「N terminal」の共起表現(1語右で並び替え)

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共起
表現

「N terminal」の共起表現一覧(1語右で並び替え)

N terminal

1語右で並び替え

該当件数:186件

dition to NBD and LRR, NLRP1 contains at its N-terminal a pyrin domain(PYD) and at its C-terminal an
N-terminal acetylation
nsferase, peptide acetyltransferase, protein N-terminal acetyltransferase, NAT, Nalpha-acetyltransfe
that utilize a metal cofactor and remove the N-terminal amino acid from peptides with a proline resi
an amide bond to the alpha-amino group of an N-terminal amino acid of a nascent polypeptide.
Sanger described its use for determining the N-terminal amino acid in polypeptide chains, in particu
The N-terminal amino acid of a protein is an important dete
non-covalently associated subunits, [alpha] ( N-terminal) and [beta] (C-terminal).
The N-terminal and the C-terminal portions of this enzyme c
of the cytoplasmic loops to produce a larger N-terminal and a smaller C-terminal fragment which toge
lypeptides are directional and have distinct N-terminal and C-terminal ends, propagation parameters
The EcoRII monomer has two domains, N-terminal and C-terminal, linked through a hinge loop.
Both the N-terminal and C-terminal regions of this protein protr
r of the TRPA sub-family, TRPA1, contains 14 N-terminal ankyrin repeats and is believed to function
P binding, hydrolysis, and ADP release by an N-terminal ATP-hydrolizing domain to cycles of sequestr
This cationic N-terminal beta-sheet domain mediates binding of the cl
r helix propagation, v for initiation, n for N-terminal capping, and c for C-terminal capping.
These proteins have at least 1 N-terminal CARD domain followed by a centrally located
These inhibitors possess an N-terminal CDK-inhibitory domain which binds to the ATP
ulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with sub
three topologically non-equivalent domains ( N-terminal, central, and C-terminal).
The N-terminal chloroplast targeting peptide (cpTP) allows
SK1 kinase activity by direct binding to its N-terminal coiled-coil domain (NCC).
N-terminal CUB domain (for complement C1r/C1s, Uegf, Bm
The N-terminal cysteine as well as the internal cysteines a
er reacts with another peptide containing an N-terminal cysteine residue, in the presence of an adde
re considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal m
sed of several domains starting with a short N-terminal cytoplasmic portion connected to an extracel
The N-terminal, cytoplasmic tetramerization domain (T1) of
ion transporter 1. Steap3 is composed of an N-terminal cytosolic oxidoreductase domain and a C-term
Transgenic mice with N-terminal deletion of Gli2, developed the benign trich
The gene product contains an N-terminal DNA binding domain and C-terminal ligand bin
IS restriction endonuclease consisting of an N-terminal DNA-binding domain and a non-specific DNA cl
TM1602 has an N-terminal DNA-binding domain and a C-terminal 3H regul
The N-terminal domain of alpha-crystallin is not necessary
, however, for a truncated PheOH lacking the N-terminal domain or if the full-length enzyme is pre-i
It consists of an N-terminal domain L and four repetitive calpain-inhibit
The central part of the N-terminal domain consists of a variable number (3 in v
n prokaryotes, the FEN enzyme is found as an N-terminal domain of DNA polymerase I, but some prokary
with contributions from residues within the N-terminal domain and the linker region.
The N-terminal domain is also found in the PROSC (proline s
The N-terminal domain of APOBEC like proteins is the cataly
The N-terminal domain of three proteins share low sequence
in Drosophila, mice, and humans, contains an N-terminal domain not found in other isoforms that show
Deletion of the N-terminal domain also eliminates the lag time while in
The N-terminal domain appears to bind to the NAD promoter r
ructurally the protein consists of an acidic N-terminal domain of about 90 kDa separated from a basi
resent a similar domain organization, with a N-terminal domain of 39 to 129 residues in length, a pr
The N-terminal domain of the mature protein forms an alpha-
a 50-residue flexible linker peptide, and an N-terminal domain predicted to adopt a cystatin-like fo
C5a and acidic residues in the extracellular N-terminal domain allows the C-terminus of C5a to bind
The N-terminal domain has phospholipase activity.
The N-terminal domain is called a MENTAL (MLN64 N-terminal)
Its N-terminus consists of a MENTAL (MLN64 N-terminal) domain similar to the protein MLN64 N-termi
The regulatory nature of the N-terminal domain (residues 1-117) is conferred by its
The N-terminal domain consists of a seven-bladed β-propelle
The N-terminal domain of cytochrome C oxidase contains two
The N-terminal domain of yeast ECM25 protein has been ident
consisting of two domains: an alpha helical N-terminal domain, and a C-terminal domain composed of
into multiple subdomains, starting with the N-terminal domain, followed by the ankle, distal leg, k
a shorter all-alpha N-terminal domain,
ase has two clearly defined domains, a small N-terminal domain, and a large C-terminal domain.
clathrin-binding domain, and a tension-like N-terminal domain.
, Ala64, Ser64, Val103, Cys48, His102 at the N-terminal domain.
s consist of a conserved extracellular large N-terminal domain; three highly conserved transmembrane
alyse extracellular matrix degradation, have N-terminal domains that resemble PGBD.
n apo structure are spatially blocked by the N-terminal domains.
structure composed of 3 protein domains: an N-terminal effector domain containing a mitochondrion l
this protein with the receptors unmasks the N-terminal effector domain(see structural image on the
tide end-group analysis: A derivatization of N-terminal end with Sanger's reagent (DNFB), B total ac
o acid sequence of xenin is identical to the N-terminal end of cytoplasmic coatomer subunit alpha, f
protein with a tyrosine kinase domain at the N-terminal end and a proline-rich domain at the C-termi
ts of two globular structural domains at the N-terminal end and one globular domain at the C-termina
span the cellular membrane 4 times, with the N-terminal end and the C-terminal end both located in t
The N-terminal end is usually very short (4-10 amino acids)
M Jope, "The Protein of Brachiopod Shell V: N-terminal End Groups", Comp.
C-terminal end, dentin sialoprotein from the N-terminal end, and dentin glycoprotein from the middle
tracellular region with a variable number of N-terminal epidermal growth factor (EGF)-like domains c
n extended extracellular region with several N-terminal epidermal growth factor (EGF)-like domains,
ro-Val-Asn-Phe-Lys-Leu-Leu-Ser-His and is an N-terminal extended form of hemopressin, a 9-AA polypep
the targeting peptide are often found at the N-terminal extension and is composed of between 6-136 b
architecture comprising a signal peptide, an N-terminal extracellular domain, a single transmembrane
ts have a characteristic cys-cys pair in the N-terminal extracellular domain, this is shown to be es
d C2 type immunoglobulin-like domains at the N-terminal extracellular portion.
ed structure for each subunit is a conserved N-terminal extracellular domain followed by three conse
highly conserved amino acids apart near the N-terminal extracellular domain of the alpha subunit.
n-1 is a glycoprotein which contains a large N-terminal extracellular region, multiple transmembrane
The subunits of tPRAI associate via the N-terminal faces of their central beta-barrels.
In addition, N-terminal FLAG tags can be removed readily from protei
coded by the MBTPS2 gene which liberates the N-terminal fragment of sterol regulatory element bindin
An N-terminal fragment of PCI is a possible serum biomarke
tides, one bearing a C-terminal α-thioester ( N-terminal fragment 1) and the other an N-terminal cyst
The linker domain between the N-terminal globular domains, called the interglobular d
N-terminal glutamine residues can spontaneously cyclize
320 amino acids, and contains 3 domains, an N-terminal Gly/Arg-rich region; a central domain resemb
The N-terminal half (domains 1 and 2) contains the 'Rossman
xin:NADP+ reductase: the FAD-binding domain ( N-terminal) has the topology of an anti-parallel beta-b
sed of three distinct structural domains: an N-terminal helical bundle domain (IPR005639) involved i
ially equivalent; PGHS contains 5 additional N-terminal helices that have no equivalent in MPO.
n oligomerisation domain consists of a short N-terminal helix (alpha-1), a flexible loop and a long
The N-terminal heparin-binding domain of TSP1, when isolate
rnate name implies, MENTHO, short for "MLN64 N-terminal homologue", contains a region in its N-termi
The gene product has an N-terminal hydrophobic domain that is not present in ot
nce sialoadhesin binds sialic acids with its N-terminal IgV-domain, it is also a member of the SIGLE
immunoglobulin superfamily and possesses one N-terminal immunoglobulin (Ig)-variable (V) domain, one
the presence of two leucine residues in its N-terminal intracellular domain, which influences intra
emonstrated that ERK, p38 MAP kinase and Jun N-terminal kinase were all able to phosphorylate and ac
The N-terminal kinase domain is able to phosphorylate histo
biochemical studies as an inhbitor of c-Jun N-terminal kinases (JNKs).
cted including: two ERK3 isoforms, ERK4, Jun N-terminal kinases/stress-activated protein kinases (JN
N-terminal labelling
MENTHO or STARD3 N-terminal like protein (STARD3NL) is an integral membr
all subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase d
The β subunit consists of a long N-terminal loop that wraps around the α subunit; a heli
ine residues exposed during co-translational N-terminal methionine removal.
bout the presence of programmed frameshifts, N-terminal methionine excision, signal peptides, proteo
Moreover, the side chains of the N-terminal methionines and the C-terminal leucines of b
, almost all coronins have a short conserved N-terminal motif and coiled coil motif of 50aa at C-ter
AAA proteins have an N-terminal Non-ATPase domain which is followed by eithe
esidues which are added at the C-terminal or N-terminal of the protein of interest.
Itk and Tec are able to bind to the N-terminal of these two motifs which immediately succee
egion in the potassium channel (flanking the N-terminal of SloTx) is situated in the face opposite t
The N-terminal passenger domain is translocated across the
A glycosylated form of the N-terminal peptide may be associated with cachexia (mus
The N-terminal peptide, also known as diffusible survival e
transmembrane and extramembrane regions: an N-terminal periplasmic region, a transmembrane region,
There are three sub-families - all share an N-terminal PITP-like domain, whose sequence is highly c
C-terminal region of the RET protein with an N-terminal portion of another protein, can also lead to
equence, methionine is incorporated into the N-terminal position of all proteins in eukaryotes and a
finger transcription factor and contains an N-terminal POZ domain.
Alternatively, the N-terminal pro-sequence of proteases which must be clea
o the secreted C-terminal peptide, while the N-terminal product may play a role in cell cycle contro
The N-terminal prohormone of brain natriuretic peptide (NT-
sists of four subunits, each composed of the N-terminal proregion fragment, the heavy chain and the
eins, such as NALP2, are characterized by an N-terminal pyrin (MIM 608107) domain (PYD) and are invo
Most short NALPs, such as NALP12, have an N-terminal pyrin (MEFV; MIM 608107) domain (PYD), follo
Most short NALPs, such as NALP7, have an N-terminal pyrin (MEFV) domain (PYD), followed by a NAC
he adaptor molecule ASC) is mediated via the N-terminal pyrin (PYD) domain.
y reported that acetylation of Lys5 near the N-terminal region and Lys29 in the beta-turn region led
ein structure prediction methods suggest the N-terminal region of CLCA3 protein is a zinc metallopro
The N-terminal region is thought to bind the lipid and cont
The N-terminal region contains the conserved Y-G-N-G-V/L 'p
The N-terminal region contains 12 basic aa which can be tak
RecQ helicase with topoisomerase III at the N-terminal region is involved in the suppression of spo
the deacetylation of lysine residues on the N-terminal region of the core histones (H2A, H2B, H3 an
Opiorphin pentapeptide originates from the N-terminal region of the protein PROL1 (proline rich, l
ein structure prediction methods suggest the N-terminal region of CLCA1 protein is a zinc metallopro
The N-terminal region of PKC, known as C1, has been shown
ein structure prediction methods suggest the N-terminal region of CLCA2 protein is a zinc metallopro
Residues 1-60: An amphipathic N-terminal region dominated by four 11-residue repeats
The N-terminal region of PKC, known as C1, binds PMA and DA
a hydrophilic, cationic and highly conserved N-terminal region, and a less conserved hydrophobic/amp
It has been found that N-terminal regions of Gli1 recruit histone deacetylase
This N-terminal regulatory domain is not observed in bacteri
N-terminal residue sequencing resulting in five to ten
N-end rule pathway, in which a destabilizing N-terminal residue dramatically decreases the in vivo h
either side of a proline residue, (iii) the N-terminal residue is lysine or arginine, or (iv) the s
Citrus lacking the 21 amino sequence on the N-terminal results in extensive chlorophyll breakdown a
B share a region of high similarity in their N-terminal section; this region includes two cysteine r
smembrane receptor domain, whereas the large N-terminal segment (5900 residues) includes 35 calcium
roteases in that it contains this additional N-terminal segment predicted to share structural simila
It has two cysteine residues on the N-terminal segment, a hydrophilic loop near the carbohy
th its substrate more readily because of the N-terminal sequence and some natural regulation occurs
cked N-terminals which present a problem for N-terminal sequencing using Edman chemistry, which requ
CHN1 is a three-domain protein with the N-terminal SH2 domain, the C-terminal RhoGAP domain and
It is blocked by pGlu at its N-terminal side and amidated at its C-terminus.
s recognition event is based upon a specific N-terminal signal sequence that is in the first few cod
d a single transmembrane domain but lacks an N-terminal signal peptide.
ells, and is activated by the cleavage of an N-terminal signal sequence.
s, a complete vitellinogen is composed of an N-terminal signal peptide for export, followed by four
the protein and consists of two subdomains: N-terminal subdomain (Cys 167 to Cys 179) and C-termina
The N-terminal subdomain is connected with N-terminal domai
The N-terminal tail of Lck is myristoylated and palmitoylat
histones of the histone octamer all contain N-terminal tails that emanate from their central histon
tylated lysine residues such as those on the N-terminal tails of histones.
In bone physiology, the N-terminal telopeptide (or more formally, amino-termina
o acids in Chenopodium album) located on the N-terminal that was absent from the mature protein.
tidases can only remove the His-tag from the N-terminal, therefore removing the tag from the C-termi
ction involving a nucleophilic attack of the N-terminal thiol group of peptide 2 at the α-thioester
sins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains an
to all nuclear hormone receptors, namely an N-terminal transcriptional activation domain (A/B domai
The name 'YKL' stands for its N-terminal tripeptide sequence, and unlike the other me
protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker
The N-terminal two helices are antiparallel and the longer
y are transmembrane proteins that contain an N-terminal V-like immunoglobulin (IgV) domain that bind
3-phosphoglycerate (3-PG) binds to the N-terminal, while the nucleotide substrates, MgATP or M