「Transmembrane」の共起表現(1語右で並び替え)

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共起表現

「Transmembrane」の共起表現一覧(1語右で並び替え)

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Members of this family possess twelve	transmembrane a-helical spanners (TMSs).
Each hERG subunit consists of 6	transmembrane alpha helices, numbered S1-S6, a pore heli
teins had well defined structures and that	transmembrane alpha-helices could occur.
omain of cytochrome C oxidase contains two	transmembrane alpha-helices.
It has a C-terminal	transmembrane alpha-helix.
This domain acts as a	transmembrane anchor, allowing the conduction of electro
a tripartite structure with extracellular,	transmembrane, and cytoplasmic regions.
cylindrical shape, and can be divided into	transmembrane and extramembrane regions: an N-terminal p
cluster of differentiation 318) and Trask (	Transmembrane and associated with src kinases).
a beta-ribbon arm that forms an oligomeric	transmembrane barrel.
(Cluster of Differentiation 69) is a human	transmembrane C-Type lectin protein encoded by the CD69
ucose transporter), member 2 (SLC2A2) is a	transmembrane carrier protein that enables passive gluco
The two paralogous enzymes-	transmembrane CD38 and GPI anchored CD157, that produce
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
ponent of fungal cell membranes, forming a	transmembrane channel that leads to monovalent ion (K+,
been shown to predominantly exist as large	transmembrane channels connecting the intracellular and
	Transmembrane Channels are channels created by the membr
The membrane-attack complex (MAC) forms	transmembrane channels.
protein in glioma cells, so this prevents	transmembrane chloride fluxes but this interaction does
The Frizzled genes belong to the seven	transmembrane class of receptors (7TMR) and have in thei
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
dent kinase-1, EZR, PODXL, Cystic fibrosis	transmembrane conductance regulator and PLCB3.
y targeting the intestinal cystic fibrosis	transmembrane conductance regulator Cl- transport inhibi
shown to interact with the cystic fibrosis	transmembrane conductance regulator.
tiporter 3 regulator 1 and Cystic fibrosis	transmembrane conductance regulator.
It is a	transmembrane copper-dependent ferroxidase responsible f
retically is inversely proportional to the	transmembrane current.
cross the membrane, helping to establish a	transmembrane difference of proton electrochemical poten
CALCRL is linked to one of three single	transmembrane domain receptor activity-modifying protein
N-terminal extracellular domain, a single	transmembrane domain and an intracellular domain.
hibits osteoclast formation and contains a	transmembrane domain near the N-terminus as well as the
receptor tyrosine kinase having a putative	transmembrane domain and an extracellular domain.
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.
y glycosylated mucin-like domain, a unique	transmembrane domain and a short cytoplasmic tail.
XC chemokine domain, a mucin-like stalk, a	transmembrane domain and a cytoplasmic tail containing a
ntually, it was discovered that the second	transmembrane domain is not in fact trans at all, but ki
ber of this subfamily contains a potential	transmembrane domain suggesting that these proteins are
The	transmembrane domain of the beta subunit of formate dehy
These proteins are related to OmpA-like	transmembrane domain family.
1. a membrane protein with one	transmembrane domain
A unique	transmembrane domain (S0) that precedes the 6 transmembr
S2P cleaves the	transmembrane domain of SREPB, making it a member of the
The signals are initiated at the 7	transmembrane domain and transmitted through receptor co
s elegans sel-12 gene encodes a multi-pass	transmembrane domain protein that is similar to human pr
ure: a leucine-rich repeat (LRR) region, a	transmembrane domain, and a Toll/Interleukin-1 receptor
ur extracellular immunoglobulin domains, a	transmembrane domain, and two to four cytoplasmic immuno
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
acellular immunoglobulin domains, a single	transmembrane domain, and a short, C-terminal cytoplasmi
se domain and a C-terminal heme-containing	transmembrane domain.
electivity were are also identified in the	transmembrane domain.
n Toxoplasma gondii that contains a single	transmembrane domain.
rters and the encoded protein contains two	transmembrane domains and two nucleotide binding folds.
upled receptors (GPCRs, or GPRs) contain 7	transmembrane domains and transduce extracellular signal
roteins, including SLC2A6, that contain 12	transmembrane domains and a number of critical conserved
h it appears to do by interacting with the	transmembrane domains from within the lipid bilayer.
However, if each of the four	transmembrane domains went all the way through the plasm
protein and are hydrolysed to ADP) and two	transmembrane domains (parts of the protein which span t
nit indicated that there seemed to be four	transmembrane domains (parts of the protein that pass th
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 synaptic vesicle glycoprotein with four	transmembrane domains weighing 38kDa.
N-terminal extracellular region, multiple	transmembrane domains and a cytoplasmic C-tail.
ers are characterized by the presence of 7	transmembrane domains and numerous conserved amino acids
r SSSF proteins predicts 11 to 15 putative	transmembrane domains (TMs) in alpha-helical conformatio
onnexins are very similar, consisting of 4	transmembrane domains, 2 extracellular and 1 intracellul
termine the three-dimensional structure of	transmembrane domains, as well as positively charged res
They also have seven	transmembrane domains, a characteristic unique to this s
They have four	transmembrane domains, with the N-terminus and the C-ter
ellular domain followed by three conserved	transmembrane domains, a variable cytoplasmic loop, a fo
MotA has four	transmembrane domains.
of C5a to bind to residues in the receptor	transmembrane domains.
of receptors possessing seven hydrophobic	transmembrane domains.
um dependent chloride channel and has five	transmembrane domains.
amino acid protein (CLC-5), with 12 to 13	transmembrane domains; it manifests itself through low m
N-terminal domain; three highly conserved	transmembrane domains; a cytoplasmic loop of variable si
There is a very large	transmembrane electrochemical gradient of Ca2+ driving t
The	transmembrane electrochemical potential gradient may ena
The protein encoded by this gene is a	transmembrane endopeptidase that belongs to the type II
All are members of the 7	transmembrane G-protein coupled receptor family and indu
(ADC) that targets cancer cells expressing	transmembrane glycoprotein NMB (GPNMB).
The receptor is a	transmembrane glycoprotein present on the surface of mye
CDCP1/Trask is a 140 kD	transmembrane glycoprotein with a large extracellular do
N-cadherin, a cell- surface	transmembrane glycoprotein of the cadherin superfamily o
The protein encoded by this gene is a	transmembrane glycoprotein that functions as a sulfate t
CD155 is a Type I	transmembrane glycoprotein in the immunoglobulin superfa
ubunits, that are noncovalently associated	transmembrane glycoprotein receptors.
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
It is a member of pentaspan	transmembrane glycoproteins (5-transmembrane, 5-TM), whi
l immunoglobulin-like receptors (KIRs) are	transmembrane glycoproteins expressed by natural killer
l immunoglobulin-like receptors (KIRs) are	transmembrane glycoproteins expressed by natural killer
gene encodes a member of the CD1 family of	transmembrane glycoproteins, which are structurally rela
All ICAM proteins are type I	transmembrane glycoproteins, contain 2-9 immunoglobulin-
amily of proteins, predicted to have seven	transmembrane helical domains of largely hydrophobic ami
mily has a common structure of 12 presumed	transmembrane helices and includes carriers for gamma-am
Only	transmembrane helices of HtrII are resolved.
are integral membrane proteins with seven	transmembrane helices, the last of which contains the at
for bR showing the protein to consist of 7	transmembrane helices.
The monomeric complex contains 15	transmembrane helices.
tches of hydrophobic residues may indicate	transmembrane helices.
s family of ion channels contains 10 or 12	transmembrane helices.
encodes a plasma membrane protein with 11	transmembrane helices.
figure for structure) is a member of the 6	transmembrane helix structural class of potassium ion ch
ain, which has a Catalytic function; and a	transmembrane helix.
ct electron transfer from the cytosol to a	transmembrane heme moiety.
Ionophores disrupt	transmembrane ion concentration gradients, required for
muscle the dystroglycan complex works as a	transmembrane linkage between the extracellular matrix a
hose acting on acid anhydrides to catalyse	transmembrane movement of substances.
A vesicular transport protein is a	transmembrane or membrane associated protein.
gely based on the study and engineering of	transmembrane pore-forming proteins, as well as interest
ential, a type of graded potential, is the	transmembrane potential difference of a sensory receptor
It is synthesized primarily as a	transmembrane precursor, which is then processed to matu
The	transmembrane pressure (pressure drop across the membran
ΔP:	transmembrane pressure (should also include effects of o
Flux and	transmembrane pressure (TMP) are the best indicators of
This gene encodes a	transmembrane protein that is located in the endoplasmic
cific angiogenesis inhibitor, a seven-span	transmembrane protein and is thought to be a member of t
Patched (Ptc) is a conserved 12-pass	transmembrane protein receptor that plays an obligate ne
1 receptor accessory protein (IL1RAP) is a	transmembrane protein that interacts with IL-1R and is r
glycoprotein Ib (GPIb) is a heterodimeric	transmembrane protein consisting of a disulfide-linked 1
t the lipid bilayer-spanning portions of a	transmembrane protein will assume an alpha-helical secon
receptor, which is predicted to be a seven	transmembrane protein similar to G protein-coupled recep
carrier family and encodes a cell surface,	transmembrane protein with an alpha-amylase domain.
r family, which is predicted to be a seven	transmembrane protein similar to G protein-coupled recep
e is a receptor for BAFF and is a type III	transmembrane protein containing a single extracellular
The gene product is a glycosylated	transmembrane protein that functions in both the periphe
This	transmembrane protein localizes to lipid rafts (also kno
They can activate a	transmembrane protein if it is a receptor (e.g., HER2),
transporter, also called an ion pump, is a	transmembrane protein that moves ions across a plasma me
e absence of Hh (Figure 3), a cell-surface	transmembrane protein called Patched (PTCH) acts to prev
biochemistry, the membrane topology of an	transmembrane protein describes which portions of the am
t membrane, while [beta]-dystroglycan is a	transmembrane protein and binds to dystrophin, which is
CD79 (Cluster of Differentiation 79) is a	transmembrane protein that forms a complex with the B-ce
It is a type I	transmembrane protein present on activated T cells, acti
in of the interleukin-4 receptor, a type I	transmembrane protein that can bind interleukin 4 and in
protein product is a type III (leaderless)	transmembrane protein of 262 aminoacids (long form) or 2
When the hydrophobic part of a	transmembrane protein is too large to match the hydropho
CD11c is a type I	transmembrane protein found at high levels on most human
SLC39A4 is a	transmembrane protein associated with acrodermatitis ent
	Transmembrane protein C2orf18 is a protein that in human
This protein is a type I	transmembrane protein implicated in asthma and bronchial
This putative	transmembrane protein is thought to play a role in carbo
Adhesion Molecule-Like, or AMICA1 is a JAM	transmembrane protein family member.
LMP-1 is a six-span	transmembrane protein that is also essential for EBV-med
Fractalkine is a	transmembrane protein and chemokine involved in the adhe
It is predicted to be a seven	transmembrane protein similar to G protein-coupled recep
This gene encodes a single-pass	transmembrane protein that shares limited similarity wit
This protein is a type III	transmembrane protein of the TNFR (tumor necrosis factor
CD155 is a	transmembrane protein with 3 extracellular immunoglobuli
caffolding protein with a role in synaptic	transmembrane protein anchoring and ion channel traffick
The encoded	transmembrane protein directs phagocytosis of several ba
It is a	transmembrane protein expressed on the surface of oligod
ylglycerol monooxygenase was discovered as	transmembrane protein 195 (TMEM195) on chromosome 7.
CD22 is a sugar binding	transmembrane protein, which specifically binds sialic a
via the viral protein gp120; gp41, a viral	transmembrane protein, then undergoes a conformational c
“MOG is a quantitatively minor type I	transmembrane protein, and is found exclusively in the C
it is a GPI-anchored protein rather than a	transmembrane protein.
Unlike most collagens, collagen XVII is a	transmembrane protein.
The full length form is the	transmembrane protein.
n Golgi 1,2-mannosidase which is a type II	transmembrane protein.
sible for the intramembrane proteolysis of	transmembrane proteins such as the Notch protein and amy
They are	transmembrane proteins that contain an N-terminal V-like
ight-harvesting proteins are the intrinsic	transmembrane proteins CP43 (PsbC) and CP47 (PsbB) occur
Connexins are four-pass	transmembrane proteins with both C and N cytoplasmic ter
Rh family proteins are all predicted to be	transmembrane proteins with 12 membrane spanning domains
e transport proteins, a class of multipass	transmembrane proteins that facilitate the diffusion of
laudins are small (20-27 kilodalton (kDa))	transmembrane proteins which are found in many organisms
istic of extracellular matrix proteins and	transmembrane proteins suggests that this protein is a r
s and actin microfilaments are attached to	transmembrane proteins by attachment proteins between th
membrane protein, that cleaves single-pass	transmembrane proteins at residues within the transmembr
Other members of the JAM family of	transmembrane proteins include JAM1, JAM2 and JAM3.
Calsyntenins (Csts, CLSTN) are type I	transmembrane proteins that belong to the cadherin super
These domains help anchor	transmembrane proteins to the cytoskeleton and hold toge
LMP-2A/LMP-2B are	transmembrane proteins that act to block tyrosine kinase
noid and Glutathione metabolism) family of	transmembrane proteins with highly divergent functions .
Bestrophins are	transmembrane proteins that contain a homologous region
Notch (DSL) proteins are a family of	transmembrane proteins with repeated extracellular EGF d
More than 40 highly divergent	transmembrane proteins that could contribute to this fun
The protein, interferon-inducible	transmembrane proteins (IFITM), was discovered about 25
viral hemagglutinin, neuraminidase and M2	transmembrane proteins, and facilitates budding of the m
, which are a large family of secreted and	transmembrane proteins, some of which function as repell
TLRs are	transmembrane proteins, expressed on the cell surface an
These receptors are all	transmembrane proteins, composed of a ligand-binding ext
ymes that cleave extracellular portions of	transmembrane proteins, releasing the soluble ectodomain
Peptide hormone receptors are often	transmembrane proteins.
This is a member of MAPEG family of	transmembrane proteins.
ia to invade mammalian cells via cadherins	transmembrane proteins.
cut off or shed extracellular portions of	transmembrane proteins.
Some terminal oxidases generate a	transmembrane proton gradient across the plasma membrane
The vacuolar (V-type) ATPases have a	transmembrane proton-conducting sector and an extramembr
ember 13B (more commonly known as TACI), a	transmembrane receptor protein found predominantly on th
ptor 1 (BLR1) is a G protein-coupled seven	transmembrane receptor for chemokine CXCL13 (also known
lecular biology, the insulin receptor is a	transmembrane receptor that is activated by insulin.
The B-cell receptor is a	transmembrane receptor protein located on the outer surf
An enzyme-linked receptor is a	transmembrane receptor, where the binding of an extracel
CD93 is a C-type lectin	transmembrane receptors which play a role not only in ce

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共起表現

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「Transmembrane」の共起表現一覧(1語右で並び替え)