Atomistry » Zinc » PDB 4mhy-4mtd » 4msq
Atomistry »
  Zinc »
    PDB 4mhy-4mtd »
      4msq »

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

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy