Zinc in PDB 5kl7: Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna
Protein crystallography data
The structure of Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna, PDB code: 5kl7
was solved by
H.Hashimoto,
X.Cheng,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
29.23 /
1.58
|
Space group
|
P 21 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
67.458,
77.797,
35.683,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
16.4 /
19.4
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna
(pdb code 5kl7). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 3 binding sites of Zinc where determined in the
Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna, PDB code: 5kl7:
Jump to Zinc binding site number:
1;
2;
3;
Zinc binding site 1 out
of 3 in 5kl7
Go back to
Zinc Binding Sites List in 5kl7
Zinc binding site 1 out
of 3 in the Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn501
b:16.3
occ:1.00
|
NE2
|
A:HIS373
|
2.0
|
13.9
|
1.0
|
NE2
|
A:HIS377
|
2.1
|
15.7
|
1.0
|
SG
|
A:CYS360
|
2.3
|
16.8
|
1.0
|
SG
|
A:CYS355
|
2.3
|
17.0
|
1.0
|
CE1
|
A:HIS373
|
2.9
|
14.9
|
1.0
|
CD2
|
A:HIS373
|
3.0
|
14.5
|
1.0
|
CD2
|
A:HIS377
|
3.0
|
16.4
|
1.0
|
CE1
|
A:HIS377
|
3.1
|
20.8
|
1.0
|
HB3
|
A:CYS355
|
3.1
|
21.7
|
1.0
|
HE1
|
A:HIS373
|
3.1
|
17.9
|
1.0
|
HB3
|
A:CYS360
|
3.1
|
21.6
|
1.0
|
CB
|
A:CYS360
|
3.1
|
18.0
|
1.0
|
HD2
|
A:HIS377
|
3.2
|
19.6
|
1.0
|
CB
|
A:CYS355
|
3.2
|
18.1
|
1.0
|
HD2
|
A:HIS373
|
3.2
|
17.4
|
1.0
|
HB2
|
A:CYS360
|
3.2
|
21.6
|
1.0
|
HE1
|
A:HIS377
|
3.3
|
25.0
|
1.0
|
HB2
|
A:CYS355
|
3.3
|
21.7
|
1.0
|
HB2
|
A:PHE357
|
3.5
|
20.6
|
1.0
|
HB2
|
A:ARG362
|
3.7
|
20.6
|
1.0
|
O
|
A:HOH604
|
4.0
|
30.7
|
0.5
|
HG3
|
A:ARG362
|
4.0
|
23.9
|
1.0
|
ND1
|
A:HIS373
|
4.1
|
14.6
|
1.0
|
CG
|
A:HIS373
|
4.1
|
13.3
|
1.0
|
ND1
|
A:HIS377
|
4.2
|
22.1
|
1.0
|
CG
|
A:HIS377
|
4.2
|
15.7
|
1.0
|
H
|
A:ARG362
|
4.3
|
21.0
|
1.0
|
H
|
A:PHE357
|
4.4
|
25.3
|
1.0
|
CB
|
A:PHE357
|
4.4
|
17.2
|
1.0
|
HG2
|
A:GLN374
|
4.5
|
17.9
|
1.0
|
HG2
|
A:ARG362
|
4.5
|
23.9
|
1.0
|
CB
|
A:ARG362
|
4.5
|
17.2
|
1.0
|
CG
|
A:ARG362
|
4.5
|
20.0
|
1.0
|
CA
|
A:CYS360
|
4.6
|
19.6
|
1.0
|
CA
|
A:CYS355
|
4.6
|
18.6
|
1.0
|
HA
|
A:GLN374
|
4.7
|
17.7
|
1.0
|
HD1
|
A:PHE357
|
4.7
|
32.6
|
1.0
|
HB3
|
A:PHE357
|
4.8
|
20.6
|
1.0
|
HD1
|
A:HIS373
|
4.8
|
17.5
|
1.0
|
HA
|
A:CYS360
|
4.9
|
23.5
|
1.0
|
HA
|
A:CYS355
|
4.9
|
22.4
|
1.0
|
CG
|
A:PHE357
|
4.9
|
18.0
|
1.0
|
HD3
|
A:ARG376
|
4.9
|
63.3
|
1.0
|
HD1
|
A:HIS377
|
5.0
|
26.5
|
1.0
|
HG3
|
A:GLN374
|
5.0
|
17.9
|
1.0
|
HG2
|
A:ARG376
|
5.0
|
34.3
|
1.0
|
C
|
A:CYS355
|
5.0
|
19.8
|
1.0
|
CD1
|
A:PHE357
|
5.0
|
27.2
|
1.0
|
|
Zinc binding site 2 out
of 3 in 5kl7
Go back to
Zinc Binding Sites List in 5kl7
Zinc binding site 2 out
of 3 in the Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn502
b:18.8
occ:1.00
|
NE2
|
A:HIS405
|
2.0
|
18.2
|
1.0
|
NE2
|
A:HIS401
|
2.1
|
17.0
|
1.0
|
SG
|
A:CYS388
|
2.3
|
20.1
|
1.0
|
SG
|
A:CYS385
|
2.3
|
19.8
|
1.0
|
CD2
|
A:HIS405
|
3.0
|
20.7
|
1.0
|
CD2
|
A:HIS401
|
3.0
|
16.6
|
1.0
|
CE1
|
A:HIS405
|
3.0
|
26.2
|
1.0
|
HB3
|
A:CYS388
|
3.1
|
27.2
|
1.0
|
CE1
|
A:HIS401
|
3.1
|
19.8
|
1.0
|
HB3
|
A:CYS385
|
3.1
|
21.0
|
1.0
|
HD2
|
A:HIS401
|
3.1
|
19.9
|
1.0
|
HD2
|
A:HIS405
|
3.1
|
24.8
|
1.0
|
CB
|
A:CYS385
|
3.2
|
17.5
|
1.0
|
H
|
A:CYS388
|
3.2
|
28.7
|
1.0
|
HE1
|
A:HIS405
|
3.2
|
31.4
|
1.0
|
CB
|
A:CYS388
|
3.3
|
22.6
|
1.0
|
HB2
|
A:CYS385
|
3.3
|
21.0
|
1.0
|
HE1
|
A:HIS401
|
3.3
|
23.8
|
1.0
|
HB
|
A:THR387
|
3.6
|
29.9
|
1.0
|
N
|
A:CYS388
|
3.8
|
23.9
|
1.0
|
HB2
|
A:CYS388
|
4.1
|
27.2
|
1.0
|
CA
|
A:CYS388
|
4.1
|
22.4
|
1.0
|
ND1
|
A:HIS405
|
4.1
|
25.5
|
1.0
|
CG
|
A:HIS405
|
4.1
|
21.5
|
1.0
|
CG
|
A:HIS401
|
4.2
|
13.5
|
1.0
|
ND1
|
A:HIS401
|
4.2
|
16.0
|
1.0
|
HB3
|
A:ARG390
|
4.2
|
20.5
|
1.0
|
H
|
A:ARG390
|
4.3
|
23.8
|
1.0
|
H
|
A:THR387
|
4.4
|
26.1
|
1.0
|
CB
|
A:THR387
|
4.5
|
24.9
|
1.0
|
HE2
|
A:PHE392
|
4.5
|
20.6
|
1.0
|
H
|
A:GLN389
|
4.5
|
27.0
|
1.0
|
HA
|
A:THR402
|
4.6
|
21.1
|
1.0
|
HG22
|
A:THR387
|
4.6
|
30.8
|
1.0
|
CA
|
A:CYS385
|
4.6
|
19.1
|
1.0
|
C
|
A:CYS388
|
4.7
|
27.0
|
1.0
|
C
|
A:THR387
|
4.8
|
27.0
|
1.0
|
HZ
|
A:PHE392
|
4.8
|
23.0
|
1.0
|
HG1
|
A:THR404
|
4.9
|
31.2
|
1.0
|
HA
|
A:CYS388
|
4.9
|
26.9
|
1.0
|
N
|
A:GLN389
|
4.9
|
22.5
|
1.0
|
HD1
|
A:HIS405
|
4.9
|
30.6
|
1.0
|
CG2
|
A:THR387
|
4.9
|
25.7
|
1.0
|
HG21
|
A:THR387
|
5.0
|
30.8
|
1.0
|
HA
|
A:CYS385
|
5.0
|
22.9
|
1.0
|
HD1
|
A:HIS401
|
5.0
|
19.2
|
1.0
|
HB2
|
A:ARG390
|
5.0
|
20.5
|
1.0
|
HG22
|
A:THR402
|
5.0
|
20.6
|
1.0
|
|
Zinc binding site 3 out
of 3 in 5kl7
Go back to
Zinc Binding Sites List in 5kl7
Zinc binding site 3 out
of 3 in the Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Wilms Tumor Protein (WT1) ZNF2-4Q369R in Complex with Carboxylated Dna within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn503
b:22.9
occ:1.00
|
NE2
|
A:HIS435
|
2.0
|
25.4
|
1.0
|
NE2
|
A:HIS431
|
2.0
|
18.9
|
1.0
|
SG
|
A:CYS418
|
2.2
|
28.1
|
1.0
|
SG
|
A:CYS413
|
2.3
|
23.0
|
1.0
|
CD2
|
A:HIS431
|
3.0
|
19.7
|
1.0
|
CD2
|
A:HIS435
|
3.0
|
22.1
|
1.0
|
HB3
|
A:CYS418
|
3.0
|
33.3
|
1.0
|
CE1
|
A:HIS435
|
3.0
|
35.5
|
1.0
|
CE1
|
A:HIS431
|
3.1
|
22.3
|
1.0
|
HD2
|
A:HIS431
|
3.1
|
23.7
|
1.0
|
HB2
|
A:CYS413
|
3.1
|
28.2
|
1.0
|
CB
|
A:CYS418
|
3.1
|
27.8
|
1.0
|
HD2
|
A:HIS435
|
3.2
|
26.5
|
1.0
|
CB
|
A:CYS413
|
3.2
|
23.5
|
1.0
|
HE1
|
A:HIS435
|
3.2
|
42.6
|
1.0
|
HB3
|
A:CYS413
|
3.3
|
28.2
|
1.0
|
HE1
|
A:HIS431
|
3.3
|
26.8
|
1.0
|
HB2
|
A:CYS418
|
3.4
|
33.3
|
1.0
|
HB2
|
A:TRP415
|
3.4
|
39.4
|
1.0
|
HB2
|
A:LYS420
|
3.7
|
23.9
|
1.0
|
HG3
|
A:LYS420
|
4.1
|
39.1
|
1.0
|
CG
|
A:HIS431
|
4.1
|
18.2
|
1.0
|
ND1
|
A:HIS435
|
4.1
|
33.4
|
1.0
|
ND1
|
A:HIS431
|
4.1
|
20.2
|
1.0
|
CG
|
A:HIS435
|
4.1
|
26.4
|
1.0
|
HD1
|
A:TRP415
|
4.2
|
78.1
|
1.0
|
H
|
A:LYS420
|
4.3
|
41.3
|
1.0
|
CB
|
A:TRP415
|
4.4
|
32.9
|
1.0
|
H
|
A:TRP415
|
4.4
|
27.6
|
1.0
|
HG2
|
A:LYS420
|
4.4
|
39.1
|
1.0
|
HE1
|
A:MET434
|
4.5
|
42.9
|
1.0
|
CB
|
A:LYS420
|
4.5
|
19.9
|
1.0
|
CG
|
A:LYS420
|
4.5
|
32.6
|
1.0
|
CA
|
A:CYS418
|
4.5
|
29.5
|
1.0
|
CA
|
A:CYS413
|
4.6
|
17.6
|
1.0
|
HD2
|
A:HIS432
|
4.7
|
24.0
|
1.0
|
HB3
|
A:TRP415
|
4.7
|
39.4
|
1.0
|
CD1
|
A:TRP415
|
4.8
|
65.1
|
1.0
|
O
|
A:CYS418
|
4.8
|
45.6
|
1.0
|
HA
|
A:CYS413
|
4.8
|
21.1
|
1.0
|
C
|
A:CYS418
|
4.9
|
31.5
|
1.0
|
CG
|
A:TRP415
|
4.9
|
38.0
|
1.0
|
HA
|
A:CYS418
|
4.9
|
35.4
|
1.0
|
HD1
|
A:HIS435
|
4.9
|
40.0
|
1.0
|
HD1
|
A:HIS431
|
4.9
|
24.3
|
1.0
|
HE3
|
A:MET434
|
4.9
|
42.9
|
1.0
|
|
Reference:
H.Hashimoto,
X.Zhang,
Y.Zheng,
G.G.Wilson,
X.Cheng.
Denys-Drash Syndrome Associated WT1 Glutamine 369 Mutants Have Altered Sequence-Preferences and Altered Responses to Epigenetic Modifications. Nucleic Acids Res. V. 44 10165 2016.
ISSN: ESSN 1362-4962
PubMed: 27596598
DOI: 10.1093/NAR/GKW766
Page generated: Sun Oct 27 20:35:00 2024
|