Calcium in PDB 7bvh: Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose

Enzymatic activity of Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose

All present enzymatic activity of Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose:
2.4.2.34;

Protein crystallography data

The structure of Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose, PDB code: 7bvh was solved by Y.Zhao, L.Zhang, L.J.Wu, Q.Wang, J.Li, G.S.Besra, Z.H.Rao, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.67 / 3.30
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 121.080, 176.330, 207.770, 90.00, 90.00, 90.00
R / Rfree (%) 23.2 / 26.5

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose (pdb code 7bvh). 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 Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose, PDB code: 7bvh:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 7bvh

Go back to Calcium Binding Sites List in 7bvh
Calcium binding site 1 out of 2 in the Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose


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 Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca1201

b:88.5
occ:1.00
O A:ASP931 2.6 1.0 1.0
O A:HIS936 2.7 97.2 1.0
OD1 A:ASP929 2.8 0.6 1.0
OD2 A:ASP929 2.9 0.1 1.0
CG A:ASP929 3.2 0.2 1.0
C A:HIS936 3.6 94.5 1.0
C A:ASP931 3.8 0.5 1.0
OG A:SER835 3.9 0.8 1.0
CA A:TRP937 3.9 88.1 1.0
N A:TRP937 4.1 87.0 1.0
N A:ASP931 4.2 0.8 1.0
CA A:ASP931 4.4 0.4 1.0
CB A:TRP937 4.4 86.2 1.0
CD2 A:HIS936 4.5 0.4 1.0
O A:SER835 4.5 0.7 1.0
CB A:HIS936 4.6 95.5 1.0
CB A:ASP931 4.6 1.0 1.0
CB A:ASP929 4.6 0.6 1.0
CG A:HIS936 4.7 0.4 1.0
CA A:HIS936 4.7 92.5 1.0
O A:ALA933 4.8 0.9 1.0
N A:LEU932 4.9 0.4 1.0
NE2 A:GLN841 4.9 0.2 1.0

Calcium binding site 2 out of 2 in 7bvh

Go back to Calcium Binding Sites List in 7bvh
Calcium binding site 2 out of 2 in the Crystal Structure of Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose


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 Arabinosyltransferase EMBC2-ACPM2 Complex From Mycobacterium Smegmatis Complexed with Di-Arabinose within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca1201

b:0.3
occ:1.00
OD2 B:ASP929 2.5 0.2 1.0
OD1 B:ASP929 2.8 0.6 1.0
O B:ASP931 3.0 0.2 1.0
CG B:ASP929 3.0 0.2 1.0
O B:ALA933 3.2 0.6 1.0
O B:HIS936 3.5 98.6 1.0
N B:ALA933 3.7 0.4 1.0
OE1 B:GLN841 3.8 1.0 1.0
C B:ASP931 4.1 0.6 1.0
C B:ALA933 4.1 0.5 1.0
CB B:GLN841 4.4 0.2 1.0
CA B:ALA933 4.5 0.5 1.0
O B:ASP929 4.5 0.2 1.0
CB B:ASP929 4.5 0.6 1.0
CA B:LEU932 4.5 1.0 1.0
CD B:GLN841 4.6 0.8 1.0
C B:LEU932 4.6 0.9 1.0
CG B:GLN841 4.6 0.4 1.0
C B:HIS936 4.7 97.1 1.0
N B:LEU932 4.8 0.9 1.0
O B:GLN842 4.8 0.6 1.0
NE2 B:HIS936 4.9 1.0 1.0
CD2 B:HIS936 4.9 0.6 1.0

Reference:

L.Zhang, Y.Zhao, Y.Gao, L.Wu, R.Gao, Q.Zhang, Y.Wang, C.Wu, F.Wu, S.S.Gurcha, N.Veerapen, S.M.Batt, W.Zhao, L.Qin, X.Yang, M.Wang, Y.Zhu, B.Zhang, L.Bi, X.Zhang, H.Yang, L.W.Guddat, W.Xu, Q.Wang, J.Li, G.S.Besra, Z.Rao. Structures of Cell Wall Arabinosyltransferases with the Anti-Tuberculosis Drug Ethambutol Science 2020.
ISSN: ESSN 1095-9203
DOI: 10.1126/SCIENCE.ABA9102
Page generated: Sat Dec 12 08:03:15 2020

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