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Calcium in PDB 3svw: Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex

Enzymatic activity of Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex

All present enzymatic activity of Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex:
1.4.99.3;

Protein crystallography data

The structure of Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex, PDB code: 3svw was solved by L.M.R.Jensen, C.M.Wilmot, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 33.89 / 1.86
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 55.606, 89.001, 104.812, 67.05, 79.51, 79.72
R / Rfree (%) 13.1 / 17.4

Other elements in 3svw:

The structure of Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex also contains other interesting chemical elements:

Iron (Fe) 4 atoms
Sodium (Na) 4 atoms

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex (pdb code 3svw). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex, PDB code: 3svw:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 3svw

Go back to Calcium Binding Sites List in 3svw
Calcium binding site 1 out of 2 in the Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca400

b:17.4
occ:1.00
O A:HOH386 2.2 10.2 1.0
O A:PRO277 2.3 15.2 1.0
O A:HOH394 2.3 12.9 1.0
O A:THR275 2.4 15.3 1.0
O A:HOH379 2.5 9.0 1.0
OD1 A:ASN66 2.5 17.2 1.0
O A:HOH378 2.6 15.3 1.0
C A:PRO277 3.5 15.4 1.0
CG A:ASN66 3.6 16.2 1.0
C A:THR275 3.6 14.8 1.0
ND2 A:ASN66 4.0 16.5 1.0
O A:HOH2279 4.1 32.9 1.0
C A:GLY276 4.1 16.7 1.0
N A:PRO277 4.2 17.2 1.0
O A:HOH420 4.3 12.4 1.0
CA A:GLY276 4.3 15.8 1.0
CA A:TYR278 4.3 15.4 1.0
O A:THR67 4.4 14.0 1.0
N A:TYR278 4.4 14.4 1.0
CB A:THR275 4.4 13.9 1.0
N A:GLY276 4.4 16.0 1.0
OG1 A:THR275 4.4 14.5 1.0
O1A A:HEC600 4.5 14.6 1.0
CA A:PRO277 4.5 16.8 1.0
O A:GLY276 4.5 17.2 1.0
O2A A:HEC600 4.6 14.1 1.0
CA A:THR275 4.6 14.2 1.0
CD2 A:TYR278 4.7 14.8 1.0
O A:HOH396 4.7 10.3 1.0
O A:HOH456 4.7 22.8 1.0
CD A:PRO277 4.8 18.6 1.0
CB A:ASN66 4.8 12.4 1.0
CGA A:HEC600 4.9 14.8 1.0

Calcium binding site 2 out of 2 in 3svw

Go back to Calcium Binding Sites List in 3svw
Calcium binding site 2 out of 2 in the Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Crystal Structure of the P107V-Maug/Pre-Methylamine Dehydrogenase Complex within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca400

b:13.0
occ:1.00
OD1 B:ASN66 2.4 14.0 1.0
O B:HOH385 2.4 8.9 1.0
O B:PRO277 2.4 12.1 1.0
O B:THR275 2.4 13.3 1.0
O B:HOH403 2.4 6.7 1.0
O B:HOH414 2.4 7.4 1.0
O B:HOH443 2.5 9.4 1.0
CG B:ASN66 3.4 15.3 1.0
C B:PRO277 3.6 13.1 1.0
C B:THR275 3.6 14.1 1.0
ND2 B:ASN66 3.9 12.2 1.0
C B:GLY276 4.1 14.4 1.0
CA B:GLY276 4.3 14.0 1.0
N B:PRO277 4.3 13.6 1.0
O B:THR67 4.3 12.8 1.0
O B:HOH432 4.4 11.4 1.0
OG1 B:THR275 4.4 13.1 1.0
CA B:TYR278 4.4 11.5 1.0
CB B:THR275 4.4 14.1 1.0
N B:GLY276 4.4 14.6 1.0
N B:TYR278 4.5 12.9 1.0
O1A B:HEC600 4.5 10.1 1.0
O B:GLY276 4.5 14.4 1.0
CA B:PRO277 4.6 13.3 1.0
O B:HOH475 4.6 9.4 1.0
CB B:ASN66 4.7 11.3 1.0
CA B:THR275 4.7 15.1 1.0
O2A B:HEC600 4.7 11.8 1.0
CD2 B:TYR278 4.8 14.2 1.0
CD B:PRO277 4.9 13.5 1.0
O B:HOH419 4.9 12.8 1.0

Reference:

M.Feng, L.M.Jensen, E.T.Yukl, X.Wei, A.Liu, C.M.Wilmot, V.L.Davidson. Proline 107 Is A Major Determinant in Maintaining the Structure of the Distal Pocket and Reactivity of the High-Spin Heme of Maug. Biochemistry V. 51 1598 2012.
ISSN: ISSN 0006-2960
PubMed: 22299652
DOI: 10.1021/BI201882E
Page generated: Tue Jul 8 16:46:46 2025

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