Zinc in PDB 1kbp: Kidney Bean Purple Acid Phosphatase
Enzymatic activity of Kidney Bean Purple Acid Phosphatase
All present enzymatic activity of Kidney Bean Purple Acid Phosphatase:
3.1.3.2;
Protein crystallography data
The structure of Kidney Bean Purple Acid Phosphatase, PDB code: 1kbp
was solved by
T.Klabunde,
N.Strater,
B.Krebs,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
10.00 /
2.65
|
Space group
|
C 2 2 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
132.700,
347.300,
128.700,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
19.5 /
23.3
|
Other elements in 1kbp:
The structure of Kidney Bean Purple Acid Phosphatase also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Kidney Bean Purple Acid Phosphatase
(pdb code 1kbp). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the
Kidney Bean Purple Acid Phosphatase, PDB code: 1kbp:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 1kbp
Go back to
Zinc Binding Sites List in 1kbp
Zinc binding site 1 out
of 4 in the Kidney Bean Purple Acid Phosphatase
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Kidney Bean Purple Acid Phosphatase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn439
b:40.6
occ:1.00
|
NE2
|
A:HIS286
|
2.1
|
16.2
|
1.0
|
ND1
|
A:HIS323
|
2.2
|
26.3
|
1.0
|
OD1
|
A:ASN201
|
2.3
|
31.6
|
1.0
|
OD2
|
A:ASP164
|
2.3
|
29.8
|
1.0
|
CE1
|
A:HIS323
|
3.0
|
23.8
|
1.0
|
CD2
|
A:HIS286
|
3.1
|
14.1
|
1.0
|
CE1
|
A:HIS286
|
3.1
|
20.1
|
1.0
|
CG
|
A:ASP164
|
3.2
|
28.9
|
1.0
|
FE
|
A:FE438
|
3.3
|
33.8
|
1.0
|
CG
|
A:ASN201
|
3.3
|
25.3
|
1.0
|
CG
|
A:HIS323
|
3.4
|
21.8
|
1.0
|
OD1
|
A:ASP164
|
3.4
|
32.2
|
1.0
|
CA
|
A:HIS323
|
3.6
|
16.5
|
1.0
|
ND2
|
A:ASN201
|
3.8
|
29.2
|
1.0
|
CB
|
A:HIS323
|
3.8
|
16.3
|
1.0
|
OD2
|
A:ASP135
|
3.9
|
31.2
|
1.0
|
ND1
|
A:HIS286
|
4.2
|
17.6
|
1.0
|
NE2
|
A:HIS323
|
4.2
|
28.8
|
1.0
|
CG
|
A:HIS286
|
4.2
|
11.2
|
1.0
|
N
|
A:ASN201
|
4.3
|
21.1
|
1.0
|
CD2
|
A:HIS202
|
4.3
|
14.8
|
1.0
|
CD2
|
A:HIS323
|
4.4
|
22.6
|
1.0
|
N
|
A:HIS323
|
4.4
|
17.6
|
1.0
|
O
|
A:HIS323
|
4.4
|
31.4
|
1.0
|
CB
|
A:ASP164
|
4.5
|
22.1
|
1.0
|
C
|
A:HIS323
|
4.6
|
19.8
|
1.0
|
CB
|
A:ASN201
|
4.6
|
27.3
|
1.0
|
CA
|
A:ASN201
|
5.0
|
25.8
|
1.0
|
CG
|
A:ASP135
|
5.0
|
30.9
|
1.0
|
|
Zinc binding site 2 out
of 4 in 1kbp
Go back to
Zinc Binding Sites List in 1kbp
Zinc binding site 2 out
of 4 in the Kidney Bean Purple Acid Phosphatase
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Kidney Bean Purple Acid Phosphatase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn439
b:49.6
occ:1.00
|
NE2
|
B:HIS286
|
2.2
|
32.9
|
1.0
|
ND1
|
B:HIS323
|
2.2
|
37.1
|
1.0
|
OD1
|
B:ASN201
|
2.2
|
46.3
|
1.0
|
OD2
|
B:ASP164
|
2.3
|
42.4
|
1.0
|
CE1
|
B:HIS323
|
3.0
|
33.6
|
1.0
|
CD2
|
B:HIS286
|
3.1
|
34.8
|
1.0
|
CE1
|
B:HIS286
|
3.2
|
36.8
|
1.0
|
CG
|
B:ASP164
|
3.2
|
43.2
|
1.0
|
CG
|
B:ASN201
|
3.3
|
43.9
|
1.0
|
FE
|
B:FE438
|
3.3
|
52.5
|
1.0
|
CG
|
B:HIS323
|
3.3
|
34.9
|
1.0
|
OD1
|
B:ASP164
|
3.4
|
46.9
|
1.0
|
CA
|
B:HIS323
|
3.6
|
36.2
|
1.0
|
ND2
|
B:ASN201
|
3.7
|
45.0
|
1.0
|
CB
|
B:HIS323
|
3.8
|
35.5
|
1.0
|
OD2
|
B:ASP135
|
3.9
|
35.6
|
1.0
|
NE2
|
B:HIS323
|
4.2
|
35.9
|
1.0
|
CG
|
B:HIS286
|
4.3
|
31.8
|
1.0
|
ND1
|
B:HIS286
|
4.3
|
30.9
|
1.0
|
CD2
|
B:HIS202
|
4.3
|
49.7
|
1.0
|
CD2
|
B:HIS323
|
4.4
|
37.0
|
1.0
|
O
|
B:HIS323
|
4.4
|
40.2
|
1.0
|
N
|
B:ASN201
|
4.4
|
34.5
|
1.0
|
N
|
B:HIS323
|
4.5
|
31.8
|
1.0
|
C
|
B:HIS323
|
4.5
|
38.8
|
1.0
|
CB
|
B:ASP164
|
4.5
|
36.8
|
1.0
|
CB
|
B:ASN201
|
4.6
|
41.9
|
1.0
|
CG
|
B:ASP135
|
4.9
|
31.5
|
1.0
|
CA
|
B:ASN201
|
5.0
|
37.6
|
1.0
|
NE2
|
B:HIS202
|
5.0
|
54.6
|
1.0
|
|
Zinc binding site 3 out
of 4 in 1kbp
Go back to
Zinc Binding Sites List in 1kbp
Zinc binding site 3 out
of 4 in the Kidney Bean Purple Acid Phosphatase
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Kidney Bean Purple Acid Phosphatase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn439
b:42.6
occ:1.00
|
NE2
|
C:HIS286
|
2.2
|
21.9
|
1.0
|
ND1
|
C:HIS323
|
2.3
|
27.6
|
1.0
|
OD1
|
C:ASN201
|
2.3
|
32.8
|
1.0
|
OD2
|
C:ASP164
|
2.3
|
29.1
|
1.0
|
CE1
|
C:HIS323
|
3.0
|
27.8
|
1.0
|
FE
|
C:FE438
|
3.2
|
30.4
|
1.0
|
CE1
|
C:HIS286
|
3.2
|
26.3
|
1.0
|
CD2
|
C:HIS286
|
3.2
|
24.8
|
1.0
|
CG
|
C:ASP164
|
3.2
|
27.6
|
1.0
|
CG
|
C:ASN201
|
3.3
|
28.8
|
1.0
|
CG
|
C:HIS323
|
3.4
|
20.7
|
1.0
|
OD1
|
C:ASP164
|
3.5
|
28.7
|
1.0
|
CA
|
C:HIS323
|
3.6
|
20.7
|
1.0
|
ND2
|
C:ASN201
|
3.7
|
31.1
|
1.0
|
CB
|
C:HIS323
|
3.9
|
18.9
|
1.0
|
OD2
|
C:ASP135
|
4.0
|
26.3
|
1.0
|
NE2
|
C:HIS323
|
4.2
|
24.9
|
1.0
|
CD2
|
C:HIS202
|
4.3
|
27.5
|
1.0
|
ND1
|
C:HIS286
|
4.3
|
23.6
|
1.0
|
O
|
C:HIS323
|
4.4
|
34.1
|
1.0
|
CG
|
C:HIS286
|
4.4
|
18.4
|
1.0
|
N
|
C:ASN201
|
4.4
|
15.1
|
1.0
|
N
|
C:HIS323
|
4.4
|
23.0
|
1.0
|
CD2
|
C:HIS323
|
4.4
|
24.7
|
1.0
|
C
|
C:HIS323
|
4.5
|
24.5
|
1.0
|
CB
|
C:ASP164
|
4.5
|
25.4
|
1.0
|
CB
|
C:ASN201
|
4.6
|
24.6
|
1.0
|
NE2
|
C:HIS325
|
5.0
|
28.0
|
1.0
|
OH
|
C:TYR167
|
5.0
|
32.9
|
1.0
|
NE2
|
C:HIS202
|
5.0
|
34.0
|
1.0
|
CG
|
C:ASP135
|
5.0
|
29.4
|
1.0
|
|
Zinc binding site 4 out
of 4 in 1kbp
Go back to
Zinc Binding Sites List in 1kbp
Zinc binding site 4 out
of 4 in the Kidney Bean Purple Acid Phosphatase
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Kidney Bean Purple Acid Phosphatase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Zn439
b:44.3
occ:1.00
|
NE2
|
D:HIS286
|
2.1
|
18.5
|
1.0
|
OD2
|
D:ASP164
|
2.2
|
28.0
|
1.0
|
ND1
|
D:HIS323
|
2.3
|
29.5
|
1.0
|
OD1
|
D:ASN201
|
2.3
|
36.3
|
1.0
|
CE1
|
D:HIS286
|
3.1
|
17.8
|
1.0
|
CE1
|
D:HIS323
|
3.1
|
29.3
|
1.0
|
CG
|
D:ASP164
|
3.1
|
27.5
|
1.0
|
CD2
|
D:HIS286
|
3.1
|
19.7
|
1.0
|
FE
|
D:FE438
|
3.3
|
33.8
|
1.0
|
OD1
|
D:ASP164
|
3.3
|
27.7
|
1.0
|
CG
|
D:ASN201
|
3.4
|
34.4
|
1.0
|
CG
|
D:HIS323
|
3.4
|
27.5
|
1.0
|
CA
|
D:HIS323
|
3.6
|
27.9
|
1.0
|
ND2
|
D:ASN201
|
3.8
|
32.9
|
1.0
|
CB
|
D:HIS323
|
3.9
|
24.6
|
1.0
|
OD2
|
D:ASP135
|
3.9
|
26.7
|
1.0
|
ND1
|
D:HIS286
|
4.2
|
17.1
|
1.0
|
CG
|
D:HIS286
|
4.3
|
16.1
|
1.0
|
NE2
|
D:HIS323
|
4.3
|
29.1
|
1.0
|
CD2
|
D:HIS202
|
4.3
|
26.8
|
1.0
|
N
|
D:ASN201
|
4.3
|
20.2
|
1.0
|
N
|
D:HIS323
|
4.4
|
18.8
|
1.0
|
CB
|
D:ASP164
|
4.4
|
28.8
|
1.0
|
CD2
|
D:HIS323
|
4.5
|
29.4
|
1.0
|
O
|
D:HIS323
|
4.5
|
35.4
|
1.0
|
C
|
D:HIS323
|
4.6
|
30.6
|
1.0
|
CB
|
D:ASN201
|
4.6
|
30.4
|
1.0
|
CG
|
D:ASP135
|
4.9
|
28.4
|
1.0
|
CA
|
D:ASN201
|
5.0
|
25.9
|
1.0
|
|
Reference:
T.Klabunde,
N.Strater,
R.Frohlich,
H.Witzel,
B.Krebs.
Mechanism of Fe(III)-Zn(II) Purple Acid Phosphatase Based on Crystal Structures. J.Mol.Biol. V. 259 737 1996.
ISSN: ISSN 0022-2836
PubMed: 8683579
DOI: 10.1006/JMBI.1996.0354
Page generated: Sun Oct 13 04:18:09 2024
|