Zinc in PDB 4pnt: Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
Enzymatic activity of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
All present enzymatic activity of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.:
2.4.2.30;
Protein crystallography data
The structure of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd., PDB code: 4pnt
was solved by
W.Qiu,
R.Lam,
V.Romanov,
R.Gordon,
S.Gebremeskel,
J.Vodsedalek,
C.Thompson,
I.Beletskaya,
K.P.Battaile,
E.F.Pai,
N.Y.Chirgadze,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
76.74 /
1.60
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
73.980,
79.590,
153.480,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
19.1 /
22.6
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
(pdb code 4pnt). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the
Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd., PDB code: 4pnt:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 4pnt
Go back to
Zinc Binding Sites List in 4pnt
Zinc binding site 1 out
of 4 in the Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn1201
b:28.9
occ:1.00
|
SG
|
A:CYS1089
|
2.0
|
25.5
|
1.0
|
ND1
|
A:HIS1084
|
2.1
|
39.5
|
1.0
|
SG
|
A:CYS1081
|
2.2
|
26.4
|
1.0
|
SG
|
A:CYS1092
|
2.3
|
27.9
|
1.0
|
CE1
|
A:HIS1084
|
3.0
|
39.3
|
1.0
|
CB
|
A:CYS1092
|
3.2
|
24.2
|
1.0
|
CB
|
A:CYS1081
|
3.2
|
23.4
|
1.0
|
CG
|
A:HIS1084
|
3.2
|
38.1
|
1.0
|
CB
|
A:CYS1089
|
3.3
|
22.8
|
1.0
|
CB
|
A:HIS1084
|
3.6
|
35.0
|
1.0
|
N
|
A:HIS1084
|
3.8
|
34.8
|
1.0
|
N
|
A:CYS1092
|
4.0
|
23.9
|
1.0
|
CA
|
A:CYS1092
|
4.2
|
23.7
|
1.0
|
NE2
|
A:HIS1084
|
4.2
|
39.6
|
1.0
|
CA
|
A:HIS1084
|
4.3
|
33.8
|
1.0
|
CD2
|
A:HIS1084
|
4.3
|
39.5
|
1.0
|
CB
|
A:VAL1083
|
4.5
|
39.4
|
1.0
|
O
|
A:HOH1355
|
4.5
|
40.8
|
1.0
|
CA
|
A:CYS1081
|
4.6
|
24.1
|
1.0
|
CA
|
A:CYS1089
|
4.7
|
23.4
|
1.0
|
C
|
A:VAL1083
|
4.8
|
40.0
|
1.0
|
O
|
A:HOH1345
|
4.9
|
45.7
|
1.0
|
CA
|
A:VAL1083
|
4.9
|
36.1
|
1.0
|
CB
|
A:ILE1091
|
4.9
|
28.3
|
1.0
|
CG1
|
A:VAL1083
|
4.9
|
39.2
|
1.0
|
O
|
A:HOH1486
|
5.0
|
23.6
|
1.0
|
N
|
A:VAL1083
|
5.0
|
36.8
|
1.0
|
|
Zinc binding site 2 out
of 4 in 4pnt
Go back to
Zinc Binding Sites List in 4pnt
Zinc binding site 2 out
of 4 in the Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn1201
b:30.1
occ:1.00
|
ND1
|
B:HIS1084
|
2.1
|
35.9
|
1.0
|
SG
|
B:CYS1089
|
2.2
|
25.1
|
1.0
|
SG
|
B:CYS1081
|
2.3
|
25.8
|
1.0
|
SG
|
B:CYS1092
|
2.4
|
28.4
|
1.0
|
CE1
|
B:HIS1084
|
3.0
|
35.4
|
1.0
|
CG
|
B:HIS1084
|
3.2
|
34.6
|
1.0
|
CB
|
B:CYS1081
|
3.2
|
22.7
|
1.0
|
CB
|
B:CYS1089
|
3.2
|
21.0
|
1.0
|
CB
|
B:CYS1092
|
3.3
|
24.4
|
1.0
|
CB
|
B:HIS1084
|
3.5
|
30.9
|
1.0
|
N
|
B:HIS1084
|
3.8
|
32.0
|
1.0
|
N
|
B:CYS1092
|
3.9
|
23.9
|
1.0
|
O
|
B:HOH1374
|
4.1
|
39.3
|
1.0
|
NE2
|
B:HIS1084
|
4.2
|
35.8
|
1.0
|
CA
|
B:CYS1092
|
4.2
|
23.4
|
1.0
|
CA
|
B:HIS1084
|
4.2
|
30.0
|
1.0
|
CD2
|
B:HIS1084
|
4.3
|
36.2
|
1.0
|
O
|
B:HOH1463
|
4.4
|
42.6
|
1.0
|
CB
|
B:VAL1083
|
4.6
|
36.5
|
1.0
|
CA
|
B:CYS1081
|
4.6
|
22.6
|
1.0
|
CA
|
B:CYS1089
|
4.6
|
20.2
|
1.0
|
C
|
B:VAL1083
|
4.8
|
37.5
|
1.0
|
CB
|
B:ILE1091
|
4.8
|
27.0
|
1.0
|
N
|
B:VAL1083
|
4.9
|
32.4
|
1.0
|
CA
|
B:VAL1083
|
4.9
|
32.7
|
1.0
|
C
|
B:CYS1081
|
5.0
|
31.0
|
1.0
|
|
Zinc binding site 3 out
of 4 in 4pnt
Go back to
Zinc Binding Sites List in 4pnt
Zinc binding site 3 out
of 4 in the Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn1202
b:29.4
occ:1.00
|
ND1
|
C:HIS1084
|
2.1
|
38.5
|
1.0
|
SG
|
C:CYS1089
|
2.2
|
26.1
|
1.0
|
SG
|
C:CYS1081
|
2.2
|
27.8
|
1.0
|
SG
|
C:CYS1092
|
2.3
|
28.1
|
1.0
|
CE1
|
C:HIS1084
|
3.1
|
38.2
|
1.0
|
CB
|
C:CYS1089
|
3.1
|
22.5
|
1.0
|
CG
|
C:HIS1084
|
3.2
|
37.2
|
1.0
|
CB
|
C:CYS1081
|
3.2
|
24.2
|
1.0
|
CB
|
C:CYS1092
|
3.3
|
24.0
|
1.0
|
CB
|
C:HIS1084
|
3.6
|
33.6
|
1.0
|
N
|
C:HIS1084
|
3.9
|
35.1
|
1.0
|
N
|
C:CYS1092
|
3.9
|
23.8
|
1.0
|
CA
|
C:CYS1092
|
4.2
|
23.3
|
1.0
|
NE2
|
C:HIS1084
|
4.2
|
38.5
|
1.0
|
O
|
C:HOH1512
|
4.2
|
37.7
|
1.0
|
CA
|
C:HIS1084
|
4.3
|
33.0
|
1.0
|
CD2
|
C:HIS1084
|
4.3
|
38.6
|
1.0
|
CB
|
C:VAL1083
|
4.5
|
42.6
|
1.0
|
CA
|
C:CYS1089
|
4.5
|
22.4
|
1.0
|
CA
|
C:CYS1081
|
4.6
|
24.4
|
1.0
|
O
|
C:HOH1515
|
4.8
|
22.1
|
1.0
|
C
|
C:VAL1083
|
4.9
|
41.9
|
1.0
|
CB
|
C:ILE1091
|
4.9
|
26.2
|
1.0
|
C
|
C:ILE1091
|
5.0
|
27.7
|
1.0
|
O
|
C:HOH1416
|
5.0
|
34.8
|
1.0
|
CA
|
C:VAL1083
|
5.0
|
38.2
|
1.0
|
|
Zinc binding site 4 out
of 4 in 4pnt
Go back to
Zinc Binding Sites List in 4pnt
Zinc binding site 4 out
of 4 in the Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd.
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Crystal Structure of Human Tankyrase 2 in Complex with 1,5-Iqd. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Zn1200
b:33.8
occ:1.00
|
SG
|
D:CYS1089
|
2.1
|
29.5
|
1.0
|
ND1
|
D:HIS1084
|
2.2
|
47.3
|
1.0
|
SG
|
D:CYS1081
|
2.4
|
33.9
|
1.0
|
SG
|
D:CYS1092
|
2.4
|
33.4
|
1.0
|
CE1
|
D:HIS1084
|
3.1
|
46.7
|
1.0
|
CB
|
D:CYS1092
|
3.2
|
29.0
|
1.0
|
CB
|
D:CYS1089
|
3.2
|
25.9
|
1.0
|
CB
|
D:CYS1081
|
3.3
|
30.4
|
1.0
|
CG
|
D:HIS1084
|
3.3
|
45.3
|
1.0
|
CB
|
D:HIS1084
|
3.7
|
41.4
|
1.0
|
N
|
D:CYS1092
|
3.8
|
28.7
|
1.0
|
N
|
D:HIS1084
|
3.9
|
40.6
|
1.0
|
CA
|
D:CYS1092
|
4.1
|
27.9
|
1.0
|
NE2
|
D:HIS1084
|
4.3
|
46.7
|
1.0
|
O
|
D:HOH1500
|
4.4
|
50.4
|
1.0
|
CA
|
D:HIS1084
|
4.4
|
40.1
|
1.0
|
CD2
|
D:HIS1084
|
4.4
|
46.9
|
1.0
|
CB
|
D:VAL1083
|
4.6
|
44.0
|
1.0
|
CA
|
D:CYS1089
|
4.6
|
26.1
|
1.0
|
CA
|
D:CYS1081
|
4.7
|
30.5
|
1.0
|
O
|
D:HOH1466
|
4.7
|
27.8
|
1.0
|
CB
|
D:ILE1091
|
4.8
|
29.7
|
1.0
|
C
|
D:VAL1083
|
4.9
|
44.6
|
1.0
|
C
|
D:ILE1091
|
4.9
|
31.9
|
1.0
|
|
Reference:
W.Qiu,
R.Lam,
O.Voytyuk,
V.Romanov,
R.Gordon,
S.Gebremeskel,
J.Vodsedalek,
C.Thompson,
I.Beletskaya,
K.P.Battaile,
E.F.Pai,
R.Rottapel,
N.Y.Chirgadze.
Insights Into the Binding of Parp Inhibitors to the Catalytic Domain of Human Tankyrase-2 Acta Crystallogr.,Sect.D V. D70 2740 2014.
ISSN: ESSN 1399-0047
DOI: 10.1107/S1399004714017660
Page generated: Sun Oct 27 06:00:43 2024
|