CYTOCHROME bc 1 : A BACTERIAL CYTOCHROME 401
Q
Site o
PDB No.(Substrate/Inhibitor)
Ar - Ar or
hydrophobic
contacts
his161 (H161)
(from ISP, [2Fe - 2S]
ligand) (
Å )
glu271 (E271) (from cyto b, EF loop) ( Å )
tyr273 (Y273) (from cyto b, EF loop) ( Å )
Q
Site i
PDB(substrate/inhibitor)
Ar - Ar or
hydrophobic
contacts
ser35 S35
(from helix A)
his201 H201(from helix D)
ser205 S205
(from helix D)
lys227 K227(from helix E)
asp228 D228(from helix E)
1NTZ(substrate
ubiquinone - 2 (UQ2)
Ar - Ar with
phe220
O
· · · H 4
O = 3.4, 2
H
O · · · H201 N 2
= 2.6 ε 2
O
· · · S205 O 4
= γ
4.0,
O
· · · S205 O 3
= γ
2.7 Å
O
· · · H 1
O = 3.6, 2
H
O · · · K227 N 2
ζ
= 3.3
O
· · · D228 O 1
δ^2
= 2.5
a
1SQX(substrate
ubiquinone - 2, UQ2)
O
· · · S35 O 1
= 4.3 γ
O
· · · H 4
O = 2.5, 2
H
O · · · H201 N 2
= 2.6 ε 2
O
· · · S205 O 3
= γ
3.5
not involved
O
· · · D228 O 1
δ^2
= 2.7
a
1PP9(substrate
ubiquinone - 10, UQ)
Ar - Ar with
phe220
O
· · · H 1
O = 3.2, 2
H
O · · · S35 O 2
= 3.0 γ
O
· · · H201 N 4
= 2.3 ε 2
O
· · · S205 O 3
= γ
3.7
not involved
O
· · · D228 O 1
δ^2
= 2.2
a
1NTK(inhibitor
anitmycin A, AY1)
Ar - Ar with
phe220
O
· · · S35 O 3
= 3.0,γ
O
· · · S35 O 7
= 3.7 γ
N
· · · H 2
O = 2.5, 2
H
O · · · H 2
O = 2.8, 2
H
O · · · H201 N 2
= 2.5 ε 2
not involved
O
· · · K227 N 1
= ζ
3.7
O
· · · D228 O 2
δ^2
= 2.3
b
N
· · · D228 O 1
δ^1
= 3.0
1PPJ(inhibitor
antimycin A, ANY)
O
· · · H 1
O 2
222
= 2.9,
H
O 2
222
· · · S35 O
= γ
3.0
O
· · · H 3
O = 2.8 2
H
O 2
1473
· · · H201 N
= ε 2
2.7
not involved
O
· · · H 2
O 2
119
=
2.6,
H
O 2
119
· · · K227
N
= 2.7 ζ
O
· · · D228 O 1
δ^2
= 2.6,
N
· · · D228 O 1
δ^1
= 2.8
a The H - donor is questionable in these hydrogen bonds. b The H atoms of the salicylamine hydroxyl OH (O
) must be the H - donor for both the intramolecular hydrogen bond with the amide linker carbonyl 2
group (O
) and the O 3
carboxylic acid oxygen of asp228 assuming the carboxylic acid group is deprotonated. δ 2