「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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