「transmembrane」の共起表現(2語右で並び替え)

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共起表現

「transmembrane」の共起表現一覧(2語右で並び替え)

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racellular ligand-binding domain, a single	transmembrane region, a region with sequence similar to
They also have seven	transmembrane domains, a characteristic unique to this s
ellular domain followed by three conserved	transmembrane domains, a variable cytoplasmic loop, a fo
N-terminal domain; three highly conserved	transmembrane domains; a cytoplasmic loop of variable si
This domain acts as a	transmembrane anchor, allowing the conduction of electro
caffolding protein with a role in synaptic	transmembrane protein anchoring and ion channel traffick
rters and the encoded protein contains two	transmembrane domains and two nucleotide binding folds.
cific angiogenesis inhibitor, a seven-span	transmembrane protein and is thought to be a member of t
of five extracellular cadherin repeats, a	transmembrane region and a highly conserved cytoplasmic
upled receptors (GPCRs, or GPRs) contain 7	transmembrane domains and transduce extracellular signal
N-terminal extracellular domain, a single	transmembrane domain and an intracellular domain.
receptor tyrosine kinase having a putative	transmembrane domain and an extracellular domain.
es with multiple subunits, each possessing	transmembrane regions, and all arranged to form a ligand
an extra cytoplasmic N terminal domain, a	transmembrane region, and a cytoplasmic C-terminal domai
s in cell shape, cell motility, secretion,	transmembrane transport, and regulation of the cell cycl
roteins, including SLC2A6, that contain 12	transmembrane domains and a number of critical conserved
ure: a leucine-rich repeat (LRR) region, a	transmembrane domain, and a Toll/Interleukin-1 receptor
The two paralogous enzymes-	transmembrane CD38 and GPI anchored CD157, that produce
1 extracellular calcium-binding domains, a	transmembrane domain and a unique cytoplasmic domain.
extracellular domains, exon 4 encodes the	transmembrane domain and the cytoplasmic tail.
ur extracellular immunoglobulin domains, a	transmembrane domain, and two to four cytoplasmic immuno
y glycosylated mucin-like domain, a unique	transmembrane domain and a short cytoplasmic tail.
acellular N and C termini, two hydrophobic	transmembrane regions, and a large extracellular loop, w
XC chemokine domain, a mucin-like stalk, a	transmembrane domain and a cytoplasmic tail containing a
viral hemagglutinin, neuraminidase and M2	transmembrane proteins, and facilitates budding of the m
t membrane, while [beta]-dystroglycan is a	transmembrane protein and binds to dystrophin, which is
llular protein domains, exon 4 encodes the	transmembrane domain, and exon 5 encodes the cytoplasmic
r peptide hormones such as BNP and ANP), a	transmembrane domain, and an internal catalytic domain h
ccessory molecules have negatively charged	transmembrane regions and are vital to propagating the s
mily has a common structure of 12 presumed	transmembrane helices and includes carriers for gamma-am
G protein-coupled receptors contain 7	transmembrane domains and transduce extracellular signal
e encoded protein contains twelve putative	transmembrane domains and is a plasma integral membrane
: a periplasmic ligand-binding domain, two	transmembrane segments, and a cytoplasmic domain.
Fractalkine is a	transmembrane protein and chemokine involved in the adhe
“MOG is a quantitatively minor type I	transmembrane protein, and is found exclusively in the C
The signals are initiated at the 7	transmembrane domain and transmitted through receptor co
The alpha-1 subunit has 24	transmembrane segments and forms the pore through which
N-terminal extracellular region, multiple	transmembrane domains and a cytoplasmic C-tail.
Additionally, SynechoNET provides	transmembrane topology and domain information, as well a
ers are characterized by the presence of 7	transmembrane domains and numerous conserved amino acids
acellular immunoglobulin domains, a single	transmembrane domain, and a short, C-terminal cytoplasmi
Like C9, this protein creates	transmembrane tubules and is capable of lysing non-speci
	Transmembrane Channels are channels created by the membr
pore was identified, made up of the second	transmembrane segment, as shown also later by the groups
termine the three-dimensional structure of	transmembrane domains, as well as positively charged res
SLC39A4 is a	transmembrane protein associated with acrodermatitis ent
cluster of differentiation 318) and Trask (	Transmembrane and associated with src kinases).
membrane protein, that cleaves single-pass	transmembrane proteins at residues within the transmembr
muscle the dystroglycan complex works as a	transmembrane linkage between the extracellular matrix a
s and actin microfilaments are attached to	transmembrane proteins by attachment proteins between th
	Transmembrane protein C2orf18 is a protein that in human
e absence of Hh (Figure 3), a cell-surface	transmembrane protein called Patched (PTCH) acts to prev
These receptors are all	transmembrane proteins, composed of a ligand-binding ext
Ionophores disrupt	transmembrane ion concentration gradients, required for
been shown to predominantly exist as large	transmembrane channels connecting the intracellular and
glycoprotein Ib (GPIb) is a heterodimeric	transmembrane protein consisting of a disulfide-linked 1
All ICAM proteins are type I	transmembrane glycoproteins, contain 2-9 immunoglobulin-
e is a receptor for BAFF and is a type III	transmembrane protein containing a single extracellular
teins had well defined structures and that	transmembrane alpha-helices could occur.
All are members of the 7	transmembrane G-protein coupled receptor family and indu
ight-harvesting proteins are the intrinsic	transmembrane proteins CP43 (PsbC) and CP47 (PsbB) occur
a tripartite structure with extracellular,	transmembrane, and cytoplasmic regions.
biochemistry, the membrane topology of an	transmembrane protein describes which portions of the am
ential, a type of graded potential, is the	transmembrane potential difference of a sensory receptor
The encoded	transmembrane protein directs phagocytosis of several ba
amily of proteins, predicted to have seven	transmembrane helical domains of largely hydrophobic ami
The 7	transmembrane spanning domains, with an external amino t
pled receptors, the CB2 receptor has seven	transmembrane spanning domains.
Type I cytokine receptors are	transmembrane receptors expressed on the surface of cell
TLRs are	transmembrane proteins, expressed on the cell surface an
l immunoglobulin-like receptors (KIRs) are	transmembrane glycoproteins expressed by natural killer
l immunoglobulin-like receptors (KIRs) are	transmembrane glycoproteins expressed by natural killer
It is a	transmembrane protein expressed on the surface of oligod
cylindrical shape, and can be divided into	transmembrane and extramembrane regions: an N-terminal p
ndoplasmic reticulum (ER) stress-regulated	transmembrane transcription factor that activates the tr
Adhesion Molecule-Like, or AMICA1 is a JAM	transmembrane protein family member.
These proteins are related to OmpA-like	transmembrane domain family.
It is a	transmembrane copper-dependent ferroxidase responsible f
protein in glioma cells, so this prevents	transmembrane chloride fluxes but this interaction does
GABAB receptors (GABABR) are metabotropic	transmembrane receptors for gamma-aminobutyric acid (GAB
ptor 1 (BLR1) is a G protein-coupled seven	transmembrane receptor for chemokine CXCL13 (also known
CD11c is a type I	transmembrane protein found at high levels on most human
as been shown to be important in recycling	transmembrane receptors from endosomes to the trans-Golg
h it appears to do by interacting with the	transmembrane domains from within the lipid bilayer.
There is a very large	transmembrane electrochemical gradient of Ca2+ driving t
Some terminal oxidases generate a	transmembrane proton gradient across the plasma membrane
Each hERG subunit consists of 6	transmembrane alpha helices, numbered S1-S6, a pore heli
d to an extracellular sensing domain via a	transmembrane α helix.
The protein encoded by this gene is a	transmembrane (type I) heparan sulfate proteoglycan and
They can activate a	transmembrane protein if it is a receptor (e.g., HER2),
This protein is a type I	transmembrane protein implicated in asthma and bronchial
ligand) binds to a receptor that has seven	transmembrane regions; in this case, the ligand is ACh.
papillomaviruses, outer membrane proteins,	transmembrane regions in protein, protein secondary stru
CD155 is a Type I	transmembrane glycoprotein in the immunoglobulin superfa
Other members of the JAM family of	transmembrane proteins include JAM1, JAM2 and JAM3.
ntually, it was discovered that the second	transmembrane domain is not in fact trans at all, but ki
When the hydrophobic part of a	transmembrane protein is too large to match the hydropho
This putative	transmembrane protein is thought to play a role in carbo
amino acid protein (CLC-5), with 12 to 13	transmembrane domains; it manifests itself through low m
ic protein (BMP) receptors are a family of	transmembrane serine/threonine kinases that include the
hogenetic protein (BMP) receptor family of	transmembrane serine/threonine kinases.
SIRP family members are receptor-type	transmembrane glycoproteins known to be involved in the
ADAM family members are type I	transmembrane glycoproteins known to be involved in cell
(Cluster of Differentiation 69) is a human	transmembrane C-Type lectin protein encoded by the CD69
This	transmembrane protein localizes to lipid rafts (also kno
A vesicular transport protein is a	transmembrane or membrane associated protein.
ct electron transfer from the cytosol to a	transmembrane heme moiety.
the EGF-TM7 family of class II seven-span	transmembrane (7-TM) molecules, likely encoded by a gene
hibits osteoclast formation and contains a	transmembrane domain near the N-terminus as well as the
(ADC) that targets cancer cells expressing	transmembrane glycoprotein NMB (GPNMB).
The SecY protein is the main	transmembrane subunit of the eubacterial protein secreto
se, subunit C of F0/V0 complex is the main	transmembrane subunit of V-type , A-type and F-type ATP
end of the Aβ peptide, cleaves within the	transmembrane region of APP and can generate a number of
The Frizzled genes belong to the seven	transmembrane class of receptors (7TMR) and have in thei
protein product is a type III (leaderless)	transmembrane protein of 262 aminoacids (long form) or 2
N-cadherin, a cell- surface	transmembrane glycoprotein of the cadherin superfamily o
Only	transmembrane helices of HtrII are resolved.
cross the membrane, helping to establish a	transmembrane difference of proton electrochemical poten
The	transmembrane domain of the beta subunit of formate dehy
hrome c oxidase subunit III is one of main	transmembrane subunits of cytochrome c oxidase
protein has been found associated with the	transmembrane sector of the V-type ATPases.
The	transmembrane region of the TCR is composed of positivel
This protein is a type III	transmembrane protein of the TNFR (tumor necrosis factor
hose acting on acid anhydrides to catalyse	transmembrane movement of substances.
S2P cleaves the	transmembrane domain of SREPB, making it a member of the
shown frequently to bind the C-termini of	transmembrane receptors or ion channels.
The	transmembrane electrochemical potential gradient may ena
The receptor is a	transmembrane glycoprotein present on the surface of mye
It is a type I	transmembrane protein present on activated T cells, acti
ember 13B (more commonly known as TACI), a	transmembrane receptor protein found predominantly on th
ucose transporter), member 2 (SLC2A2) is a	transmembrane carrier protein that enables passive gluco
s elegans sel-12 gene encodes a multi-pass	transmembrane domain protein that is similar to human pr
The B-cell receptor is a	transmembrane receptor protein located on the outer surf
Bestrophins are	transmembrane (TM) proteins that share a homology region
r gradients involves chemotaxis receptors,	transmembrane (TM) proteins that detect stimuli through
gely based on the study and engineering of	transmembrane pore-forming proteins, as well as interest
CALCRL is linked to one of three single	transmembrane domain receptor activity-modifying protein
Patched (Ptc) is a conserved 12-pass	transmembrane protein receptor that plays an obligate ne
encodes a member of the class B seven-span	transmembrane (TM7) receptor family expressed predominan
ubunits, that are noncovalently associated	transmembrane glycoprotein receptors.
R583Q is present in the 4th	transmembrane spanning region of domain 2 while the I171
of 7 immunoglobulin-like domains, a single	transmembrane spanning region and an intracellular porti
They also possess a single	transmembrane spanning region and an intracellular porti
dent kinase-1, EZR, PODXL, Cystic fibrosis	transmembrane conductance regulator and PLCB3.
y targeting the intestinal cystic fibrosis	transmembrane conductance regulator Cl- transport inhibi
the chloride channel CFTR (cystic fibrosis	transmembrane conductance regulator) on epithelial cells
by a defect in a protein, cystic fibrosis	transmembrane conductance regulator, which regulates flu
shown to interact with the cystic fibrosis	transmembrane conductance regulator.
tiporter 3 regulator 1 and Cystic fibrosis	transmembrane conductance regulator.
ymes that cleave extracellular portions of	transmembrane proteins, releasing the soluble ectodomain
The vacuolar (V-type) ATPases have a	transmembrane proton-conducting sector and an extramembr
R1664Q is in the 4th	transmembrane spanning segment of domain 4 and, presumab
receptor, which is predicted to be a seven	transmembrane protein similar to G protein-coupled recep
r family, which is predicted to be a seven	transmembrane protein similar to G protein-coupled recep
The KCa channel α subunits have six	transmembrane segments similar to the KVs, except KCa1,
It is predicted to be a seven	transmembrane protein similar to G protein-coupled recep
and polyarthritis, and the contribution of	transmembrane versus soluble TNF in the pathogenic proce
ins are predicted to have 12 alpha-helical	transmembrane regions, some of the animal proteins may h
, which are a large family of secreted and	transmembrane proteins, some of which function as repell
Members of this family possess twelve	transmembrane a-helical spanners (TMSs).
figure for structure) is a member of the 6	transmembrane helix structural class of potassium ion ch
The seven	transmembrane α-helix structure of a G-protein-coupled r
sible for the intramembrane proteolysis of	transmembrane proteins such as the Notch protein and amy
been shown to mediate retrieval of various	transmembrane receptors, such as the cation-independent
ber of this subfamily contains a potential	transmembrane domain suggesting that these proteins are
istic of extracellular matrix proteins and	transmembrane proteins suggests that this protein is a r
known to complex with integrins and other	transmembrane 4 superfamily proteins.
in encoded by this gene is a member of the	transmembrane 4 superfamily, also known as the tetraspan
brane glycoprotein that is a member of the	transmembrane 4 superfamily.
CD43 (cluster of differentiation 43) is a	transmembrane cell surface protein that in humans is enc
Langerin is a type II	transmembrane cell surface receptor produced by Langerha
This gene encodes a	transmembrane protein that is located in the endoplasmic
1 receptor accessory protein (IL1RAP) is a	transmembrane protein that interacts with IL-1R and is r
receptor, Tar, is a member of a family of	transmembrane receptors that mediate chemotactic respons
They are	transmembrane proteins that contain an N-terminal V-like
These proteins are type-I	transmembrane receptors that share an intracellular 200
The gene product is a glycosylated	transmembrane protein that functions in both the periphe
The protein encoded by this gene is a	transmembrane endopeptidase that belongs to the type II
transporter, also called an ion pump, is a	transmembrane protein that moves ions across a plasma me
e transport proteins, a class of multipass	transmembrane proteins that facilitate the diffusion of
CD79 (Cluster of Differentiation 79) is a	transmembrane protein that forms a complex with the B-ce
in of the interleukin-4 receptor, a type I	transmembrane protein that can bind interleukin 4 and in
ponent of fungal cell membranes, forming a	transmembrane channel that leads to monovalent ion (K+,
The protein encoded by this gene is a	transmembrane glycoprotein that functions as a sulfate t
CD164 is a type I integral	transmembrane sialomucin that functions as an adhesion r
LMP-1 is a six-span	transmembrane protein that is also essential for EBV-med
Calsyntenins (Csts, CLSTN) are type I	transmembrane proteins that belong to the cadherin super
lecular biology, the insulin receptor is a	transmembrane receptor that is activated by insulin.
This gene encodes a single-pass	transmembrane protein that shares limited similarity wit
LMP-2A/LMP-2B are	transmembrane proteins that act to block tyrosine kinase
Bestrophins are	transmembrane proteins that contain a homologous region
More than 40 highly divergent	transmembrane proteins that could contribute to this fun
are integral membrane proteins with seven	transmembrane helices, the last of which contains the at
via the viral protein gp120; gp41, a viral	transmembrane protein, then undergoes a conformational c
ession of the receptor and participates in	transmembrane signaling through phosphorylation of its i
These domains help anchor	transmembrane proteins to the cytoskeleton and hold toge
ThTr-2 is a ubiquitously expressed	transmembrane thiamine transporter that lacks folate tra
80 amino acids which seems to contain four	transmembrane segments, two disulfide bonds and which co
a synaptic vesicle glycoprotein with four	transmembrane domains weighing 38kDa.
However, if each of the four	transmembrane domains went all the way through the plasm

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共起表現

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「transmembrane」の共起表現一覧(2語右で並び替え)