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Zinc in PDB 4buz: SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad

Protein crystallography data

The structure of SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad, PDB code: 4buz was solved by M.Weyand, M.Lakshminarasimhan, M.Gertz, C.Steegborn, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.32 / 1.90
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 46.750, 59.920, 109.030, 90.00, 90.00, 90.00
R / Rfree (%) 15.93 / 19.357

Other elements in 4buz:

The structure of SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad also contains other interesting chemical elements:

Chlorine (Cl) 1 atom

Zinc Binding Sites:

The binding sites of Zinc atom in the SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad (pdb code 4buz). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad, PDB code: 4buz:

Zinc binding site 1 out of 1 in 4buz

Go back to Zinc Binding Sites List in 4buz
Zinc binding site 1 out of 1 in the SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of SIR2 Complex Structure Mixture of Ex-527 Inhibitor and Reaction Products or of Reaction Substrates P53 Peptide and Nad within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn1250

b:37.2
occ:1.00
SG A:CYS148 2.3 31.8 1.0
SG A:CYS127 2.3 40.9 1.0
SG A:CYS124 2.3 32.2 1.0
SG A:CYS151 2.4 37.6 1.0
CB A:CYS124 3.0 27.5 1.0
CB A:CYS148 3.2 31.2 1.0
CB A:CYS127 3.5 39.0 1.0
CB A:CYS151 3.7 40.7 1.0
N A:CYS127 3.8 32.6 1.0
N A:CYS151 3.9 42.8 1.0
CA A:CYS127 4.2 35.4 1.0
CA A:CYS151 4.3 41.4 1.0
CB A:ASP150 4.5 46.1 1.0
CA A:CYS124 4.5 23.2 1.0
CA A:CYS148 4.7 30.1 1.0
C A:CYS127 4.7 35.2 1.0
CB A:LYS129 4.7 36.3 1.0
CB A:ARG126 4.7 33.4 1.0
N A:GLU128 4.8 33.0 1.0
C A:CYS151 4.8 40.3 1.0
CB A:SER153 4.8 33.3 1.0
C A:ASP150 4.9 46.0 1.0
C A:ARG126 4.9 34.0 1.0
N A:SER153 4.9 35.0 1.0
N A:ASN152 4.9 38.1 1.0
N A:ASP150 5.0 44.2 1.0

Reference:

M.Gertz, F.Fischer, G.T.T.Nguyen, M.Lakshminarasimhan, M.Schutkowski, M.Weyand, C.Steegborn. Ex-527 Inhibits Sirtuins By Exploiting Their Unique Nad+-Dependent Deacetylation Mechanism Proc.Natl.Acad.Sci.Usa V. 110 E2772 2013.
ISSN: ISSN 0027-8424
PubMed: 23840057
DOI: 10.1073/PNAS.1303628110
Page generated: Sat Oct 26 20:05:41 2024

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