Atomistry » Fluorine » PDB 5vd4-5vsr » 5vrl
Atomistry »
  Fluorine »
    PDB 5vd4-5vsr »
      5vrl »

Fluorine in PDB 5vrl: Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333.

Enzymatic activity of Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333.

All present enzymatic activity of Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333.:
1.3.1.9;

Protein crystallography data

The structure of Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333., PDB code: 5vrl was solved by J.Abendroth, T.E.Edwards, D.Lorimer, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 41.90 / 2.65
Space group I 41 2 2
Cell size a, b, c (Å), α, β, γ (°) 94.080, 94.080, 184.430, 90.00, 90.00, 90.00
R / Rfree (%) 17.2 / 19.8

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333. (pdb code 5vrl). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333., PDB code: 5vrl:
Jump to Fluorine binding site number: 1; 2; 3;

Fluorine binding site 1 out of 3 in 5vrl

Go back to Fluorine Binding Sites List in 5vrl
Fluorine binding site 1 out of 3 in the Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333.


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F300

b:48.7
occ:1.00
F25 A:9JA300 0.0 48.7 1.0
C24 A:9JA300 1.3 50.1 1.0
F26 A:9JA300 2.2 58.2 1.0
F27 A:9JA300 2.2 49.6 1.0
C23 A:9JA300 2.4 43.0 1.0
C22 A:9JA300 2.8 40.9 1.0
C28 A:9JA300 3.6 40.3 1.0
CD2 A:LEU221 3.6 45.7 1.0
CD1 A:LEU221 3.7 46.7 1.0
CG2 A:ILE218 3.9 62.6 1.0
CG1 A:ILE218 4.0 66.7 1.0
CG A:LEU221 4.0 45.7 1.0
C18 A:9JA300 4.1 45.2 1.0
CB A:LEU221 4.2 44.9 1.0
CB A:ILE218 4.3 66.4 1.0
CA A:ILE218 4.3 63.3 1.0
CD1 A:ILE218 4.5 65.2 1.0
O A:PRO159 4.6 40.9 1.0
C29 A:9JA300 4.7 37.9 1.0
O A:ILE218 4.8 61.2 1.0
C17 A:9JA300 4.9 40.8 1.0
CB A:ALA160 4.9 44.1 1.0
N20 A:9JA300 5.0 49.2 1.0

Fluorine binding site 2 out of 3 in 5vrl

Go back to Fluorine Binding Sites List in 5vrl
Fluorine binding site 2 out of 3 in the Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333.


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F300

b:58.2
occ:1.00
F26 A:9JA300 0.0 58.2 1.0
C24 A:9JA300 1.3 50.1 1.0
F27 A:9JA300 2.2 49.6 1.0
F25 A:9JA300 2.2 48.7 1.0
C23 A:9JA300 2.3 43.0 1.0
C28 A:9JA300 2.7 40.3 1.0
CB A:TYR161 3.4 40.4 1.0
SD A:MET158 3.6 58.3 1.0
C22 A:9JA300 3.6 40.9 1.0
CG A:TYR161 3.8 42.3 1.0
CE2 A:PHE152 3.9 36.4 1.0
CD1 A:LEU221 3.9 46.7 1.0
O A:PRO159 3.9 40.9 1.0
CD1 A:TYR161 3.9 45.7 1.0
C29 A:9JA300 4.1 37.9 1.0
CG A:MET158 4.2 47.9 1.0
N A:TYR161 4.3 38.4 1.0
CA A:TYR161 4.3 42.2 1.0
CZ A:PHE152 4.4 33.8 1.0
CD2 A:LEU221 4.5 45.7 1.0
CD2 A:TYR161 4.6 39.9 1.0
CD2 A:PHE152 4.7 35.2 1.0
C18 A:9JA300 4.7 45.2 1.0
CG A:LEU221 4.8 45.7 1.0
CE1 A:TYR161 4.9 46.2 1.0
C17 A:9JA300 4.9 40.8 1.0

Fluorine binding site 3 out of 3 in 5vrl

Go back to Fluorine Binding Sites List in 5vrl
Fluorine binding site 3 out of 3 in the Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333.


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 3 of Crystal Structure of the Inha From Mycobacterium Tuberculosis in Complex with AN12855, Ebsi 4333. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F300

b:49.6
occ:1.00
F27 A:9JA300 0.0 49.6 1.0
C24 A:9JA300 1.3 50.1 1.0
F26 A:9JA300 2.2 58.2 1.0
F25 A:9JA300 2.2 48.7 1.0
C23 A:9JA300 2.3 43.0 1.0
C22 A:9JA300 3.2 40.9 1.0
C28 A:9JA300 3.2 40.3 1.0
N A:TYR161 3.8 38.4 1.0
CE A:MET202 3.8 43.6 1.0
CD1 A:TYR161 3.8 45.7 1.0
CB A:ALA160 3.9 44.1 1.0
CB A:TYR161 3.9 40.4 1.0
CA A:TYR161 4.0 42.2 1.0
CD1 A:ILE218 4.1 65.2 1.0
O A:PRO159 4.1 40.9 1.0
CG1 A:ILE218 4.2 66.7 1.0
CG A:TYR161 4.2 42.3 1.0
C A:ALA160 4.3 43.5 1.0
C18 A:9JA300 4.4 45.2 1.0
C29 A:9JA300 4.4 37.9 1.0
CA A:ALA160 4.7 46.6 1.0
CE1 A:TYR161 4.8 46.2 1.0
CG2 A:ILE218 4.9 62.6 1.0
C17 A:9JA300 4.9 40.8 1.0
O A:ALA160 5.0 43.4 1.0

Reference:

Y.Xia, Y.Zhou, D.S.Carter, M.B.Mcneil, W.Choi, J.Halladay, P.W.Berry, W.Mao, V.Hernandez, T.O'malley, A.Korkegian, B.Sunde, L.Flint, L.K.Woolhiser, M.S.Scherman, V.Gruppo, C.Hastings, G.T.Robertson, T.R.Ioerger, J.Sacchettini, P.J.Tonge, A.J.Lenaerts, T.Parish, M.Alley. Discovery of A Cofactor-Independent Inhibitor Ofmycobacterium Tuberculosisinha. Life Sci Alliance V. 1 00025 2018.
ISSN: ESSN 2575-1077
PubMed: 30456352
DOI: 10.26508/LSA.201800025
Page generated: Thu Aug 1 16:16:07 2024

Last articles

Zn in 9MJ5
Zn in 9HNW
Zn in 9G0L
Zn in 9FNE
Zn in 9DZN
Zn in 9E0I
Zn in 9D32
Zn in 9DAK
Zn in 8ZXC
Zn in 8ZUF
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy