「residues」の共起表現一覧(1語右で並び替え)
該当件数 : 428件
s not present in cells, the abnormal aspartyl | residues accumulate, creating abnormal proteins that h |
that liquids are incrementally separated from | residues across a range of pressures and subsequently |
The phosphorylated serine and threonine | residues act as binding sites for arrestin proteins wh |
Absorbed glycols from the flux | residues aggravate the problem. |
te cells (because of affinity for sialic acid | residues), allowing preferential protection of host (a |
zyme is coordinated by at least two histidine | residues, an aspartate residue, a glutamine residue, a |
chain (e.g., iodoacetamide to modify cysteine | residues), an isotopically coded linker, and a tag (e. |
double strand breaks, 8-hydroxydeoxyguanosine | residues and polycyclic aromatic hydrocarbon adducts. |
recycling (for one, through decomposing plant | residues) and other soil building and maintaining acti |
due range and known to contain eight cysteine | residues; and the ‘short chain neurotoxins' (SCN) with |
This C2 domain is about 116 amino-acid | residues and is located between the two copies of the |
The protein contains 5058 | residues, and is currently the largest known protein o |
pper atoms are coordinated by seven histidine | residues and bridged by a sulfur atom. |
lmost completely homologous for the first ~36 | residues and similar in tertiary structure for the fir |
ining 1,4-linked D-glucuronate or L-iduronate | residues and 1,4-alpha-linked 2-sulfoamino-2-deoxy-6-s |
of hydrogen bonds connect distant amino acid | residues and are not involved in secondary structure s |
rylation/dephosphorylation of targeted serine | residues and by allosteric transformation by citrate o |
nd their source can include slag, dross, flux | residues, and pieces of the mold. |
sistin pre-peptide in human is 108 amino acid | residues and in the mouse and rat it is 114 aa; the mo |
Curdlan consists of β-(1,3)-linked glucose | residues and forms elastic gels upon heating in aqueou |
is a peptide hormone containing 28 amino acid | residues and is produced in many areas of the human bo |
nt, yet the pseudoknot region lacks conserved | residues and pseudoknots are among the first structure |
aging, animal welfare, wildlife conservation, | residues and additives in order to reassure the buying |
ic bonds in protein (especially, like proline | residues) and that is why it can precipitate tannins t |
bonds from trans form to cis form at proline | residues and facilitates protein folding. |
c ion (green) is coordinated by two histidine | residues and two cysteine residues. |
inases that phosphorylate serine or threonine | residues and can discriminate between the kinase domai |
ine kinases, but instead phosphorylate serine | residues, and probably do not use a phospho-histidine |
Hydrogen bonds between binding pocket | residues and pepstatin are highlighted. |
for example in the distribution of quadratic | residues, and in particular in the classical question |
no central pore and contains both hydrophobic | residues and charged residues neutralized by salt brid |
The κ- Hefutoxin1 consists of 22 | residues and one amidated C terminus and is therefore |
tal is composed of 50% helical (9 helices; 97 | residues) and 10% beta sheet (6 strands; 21 residues). |
hat cleaves the link between N-acetylmuramoyl | residues and L-amino acid residues in certain cell-wal |
sh fruit should be washed to remove pesticide | residues, and ideally be organic fruit |
boxypeptidase E cleaves C-terminal amino acid | residues and is involved in neuropeptide processing. |
s hero is obsessed with “surplus matter”: the | residues and traces of events. |
It has 191 amino acid | residues and a molecular weight of 22,125 daltons. |
Just two histidine | residues and one aspartic acid residue are entirely co |
acid sequence (i.e., they are more than three | residues apart in the primary sequence) but are spatia |
th the aspartic acid and arginine active site | residues are highly conserved among galactokinases. |
If terminal sialic acid | residues are removed from glycoproteins, the resulting |
eptidoglycan or pseudomurein, where the sugar | residues are β-(1,3) linked N-acetylglucosamine and N- |
The xylose | residues are often capped with a galactose residue som |
nment to determine which conserved amino acid | residues are critical for folding and stability. |
turing varieties, and the destruction of crop | residues are well-established methods for suppressing |
A recent study shows that these basic | residues are involved in actin binding. |
K-65 | residues are the very radioactive mill residues result |
uct of the chlorination of water when organic | residues are present in the water, though concentratio |
with high hydrophilicity indicate that these | residues are in contact with solvent, or water, and th |
Amino-acid | residues are attached with their N-terminus protected, |
al cells in the matrix can be shaded black if | residues are identical, so that matching sequence segm |
The active site | residues are exposed on the exterior of the flat face |
eaction in which at least one alpha-D-mannose | residues are transferred from GDP-mannose to positions |
Specifically 2 helices and 7 | residues are formed. |
he catalytic histidine and stabilizing serine | residues are colored orange. |
These | residues are all conserved in the Clostridium alpha-to |
Certain sequences of amino acid | residues are able to recognise and are specific to an |
e mRNA has been cleaved, around 250 adenosine | residues are added to the free 3' end at the cleavage |
The active site Asp-25 | residues are colored red. |
ligosaccharides with three sequential glucose | residues are added to asparagine residues of the nasce |
Proline | residues are known to be structure-breaking residues, |
to determine which | residues are important for a particular phenotype, e.g |
A different representation: polyacrylic acid | residues are shown in red, residues of the cross-linke |
The active site His and Ser | residues are located at the exterior of the beta-barre |
age areas are kept clean and tidy and that no | residues are left over. |
mon post-translational modification, cysteine | residues are converted into thiazolines. |
andran plot shows 66 out of 67 (98.5%) of all | residues are in the favored regions with no outliers p |
Fuel made of | residues as CO2 produced by using a primary fuel. |
ting covalently with DNA guanine and cytosine | residues as well as protein. |
pin has the same amino acid sequence with 191 | residues as the native human growth hormone produced i |
on process is unable to sequence more than 70 | residues at a time. |
ecause of specificity for aromatic amino acid | residues at the active site (as in chymotrypsin, in wh |
The fourth TM domain has positively charged | residues at every third residue and acts as a voltage |
e leucine zipper consists of multiple leucine | residues at approximately 7-residue intervals, which f |
report, "Safety of the High-Level Uranium Ore | Residues at the Niagara Falls Storage Site, Lewiston, |
f two geranylgeranyl groups onto two cysteine | residues at the C-terminal consensus sequence CXC or X |
for example when previously internal glycine | residues become exposed by caspase cleavage during apo |
ng, hydrophobic methyl groups from methionine | residues become exposed on the protein via conformatio |
se sugars in O linkage to serine or threonine | residues between the second and third conserved cystei |
ontacts, ΔSi,j is the sequence separation, in | residues, between contacting residues i and j, and L i |
kely, apamin acts as a pore blocker, although | residues both inside and outside of the pore region of |
It is more common on glycine | residues but also occurs on other amino acids. |
blems, such as the proton exchange of protein | residues by deuterons. |
nexin result from the trimming of two glucose | residues by the sequential action of two glucosidases, |
β subunit becomes phosphorylated on tyrosine | residues by members of the Janus kinase (JAK) family. |
e late 1990s have suggested that neonicotinic | residues can accumulate in pollen and nectar of treate |
N-terminal glutamine | residues can spontaneously cyclize to become pyrogluta |
Liskamp have shown that scaffolded histidine | residues can be used as mimics of certain metalloprote |
sion of carbon monoxide in path B two organic | residues can recombine with formation of a new carbon |
It takes a band of 32 | residues centered on the init1 region of step2 for cal |
The guanidine group of arginine | residues condense with MDA to give 2-aminopyrimidines. |
It is a disaccharide made of two glucose | residues, connected with a 1->3 link. |
atory domain of the enzyme, and the remaining | residues constitute the catalytic domain. |
The | residues constituting the MIDAS motif in the CD11b and |
d process for treating and recovering mineral | residues contaminated with heavy metals. |
BglII active site | residues coordinate with Mg2+ cation and water molecul |
eptide with its abudance of charged and polar | residues could improve solubility of proteins it is at |
h variations in assignment of single terminal | residues, current implementations of STRIDE and DSSP a |
tive site sequence with two reactive cysteine | residues: Cys-X-Y-Cys, where X and Y are often but not |
To consider three consecutive | residues each with two states (helix and coil), the Li |
LDL receptor type A (LA) repeats of 40 | residues each, displaying a triple-disulfide-bond-stab |
ndenses to form a cross-linked structure of 4 | residues, either Desmosine or Isodesmosine. |
the flat side of the beta-barrel, with polar | residues embedded in an apolar environment forming the |
This protein contains selenocysteine (Sec) | residues encoded by the UGA codon, which normally sign |
and commensurately lower in other hydrophobic | residues, esp. |
een these two forms is the number of cysteine | residues exposed at the surface of the enzyme. |
se (NMT), and occurs most commonly on glycine | residues exposed during co-translational N-terminal me |
up three of every four amino acids and other | residues falling periodically into the fourth spot. |
ts, Q1 and Q2, composed mainly of hydrophobic | residues flanking the saddle. |
36-38) rapidly phosphorylated on tyrosine | residues following TCR ligation. |
h can then be mixed with biomass such as crop | residues, food waste, manure and / or other, and burie |
that of thermolysin the predicted active site | residues for members of this family and thermolysin oc |
contains Walker A and Walker B. The important | residues for ATP hydrolysis and/or binding are located |
activating proteins are quite large (from 765 | residues for sar1 to 3079 residues for IRA2) but share |
glycoprotein with 4 lysine | residues for conjugation to a labeled molecule. |
cal domains of largely hydrophobic amino acid | residues, forming three intra- and three extra-cellula |
The primary structure contains 28 cysteine | residues forming multiple disulfide bonds. |
of 18 amino acids, six of which are arginine | residues, forms two antiparallel β-sheets with a β-tur |
ssion from the works incinerator which burned | residues from the chlorination plant. |
ccharide binding site in which four conserved | residues from four separate regions in the protein con |
y for designing pramlintide was to substitute | residues from rat amylin, which is not amyloidogenic ( |
Exolytic cleavage of disaccharide | residues from the non-reducing ends of both polymeric |
Fuel for the plant is derived from wood | residues from Erie Flooring and Wood Products that are |
Organic | residues from these extinction boundaries indicate tha |
n catalyzes the removal of 3 distinct mannose | residues from peptide-bound Man(9)-GlcNAc(2) oligosacc |
eedstocks such as tobacco, flax straw and the | residues from the production of bioethanol. |
samples, especially when finely divided, and | residues from reactions can be pyrophoric, which can i |
and provided by a methionine residue about 40 | residues further on towards the C-terminus. |
Fly ash is one of the | residues generated in combustion, and comprises the fi |
not always, substituted with D-alanine ester | residues, giving the molecule zwitterionic properties. |
On the interacting helices are | residues Glu144 and Arg145, which interact together fo |
ptors contain high proportions of hydrophobic | residues grouped into 7 domains, in a manner reminisce |
ptors contain high proportions of hydrophobic | residues grouped into 7 domains, in a manner reminisce |
onally, acid/base catalysis by the amino acid | residues has been suggested. |
((-CYS*-TRY-LYS-TRP-PHE-CYS*-), (*bridged CYS | residues)), has been conserved through evolution from |
DBCP | residues have persisted in contaminated soil and groun |
y a hydrogen bond only once three consecutive | residues have adopted the helical conformation. |
demonstrated to persist for several years and | residues have been detected in plants for several year |
onds and unusual pKa values for the catalytic | residues have been proposed as the basis for the fast |
s highly significant that these two histidine | residues, His214 and His270, and one aspartic acid res |
For two | residues i and j, the ij element of the matrix is 1 if |
hat cleaves single-stranded RNA after guanine | residues, i.e., on their 3' end; the most commonly stu |
Residues important for catalysis are shown in magenta. | |
Putative CB1 receptor amino acid side chain | residues in receptor-ligand interaction are shown. |
als and at side-chains of arginine and lysine | residues in hemoglobin. |
tive dyes, as a specific reagent for tyrosine | residues in enzymes, and as a fluorinating agent. |
Side view of an 310-helix of alanine | residues in atomic detail. |
ks in the spectrum should match the number of | residues in the protein (though sidechains with nitrog |
phosphate group to the sidechain of histidine | residues in proteins (protein-histidine kinases). |
ylglucoamine groups from serine and threonine | residues in the cytoplasm and nucleus of the cell. |
ein domain which recognises methylated lysine | residues in histone tails. |
rate a number of isoforms of 36-43 amino acid | residues in length. |
sidechain oxygen atom of serine or threonine | residues in proteins (protein-serine/threonine kinases |
Dermaseptins are typically 27-34 amino acid | residues in length and were the first vertebrate pepti |
The two amino acid cysteine | residues in contryphans are linked by a disulfide bond |
ons of RNA are formed by base-pairing between | residues in the close to region of the editing site wi |
as its half-life is lower, leading to reduced | residues in the food, and the dose required to affect |
zation, with a N-terminal domain of 39 to 129 | residues in length, a protein kinase domain and a shor |
he dcm gene) methylated the internal cytosine | residues in the sequences CCAGG and CCTGG. |
The continuous stretch of amino acid | residues in the chain that enables targeting are calle |
s that provide single dihedral values for all | residues in the π-helix are misleading. |
characterized by the presence of two leucine | residues in its N-terminal intracellular domain, which |
e the amine group of the side chain of lysine | residues in proteins, causing cross-linking and a loss |
ent kinases by the removal of phosphates from | residues in the Cdk active site. |
These molecules covalently modify active site | residues in order to elucidate the structure of the ac |
amino acid sequence demonstrated the leucine | residues in a predicted leucine zipper motif were requ |
teine disulfide bridges and lysine amino acid | residues in proteins, gradually affecting function and |
lyzes the hydrolysis of terminal non-reducing | residues in beta-D-glucosides with release of glucose. |
cted to guides the methylation of 2'-O-ribose | residues in 28S ribosomal RNA (rRNA). |
Chloramphenicol binds to A2451 and A2452 | residues in the 23S rRNA of the ribosome and inhibits |
viruses, such as HIV, by deaminating cytosine | residues in nascent retroviral cDNA. |
-ribosyltransferases, which modify amino acid | residues in proteins such as histones by adding a sing |
o-stage process: an interaction between basic | residues in the helical core of C5a and acidic residue |
One of the active site | residues in the protein kinase domain of this protein |
ng contiguous stretches of un-esterified GalA | residues in homogalacturonan domains of pectin. |
In general, aspartic or glutamic acid | residues in the active site of the enzyme catalyze the |
It leaves no | residues in tissues. |
yl group from S-adenosylmethionine to adenine | residues in the sequence GATC. |
minated sites in New Zealand due to pesticide | residues in the soils from a now defunct factory. |
It reacts with cysteine | residues in proteins. |
to a different number of ionizable amino acid | residues in the protein portion of hemoglobin (which w |
ored in red are positively-charged amino acid | residues in the N-terminus and the β-turn region that |
ce transported, the translated protein is 396 | residues in length, with an N-terminus located at amin |
be storing thousands of cubic metres of wood | residues in one place, so the issue becomes one of con |
Pint: A server for predicting ATP interacting | residues in proteins. |
ny benefits, including avoiding petrochemical | residues in the product and the loss of some "top note |
onversion of thiol groups, including cysteine | residues in proteins, to form S-nitrosothiols (RSNOs). |
ut does not hydrolyze palmitate from cysteine | residues in proteins. |
is colleagues had hoped, as the amount of DDT | residues in the environment dropped, osprey numbers on |
where m is number of | residues in the helix. |
Apiose is a branched-chain sugar found as | residues in galacturonans-type pectins; that occurs in |
It is a polypeptide chain 64 | residues in length. |
oups such as palmitate from modified cysteine | residues in proteins or peptides during lysosomal degr |
For example, cysteine | residues in the peptide may be temporarily blocked fro |
of separating the 1,6-linked alpha-D-mannose | residues in alpha-D-Manp-(1->6)-D-Manp. |
s absent includes the same order of catalytic | residues in the sequences. |
red, the alpha carbons of the eight cysteine | residues in green, and the disulfide bridges in yellow |
as nucleotide sugars act as donors for sugar | residues in the glycosylation reactions that produce p |
ugustin-Louis Cauchy introduces the theory of | residues in complex analysis. |
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