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Zinc in PDB 7d1h: Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation

Enzymatic activity of Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation

All present enzymatic activity of Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation:
2.3.2.5;

Protein crystallography data

The structure of Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation, PDB code: 7d1h was solved by K.-F.Huang, J.-S.Huang, M.-L.Wu, W.-L.Hsieh, A.H.-J.Wang, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 21.41 / 1.69
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 55.534, 71.403, 80.225, 90, 90, 90
R / Rfree (%) 18.3 / 21.8

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation (pdb code 7d1h). 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 Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation, PDB code: 7d1h:

Zinc binding site 1 out of 1 in 7d1h

Go back to Zinc Binding Sites List in 7d1h
Zinc binding site 1 out of 1 in the Crystal Structure of Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation


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 Ixodes Scapularis Glutaminyl Cyclase with D238A Mutation within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn400

b:13.8
occ:1.00
O A:HOH730 1.9 24.3 1.0
OE2 A:GLU184 2.0 12.7 1.0
OD2 A:ASP144 2.0 11.7 1.0
NE2 A:HIS322 2.0 12.5 1.0
CG A:ASP144 2.8 10.8 1.0
CD A:GLU184 2.8 12.2 1.0
OE1 A:GLU184 2.9 13.4 1.0
OD1 A:ASP144 2.9 11.4 1.0
CD2 A:HIS322 2.9 13.0 1.0
CE1 A:HIS322 3.1 13.7 1.0
O A:HOH565 4.0 11.3 1.0
NE1 A:TRP321 4.0 13.6 1.0
O A:HOH800 4.1 40.0 1.0
CG A:HIS322 4.1 13.5 1.0
ND1 A:HIS322 4.1 13.5 1.0
O A:HOH658 4.2 32.9 1.0
CB A:ASP144 4.2 11.2 1.0
CG A:GLU184 4.2 12.2 1.0
OE1 A:GLU183 4.2 14.7 1.0
O A:HOH777 4.3 28.1 1.0
O A:HOH614 4.6 12.0 1.0
CD1 A:TRP321 4.7 13.3 1.0
CE2 A:TRP321 4.7 13.8 1.0
NE2 A:HIS128 4.7 11.3 1.0
CD2 A:LEU239 4.8 10.6 1.0
CE1 A:HIS128 4.9 11.4 1.0
CZ2 A:TRP321 5.0 14.5 1.0
O A:ASP144 5.0 12.2 1.0

Reference:

K.F.Huang, J.S.Huang, M.L.Wu, W.L.Hsieh, K.C.Hsu, H.L.Hsu, T.P.Ko, A.H-J Wang. A Unique Carboxylic-Acid Hydrogen-Bond Network (Cahbn) Confers Glutaminyl Cyclase Activity on M28 Family Enzymes. J.Mol.Biol. 66960 2021.
ISSN: ESSN 1089-8638
PubMed: 33774034
DOI: 10.1016/J.JMB.2021.166960
Page generated: Tue Oct 29 18:36:22 2024

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