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Fluorine in PDB 2dqt: High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog

Protein crystallography data

The structure of High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog, PDB code: 2dqt was solved by O.Kristensen, D.G.Vassylyev, F.Tanaka, N.Ito, K.Morikawa, I.Fujii, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 6.00 / 1.80
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 55.906, 61.662, 66.673, 90.00, 104.68, 90.00
R / Rfree (%) 18.7 / 24.6

Other elements in 2dqt:

The structure of High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms

Fluorine Binding Sites:

The binding sites of Fluorine atom in the High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog (pdb code 2dqt). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog, PDB code: 2dqt:
Jump to Fluorine binding site number: 1; 2; 3;

Fluorine binding site 1 out of 3 in 2dqt

Go back to Fluorine Binding Sites List in 2dqt
Fluorine binding site 1 out of 3 in the High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog within 5.0Å range:
probe atom residue distance (Å) B Occ
H:F501

b:18.8
occ:1.00
F1 H:CPD501 0.0 18.8 1.0
C20 H:CPD501 1.4 18.8 1.0
F3 H:CPD501 2.2 15.8 1.0
F2 H:CPD501 2.2 20.9 1.0
C19 H:CPD501 2.4 13.5 1.0
O8 H:CPD501 3.0 15.2 1.0
N3 H:CPD501 3.3 12.5 1.0
CG1 H:VAL95 3.4 13.6 1.0
CD1 H:TRP100I 3.7 16.1 1.0
O3 H:CPD501 3.8 18.6 1.0
CG2 H:VAL95 4.1 9.4 1.0
CE1 H:PHE100K 4.2 18.6 1.0
CB H:VAL95 4.3 9.7 1.0
OG H:SER50 4.3 6.8 1.0
CG H:TRP100I 4.4 14.1 1.0
CB H:TRP100I 4.4 10.0 1.0
CZ H:PHE100K 4.6 8.1 1.0
NE1 H:TRP100I 4.6 14.7 1.0
C18 H:CPD501 4.6 12.3 1.0
N2 H:CPD501 4.7 14.8 1.0
CD1 H:PHE100K 4.9 9.7 1.0
C10 H:CPD501 4.9 13.6 1.0
C H:TRP100I 4.9 16.1 1.0
N H:TYR100J 5.0 14.1 1.0

Fluorine binding site 2 out of 3 in 2dqt

Go back to Fluorine Binding Sites List in 2dqt
Fluorine binding site 2 out of 3 in the High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog within 5.0Å range:
probe atom residue distance (Å) B Occ
H:F501

b:20.9
occ:1.00
F2 H:CPD501 0.0 20.9 1.0
C20 H:CPD501 1.4 18.8 1.0
F1 H:CPD501 2.2 18.8 1.0
F3 H:CPD501 2.2 15.8 1.0
C19 H:CPD501 2.4 13.5 1.0
O8 H:CPD501 2.8 15.2 1.0
CZ H:PHE100K 3.4 8.1 1.0
N3 H:CPD501 3.5 12.5 1.0
OG H:SER50 3.6 6.8 1.0
CE1 H:PHE100K 3.6 18.6 1.0
NE1 H:TRP47 3.7 5.8 1.0
CG L:PRO96 3.8 10.2 1.0
CD1 H:TRP47 3.8 9.7 1.0
CZ L:PHE89 4.0 22.1 1.0
CB L:PRO96 4.1 10.3 1.0
CE2 H:PHE100K 4.4 6.4 1.0
CE2 H:TRP47 4.6 4.1 1.0
CG H:TRP47 4.7 10.8 1.0
CD1 H:PHE100K 4.7 9.7 1.0
OG H:SER35 4.8 16.3 1.0
CE1 L:PHE89 4.8 15.3 1.0
C18 H:CPD501 4.9 12.3 1.0
CE2 L:PHE89 4.9 13.9 1.0
CB H:SER50 4.9 1.2 1.0

Fluorine binding site 3 out of 3 in 2dqt

Go back to Fluorine Binding Sites List in 2dqt
Fluorine binding site 3 out of 3 in the High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 3 of High Resolution Crystal Structure of the Complex of the Hydrolytic Antibody Fab 6D9 and A Transition-State Analog within 5.0Å range:
probe atom residue distance (Å) B Occ
H:F501

b:15.8
occ:1.00
F3 H:CPD501 0.0 15.8 1.0
C20 H:CPD501 1.4 18.8 1.0
F1 H:CPD501 2.2 18.8 1.0
F2 H:CPD501 2.2 20.9 1.0
C19 H:CPD501 2.4 13.5 1.0
N3 H:CPD501 2.7 12.5 1.0
CD1 H:TRP100I 3.5 16.1 1.0
O8 H:CPD501 3.5 15.2 1.0
CA L:GLY91 3.7 10.7 1.0
CZ L:PHE89 3.7 22.1 1.0
O L:GLY91 3.8 14.8 1.0
NE1 H:TRP100I 3.9 14.7 1.0
CE1 L:PHE89 4.0 15.3 1.0
O L:HOH215 4.0 12.3 1.0
CG L:PRO96 4.0 10.2 1.0
C18 H:CPD501 4.1 12.3 1.0
CB L:PRO96 4.2 10.3 1.0
C L:GLY91 4.2 14.3 1.0
CG H:TRP100I 4.7 14.1 1.0
C17 H:CPD501 4.7 9.3 1.0
CZ H:PHE100K 4.8 8.1 1.0
N L:GLY91 4.9 10.1 1.0
CE2 L:PHE89 4.9 13.9 1.0

Reference:

M.Oda, N.Ito, T.Tsumuraya, K.Suzuki, M.Sakakura, I.Fujii. Thermodynamic and Structural Basis For Transition-State Stabilization in Antibody-Catalyzed Hydrolysis J.Mol.Biol. V. 369 198 2007.
ISSN: ISSN 0022-2836
PubMed: 17428500
DOI: 10.1016/J.JMB.2007.03.023
Page generated: Sun Dec 13 11:35:34 2020

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