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Fluorine in PDB 6tiw: Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2)

Other elements in 6tiw:

The structure of Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2) also contains other interesting chemical elements:

Magnesium (Mg) 2 atoms

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2) (pdb code 6tiw). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2), PDB code: 6tiw:
Jump to Fluorine binding site number: 1; 2; 3;

Fluorine binding site 1 out of 3 in 6tiw

Go back to Fluorine Binding Sites List in 6tiw
Fluorine binding site 1 out of 3 in the Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2)


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2) within 5.0Å range:
probe atom residue distance (Å) B Occ
K:F501

b:0.0
occ:1.00
F1 K:MZK501 0.0 0.0 1.0
C16 K:MZK501 1.4 0.0 1.0
F2 K:MZK501 2.2 0.0 1.0
F3 K:MZK501 2.2 0.0 1.0
C13 K:MZK501 2.4 0.0 1.0
C14 K:MZK501 2.7 0.0 1.0
CG K:ARG355 3.3 0.7 1.0
O K:GLY296 3.5 0.7 1.0
C15 K:MZK501 3.7 0.0 1.0
CA K:GLY296 3.7 0.7 1.0
NH1 K:ARG355 3.7 0.7 1.0
CG2 K:THR300 3.8 0.8 1.0
CB K:ILE299 3.9 0.7 1.0
CZ K:ARG355 3.9 0.7 1.0
C K:GLY296 3.9 0.7 1.0
NE K:ARG355 4.1 0.7 1.0
C11 K:MZK501 4.1 0.0 1.0
CD K:ARG355 4.1 0.7 1.0
CB K:ARG355 4.2 0.7 1.0
CG2 K:ILE299 4.2 0.7 1.0
N K:THR300 4.5 0.8 1.0
NH2 K:ARG355 4.5 0.7 1.0
CG1 K:ILE299 4.6 0.7 1.0
CA K:TYR352 4.7 0.7 1.0
C12 K:MZK501 4.8 0.0 1.0
CD2 K:TYR352 4.9 0.7 1.0
N K:TYR352 4.9 0.7 1.0
C K:ILE299 4.9 0.7 1.0
C K:GLU351 5.0 0.7 1.0
C9 K:MZK501 5.0 0.0 1.0

Fluorine binding site 2 out of 3 in 6tiw

Go back to Fluorine Binding Sites List in 6tiw
Fluorine binding site 2 out of 3 in the Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2)


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2) within 5.0Å range:
probe atom residue distance (Å) B Occ
K:F501

b:0.0
occ:1.00
F2 K:MZK501 0.0 0.0 1.0
C16 K:MZK501 1.4 0.0 1.0
F1 K:MZK501 2.2 0.0 1.0
F3 K:MZK501 2.2 0.0 1.0
C13 K:MZK501 2.4 0.0 1.0
CG2 K:ILE299 2.7 0.7 1.0
CB K:ILE299 2.7 0.7 1.0
C15 K:MZK501 2.9 0.0 1.0
CD2 K:TYR352 3.0 0.7 1.0
CE2 K:TYR352 3.1 0.7 1.0
CG1 K:ILE299 3.1 0.7 1.0
CG K:ARG355 3.3 0.7 1.0
CB K:ARG355 3.4 0.7 1.0
C14 K:MZK501 3.5 0.0 1.0
CA K:TYR352 3.9 0.7 1.0
CG K:TYR352 4.0 0.7 1.0
CZ K:TYR352 4.0 0.7 1.0
O K:GLY296 4.1 0.7 1.0
CA K:GLY296 4.1 0.7 1.0
CA K:ILE299 4.2 0.7 1.0
C12 K:MZK501 4.3 0.0 1.0
CB K:TYR352 4.3 0.7 1.0
CD1 K:ILE299 4.3 0.7 1.0
O K:TYR352 4.5 0.7 1.0
C K:ILE299 4.6 0.7 1.0
CD1 K:TYR352 4.6 0.7 1.0
C K:GLY296 4.6 0.7 1.0
CE1 K:TYR352 4.6 0.7 1.0
OH K:TYR352 4.7 0.7 1.0
CD2 K:LEU295 4.7 0.7 1.0
CD K:ARG355 4.7 0.7 1.0
C11 K:MZK501 4.7 0.0 1.0
C K:TYR352 4.7 0.7 1.0
N K:THR300 4.7 0.8 1.0
N K:TYR352 4.8 0.7 1.0
CA K:ARG355 4.9 0.7 1.0
N K:ILE299 4.9 0.7 1.0
C9 K:MZK501 5.0 0.0 1.0
O K:LEU295 5.0 0.7 1.0

Fluorine binding site 3 out of 3 in 6tiw

Go back to Fluorine Binding Sites List in 6tiw
Fluorine binding site 3 out of 3 in the Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2)


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 3 of Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2) within 5.0Å range:
probe atom residue distance (Å) B Occ
K:F501

b:0.0
occ:1.00
F3 K:MZK501 0.0 0.0 1.0
C16 K:MZK501 1.4 0.0 1.0
F2 K:MZK501 2.2 0.0 1.0
F1 K:MZK501 2.2 0.0 1.0
CG K:ARG355 2.3 0.7 1.0
C13 K:MZK501 2.4 0.0 1.0
CA K:TYR352 2.6 0.7 1.0
N K:TYR352 2.9 0.7 1.0
C15 K:MZK501 3.1 0.0 1.0
C K:GLU351 3.1 0.7 1.0
CB K:ARG355 3.2 0.7 1.0
O K:GLU351 3.2 0.7 1.0
C14 K:MZK501 3.4 0.0 1.0
CD K:ARG355 3.4 0.7 1.0
CD2 K:TYR352 3.4 0.7 1.0
NE K:ARG355 3.5 0.7 1.0
CB K:TYR352 3.5 0.7 1.0
C K:TYR352 3.6 0.7 1.0
O K:TYR352 3.7 0.7 1.0
CZ K:ARG355 4.0 0.7 1.0
CB K:GLU351 4.0 0.7 1.0
CG K:TYR352 4.1 0.7 1.0
CA K:GLU351 4.2 0.7 1.0
CE2 K:TYR352 4.3 0.7 1.0
CG2 K:ILE299 4.3 0.7 1.0
NH1 K:ARG355 4.3 0.7 1.0
C12 K:MZK501 4.3 0.0 1.0
N K:ARG355 4.4 0.7 1.0
CA K:ARG355 4.4 0.7 1.0
C11 K:MZK501 4.6 0.0 1.0
NH2 K:ARG355 4.6 0.7 1.0
N K:ALA353 4.7 0.7 1.0
CB K:ILE299 4.7 0.7 1.0
O K:SER348 4.8 0.7 1.0
C9 K:MZK501 5.0 0.0 1.0

Reference:

A.Pena, A.Sweeney, A.D.Cook, M.Topf, C.A.Moores. Structure of Microtubule-Trapped Human Kinesin-5 and Its Mechanism of Inhibition Revealed Using Cryoelectron Microscopy. Structure 2020.
ISSN: ISSN 0969-2126
PubMed: 32084356
DOI: 10.1016/J.STR.2020.01.013
Page generated: Fri Aug 2 02:05:00 2024

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