Calcium in PDB 1jrq: X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
Enzymatic activity of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
All present enzymatic activity of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase:
1.4.3.4;
Protein crystallography data
The structure of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase, PDB code: 1jrq
was solved by
J.M.Murray,
C.R.Kurtis,
W.Tambarajah,
C.G.Saysell,
C.M.Wilmot,
M.R.Parsons,
S.E.V.Phillips,
P.F.Knowles,
M.J.Mcpherson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
2.15
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
134.540,
166.450,
79.380,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
19.5 /
23.5
|
Other elements in 1jrq:
The structure of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
(pdb code 1jrq). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 4 binding sites of Calcium where determined in the
X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase, PDB code: 1jrq:
Jump to Calcium binding site number:
1;
2;
3;
4;
Calcium binding site 1 out
of 4 in 1jrq
Go back to
Calcium Binding Sites List in 1jrq
Calcium binding site 1 out
of 4 in the X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 1 of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca802
b:26.4
occ:1.00
|
O
|
A:ALA679
|
2.4
|
18.1
|
1.0
|
OD1
|
A:ASP535
|
2.4
|
18.8
|
1.0
|
OD1
|
A:ASP533
|
2.4
|
26.7
|
1.0
|
OD1
|
A:ASP678
|
2.4
|
26.0
|
1.0
|
O
|
A:LEU534
|
2.5
|
24.4
|
1.0
|
O
|
A:HOH948
|
2.6
|
15.3
|
1.0
|
C
|
A:LEU534
|
3.4
|
22.2
|
1.0
|
C
|
A:ALA679
|
3.5
|
20.6
|
1.0
|
CG
|
A:ASP535
|
3.6
|
21.1
|
1.0
|
NZ
|
A:LYS133
|
3.6
|
22.6
|
1.0
|
CG
|
A:ASP678
|
3.6
|
29.3
|
1.0
|
CG
|
A:ASP533
|
3.6
|
26.0
|
1.0
|
N
|
A:ALA679
|
3.6
|
22.8
|
1.0
|
C
|
A:ASP533
|
4.0
|
22.1
|
1.0
|
CA
|
A:ASP535
|
4.1
|
22.0
|
1.0
|
N
|
A:LEU534
|
4.1
|
23.5
|
1.0
|
N
|
A:ASP535
|
4.1
|
21.4
|
1.0
|
CA
|
A:ALA679
|
4.1
|
21.2
|
1.0
|
C
|
A:ASP678
|
4.1
|
23.6
|
1.0
|
O
|
A:ASP533
|
4.2
|
20.1
|
1.0
|
OD2
|
A:ASP533
|
4.2
|
26.4
|
1.0
|
OD2
|
A:ASP678
|
4.3
|
29.8
|
1.0
|
CA
|
A:ASP678
|
4.4
|
24.9
|
1.0
|
CB
|
A:ASP535
|
4.4
|
21.1
|
1.0
|
CA
|
A:LEU534
|
4.4
|
23.2
|
1.0
|
CA
|
A:ASP533
|
4.4
|
22.0
|
1.0
|
OD2
|
A:ASP535
|
4.4
|
20.6
|
1.0
|
O
|
A:GLU539
|
4.5
|
26.6
|
1.0
|
N
|
A:VAL680
|
4.6
|
18.2
|
1.0
|
CB
|
A:ASP678
|
4.6
|
27.3
|
1.0
|
CB
|
A:ASP533
|
4.6
|
23.4
|
1.0
|
ND2
|
A:ASN541
|
4.7
|
19.6
|
1.0
|
O
|
A:ASP678
|
4.8
|
23.9
|
1.0
|
CA
|
A:VAL680
|
4.8
|
21.9
|
1.0
|
CG2
|
A:VAL680
|
4.9
|
22.1
|
1.0
|
CE
|
A:LYS133
|
4.9
|
23.9
|
1.0
|
CB
|
A:ALA679
|
4.9
|
19.8
|
1.0
|
|
Calcium binding site 2 out
of 4 in 1jrq
Go back to
Calcium Binding Sites List in 1jrq
Calcium binding site 2 out
of 4 in the X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 2 of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca803
b:54.8
occ:1.00
|
O
|
A:TYR667
|
2.5
|
28.2
|
1.0
|
OE2
|
A:GLU573
|
2.6
|
28.5
|
1.0
|
O
|
A:HOH974
|
2.6
|
28.7
|
1.0
|
OE1
|
A:GLU672
|
2.7
|
39.8
|
1.0
|
O
|
A:HOH979
|
2.8
|
30.7
|
1.0
|
O
|
A:HOH1523
|
2.8
|
35.2
|
1.0
|
OE1
|
A:GLU573
|
3.1
|
25.9
|
1.0
|
CD
|
A:GLU573
|
3.2
|
30.4
|
1.0
|
CD
|
A:GLU672
|
3.7
|
41.1
|
1.0
|
C
|
A:TYR667
|
3.7
|
27.3
|
1.0
|
CE1
|
A:HIS644
|
3.8
|
49.6
|
1.0
|
CG
|
A:GLU672
|
4.0
|
40.2
|
1.0
|
O
|
A:HOH1033
|
4.0
|
47.4
|
1.0
|
ND1
|
A:HIS644
|
4.0
|
48.8
|
1.0
|
OE1
|
A:GLU647
|
4.3
|
26.1
|
1.0
|
N
|
A:ARG642
|
4.3
|
25.5
|
1.0
|
CB
|
A:ARG642
|
4.4
|
31.8
|
1.0
|
CA
|
A:TYR667
|
4.6
|
27.6
|
1.0
|
CB
|
A:GLU672
|
4.6
|
35.8
|
1.0
|
OE2
|
A:GLU647
|
4.6
|
28.6
|
1.0
|
CB
|
A:THR641
|
4.6
|
24.6
|
1.0
|
N
|
A:SER668
|
4.6
|
29.2
|
1.0
|
CG
|
A:ARG642
|
4.7
|
33.5
|
1.0
|
CG
|
A:GLU573
|
4.7
|
28.8
|
1.0
|
CA
|
A:SER668
|
4.7
|
30.4
|
1.0
|
O
|
A:ARG642
|
4.8
|
25.7
|
1.0
|
OE2
|
A:GLU672
|
4.8
|
42.2
|
1.0
|
CD
|
A:GLU647
|
4.9
|
28.0
|
1.0
|
CA
|
A:ARG642
|
5.0
|
27.8
|
1.0
|
|
Calcium binding site 3 out
of 4 in 1jrq
Go back to
Calcium Binding Sites List in 1jrq
Calcium binding site 3 out
of 4 in the X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 3 of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ca802
b:29.6
occ:1.00
|
OD1
|
B:ASP535
|
2.4
|
28.6
|
1.0
|
OD1
|
B:ASP533
|
2.4
|
20.6
|
1.0
|
O
|
B:ALA679
|
2.4
|
28.7
|
1.0
|
OD1
|
B:ASP678
|
2.5
|
27.2
|
1.0
|
O
|
B:LEU534
|
2.5
|
26.1
|
1.0
|
O
|
B:HOH981
|
2.7
|
25.3
|
1.0
|
C
|
B:ALA679
|
3.4
|
28.2
|
1.0
|
C
|
B:LEU534
|
3.5
|
28.0
|
1.0
|
N
|
B:ALA679
|
3.5
|
27.9
|
1.0
|
CG
|
B:ASP533
|
3.6
|
23.2
|
1.0
|
CG
|
B:ASP535
|
3.6
|
27.6
|
1.0
|
CG
|
B:ASP678
|
3.7
|
30.5
|
1.0
|
NZ
|
B:LYS133
|
3.7
|
23.1
|
1.0
|
CA
|
B:ALA679
|
4.0
|
26.9
|
1.0
|
C
|
B:ASP678
|
4.0
|
28.2
|
1.0
|
C
|
B:ASP533
|
4.1
|
24.7
|
1.0
|
CA
|
B:ASP535
|
4.1
|
27.3
|
1.0
|
N
|
B:ASP535
|
4.1
|
27.3
|
1.0
|
N
|
B:LEU534
|
4.2
|
26.4
|
1.0
|
OD2
|
B:ASP533
|
4.2
|
22.2
|
1.0
|
O
|
B:ASP533
|
4.3
|
24.5
|
1.0
|
CA
|
B:ASP678
|
4.3
|
28.6
|
1.0
|
OD2
|
B:ASP678
|
4.4
|
30.4
|
1.0
|
OD2
|
B:ASP535
|
4.4
|
28.4
|
1.0
|
O
|
B:GLU539
|
4.4
|
31.8
|
1.0
|
CB
|
B:ASP535
|
4.4
|
27.4
|
1.0
|
CA
|
B:LEU534
|
4.5
|
25.6
|
1.0
|
CA
|
B:ASP533
|
4.5
|
23.9
|
1.0
|
N
|
B:VAL680
|
4.6
|
28.7
|
1.0
|
CB
|
B:ASP678
|
4.6
|
29.1
|
1.0
|
ND2
|
B:ASN541
|
4.7
|
28.1
|
1.0
|
CB
|
B:ASP533
|
4.7
|
23.0
|
1.0
|
CG2
|
B:VAL680
|
4.8
|
24.3
|
1.0
|
O
|
B:ASP678
|
4.8
|
28.3
|
1.0
|
CB
|
B:ALA679
|
4.8
|
27.2
|
1.0
|
CA
|
B:VAL680
|
4.9
|
24.8
|
1.0
|
CE
|
B:LYS133
|
5.0
|
27.0
|
1.0
|
|
Calcium binding site 4 out
of 4 in 1jrq
Go back to
Calcium Binding Sites List in 1jrq
Calcium binding site 4 out
of 4 in the X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 4 of X-Ray Structure Analysis of the Role of the Conserved Tyrosine-369 in Active Site of E. Coli Amine Oxidase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ca803
b:54.5
occ:1.00
|
O
|
B:TYR667
|
2.5
|
28.8
|
1.0
|
O
|
B:HOH1007
|
2.7
|
35.7
|
1.0
|
OE2
|
B:GLU573
|
2.7
|
29.1
|
1.0
|
OE2
|
B:GLU672
|
2.7
|
48.8
|
1.0
|
O
|
B:HOH1012
|
2.9
|
35.5
|
1.0
|
OE1
|
B:GLU573
|
3.0
|
32.0
|
1.0
|
CD
|
B:GLU573
|
3.2
|
33.8
|
1.0
|
CD
|
B:GLU672
|
3.5
|
48.8
|
1.0
|
CG
|
B:GLU672
|
3.6
|
45.6
|
1.0
|
O
|
B:HOH1064
|
3.7
|
44.1
|
1.0
|
C
|
B:TYR667
|
3.8
|
29.7
|
1.0
|
NE2
|
B:HIS644
|
4.2
|
53.6
|
1.0
|
CD2
|
B:HIS644
|
4.3
|
52.6
|
1.0
|
CB
|
B:GLU672
|
4.4
|
40.6
|
1.0
|
OE1
|
B:GLU647
|
4.5
|
35.5
|
1.0
|
N
|
B:ARG642
|
4.5
|
29.7
|
1.0
|
CB
|
B:ARG642
|
4.6
|
32.1
|
1.0
|
CA
|
B:TYR667
|
4.6
|
30.6
|
1.0
|
CA
|
B:SER668
|
4.6
|
32.4
|
1.0
|
N
|
B:SER668
|
4.7
|
31.2
|
1.0
|
OE1
|
B:GLU672
|
4.7
|
50.3
|
1.0
|
CG
|
B:GLU573
|
4.7
|
31.6
|
1.0
|
OE2
|
B:GLU647
|
4.8
|
37.1
|
1.0
|
CB
|
B:THR641
|
4.9
|
28.9
|
1.0
|
O
|
B:ARG642
|
5.0
|
28.8
|
1.0
|
|
Reference:
J.M.Murray,
C.R.Kurtis,
W.Tambyrajah,
C.G.Saysell,
C.M.Wilmot,
M.R.Parsons,
S.E.Phillips,
P.F.Knowles,
M.J.Mcpherson.
Conserved Tyrosine-369 in the Active Site of Escherichia Coli Copper Amine Oxidase Is Not Essential. Biochemistry V. 40 12808 2001.
ISSN: ISSN 0006-2960
PubMed: 11669617
DOI: 10.1021/BI011187P
Page generated: Thu Jul 11 10:52:39 2024
|