Zinc in PDB 4msm: Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant Bound to Ubiquitin
Protein crystallography data
The structure of Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant Bound to Ubiquitin, PDB code: 4msm
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)
|
72.85 /
1.74
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
57.017,
95.322,
112.944,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
19.5 /
22.5
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant Bound to Ubiquitin
(pdb code 4msm). 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 E286A Mutant Bound to Ubiquitin, PDB code: 4msm:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 4msm
Go back to
Zinc Binding Sites List in 4msm
Zinc binding site 1 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant 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 E286A Mutant Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn501
b:21.1
occ:1.00
|
O
|
A:HOH694
|
1.4
|
17.0
|
1.0
|
OD2
|
A:ASP354
|
1.9
|
19.7
|
1.0
|
NE2
|
A:HIS343
|
2.1
|
24.6
|
1.0
|
NE2
|
A:HIS341
|
2.1
|
19.8
|
1.0
|
CG
|
A:ASP354
|
2.6
|
16.7
|
1.0
|
OD1
|
A:ASP354
|
2.7
|
17.7
|
1.0
|
CD2
|
A:HIS343
|
3.0
|
23.8
|
1.0
|
CE1
|
A:HIS341
|
3.0
|
18.8
|
1.0
|
CE1
|
A:HIS343
|
3.1
|
27.0
|
1.0
|
CD2
|
A:HIS341
|
3.2
|
19.2
|
1.0
|
O
|
B:GLY76
|
3.8
|
29.8
|
1.0
|
CB
|
A:ASP354
|
4.1
|
18.4
|
1.0
|
OG
|
A:SER351
|
4.1
|
22.9
|
1.0
|
CG
|
A:HIS343
|
4.2
|
23.7
|
1.0
|
ND1
|
A:HIS343
|
4.2
|
25.6
|
1.0
|
ND1
|
A:HIS341
|
4.2
|
18.4
|
1.0
|
O
|
A:HOH634
|
4.3
|
34.8
|
1.0
|
CG
|
A:HIS341
|
4.3
|
15.9
|
1.0
|
N
|
B:GLY76
|
4.3
|
24.4
|
1.0
|
O
|
A:PHE349
|
4.4
|
21.8
|
1.0
|
CB
|
A:SER351
|
4.6
|
20.5
|
1.0
|
N
|
A:SER351
|
4.6
|
19.8
|
1.0
|
C
|
B:GLY76
|
4.8
|
29.1
|
1.0
|
CG1
|
A:VAL372
|
4.8
|
22.0
|
1.0
|
CA
|
B:GLY75
|
4.9
|
23.1
|
1.0
|
O
|
A:HOH721
|
4.9
|
37.3
|
1.0
|
C
|
B:GLY75
|
5.0
|
22.0
|
1.0
|
CA
|
B:GLY76
|
5.0
|
29.0
|
1.0
|
|
Zinc binding site 2 out
of 4 in 4msm
Go back to
Zinc Binding Sites List in 4msm
Zinc binding site 2 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant 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 E286A Mutant Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn502
b:20.7
occ:1.00
|
NE2
|
A:HIS404
|
2.0
|
21.8
|
1.0
|
NE2
|
A:HIS406
|
2.0
|
22.6
|
1.0
|
NE2
|
A:HIS356
|
2.1
|
22.0
|
1.0
|
SG
|
A:CYS397
|
2.3
|
20.4
|
1.0
|
CD2
|
A:HIS404
|
2.9
|
22.7
|
1.0
|
CE1
|
A:HIS356
|
3.0
|
19.1
|
1.0
|
CD2
|
A:HIS406
|
3.0
|
25.1
|
1.0
|
CE1
|
A:HIS406
|
3.0
|
23.6
|
1.0
|
CE1
|
A:HIS404
|
3.1
|
19.2
|
1.0
|
CD2
|
A:HIS356
|
3.1
|
19.6
|
1.0
|
CB
|
A:CYS397
|
3.3
|
18.2
|
1.0
|
O
|
A:HOH725
|
3.9
|
29.3
|
1.0
|
CG
|
A:HIS404
|
4.1
|
23.0
|
1.0
|
ND1
|
A:HIS406
|
4.1
|
25.3
|
1.0
|
ND1
|
A:HIS356
|
4.1
|
19.6
|
1.0
|
ND1
|
A:HIS404
|
4.1
|
22.0
|
1.0
|
CG
|
A:HIS406
|
4.2
|
24.4
|
1.0
|
CG
|
A:HIS356
|
4.2
|
18.9
|
1.0
|
OG
|
A:SER352
|
4.3
|
25.6
|
1.0
|
CD1
|
A:ILE394
|
4.4
|
20.8
|
1.0
|
CA
|
A:CYS397
|
4.7
|
19.6
|
1.0
|
O
|
A:HOH687
|
4.9
|
33.7
|
1.0
|
CB
|
A:LYS399
|
5.0
|
24.8
|
1.0
|
NZ
|
A:LYS399
|
5.0
|
35.0
|
1.0
|
|
Zinc binding site 3 out
of 4 in 4msm
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Zinc Binding Sites List in 4msm
Zinc binding site 3 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant 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 E286A Mutant Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn501
b:18.6
occ:1.00
|
OD2
|
C:ASP354
|
1.8
|
16.3
|
1.0
|
O
|
D:HOH240
|
2.0
|
26.4
|
1.0
|
NE2
|
C:HIS341
|
2.0
|
17.4
|
1.0
|
NE2
|
C:HIS343
|
2.1
|
17.8
|
1.0
|
OD1
|
C:ASP354
|
2.6
|
15.2
|
1.0
|
CG
|
C:ASP354
|
2.6
|
15.1
|
1.0
|
CE1
|
C:HIS341
|
2.9
|
17.5
|
1.0
|
CD2
|
C:HIS343
|
3.0
|
17.8
|
1.0
|
CE1
|
C:HIS343
|
3.1
|
20.2
|
1.0
|
CD2
|
C:HIS341
|
3.1
|
16.3
|
1.0
|
O
|
D:GLY76
|
3.7
|
32.5
|
1.0
|
OG
|
C:SER351
|
4.0
|
19.6
|
1.0
|
ND1
|
C:HIS341
|
4.1
|
14.7
|
1.0
|
CB
|
C:ASP354
|
4.1
|
15.8
|
1.0
|
CG
|
C:HIS343
|
4.1
|
18.6
|
1.0
|
ND1
|
C:HIS343
|
4.2
|
19.9
|
1.0
|
CG
|
C:HIS341
|
4.2
|
15.7
|
1.0
|
N
|
D:GLY76
|
4.3
|
29.1
|
1.0
|
CB
|
C:SER351
|
4.5
|
19.2
|
1.0
|
O
|
C:PHE349
|
4.5
|
22.6
|
1.0
|
N
|
C:SER351
|
4.6
|
15.7
|
1.0
|
O
|
C:HOH652
|
4.8
|
32.9
|
1.0
|
CG1
|
C:VAL372
|
4.8
|
17.2
|
1.0
|
C
|
D:GLY76
|
4.9
|
34.8
|
1.0
|
CA
|
D:GLY75
|
4.9
|
22.0
|
1.0
|
|
Zinc binding site 4 out
of 4 in 4msm
Go back to
Zinc Binding Sites List in 4msm
Zinc binding site 4 out
of 4 in the Crystal Structure of Schizosaccharomyces Pombe Amsh-Like Protease SST2 E286A Mutant 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 E286A Mutant Bound to Ubiquitin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn502
b:22.5
occ:1.00
|
NE2
|
C:HIS404
|
2.1
|
26.9
|
1.0
|
NE2
|
C:HIS356
|
2.1
|
19.7
|
1.0
|
NE2
|
C:HIS406
|
2.1
|
20.8
|
1.0
|
SG
|
C:CYS397
|
2.3
|
23.3
|
1.0
|
CD2
|
C:HIS404
|
3.0
|
26.6
|
1.0
|
CE1
|
C:HIS356
|
3.0
|
19.5
|
1.0
|
CE1
|
C:HIS406
|
3.0
|
21.1
|
1.0
|
CD2
|
C:HIS406
|
3.1
|
19.2
|
1.0
|
CD2
|
C:HIS356
|
3.1
|
18.4
|
1.0
|
CE1
|
C:HIS404
|
3.1
|
25.4
|
1.0
|
CB
|
C:CYS397
|
3.4
|
25.7
|
1.0
|
O1
|
C:EDO506
|
3.9
|
40.9
|
1.0
|
ND1
|
C:HIS406
|
4.1
|
20.2
|
1.0
|
ND1
|
C:HIS356
|
4.2
|
19.4
|
1.0
|
CG
|
C:HIS404
|
4.2
|
25.1
|
1.0
|
ND1
|
C:HIS404
|
4.2
|
25.9
|
1.0
|
CG
|
C:HIS406
|
4.2
|
20.1
|
1.0
|
CG
|
C:HIS356
|
4.2
|
18.0
|
1.0
|
OG
|
C:SER352
|
4.2
|
23.2
|
1.0
|
CD1
|
C:ILE394
|
4.3
|
18.3
|
1.0
|
C2
|
C:EDO506
|
4.4
|
39.5
|
1.0
|
O
|
C:HOH641
|
4.7
|
29.7
|
1.0
|
CA
|
C:CYS397
|
4.8
|
24.7
|
1.0
|
C1
|
C:EDO506
|
4.8
|
42.1
|
1.0
|
CB
|
C:LYS399
|
4.8
|
31.7
|
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 02:41:08 2024
|