|
15 -> 36
|
EADELLADMEQHLLVLQPEAPD
|
In CheAS - helical region implicated in CheZ binding (see also |CITS: [19581362][19542283]|)
|
|
64 -> 126
|
ETTHLMENLLDEARRGEMQLNTDIINLFLETKDIMQEQLDAYKQSQEPDAASFDYICQALRQL
|
|
|
165 -> 227
|
SRLKAGEVDLLEEELGHLTTLTDVVKGADSLSAILPGDIAEDDITAVLCFVIEADQITFETVE
|
|
|
275 -> 411
|
INLVGELVITQSMLAQRSSELDPVNHGDLITSMGQLQRNARDLQESVMSIRMMPMEYVFSRYPRLVRDLAGKLGKQVELTLVGSSTELDKSLIERIIDPLTHLVRNSLDHGIELPEKRLAAGKNSVGNLILSAEHQG
|
|
|
417 -> 543
|
EVTDDGAGLNRERILAKAASQGLTVSENMSDDEVAMLIFAPGFSTAEQVTDVSGRGVGMDVVKRNIQKMGGHVEIQSKQGTGTTIRILLPLTLAILDGMSVRVADEVFILPLNAVMESLQPREADLH
|
|
|
1 -> 97
|
MSMDISDFYQTFFDEADELLADMEQHLLVLQPEAPDAEQLNAIFRAAHSIKGGAGTFGFSVLQETTHLMENLLDEARRGEMQLNTDIINLFLETKDI
|
UniProt: not present in isoform cheA(S)
|
|
8 -> 106
|
FYQTFFDEADELLADMEQHLLVLQPEAPDAEQLNAIFRAAHSIKGGAGTFGFSVLQETTHLMENLLDEARRGEMQLNTDIINLFLETKDIMQEQLDAYK
|
|
|
161 -> 223
|
RIILSRLKAGEVDLLEEELGHLTTLTDVVKGADSLSAILPGDIAEDDITAVLCFVIEADQITF
|
|
|
214 -> 214
|
F
|
F → A: results in a large decrease in CheA-CheY binding affinity and slower CheA-CheY phosphotransfer kinetics; is defective in recruiting labeled CheY into signal clusters and less effective than the wild type in supporting chemotaxis
|
|
262 -> 324
|
TSIRVAVEKVDQLINLVGELVITQSMLAQRSSELDPVNHGDLITSMGQLQRNARDLQESVMSI
|
|
|
337 -> 337
|
P
|
P → L/S: elevated CheA autokinase activity and higher affinity for ATP compared to wild-type
|
|
372 -> 508
|
DPLTHLVRNSLDHGIELPEKRLAAGKNSVGNLILSAEHQGGNICIEVTDDGAGLNRERILAKAASQGLTVSENMSDDEVAMLIFAPGFSTAEQVTDVSGRGVGMDVVKRNIQKMGGHVEIQSKQGTGTTIRILLPLT
|
|
|
376 -> 376
|
H
|
H → Q
|
|
380 -> 380
|
N
|
N → D; loss of autokinase activity; moderate decrease in affinity for ATP
|
|
420 -> 420
|
D
|
D → N; loss of autokinase activity; moderate decrease in affinity for ATP
|
|
422 -> 422
|
G
|
G → A; loss of autokinase activity; moderate decrease in affinity for ATP
|
|
470 -> 470
|
G
|
G → K: lacks autokinase activity; binds ATP with wild-type affinity
|
|
499 -> 499
|
T
|
T → S/A
|
|
514 -> 640
|
GMSVRVADEVFILPLNAVMESLQPREADLHPLAGGERVLEVRGEYLPIVELWKVFNVAGAKTEATQGIVVILQSGGRRYALLVDQLIGQHQVVVKNLESNYRKVPGISAATILGDGSVALIVDVSAL
|
|