HIS434
|
4.4
|
50.3
|
1.0
|
CA
|
A:HIS434
|
4.5
|
48.6
|
1.0
|
ND1
|
A:HIS434
|
4.5
|
51.0
|
1.0
|
OH
|
A:TYR458
|
4.5
|
58.9
|
1.0
|
C
|
A:HIS434
|
4.7
|
49.0
|
1.0
|
NE2
|
A:HIS311
|
4.7
|
50.1
|
1.0
|
CE1
|
A:PHE453
|
4.8
|
44.0
|
1.0
|
OD1
|
A:ASN310
|
4.9
|
50.4
|
1.0
|
CA
|
A:ASP278
|
4.9
|
49.2
|
1.0
|
|
Iron binding site 3 out
of 4 in 3icf
Go back to
Iron Binding Sites List in 3icf
Iron binding site 3 out
of 4 in the Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe601
b:51.0
occ:1.00
|
ND1
|
B:HIS434
|
1.9
|
50.8
|
1.0
|
NE2
|
B:HIS359
|
1.9
|
47.1
|
1.0
|
O1
|
B:PO42
|
2.0
|
46.3
|
1.0
|
OD1
|
B:ASN310
|
2.1
|
49.9
|
1.0
|
OD2
|
B:ASP278
|
2.1
|
52.5
|
1.0
|
CE1
|
B:HIS434
|
2.6
|
50.2
|
1.0
|
CE1
|
B:HIS359
|
2.9
|
45.6
|
1.0
|
CD2
|
B:HIS359
|
2.9
|
46.7
|
1.0
|
CG
|
B:ASP278
|
3.0
|
49.8
|
1.0
|
CG
|
B:HIS434
|
3.1
|
50.2
|
1.0
|
CG
|
B:ASN310
|
3.2
|
50.8
|
1.0
|
FE
|
B:FE602
|
3.3
|
51.1
|
1.0
|
P
|
B:PO42
|
3.3
|
47.8
|
1.0
|
OD1
|
B:ASP278
|
3.4
|
52.4
|
1.0
|
CA
|
B:HIS434
|
3.6
|
48.7
|
1.0
|
CB
|
B:HIS434
|
3.7
|
48.6
|
1.0
|
O2
|
B:PO42
|
3.7
|
47.8
|
1.0
|
ND2
|
B:ASN310
|
3.7
|
46.7
|
1.0
|
O4
|
B:PO42
|
3.8
|
51.9
|
1.0
|
NE2
|
B:HIS434
|
3.8
|
49.5
|
1.0
|
ND1
|
B:HIS359
|
4.0
|
42.3
|
1.0
|
OD2
|
B:ASP249
|
4.0
|
53.2
|
1.0
|
CD2
|
B:HIS434
|
4.0
|
50.1
|
1.0
|
CG
|
B:HIS359
|
4.1
|
47.5
|
1.0
|
O
|
B:HIS434
|
4.1
|
50.2
|
1.0
|
CB
|
B:ASP278
|
4.3
|
48.7
|
1.0
|
C
|
B:HIS434
|
4.3
|
49.2
|
1.0
|
CB
|
B:ASN310
|
4.5
|
52.0
|
1.0
|
N
|
B:ASN310
|
4.5
|
52.0
|
1.0
|
O3
|
B:PO42
|
4.5
|
46.7
|
1.0
|
O
|
B:LEU392
|
4.6
|
49.9
|
1.0
|
N
|
B:HIS434
|
4.7
|
48.5
|
1.0
|
ND1
|
B:HIS311
|
4.7
|
51.0
|
1.0
|
NE2
|
B:HIS251
|
4.9
|
52.7
|
1.0
|
CG
|
B:ASP249
|
5.0
|
50.5
|
1.0
|
NH1
|
B:ARG407
|
5.0
|
54.0
|
1.0
|
|
Iron binding site 4 out
of 4 in 3icf
Go back to
Iron Binding Sites List in 3icf
Iron binding site 4 out
of 4 in the Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe602
b:51.1
occ:1.00
|
NE2
|
B:HIS251
|
2.0
|
52.7
|
1.0
|
O2
|
B:PO42
|
2.1
|
47.8
|
1.0
|
OD2
|
B:ASP249
|
2.1
|
53.2
|
1.0
|
OD2
|
B:ASP278
|
2.1
|
52.5
|
1.0
|
CE1
|
B:HIS251
|
2.8
|
52.3
|
1.0
|
O
|
B:HOH518
|
2.8
|
39.8
|
1.0
|
CG
|
B:ASP278
|
3.1
|
49.8
|
1.0
|
CD2
|
B:HIS251
|
3.1
|
52.9
|
1.0
|
P
|
B:PO42
|
3.1
|
47.8
|
1.0
|
O1
|
B:PO42
|
3.3
|
46.3
|
1.0
|
FE
|
B:FE601
|
3.3
|
51.0
|
1.0
|
CG
|
B:ASP249
|
3.3
|
50.5
|
1.0
|
CB
|
B:ASP278
|
3.5
|
48.7
|
1.0
|
O4
|
B:PO42
|
3.8
|
51.9
|
1.0
|
ND1
|
B:HIS251
|
4.0
|
50.4
|
1.0
|
CE1
|
B:HIS359
|
4.1
|
45.6
|
1.0
|
CB
|
B:ASP249
|
4.1
|
51.3
|
1.0
|
NH2
|
B:ARG282
|
4.1
|
48.0
|
1.0
|
OD1
|
B:ASP249
|
4.2
|
51.9
|
1.0
|
CG
|
B:HIS251
|
4.2
|
51.8
|
1.0
|
NE2
|
B:HIS359
|
4.2
|
47.1
|
1.0
|
OD1
|
B:ASP278
|
4.2
|
52.4
|
1.0
|
O3
|
B:PO42
|
4.4
|
46.7
|
1.0
|
O
|
B:HIS434
|
4.5
|
50.2
|
1.0
|
ND1
|
B:HIS434
|
4.5
|
50.8
|
1.0
|
CA
|
B:HIS434
|
4.5
|
48.7
|
1.0
|
OH
|
B:TYR458
|
4.6
|
58.8
|
1.0
|
C
|
B:HIS434
|
4.7
|
49.2
|
1.0
|
CE1
|
B:PHE453
|
4.9
|
43.8
|
1.0
|
OD1
|
B:ASN310
|
4.9
|
49.9
|
1.0
|
CA
|
B:ASP278
|
4.9
|
49.1
|
1.0
|
|
Reference:
A.U.Singer,
X.Xu,
C.Chang,
H.Cui,
A.M.Edwards,
A.Joachimiak,
A.Savchenko,
A.F.Yakunin.
Structure of Protein Serine/Threonine Phosphatase From Saccharomyces Cerevisiae with Similarity to Human Phosphatase PP5 To Be Published.
Page generated: Sun Aug 4 12:17:15 2024
|