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Magnesium in PDB 3ijq: Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding.

Protein crystallography data

The structure of Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding., PDB code: 3ijq was solved by A.A.Fedorov, E.V.Fedorov, T.Lukk, J.A.Gerlt, S.C.Almo, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 24.93 / 2.00
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 141.710, 99.865, 60.851, 90.00, 90.32, 90.00
R / Rfree (%) 24.7 / 28.7

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding. (pdb code 3ijq). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding., PDB code: 3ijq:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 3ijq

Go back to Magnesium Binding Sites List in 3ijq
Magnesium binding site 1 out of 2 in the Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding.


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg386

b:53.4
occ:1.00
O A:HOH387 2.0 49.5 1.0
OE1 A:GLU251 2.0 43.4 1.0
OD2 A:ASP276 2.1 54.1 1.0
OD2 A:ASP224 2.3 61.3 1.0
CD A:GLU251 3.1 47.3 1.0
CG A:ASP276 3.2 54.3 1.0
CG A:ASP224 3.3 59.5 1.0
O A:DGL385 3.3 52.2 1.0
OXT A:DGL385 3.6 55.7 1.0
OD1 A:ASP224 3.6 59.3 1.0
O A:HOH446 3.6 45.1 1.0
NZ A:LYS298 3.8 47.5 1.0
C A:DGL385 3.8 51.9 1.0
OE2 A:GLU251 3.9 45.7 1.0
CB A:ASP276 3.9 55.0 1.0
CG A:GLU251 4.1 50.0 1.0
OE2 A:GLU277 4.1 58.7 1.0
OD1 A:ASP276 4.2 53.5 1.0
OD1 A:ASN226 4.3 65.8 1.0
NZ A:LYS198 4.5 43.9 1.0
CB A:ASP224 4.6 58.8 1.0
ND2 A:ASN296 4.7 55.1 1.0
OE1 A:GLU277 4.9 58.5 1.0
CD A:GLU277 4.9 60.1 1.0

Magnesium binding site 2 out of 2 in 3ijq

Go back to Magnesium Binding Sites List in 3ijq
Magnesium binding site 2 out of 2 in the Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding.


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Structure of Dipeptide Epimerase From Bacteroides Thetaiotaomicron Complexed with L-Ala-D-Glu; Productive Substrate Binding. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg386

b:37.9
occ:1.00
O B:HOH388 1.7 28.9 1.0
OD2 B:ASP276 2.1 38.0 1.0
OE1 B:GLU251 2.1 39.8 1.0
OXT B:DGL385 2.4 40.0 1.0
OD2 B:ASP224 2.5 46.9 1.0
O B:DGL385 2.7 35.5 1.0
C B:DGL385 2.9 38.8 1.0
CD B:GLU251 3.1 41.3 1.0
CG B:ASP276 3.3 34.7 1.0
CG B:ASP224 3.3 50.1 1.0
NZ B:LYS298 3.5 36.5 1.0
OD1 B:ASP224 3.5 50.4 1.0
OE2 B:GLU251 3.8 40.2 1.0
CB B:ASP276 4.0 35.4 1.0
CG B:GLU251 4.1 42.2 1.0
OD1 B:ASP276 4.2 34.7 1.0
NZ B:LYS198 4.3 37.9 1.0
CA B:DGL385 4.4 35.9 1.0
ND2 B:ASN296 4.4 39.3 1.0
OE1 B:GLU277 4.4 45.6 1.0
CE B:LYS298 4.4 30.9 1.0
OE2 B:GLU277 4.5 48.9 1.0
CB B:ASP224 4.5 50.1 1.0
ND2 B:ASN226 4.7 68.2 1.0
O B:HOH405 4.8 31.2 1.0
CD B:GLU277 4.9 48.7 1.0

Reference:

T.Lukk, A.Sakai, C.Kalyanaraman, S.D.Brown, H.J.Imker, L.Song, A.A.Fedorov, E.V.Fedorov, R.Toro, B.Hillerich, R.Seidel, Y.Patskovsky, M.W.Vetting, S.K.Nair, P.C.Babbitt, S.C.Almo, J.A.Gerlt, M.P.Jacobson. Homology Models Guide Discovery of Diverse Enzyme Specificities Among Dipeptide Epimerases in the Enolase Superfamily. Proc.Natl.Acad.Sci.Usa V. 109 4122 2012.
ISSN: ISSN 0027-8424
PubMed: 22392983
DOI: 10.1073/PNAS.1112081109
Page generated: Wed Aug 14 16:09:54 2024

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