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Manganese in PDB 7cj6: Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose

Protein crystallography data

The structure of Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose, PDB code: 7cj6 was solved by H.Yoshida, A.Yoshihara, S.Kamitori, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 38.29 / 1.80
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 45.75, 80.87, 139.71, 90, 90, 90
R / Rfree (%) 18.1 / 25.5

Manganese Binding Sites:

The binding sites of Manganese atom in the Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose (pdb code 7cj6). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose, PDB code: 7cj6:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 7cj6

Go back to Manganese Binding Sites List in 7cj6
Manganese binding site 1 out of 2 in the Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn301

b:24.1
occ:1.00
OE2 A:GLU246 2.0 21.3 1.0
OE2 A:GLU152 2.0 18.1 1.0
OD2 A:ASP185 2.1 19.8 1.0
ND1 A:HIS211 2.2 16.5 1.0
O2 A:PSJ302 2.2 21.2 1.0
O3 A:PSJ302 2.4 24.7 1.0
C2 A:PSJ302 2.9 22.8 1.0
C3 A:PSJ302 2.9 26.6 1.0
CD A:GLU246 3.0 20.9 1.0
CD A:GLU152 3.1 18.1 1.0
CE1 A:HIS211 3.1 17.0 1.0
CG A:HIS211 3.2 16.1 1.0
CG A:ASP185 3.2 17.0 1.0
OE1 A:GLU246 3.3 25.4 1.0
OE1 A:GLU152 3.4 20.4 1.0
CB A:HIS211 3.5 15.9 1.0
CB A:ASP185 3.8 15.1 1.0
O A:HOH533 4.0 25.1 1.0
NH2 A:ARG217 4.1 21.0 1.0
OD1 A:ASP185 4.2 17.9 1.0
NE2 A:HIS211 4.2 16.7 1.0
CD2 A:HIS211 4.3 16.5 1.0
CG A:GLU246 4.3 20.0 1.0
C1 A:PSJ302 4.3 23.1 1.0
CG A:GLU152 4.4 17.1 1.0
C4 A:PSJ302 4.4 29.4 1.0
NE2 A:HIS188 4.4 17.2 1.0
CD2 A:HIS188 4.4 17.5 1.0
O5 A:PSJ302 4.6 39.8 1.0
O1 A:PSJ302 4.7 22.7 1.0
CB A:GLU246 4.8 20.1 1.0
NE2 A:HIS183 4.8 16.8 1.0
CE1 A:HIS183 4.9 16.5 1.0

Manganese binding site 2 out of 2 in 7cj6

Go back to Manganese Binding Sites List in 7cj6
Manganese binding site 2 out of 2 in the Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Crystal Structure of Homo Dimeric D-Allulose 3-Epimerase From Methylomonas Sp. in Complex with D-Allulose within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn301

b:19.4
occ:1.00
OD2 B:ASP185 2.0 14.2 1.0
OE2 B:GLU152 2.1 18.9 1.0
O2 B:PSJ302 2.2 23.3 1.0
ND1 B:HIS211 2.2 13.4 1.0
OE1 B:GLU246 2.2 20.3 1.0
O3 B:PSJ302 2.2 18.4 1.0
C2 B:PSJ302 2.9 25.4 1.0
CD B:GLU152 3.0 19.6 1.0
C3 B:PSJ302 3.0 26.3 1.0
CD B:GLU246 3.1 20.9 1.0
CE1 B:HIS211 3.1 13.9 1.0
CG B:ASP185 3.2 16.2 1.0
CG B:HIS211 3.2 13.9 1.0
OE2 B:GLU246 3.3 23.1 1.0
OE1 B:GLU152 3.3 20.7 1.0
CB B:HIS211 3.6 14.6 1.0
CB B:ASP185 3.8 16.5 1.0
O B:HOH472 4.1 19.6 1.0
NH1 B:ARG217 4.1 19.9 1.0
OD1 B:ASP185 4.2 17.6 1.0
NE2 B:HIS211 4.2 13.4 1.0
CD2 B:HIS211 4.3 13.5 1.0
CG B:GLU152 4.4 18.9 1.0
C4 B:PSJ302 4.4 30.0 1.0
C1 B:PSJ302 4.4 25.2 1.0
CG B:GLU246 4.4 20.3 1.0
CD2 B:HIS188 4.5 16.5 1.0
NE2 B:HIS188 4.5 17.3 1.0
O5 B:PSJ302 4.5 38.0 1.0
NE2 B:HIS183 4.7 15.5 1.0
CB B:GLU246 4.8 19.7 1.0
CE1 B:HIS183 4.9 14.8 1.0
O1 B:PSJ302 4.9 24.4 1.0

Reference:

H.Yoshida, A.Yoshihara, S.Kato, S.Mochizuki, K.Akimitsu, K.Izumori, S.Kamitori. Crystal Structure of A Novel Homodimeric L-Ribulose 3-Epimerase From Methylomonus Sp. Febs Open Bio 2021.
ISSN: ESSN 2211-5463
PubMed: 33838083
DOI: 10.1002/2211-5463.13159
Page generated: Sun Oct 6 08:13:11 2024

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