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Zinc in PDB 4s2t: Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site

Protein crystallography data

The structure of Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site, PDB code: 4s2t was solved by S.Iyer, P.La-Borde, K.A.P.Payne, M.R.Parsons, A.J.Turner, R.E.Isaac, K.R.Acharya, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 38.52 / 2.15
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 140.590, 86.810, 113.130, 90.00, 115.96, 90.00
R / Rfree (%) 20.5 / 24.7

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site (pdb code 4s2t). 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 X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site, PDB code: 4s2t:
Jump to Zinc binding site number: 1; 2; 3; 4;

Zinc binding site 1 out of 4 in 4s2t

Go back to Zinc Binding Sites List in 4s2t
Zinc binding site 1 out of 4 in the Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site


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 X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site within 5.0Å range:
probe atom residue distance (Å) B Occ
P:Zn701

b:47.5
occ:1.00
OD1 P:ASP424 2.1 36.5 1.0
OE1 P:GLU536 2.1 32.6 1.0
O2 A:01B1 2.2 39.7 0.5
OD1 P:ASP413 2.3 27.4 1.0
N2 A:01B1 2.7 46.0 0.5
OD2 P:ASP413 2.7 28.5 1.0
CG P:ASP413 2.8 26.7 1.0
CG P:ASP424 2.9 32.5 1.0
CD P:GLU536 3.0 30.6 1.0
ZN P:ZN702 3.0 55.2 1.0
OD2 P:ASP424 3.1 35.2 1.0
C2 A:01B1 3.2 43.1 0.5
OE2 P:GLU536 3.2 31.1 1.0
C1 A:01B1 3.4 45.2 0.5
OG1 P:THR426 3.5 23.6 1.0
CZ P:PHE378 3.7 30.6 1.0
OE1 P:GLU522 4.0 36.6 1.0
CB P:ASP413 4.3 27.3 1.0
CE1 P:PHE378 4.3 30.8 1.0
CB P:ASP424 4.3 30.2 1.0
CE2 P:PHE378 4.4 29.6 1.0
CG P:GLU536 4.4 27.8 1.0
N P:VAL425 4.4 27.6 1.0
C3 A:01B1 4.5 41.9 0.5
C12 A:01B1 4.5 44.8 0.5
O P:VAL425 4.6 25.4 1.0
C P:ASP424 4.7 27.9 1.0
C P:VAL425 4.7 25.2 1.0
CA P:ASP424 4.8 27.1 1.0
C6 A:01B1 4.8 46.0 0.5
C7 A:01B1 4.8 46.2 0.5
CD P:GLU522 4.9 32.2 1.0
CB P:THR426 4.9 22.7 1.0
CB P:GLU536 4.9 26.5 1.0
CA P:ASP413 4.9 25.6 1.0

Zinc binding site 2 out of 4 in 4s2t

Go back to Zinc Binding Sites List in 4s2t
Zinc binding site 2 out of 4 in the Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site


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 X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site within 5.0Å range:
probe atom residue distance (Å) B Occ
P:Zn702

b:55.2
occ:1.00
O2 A:01B1 2.0 39.7 0.5
OE2 P:GLU536 2.0 31.1 1.0
OD2 P:ASP424 2.2 35.2 1.0
NE2 P:HIS487 2.6 28.5 1.0
OE2 P:GLU522 2.7 33.3 1.0
C2 A:01B1 2.7 43.1 0.5
C1 A:01B1 2.8 45.2 0.5
ZN P:ZN701 3.0 47.5 1.0
CD P:GLU536 3.1 30.6 1.0
O3 A:01B1 3.1 44.6 0.5
OE1 P:GLU522 3.1 36.6 1.0
N2 A:01B1 3.1 46.0 0.5
C3 A:01B1 3.1 41.9 0.5
CG P:ASP424 3.2 32.5 1.0
CD P:GLU522 3.2 32.2 1.0
OE1 P:GLU536 3.4 32.6 1.0
CE1 P:HIS487 3.4 29.2 1.0
CD2 P:HIS487 3.6 27.7 1.0
OD1 P:ASP424 3.6 36.5 1.0
CG2 P:THR520 4.1 27.4 1.0
OG1 P:THR520 4.2 28.5 1.0
N A:PRO2 4.2 39.4 0.5
C6 A:01B1 4.3 46.0 0.5
CB P:ASP424 4.4 30.2 1.0
CG P:GLU536 4.4 27.8 1.0
CB P:THR520 4.4 25.6 1.0
NE2 P:HIS496 4.5 47.2 1.0
CG P:GLU522 4.6 27.6 1.0
ND1 P:HIS487 4.6 28.5 1.0
CG P:HIS487 4.7 28.1 1.0
CD2 P:HIS496 4.9 45.5 1.0

Zinc binding site 3 out of 4 in 4s2t

Go back to Zinc Binding Sites List in 4s2t
Zinc binding site 3 out of 4 in the Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site


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 X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site within 5.0Å range:
probe atom residue distance (Å) B Occ
Q:Zn701

b:48.9
occ:1.00
OE1 Q:GLU536 2.1 25.9 1.0
OD1 Q:ASP424 2.1 31.3 1.0
O2 B:01B1 2.1 40.4 0.5
OD1 Q:ASP413 2.2 26.6 1.0
OD2 Q:ASP413 2.7 24.5 1.0
CG Q:ASP413 2.8 24.6 1.0
CG Q:ASP424 2.9 29.1 1.0
N2 B:01B1 2.9 43.2 0.5
CD Q:GLU536 3.0 24.7 1.0
ZN Q:ZN702 3.1 48.2 1.0
OD2 Q:ASP424 3.1 29.4 1.0
OE2 Q:GLU536 3.2 24.4 1.0
C2 B:01B1 3.2 41.5 0.5
OG1 Q:THR426 3.5 22.4 1.0
C1 B:01B1 3.6 43.3 0.5
CZ Q:PHE378 3.7 30.0 1.0
OE1 Q:GLU522 4.0 38.9 1.0
CB Q:ASP413 4.3 24.5 1.0
CB Q:ASP424 4.3 27.3 1.0
CE1 Q:PHE378 4.3 31.2 1.0
N Q:VAL425 4.4 25.6 1.0
CG Q:GLU536 4.4 23.6 1.0
CE2 Q:PHE378 4.4 30.4 1.0
C3 B:01B1 4.5 38.3 0.5
O Q:VAL425 4.5 21.7 1.0
C12 B:01B1 4.6 52.5 0.5
C Q:ASP424 4.6 27.1 1.0
C Q:VAL425 4.6 24.3 1.0
CA Q:ASP424 4.7 25.8 1.0
CB Q:THR426 4.8 23.8 1.0
CA Q:ASP413 4.9 23.6 1.0
CB Q:GLU536 4.9 22.9 1.0
CD Q:GLU522 4.9 32.3 1.0
N Q:SER414 4.9 23.6 1.0
C6 B:01B1 4.9 48.2 0.5
CA Q:VAL425 5.0 25.1 1.0
N Q:THR426 5.0 23.6 1.0
C7 B:01B1 5.0 51.3 0.5
CD B:PRO2 5.0 32.0 0.5

Zinc binding site 4 out of 4 in 4s2t

Go back to Zinc Binding Sites List in 4s2t
Zinc binding site 4 out of 4 in the Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site


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 X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site within 5.0Å range:
probe atom residue distance (Å) B Occ
Q:Zn702

b:48.2
occ:1.00
O2 B:01B1 2.0 40.4 0.5
OE2 Q:GLU536 2.1 24.4 1.0
OD2 Q:ASP424 2.1 29.4 1.0
NE2 Q:HIS487 2.5 26.8 1.0
OE2 Q:GLU522 2.7 37.1 1.0
C2 B:01B1 2.7 41.5 0.5
C1 B:01B1 2.9 43.3 0.5
O3 B:01B1 3.1 40.4 0.5
C3 B:01B1 3.1 38.3 0.5
ZN Q:ZN701 3.1 48.9 1.0
CG Q:ASP424 3.1 29.1 1.0
CD Q:GLU536 3.1 24.7 1.0
OE1 Q:GLU522 3.2 38.9 1.0
N2 B:01B1 3.2 43.2 0.5
CD Q:GLU522 3.3 32.3 1.0
CE1 Q:HIS487 3.3 27.8 1.0
OE1 Q:GLU536 3.5 25.9 1.0
OD1 Q:ASP424 3.5 31.3 1.0
CD2 Q:HIS487 3.6 26.2 1.0
CG2 Q:THR520 4.0 23.7 1.0
N B:PRO2 4.1 33.2 0.5
OG1 Q:THR520 4.2 25.1 1.0
CB Q:ASP424 4.3 27.3 1.0
C6 B:01B1 4.4 48.2 0.5
CB Q:THR520 4.4 23.5 1.0
NE2 Q:HIS496 4.4 45.4 1.0
CG Q:GLU536 4.4 23.6 1.0
ND1 Q:HIS487 4.5 28.1 1.0
CG Q:HIS487 4.6 25.2 1.0
CG Q:GLU522 4.6 28.1 1.0
CD2 Q:HIS496 4.8 44.4 1.0
CD B:PRO2 4.8 32.0 0.5

Reference:

S.Iyer, P.J.La-Borde, K.A.Payne, M.R.Parsons, A.J.Turner, R.E.Isaac, K.R.Acharya. Crystal Structure of X-Prolyl Aminopeptidase From Caenorhabditis Elegans: A Cytosolic Enzyme with A Di-Nuclear Active Site. Febs Open Bio V. 5 292 2015.
ISSN: ESSN 2211-5463
PubMed: 25905034
DOI: 10.1016/J.FOB.2015.03.013
Page generated: Sun Oct 27 08:23:04 2024

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