Atomistry » Zinc » PDB 1lg5-1m2j » 1p6k
Atomistry »
  Zinc »
    PDB 1lg5-1m2j »
      1p6k »

Zinc in PDB 1p6k: Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound

Enzymatic activity of Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound

All present enzymatic activity of Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound:
1.14.13.39;

Protein crystallography data

The structure of Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound, PDB code: 1p6k was solved by M.L.Flinspach, H.Li, J.Jamal, W.Yang, H.Huang, J.-M.Hah, J.A.Gomez-Vidal, E.A.Litzinger, R.B.Silverman, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.38 / 1.78
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 51.770, 109.740, 164.390, 90.00, 90.00, 90.00
R / Rfree (%) 22.5 / 25

Zinc Binding Sites:

The binding sites of Zinc atom in the Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound (pdb code 1p6k). 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 Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound, PDB code: 1p6k:

Zinc binding site 1 out of 1 in 1p6k

Go back to Zinc Binding Sites List in 1p6k
Zinc binding site 1 out of 1 in the Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Rat Neuronal Nos D597N Mutant Heme Domain with L-N(Omega)- Nitroarginine-2,4-L-Diaminobutyric Amide Bound within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn900

b:34.6
occ:1.00
SG A:CYS326 2.3 37.7 1.0
SG B:CYS326 2.3 36.6 1.0
SG A:CYS331 2.3 35.8 1.0
SG B:CYS331 2.4 36.2 1.0
CB B:CYS331 3.3 38.0 1.0
CB A:CYS331 3.3 37.5 1.0
CB A:CYS326 3.4 41.3 1.0
CB B:CYS326 3.5 40.5 1.0
CA B:CYS331 3.6 38.5 1.0
CA A:CYS331 3.6 38.1 1.0
N B:MET332 4.0 38.6 1.0
N A:MET332 4.0 38.0 1.0
N A:GLY333 4.1 37.2 1.0
C B:CYS331 4.2 38.5 1.0
N B:GLY333 4.2 37.6 1.0
C A:CYS331 4.2 38.0 1.0
CA A:GLY333 4.6 37.1 1.0
CA B:GLY333 4.6 37.4 1.0
CA A:CYS326 4.8 42.3 1.0
N B:CYS331 4.8 39.3 1.0
O B:HOH1110 4.8 45.6 1.0
CA B:CYS326 4.9 41.4 1.0
N A:CYS331 4.9 39.0 1.0
C B:MET332 5.0 38.3 1.0
C A:MET332 5.0 37.7 1.0
O A:HOH1099 5.0 46.2 1.0

Reference:

M.L.Flinspach, H.Li, J.Jamal, W.Yang, H.Huang, J.M.Hah, J.A.Gomez-Vidal, E.A.Litzinger, R.B.Silverman, T.L.Poulos. Structural Basis For Dipeptide Amide Isoform-Selective Inhibition of Neuronal Nitric Oxide Synthase. Nat.Struct.Mol.Biol. V. 11 54 2004.
ISSN: ISSN 1545-9993
PubMed: 14718923
DOI: 10.1038/NSMB704
Page generated: Fri Sep 25 22:57:32 2020
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy