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Calcium in PDB 5mqm: Glycoside Hydrolase BT_0986

Protein crystallography data

The structure of Glycoside Hydrolase BT_0986, PDB code: 5mqm was solved by A.Basle, D.Ndeh, A.Rogowski, A.Cartmell, A.S.Luis, I.Venditto, A.Labourel, H.J.Gilbert, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.69 / 2.11
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 64.050, 84.810, 120.630, 90.00, 99.20, 90.00
R / Rfree (%) 19.9 / 24

Calcium Binding Sites:

The binding sites of Calcium atom in the Glycoside Hydrolase BT_0986 (pdb code 5mqm). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 3 binding sites of Calcium where determined in the Glycoside Hydrolase BT_0986, PDB code: 5mqm:
Jump to Calcium binding site number: 1; 2; 3;

Calcium binding site 1 out of 3 in 5mqm

Go back to Calcium Binding Sites List in 5mqm
Calcium binding site 1 out of 3 in the Glycoside Hydrolase BT_0986


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Glycoside Hydrolase BT_0986 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca1201

b:39.8
occ:1.00
OE1 A:GLU538 2.4 26.6 1.0
OD2 A:ASP458 2.5 35.5 1.0
OE1 A:GLU593 2.5 30.1 1.0
O3 A:RPQ1204 2.5 38.6 1.0
O2 A:RPQ1204 2.5 43.5 1.0
OG A:SER459 2.6 29.4 1.0
OE1 A:GLU561 2.8 34.2 1.0
CD A:GLU593 3.4 31.0 1.0
CD A:GLU538 3.4 28.3 1.0
C2 A:RPQ1204 3.5 41.7 1.0
CG A:ASP458 3.6 34.6 1.0
C3 A:RPQ1204 3.6 39.3 1.0
CD A:GLU561 3.6 35.5 1.0
OE2 A:GLU593 3.6 32.3 1.0
OE2 A:GLU538 3.7 29.2 1.0
CB A:SER459 3.8 29.4 1.0
OE2 A:GLU561 3.9 37.5 1.0
OD1 A:ASP458 4.0 37.3 1.0
N A:SER459 4.2 30.3 1.0
O A:HOH1354 4.3 33.0 1.0
C1 A:RPQ1204 4.3 42.9 1.0
C4 A:RPQ1204 4.6 40.0 1.0
CA A:SER459 4.7 30.5 1.0
N20 A:RPQ1204 4.7 43.7 1.0
O A:HOH1454 4.7 39.0 1.0
CG A:GLU561 4.7 34.5 1.0
CB A:GLU561 4.8 32.6 1.0
CB A:ASP458 4.8 33.0 1.0
CG A:GLU538 4.8 28.5 1.0
CG A:GLU593 4.8 30.5 1.0
NZ A:LYS571 5.0 40.4 1.0

Calcium binding site 2 out of 3 in 5mqm

Go back to Calcium Binding Sites List in 5mqm
Calcium binding site 2 out of 3 in the Glycoside Hydrolase BT_0986


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Glycoside Hydrolase BT_0986 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca1202

b:35.1
occ:1.00
NH1 A:ARG793 3.3 33.2 1.0
NH1 A:ARG701 3.3 31.5 1.0
N A:MET795 3.4 32.5 1.0
CG A:ARG701 3.6 30.2 1.0
CB A:MET795 3.6 33.7 1.0
CD A:ARG701 3.6 30.6 1.0
CG A:ARG793 3.6 31.4 1.0
CB A:ARG793 3.7 31.6 1.0
CB A:ARG701 3.8 29.3 1.0
CD A:PRO794 3.8 31.0 1.0
N A:PRO794 3.9 31.6 1.0
CG A:MET795 3.9 34.5 1.0
CD A:ARG793 3.9 31.1 1.0
CA A:MET795 4.1 32.7 1.0
CB A:PRO794 4.2 31.6 1.0
CZ A:ARG701 4.3 31.1 1.0
CZ A:ARG793 4.3 31.5 1.0
NE A:ARG701 4.4 30.2 1.0
C A:PRO794 4.4 32.2 1.0
C A:ARG793 4.4 31.6 1.0
CA A:PRO794 4.4 31.5 1.0
CG A:PRO794 4.4 30.4 1.0
O A:HOH1551 4.4 25.1 1.0
NE A:ARG793 4.6 31.2 1.0
CA A:ARG793 4.6 32.6 1.0
OD2 A:ASP310 5.0 42.2 1.0

Calcium binding site 3 out of 3 in 5mqm

Go back to Calcium Binding Sites List in 5mqm
Calcium binding site 3 out of 3 in the Glycoside Hydrolase BT_0986


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 3 of Glycoside Hydrolase BT_0986 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca1203

b:59.9
occ:1.00
ND2 A:ASN796 3.9 33.6 1.0
CA A:GLY689 3.9 32.5 1.0
O A:HOH1449 4.0 40.7 1.0
CD2 A:PHE687 4.1 34.2 1.0
CD2 A:LEU802 4.1 51.1 1.0
O A:HOH1521 4.2 32.2 1.0
O A:PRO790 4.3 31.8 1.0
CD A:PRO790 4.5 33.9 1.0
CE2 A:PHE687 4.6 35.0 1.0
N A:GLY689 4.6 32.2 1.0
N A:PRO790 4.9 33.8 1.0

Reference:

D.Ndeh, A.Rogowski, A.Cartmell, A.S.Luis, A.Basle, J.Gray, I.Venditto, J.Briggs, X.Zhang, A.Labourel, N.Terrapon, F.Buffetto, S.Nepogodiev, Y.Xiao, R.A.Field, Y.Zhu, M.A.O'neill, B.R.Urbanowicz, W.S.York, G.J.Davies, D.W.Abbott, M.C.Ralet, E.C.Martens, B.Henrissat, H.J.Gilbert. Complex Pectin Metabolism By Gut Bacteria Reveals Novel Catalytic Functions. Nature V. 544 65 2017.
ISSN: ISSN 0028-0836
PubMed: 28329766
DOI: 10.1038/NATURE21725
Page generated: Mon Jul 15 08:34:26 2024

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