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PMID: 10781583
Hou Y, Cui L, Riordan JR, Chang X
Allosteric interactions between the two non-equivalent nucleotide binding domains of multidrug resistance protein MRP1.
J Biol Chem. 2000 Jul 7;275(27):20280-7., 2000-07-07
[PubMed]
Sentences
No.
Mutations
Sentence
Comment
33
ABCC1 p.Asp793Leu
X
ABCC1 p.Asp793Leu 10781583:33:70
status:
NEW
view ABCC1 p.Asp793Leu details
ABCC1 p.Asp1454Leu
X
ABCC1 p.Asp1454Leu 10781583:33:89
status:
NEW
view ABCC1 p.Asp1454Leu details
ABCC1 p.Asp792Leu
X
ABCC1 p.Asp792Leu 10781583:33:64
status:
NEW
view ABCC1 p.Asp792Leu details
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:33:57
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Glu1455Leu
X
ABCC1 p.Glu1455Leu 10781583:33:96
status:
NEW
view ABCC1 p.Glu1455Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:33:77
status:
NEW
view ABCC1 p.Lys1333Leu details
Stable cell lines expressing wild-type and mutant MRP1s,
K684L
,
D792L
/
D793L
,
K1333L
, and
D1454L
/
E1455L
, were generated by using procedures described previously (11).
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205
ABCC1 p.Asp1454Leu
X
ABCC1 p.Asp1454Leu 10781583:205:175
status:
NEW
view ABCC1 p.Asp1454Leu details
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:205:121
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:205:156
status:
NEW
view ABCC1 p.Lys1333Leu details
Fig. 5C shows that although labeling by N3[␣-32 P]ATP was not abolished by the mutations, it was greatly reduced:
K684L
was ϳ10% of wild-type;
K1333L
, ϳ5%;
D1454L
/D1455L, ϳ15%.
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207
ABCC1 p.Asp1454Leu
X
ABCC1 p.Asp1454Leu 10781583:207:117
status:
NEW
view ABCC1 p.Asp1454Leu details
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:207:38
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Glu1455Leu
X
ABCC1 p.Glu1455Leu 10781583:207:124
status:
NEW
view ABCC1 p.Glu1455Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:207:106
status:
NEW
view ABCC1 p.Lys1333Leu details
Fig. 5D demonstrates that labeling of
K684L
by N3[␥-32 P]ATP was almost eliminated and labeling of
K1333L
and
D1454L
/
E1455L
were decreased to ϳ10% and ϳ15% of the wild-type levels, respectively.
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213
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:213:117
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:213:4
status:
NEW
view ABCC1 p.Lys1333Leu details
The
K1333L
mutation in NBD2 nearly abolished ATP-dependent uptake as did the NBD2 Walker B substitution, whereas the
K684L
substitution reduced it by approximately half.
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232
ABCC1 p.Asp1454Leu
X
ABCC1 p.Asp1454Leu 10781583:232:127
status:
NEW
view ABCC1 p.Asp1454Leu details
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:232:64
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Glu1455Leu
X
ABCC1 p.Glu1455Leu 10781583:232:135
status:
NEW
view ABCC1 p.Glu1455Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:232:95
status:
NEW
view ABCC1 p.Lys1333Leu details
Lane 1, 10 g of wild-type MRP1; lane 2, 20 g of
K684L
; lane 3, 10 g of
K1333L
; lane 4, 10 g of
D1454L
/
E1455L
.
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234
ABCC1 p.Asp1454Leu
X
ABCC1 p.Asp1454Leu 10781583:234:127
status:
NEW
view ABCC1 p.Asp1454Leu details
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:234:64
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Glu1455Leu
X
ABCC1 p.Glu1455Leu 10781583:234:135
status:
NEW
view ABCC1 p.Glu1455Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:234:95
status:
NEW
view ABCC1 p.Lys1333Leu details
Lane 1, 10 g of wild-type MRP1; lane 2, 20 g of
K684L
; lane 3, 10 g of
K1333L
; lane 4, 10 g of
D1454L
/
E1455L
.
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235
ABCC1 p.Asp1454Leu
X
ABCC1 p.Asp1454Leu 10781583:235:237
status:
NEW
view ABCC1 p.Asp1454Leu details
ABCC1 p.Lys684Leu
X
ABCC1 p.Lys684Leu 10781583:235:134
status:
NEW
view ABCC1 p.Lys684Leu details
ABCC1 p.Glu1455Leu
X
ABCC1 p.Glu1455Leu 10781583:235:245
status:
NEW
view ABCC1 p.Glu1455Leu details
ABCC1 p.Lys1333Leu
X
ABCC1 p.Lys1333Leu 10781583:235:184
status:
NEW
view ABCC1 p.Lys1333Leu details
E, ATP-dependent LTC4 uptake by membrane vesicles containing wild-type (closed diamonds) and mutant MRPs: NBD1 Walker A lysine mutant
K684L
(open circles), NBD2 Walker A lysine mutant
K1333L
(open square), NBD2 Walker B aspartate mutant
D1454L
/
E1455L
(closed circles).
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