Zinc in PDB 4msq: Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin
Protein crystallography data
The structure of Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin, PDB code: 4msq
was solved by
R.K.Shrestha,
J.A.Ronau,
C.Das,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
41.28 /
1.95
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
71.244,
57.032,
81.175,
90.00,
104.58,
90.00
|
R / Rfree (%)
|
17.7 /
20.7
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin
(pdb code 4msq). 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 Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin, PDB code: 4msq:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 4msq
Go back to
Zinc Binding Sites List in 4msq
Zinc binding site 1 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin
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 Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn501
b:21.6
occ:1.00
|
NE2
|
A:HIS406
|
2.0
|
21.9
|
1.0
|
NE2
|
A:HIS356
|
2.0
|
20.9
|
1.0
|
NE2
|
A:HIS404
|
2.1
|
20.1
|
1.0
|
SG
|
A:CYS397
|
2.3
|
20.9
|
1.0
|
CE1
|
A:HIS406
|
2.8
|
22.1
|
1.0
|
CE1
|
A:HIS356
|
2.9
|
19.7
|
1.0
|
CD2
|
A:HIS404
|
3.0
|
19.7
|
1.0
|
CD2
|
A:HIS406
|
3.1
|
16.0
|
1.0
|
CE1
|
A:HIS404
|
3.1
|
25.7
|
1.0
|
CD2
|
A:HIS356
|
3.2
|
17.9
|
1.0
|
CB
|
A:CYS397
|
3.3
|
21.2
|
1.0
|
O
|
A:HOH649
|
4.0
|
33.8
|
1.0
|
ND1
|
A:HIS406
|
4.0
|
25.5
|
1.0
|
ND1
|
A:HIS356
|
4.1
|
17.7
|
1.0
|
CG
|
A:HIS406
|
4.1
|
24.6
|
1.0
|
ND1
|
A:HIS404
|
4.2
|
21.2
|
1.0
|
CG
|
A:HIS404
|
4.2
|
26.5
|
1.0
|
CG
|
A:HIS356
|
4.2
|
14.9
|
1.0
|
OG
|
A:SER352
|
4.3
|
23.9
|
1.0
|
CD1
|
A:ILE394
|
4.5
|
21.6
|
1.0
|
O
|
A:HOH703
|
4.7
|
38.1
|
1.0
|
CA
|
A:CYS397
|
4.7
|
26.4
|
1.0
|
CB
|
A:LYS399
|
4.8
|
30.1
|
1.0
|
O
|
A:LYS399
|
4.8
|
22.8
|
1.0
|
C
|
A:CYS397
|
4.9
|
26.0
|
1.0
|
|
Zinc binding site 2 out
of 4 in 4msq
Go back to
Zinc Binding Sites List in 4msq
Zinc binding site 2 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin
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 Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn502
b:23.4
occ:1.00
|
OD2
|
A:ASP354
|
2.0
|
18.2
|
1.0
|
OXT
|
B:GLY76
|
2.0
|
24.4
|
1.0
|
NE2
|
A:HIS341
|
2.1
|
18.6
|
1.0
|
NE2
|
A:HIS343
|
2.1
|
18.7
|
1.0
|
CG
|
A:ASP354
|
2.7
|
14.1
|
1.0
|
OD1
|
A:ASP354
|
2.7
|
13.9
|
1.0
|
CE1
|
A:HIS341
|
2.9
|
16.4
|
1.0
|
C
|
B:GLY76
|
3.0
|
26.1
|
1.0
|
CD2
|
A:HIS343
|
3.0
|
19.8
|
1.0
|
CE1
|
A:HIS343
|
3.1
|
25.3
|
1.0
|
CD2
|
A:HIS341
|
3.2
|
20.8
|
1.0
|
O
|
B:GLY76
|
3.6
|
24.9
|
1.0
|
N
|
B:GLY76
|
3.7
|
22.4
|
1.0
|
OG
|
A:SER351
|
3.9
|
20.5
|
1.0
|
CA
|
B:GLY76
|
3.9
|
18.5
|
1.0
|
ND1
|
A:HIS341
|
4.1
|
19.8
|
1.0
|
CB
|
A:ASP354
|
4.1
|
16.0
|
1.0
|
CG
|
A:HIS343
|
4.2
|
21.6
|
1.0
|
ND1
|
A:HIS343
|
4.2
|
21.7
|
1.0
|
CG
|
A:HIS341
|
4.2
|
16.8
|
1.0
|
O
|
A:PHE349
|
4.3
|
22.2
|
1.0
|
CB
|
A:SER351
|
4.3
|
22.5
|
1.0
|
N
|
A:SER351
|
4.4
|
19.5
|
1.0
|
CG1
|
A:VAL372
|
4.6
|
20.1
|
1.0
|
C
|
B:GLY75
|
4.8
|
21.1
|
1.0
|
O2
|
A:EDO503
|
4.9
|
35.2
|
1.0
|
CG2
|
A:VAL372
|
5.0
|
22.7
|
1.0
|
|
Zinc binding site 3 out
of 4 in 4msq
Go back to
Zinc Binding Sites List in 4msq
Zinc binding site 3 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin
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 Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn501
b:35.6
occ:1.00
|
NE2
|
C:HIS406
|
2.0
|
32.7
|
1.0
|
NE2
|
C:HIS356
|
2.0
|
33.5
|
1.0
|
NE2
|
C:HIS404
|
2.1
|
36.2
|
1.0
|
SG
|
C:CYS397
|
2.4
|
35.0
|
1.0
|
CE1
|
C:HIS406
|
2.8
|
33.9
|
1.0
|
CE1
|
C:HIS356
|
2.9
|
29.8
|
1.0
|
CE1
|
C:HIS404
|
3.0
|
33.3
|
1.0
|
CD2
|
C:HIS356
|
3.0
|
28.4
|
1.0
|
CD2
|
C:HIS406
|
3.0
|
29.1
|
1.0
|
CD2
|
C:HIS404
|
3.1
|
35.4
|
1.0
|
CB
|
C:CYS397
|
3.3
|
32.7
|
1.0
|
ND1
|
C:HIS406
|
3.9
|
33.4
|
1.0
|
ND1
|
C:HIS356
|
4.1
|
32.9
|
1.0
|
O
|
C:HOH672
|
4.1
|
40.7
|
1.0
|
CG
|
C:HIS406
|
4.1
|
34.5
|
1.0
|
ND1
|
C:HIS404
|
4.1
|
34.7
|
1.0
|
CG
|
C:HIS356
|
4.1
|
27.1
|
1.0
|
CG
|
C:HIS404
|
4.2
|
37.0
|
1.0
|
CD1
|
C:ILE394
|
4.6
|
33.4
|
1.0
|
CA
|
C:CYS397
|
4.7
|
37.6
|
1.0
|
CB
|
C:LYS399
|
4.8
|
39.2
|
1.0
|
C
|
C:CYS397
|
4.9
|
40.7
|
1.0
|
|
Zinc binding site 4 out
of 4 in 4msq
Go back to
Zinc Binding Sites List in 4msq
Zinc binding site 4 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin
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 Schizosaccharomyces Pombe Amsh-Like Protease SST2 Catalytic Domain Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn502
b:21.6
occ:1.00
|
OD2
|
C:ASP354
|
2.0
|
15.0
|
1.0
|
O
|
D:GLY76
|
2.0
|
24.2
|
1.0
|
NE2
|
C:HIS343
|
2.0
|
13.5
|
1.0
|
NE2
|
C:HIS341
|
2.1
|
18.6
|
1.0
|
CG
|
C:ASP354
|
2.7
|
14.3
|
1.0
|
OD1
|
C:ASP354
|
2.8
|
14.7
|
1.0
|
C
|
D:GLY76
|
2.9
|
26.2
|
1.0
|
CE1
|
C:HIS341
|
2.9
|
19.8
|
1.0
|
CD2
|
C:HIS343
|
3.0
|
16.2
|
1.0
|
CE1
|
C:HIS343
|
3.1
|
18.6
|
1.0
|
CD2
|
C:HIS341
|
3.2
|
19.2
|
1.0
|
OXT
|
D:GLY76
|
3.4
|
23.1
|
1.0
|
N
|
D:GLY76
|
3.8
|
20.4
|
1.0
|
OG
|
C:SER351
|
3.9
|
20.5
|
1.0
|
CA
|
D:GLY76
|
4.0
|
20.5
|
1.0
|
O
|
C:PHE349
|
4.1
|
19.6
|
1.0
|
ND1
|
C:HIS341
|
4.1
|
20.6
|
1.0
|
CG
|
C:HIS343
|
4.2
|
19.9
|
1.0
|
ND1
|
C:HIS343
|
4.2
|
19.9
|
1.0
|
CB
|
C:ASP354
|
4.2
|
17.5
|
1.0
|
CG
|
C:HIS341
|
4.3
|
18.4
|
1.0
|
N
|
C:SER351
|
4.4
|
20.9
|
1.0
|
CB
|
C:SER351
|
4.4
|
22.6
|
1.0
|
CG1
|
C:VAL372
|
4.7
|
19.5
|
1.0
|
CG2
|
C:VAL372
|
4.9
|
15.5
|
1.0
|
O1
|
C:EDO507
|
4.9
|
36.3
|
1.0
|
C
|
D:GLY75
|
4.9
|
23.5
|
1.0
|
|
Reference:
R.K.Shrestha,
J.A.Ronau,
C.W.Davies,
R.G.Guenette,
E.R.Strieter,
L.N.Paul,
C.Das.
Insights Into the Mechanism of Deubiquitination By Jamm Deubiquitinases From Cocrystal Structures of the Enzyme with the Substrate and Product. Biochemistry V. 53 3199 2014.
ISSN: ISSN 0006-2960
PubMed: 24787148
DOI: 10.1021/BI5003162
Page generated: Sun Oct 27 02:41:58 2024
|