Zinc in PDB 5nxp: Carbonic Anhydrase II Inhibitor RA7

All present enzymatic activity of Carbonic Anhydrase II Inhibitor RA7:
4.2.1.1;

The structure of Carbonic Anhydrase II Inhibitor RA7, PDB code: 5nxp was solved by J.Brynda, P.Rezacova, M.Horejsi, J.Fanfrlik, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	40.61 / 1.25
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	41.911, 41.040, 71.519, 90.00, 104.31, 90.00
R / Rfree (%)	12.8 / 16.2

The binding sites of Zinc atom in the Carbonic Anhydrase II Inhibitor RA7 (pdb code 5nxp). 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 Carbonic Anhydrase II Inhibitor RA7, PDB code: 5nxp:

Zinc binding site 1 out of 1 in the Carbonic Anhydrase II Inhibitor RA7


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Carbonic Anhydrase II Inhibitor RA7 within 5.0Å range: probe atom residue distance (Å) B Occ A:Zn301 b:9.3 occ:1.00 NAP A:9DH302 2.0 8.4 1.0 NE2 A:HIS96 2.0 9.4 1.0 NE2 A:HIS94 2.1 9.9 1.0 ND1 A:HIS119 2.1 8.4 1.0 CE1 A:HIS119 2.9 8.8 1.0 CD2 A:HIS94 3.0 10.2 1.0 CD2 A:HIS96 3.0 9.6 1.0 SAM A:9DH302 3.0 10.0 1.0 OAO A:9DH302 3.0 9.9 1.0 CE1 A:HIS96 3.1 10.2 1.0 CE1 A:HIS94 3.1 10.1 1.0 CG A:HIS119 3.1 8.4 1.0 CB A:HIS119 3.6 9.5 1.0 O A:HOH565 3.7 16.0 1.0 OG1 A:THR199 3.8 10.1 1.0 OE1 A:GLU106 3.9 9.7 1.0 OAN A:9DH302 4.1 10.2 1.0 NE2 A:HIS119 4.1 9.2 1.0 ND1 A:HIS94 4.2 10.5 1.0 ND1 A:HIS96 4.2 10.6 1.0 CG A:HIS94 4.2 10.9 1.0 CG A:HIS96 4.2 9.3 1.0 CAJ A:9DH302 4.2 10.6 1.0 CD2 A:HIS119 4.2 9.3 1.0 O A:HOH638 4.8 32.0 1.0 CAK A:9DH302 4.8 12.0 1.0 CD A:GLU106 4.9 9.4 1.0 CAI A:9DH302 4.9 11.3 1.0

A.Pecina, J.Brynda, L.Vrzal, R.Gnanasekaran, M.Horejsi, S.M.Eyrilmez, J.Rezac, M.Lepsik, P.Rezacova, P.Hobza, P.Majer, V.Veverka, J.Fanfrlik. Ranking Power of the Sqm/Cosmo Scoring Function on Carbonic Anhydrase II-Inhibitor Complexes. Chemphyschem V. 19 873 2018.
ISSN: ISSN 1439-7641
PubMed: 29316128
DOI: 10.1002/CPHC.201701104