Zinc in PDB 8rla: RECQL5:Sfgfp Hetero Dimer Assembled By Di-Gluebody - RECQL5 Local Refinement

All present enzymatic activity of RECQL5:Sfgfp Hetero Dimer Assembled By Di-Gluebody - RECQL5 Local Refinement:
3.6.4.12;

The binding sites of Zinc atom in the RECQL5:Sfgfp Hetero Dimer Assembled By Di-Gluebody - RECQL5 Local Refinement (pdb code 8rla). 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 RECQL5:Sfgfp Hetero Dimer Assembled By Di-Gluebody - RECQL5 Local Refinement, PDB code: 8rla:

Zinc binding site 1 out of 1 in the RECQL5:Sfgfp Hetero Dimer Assembled By Di-Gluebody - RECQL5 Local Refinement


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of RECQL5:Sfgfp Hetero Dimer Assembled By Di-Gluebody - RECQL5 Local Refinement within 5.0Å range: probe atom residue distance (Å) B Occ A:Zn501 b:89.1 occ:1.00 SG A:CYS411 2.3 93.5 1.0 SG A:CYS434 2.3 74.0 1.0 SG A:CYS427 2.3 111.0 1.0 SG A:CYS431 2.3 94.3 1.0 HB3 A:CYS431 2.7 92.1 1.0 HB2 A:CYS431 2.7 91.1 1.0 CB A:CYS431 2.7 88.9 1.0 HB2 A:CYS411 3.0 85.8 1.0 CB A:CYS411 3.2 84.5 1.0 HA A:CYS411 3.4 85.5 1.0 HB2 A:CYS434 3.6 89.4 1.0 HB2 A:HIS413 3.7 78.4 1.0 H A:CYS434 3.7 90.3 1.0 CB A:CYS434 3.7 87.0 1.0 CA A:CYS411 3.8 83.6 1.0 H A:HIS413 4.0 77.3 1.0 H A:ARG412 4.0 78.0 1.0 HB3 A:CYS411 4.0 85.0 1.0 CB A:CYS427 4.1 105.2 1.0 CA A:CYS431 4.3 89.1 1.0 ND1 A:HIS413 4.3 77.7 1.0 HB3 A:CYS434 4.3 89.7 1.0 C A:CYS411 4.4 83.1 1.0 N A:ARG412 4.4 78.7 1.0 N A:CYS434 4.4 95.6 1.0 O A:CYS427 4.4 106.9 1.0 HB2 A:CYS427 4.4 101.7 1.0 H A:ALA414 4.5 74.6 1.0 HB3 A:CYS427 4.5 101.2 1.0 HB3 A:HIS433 4.5 90.3 1.0 CB A:HIS413 4.6 82.0 1.0 H A:CYS427 4.6 100.5 1.0 HA A:CYS431 4.6 90.9 1.0 N A:HIS413 4.7 71.0 1.0 CA A:CYS434 4.7 94.1 1.0 CG A:HIS413 4.9 80.2 1.0 C A:CYS431 5.0 91.7 1.0

G.Yi, D.Mamalis, M.Ye, L.Carrique, M.Fairhead, H.Li, K.Duerr, P.Zhang, D.B.Sauer, F.Von Delft, B.G.Davis, R.J.C.Gilbert. Di-Gluebodies: Rigid Modular Nanobody Protein Assemblies Enabling Simultaneous Determination of High-Resolution Cryo-Em Structures To Be Published.