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1 r membrane and one lacking the relevant SbmA membrane transport protein.
2 e region of the SLC25A40 inner mitochondrial membrane transport protein.
3 Escherichia coli (LacY) is a highly dynamic membrane transport protein.
4 omain protein that represents a new class of membrane transport protein.
5 ntrance loops are unlikely in this polytopic membrane transport protein.
6 ably blocking uptake via actions on a plasma membrane transport protein.
7 Na+-dependent L-glutamate/D,L-aspartate cell-membrane transport protein.
8 an insertion in a gene predicted to encode a membrane transport protein.
9 the lactose permease of Escherichia coli, a membrane transport protein.
10 chia coli lac permease, a well-characterized membrane transport protein.
11 +)-Li+ exchange are mediated by the same RBC membrane transport protein.
12 52 SLC-like proteins bring the total to 516 membrane transport proteins.
13 a prerequisite to understand the function of membrane transport proteins.
14 and release require vesicular and/or plasma membrane transport proteins.
15 H through the combined actions of a range of membrane transport proteins.
16 ed repeats found within the subunits of many membrane transport proteins.
17 ities of enzymes, transcription factors, and membrane transport proteins.
18 sterol-specific and reversible inhibition of membrane transport proteins.
19 formate/nitrite transporter (FNT) family of membrane transport proteins.
20 m involving secondary active Na(+)-dependent membrane transport proteins.
21 anism for this large and important family of membrane transport proteins.
22 the proper physiological functioning of many membrane transport proteins.
23 to measure rates of conformational change in membrane transport proteins.
24 and to identify putative regulatory sites of membrane transport proteins.
25 nce reconstitution, topology and activity of membrane transport proteins.
26 nd phosphatases), whereas PlantsT focuses on membrane transport proteins.
27 g, and characterization of a large number of membrane transport proteins.
28 of the Arabidopsis genome appears to encode membrane transport proteins.
29 n of bile acids is maintained by a series of membrane transport proteins.
30 n of genes encoding ribosomal, virulence and membrane transport proteins after both treatment times.
31 ivalent cation receptors modulating a plasma membrane transport protein and may lead to new insights
32 r of the ATP-binding cassette superfamily of membrane transport proteins and is a model for understan
34 nd demonstrates that several resident apical membrane transport proteins and the polymeric immunoglob
35 45,252 which is a member of a superfamily of membrane transport proteins and which is within a subgro
36 ed apical localization signal in a polytopic membrane transport protein, and suggest that this signal
37 e putative extracellular signaling proteins, membrane transport proteins, and novel secreted proteins
38 important residues in hydrophobic domains of membrane transport proteins, and several critical roles
39 ing the amount and the localization of these membrane transport proteins appears as a way to drive th
41 cation diffusion facilitator (CDF) family of membrane transport proteins are found in eukaryotes and
42 e than 400 members, the solute carrier (SLC) membrane transport proteins are the largest family of tr
44 cells, and approximately 25% of prokaryotic membrane transport proteins belong to this superfamily.
45 conducted bioinformatic analyses of integral membrane transport proteins belonging to dozens of famil
46 ithin the beta-barrel of the bacterial outer-membrane transport protein BtuB by site-directed mutagen
48 (LacY), a paradigm for the largest family of membrane transport proteins, catalyzes the coupled trans
49 (LacY), a paradigm for the largest family of membrane transport proteins, catalyzes the coupled trans
50 riers (SLC) supergroup, the largest class of membrane transport proteins, collectively termed the "SL
52 permease of Escherichia coli is a polytopic membrane transport protein containing 12 membrane-spanni
53 h programs, we suggest that related cases of membrane transport proteins containing similar motifs ar
55 cedures to isolate the effects on individual membrane transport proteins, crofelemer at 50 microM had
56 ntly modified; for example, membrane fusion, membrane transport, protein disaggregation, and protein
57 ly the Escherichia coli ferric citrate outer-membrane transport protein FecA has been characterized;
58 lipids around the crystal structure of this membrane transport protein, followed by atomistic simula
59 ise to speculation about the mechanism(s) of membrane 'transport' proteins for fatty acids and choles
60 gene, termed samt-1, coding for a candidate membrane transport protein for the presumptive donor sub
61 the gene for MDR1 (multidrug resistance), a membrane transport protein for which human polymorphisms
62 To study this issue, lactose permease, a membrane transport protein from Escherichia coli, is tra
65 of signal transduction in which an integral membrane transport protein functions to link the extrace
66 8 protein is similar to human XK, a putative membrane transport protein implicated in McLeod Syndrome
67 on the lipid bilayer itself, but rather on a membrane transport protein, implying that this is a norm
68 low nanomolar to millimolar) for an integral membrane transport protein in both detergent-solubilised
69 howcases the potential of expressing desired membrane transport proteins in cell factories to achieve
71 signed for describing the predicted cellular membrane transport proteins in organisms whose complete
72 ily that bind and deliver ligand to integral membrane transport proteins in the ATP-binding cassette,
73 eptide shows significant homology to several membrane transport proteins, including sugar and antibio
74 n Latinos, notably in SLC genes that include membrane transport proteins involved in the transport of
75 nd recognition of ligands by bacterial outer membrane transport proteins is mediated in part by inter
77 ikoshii, is an archaeal homolog of mammalian membrane transport proteins-known as excitatory amino ac
78 , which binds Hg(II) and transfers it to the membrane transport protein merT, have been determined in
79 Furthermore, we show that a cellular vesicle membrane transport protein named hVAP-33 (the human homo
80 utilizing arginine alpha-decarboxylase and a membrane transport protein necessary for delivering argi
83 of the kidney require an overlapping set of membrane transport proteins regulated by the forkhead tr
84 A gene, which encodes a putative cytoplasmic membrane transport protein required for symbiosis, was i
85 Amt proteins are the first hyperthermophilic membrane transport proteins shown to be active in a meso
86 tion to the method of MD, we use a number of membrane transport proteins studied in our laboratory as
87 as apolipoproteins E and AI, and one or more membrane transport proteins such as members of the low d
89 r family (NPF) 6.3 is a dual-affinity plasma membrane transport protein that has both high- and low-a
90 aling require Ca(2)(+) influx through plasma membrane transport proteins that are regulated by reacti
92 the family of Na+ (and Cl-)-dependent plasma membrane transport proteins that comprises transporters
93 is often mediated through overexpression of membrane transport proteins that effectively efflux anti
96 e derivatives with respect to a well studied membrane transport protein, the lactose permease of Esch
97 e bacteria involves the coupling of an outer membrane transport protein to the transperiplasmic prote
98 Granular biofilms were enriched in outer membrane transport proteins to scavenge the extracellula
99 how that overexpression of the mitochondrial membrane transport protein UCP2 in cancer cells is suffi
102 mber of the major facilitator superfamily of membrane transport proteins, which contain two domains o
103 Escherichia coli (LacY) is a highly dynamic membrane transport protein, while the Cys154-->Gly mutan
104 se as a model the lactose permease (LacY), a membrane transport protein with a known three-dimensiona