「RESIDUES」の共起表現一覧(2語左で並び替え)
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n is a large protein of 116 kDa (about a 1000 | residues). |
As a result, | residues of these chemicals find their way into the fi |
s not present in cells, the abnormal aspartyl | residues accumulate, creating abnormal proteins that h |
enzyme, as the amount of abnormal L-aspartate | residues increased when cells were treated with the in |
and provided by a methionine residue about 40 | residues further on towards the C-terminus. |
ey are single-chain polypeptides of about 100 | residues, which have neither disulfide bonds nor carbo |
t 25 kDa by a proline-rich region of about 50 | residues. |
tein domain that recognizes acetylated lysine | residues such as those on the N-terminal tails of hist |
catalyze the hydrolysis of acetylated lysine | residues restoring the positive charge to histone prot |
The two amino acid cysteine | residues in contryphans are linked by a disulfide bond |
th the aspartic acid and arginine active site | residues are highly conserved among galactokinases. |
These molecules covalently modify active site | residues in order to elucidate the structure of the ac |
BglII active site | residues coordinate with Mg2+ cation and water molecul |
The active site | residues are exposed on the exterior of the flat face |
that of thermolysin the predicted active site | residues for members of this family and thermolysin oc |
One of the active site | residues in the protein kinase domain of this protein |
this enzyme contains most of the active site | residues. |
Recently, the roles of active site | residues in human galactokinase have become understood |
the calf liver showed additional unidentified | residues, of which a new metabolite, ml, represented t |
ct by chemically reacting with adjacent thiol | residues on metabolic enzymes, creating a chelate comp |
hat cleaves single-stranded RNA after guanine | residues, i.e., on their 3' end; the most commonly stu |
is occasionally broadly applied to all glassy | residues of nuclear bomb testing, not just the Trinity |
lytic triad as the chymotrypsins although the | residues occur in a different order (His/Asp/Ser in ch |
onally, acid/base catalysis by the amino acid | residues has been suggested. |
nment to determine which conserved amino acid | residues are critical for folding and stability. |
urtoxin is a protein containing 63 amino acid | residues with a mass of 7386.1 daltons. |
rochelatase enzyme consists of 497 amino acid | residues with a m.w. of 55.4 kDa. |
es share an N-terminus of eighteen amino acid | residues. |
the proteins have from 209 to 241 amino acid | residues. |
The amino acid | residues involved in hydrogen bonding to the ligand ar |
ecause of specificity for aromatic amino acid | residues at the active site (as in chymotrypsin, in wh |
E. coli RNR2 C-terminal (7 or 33) amino acid | residues, the chimeric RNR2 subunit still binds to mou |
rate a number of isoforms of 36-43 amino acid | residues in length. |
Dermaseptins are typically 27-34 amino acid | residues in length and were the first vertebrate pepti |
to result from the absence of key amino acid | residues that produce structural differences that hind |
d 2) substitution of the consensus amino acid | residues with amino acid residues exhibiting similar h |
) is a protein of about 275 to 315 amino acid | residues that is either chromosomally encoded or found |
It is made up of amino acid | residues that are distant to one another in the primar |
The continuous stretch of amino acid | residues in the chain that enables targeting are calle |
o called S-peptide, consists of 20 amino acid | residues, of which only the first 15 are required for |
This peptide, with 35 amino acid | residues, is small enough to get inside POP while the |
teine disulfide bridges and lysine amino acid | residues in proteins, gradually affecting function and |
filter made of negatively charged amino acid | residues, which attract the positive Na+ ion and keep |
of hydrogen bonds connect distant amino acid | residues and are not involved in secondary structure s |
Altitoxin is 58 amino acid | residues long and has a molecular mass of 6598 Da; it |
sistin pre-peptide in human is 108 amino acid | residues and in the mouse and rat it is 114 aa; the mo |
ithout peptidase activity, or lack amino acid | residues that are believed to be essential for the cat |
sis relies on a handful of charged amino acid | residues positioned within the active site of the enzy |
a cleft or pocket that is lined by amino acid | residues (or nucleotides in ribozymes) that participat |
onserved disulfide bonds and three amino acid | residues involved in the catalytic activity. |
is a peptide hormone containing 28 amino acid | residues and is produced in many areas of the human bo |
-ribosyltransferases, which modify amino acid | residues in proteins such as histones by adding a sing |
The new amino acid | residues that it recruited from yellow emperor allow t |
ng signals generally contain 10-80 amino acid | residues that take on the conformation of an amphipath |
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 |
The very long (251 amino acid | residues) proregion of the cathepsin F precursor conta |
Endostatin monomer, basic amino acid | residues shown in red 1KOE |
Certain sequences of amino acid | residues are able to recognise and are specific to an |
cal domains of largely hydrophobic amino acid | residues, forming three intra- and three extra-cellula |
Structure α-PMTX consists of 13 amino acid | residues with the sequence Arg-Ile-Lys-Ile-Gly-Leu-Phe |
s altered evolutionarily conserved amino acid | residues. |
glycoproteins of about 170 to 180 amino acid | residues that contains four conserved cysteine residue |
ns code for a protein of over 3500 amino acid | residues. |
boxypeptidase E cleaves C-terminal amino acid | residues and is involved in neuropeptide processing. |
served module of approximately 230 amino acid | residues. |
0%), except for the metal-ligating amino acid | residues which are identical. |
It has 191 amino acid | residues and a molecular weight of 22,125 daltons. |
ber of positively charged lysine and arginine | residues on either side of the core sequence. |
als and at side-chains of arginine and lysine | residues in hemoglobin. |
rminals contains multiple arginine and lysine | residues that coordinate the three phosphoryl groups o |
Note the Lys and Asp | residues surrounding the 6-hydroxyl of the substrate. |
ylglucoamine groups from serine and threonine | residues in the cytoplasm and nucleus of the cell. |
g methyl-phenylalanyl and hydroxy-iso-valeryl | residues. |
e phosphoserine/threonine and phosphotyrosine | residues. |
d cleavage occurs between the Gln and Gly/Ser | residues. |
ne binding active site with Cys269 and His353 | residues showing with glutamine present |
aeces (coprolites), palynomorphs and chemical | residues. |
ting covalently with DNA guanine and cytosine | residues as well as protein. |
n, it will phosphorylate serine and threonine | residues on βARK. |
or, within the pore lumen, valine and leucine | residues (Val 255 and Leu 251) define a hydrophobic re |
diester bonds between the Adenine and Guanine | residues of both strands are hydrolyzed within the enz |
after leucine, methionine, and phenylalanine | residues. |
been identified in man of lengths 124 and 139 | residues. |
anion interaction between lysine and arginine | residues of the enzyme and phosphate groups of the nuc |
Chloramphenicol binds to A2451 and A2452 | residues in the 23S rRNA of the ribosome and inhibits |
This alters the 19th and 20th | residues of the C-terminal domain thereby altering the |
ncation of the receptor of between ten and 19 | residues. |
The phosphorylated serine and threonine | residues act as binding sites for arrestin proteins wh |
the precisely placed glutamate and histidine | residues to form the enediol, a ten- or eleven-amino a |
up three of every four amino acids and other | residues falling periodically into the fourth spot. |
titute positively-charged lysine and arginine | residues to neutral alanines. |
expense of contamination by metals and carbon | residues that shorten the life of downstream cracking |
Specifically 2 helices and 7 | residues are formed. |
to precisely target tiny minerals and organic | residues. |
rrolidone rings of proline and hydroxyproline | residues. |
ss IIa bacteriocins contain between 37 and 48 | residues. |
ence of thymidine, pseudouridine and cytidine | residues. |
eptide with its abudance of charged and polar | residues could improve solubility of proteins it is at |
e oxygen and nitrogen of interest and various | residues within the enzyme. |
echnology, the penultimate lysine and proline | residues on the C-terminal end of the B-chain are reve |
C5a receptor structure and its | residues possessing role in ligand binding or signalin |
The active site His and Ser | residues are located at the exterior of the beta-barre |
etween alpha-L-fucose and N-acetylglucosamine | residues in glycoproteins. |
eedstocks such as tobacco, flax straw and the | residues from the production of bioethanol. |
ever, methylation of some lysine and arginine | residues of histones results in transcriptional activa |
sortase B proteins that are approximately 200 | residues long. |
Type II domain is approximately forty | residues long, contains four conserved cysteines invol |
of 18 amino acids, six of which are arginine | residues, forms two antiparallel β-sheets with a β-tur |
In Bacillus cereus, there are nine | residues known to be involved in binding the zinc ions |
ysine 4 of histone 3 (H3K4), and arginine (R) | residues on H3 and H4. |
The SAM domain that spreads over around 70 | residues is found in diverse eukaryotic organisms. |
of MBL bind to specifically arranged mannose | residues on the surface of a pathogen, MASP-2 is activ |
h can then be mixed with biomass such as crop | residues, food waste, manure and / or other, and burie |
e mixed with compostable biomass such as crop | residues. |
Rava may be described as the | residues of milled material, after the flour is ground |
om four glutamic acid and seven aspartic acid | residues (in contrast to one histidine, two lysine and |
their substrates at C-terminal aspartic acid | residues. |
bonds from trans form to cis form at proline | residues and facilitates protein folding. |
on calcitonin, human calcitonin differs at 16 | residues. |
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 |
tu antigen are derived from glycophorin B and | residues 40-99 are derived from glycophorin A. Dantu i |
It cleaves base-paired nucleotide | residues. |
ons of RNA are formed by base-pairing between | residues in the close to region of the editing site wi |
length of the polypeptide was found to be 24 | residues with a secondary structure 29% helical. |
o-stage process: an interaction between basic | residues in the helical core of C5a and acidic residue |
hat cleaves the link between N-acetylmuramoyl | residues and L-amino acid residues in certain cell-wal |
Hydrogen bonds between binding pocket | residues and pepstatin are highlighted. |
are colored as follows: the ATP binding loop ( | residues 81-88), red; residue Asp301, magenta; choline |
ain information about biologically meaningful | residues, like active sites, substrate- or co-factor-b |
al cells in the matrix can be shaded black if | residues are identical, so that matching sequence segm |
kely, apamin acts as a pore blocker, although | residues both inside and outside of the pore region of |
no central pore and contains both hydrophobic | residues and charged residues neutralized by salt brid |
double strand breaks, 8-hydroxydeoxyguanosine | residues and polycyclic aromatic hydrocarbon adducts. |
suggested to form the first ring by coupling | residues 4 and 6. |
and box 3 (a conserved W surrounded by basic | residues). |
tep involving the removal of C-terminal basic | residues is required; this step is mediated by carboxy |
biquitin (truncated by two C-terminal glycine | residues). |
lcium due to the lack of calcium coordinating | residues or spatial orientation of the acidic residues |
In some cases, however, | residues on the grain result in flavours that are unac |
Activation of the 4 catalytic serine | residues within the Hin tetramer make a 2-bp double st |
and on the dihedral angles of the central two | residues. |
It is a polypeptide chain 64 | residues in length. |
which are proteins containing sugar chains or | residues) that are highly specific for their sugar moi |
nine (see image of Purine chemical structure) | residues 1492 and 1493 and the 2'OH group of the mRNA |
drogen peroxide (H2O2), used to clean organic | residues off substrates. |
Since the consensus sequence | residues of the substrate to be phosphorylated make co |
acentals also showed the high conservation of | residues thought to be involved in agonist binding and |
ediocin box' motif and two conserved cysteine | residues joined by a disulfide bridge. |
Several highly conserved histidine | residues were found in the zinc binding motif region o |
rgely acidic, contain four conserved cysteine | residues known to form two disulfide bonds, may be gly |
ed after its three highly conserved histidine | residues. |
6Ckine (because it has six conserved cysteine | residues instead of the four cysteines typical to chem |
proteolytic processing at conserved aspartic | residues to produce two subunits, large and small, tha |
if consisting of a run of conserved aspartate | residues, termed a “calcium bowl”), with their physiol |
e protein containing seven conserved cysteine | residues. |
It contains 4 conserved cysteine | residues, which probably form disulphide bridges. |
entropy lost upon making the contacts between | residues 26 and 84 and residues 58 and 110 in a polyme |
The milk shall not contain drug | residues. |
The enzymes contain ~250-300 | residues, which encode putative signal sequences and c |
polysaccharides containing beta-D-mannuronate | residues to give oligosaccharides with 4-deoxy-alpha-L |
ng chaperones for proteins containing proline | residues. |
The protein contains 5058 | residues, and is currently the largest known protein o |
ive EPPase PGM active site contains signature | residues shared by 2H-phosphatase enzymes, including a |
by the large domain, with contributions from | residues within the N-terminal domain and the linker r |
crosslinker Sulfo-SMCC, which converts lysine | residues to sulfhydryl-reactive maleimide groups. |
A fourth enzyme catalyzes the coupling of | residues 1 and 3, although where this coupling fits in |
y a disulfide bond between two cysteine (Cys) | residues 13 highly conserved amino acids apart near th |
ence motif for the c-type cytochromes, CxxCH ( | residues 21-25), which is covalently attached to the h |
not always, substituted with D-alanine ester | residues, giving the molecule zwitterionic properties. |
inates sulfate from the D-galactose 6-sulfate | residues of porphyran, producing 3,6-anhydrogalactose |
viruses, such as HIV, by deaminating cytosine | residues in nascent retroviral cDNA. |
recycling (for one, through decomposing plant | residues) and other soil building and maintaining acti |
could even be engineered to degrade existing | residues of pesticides, herbicides and other toxins. |
to determine which | residues are important for a particular phenotype, e.g |
. 14 - Incinerator and landfill disposal ban: | Residues of batteries that have gone through appropria |
Ammonia solution can dissolve silver | residues, such as that formed from Tollens' reagent. |
ated as the average sequence distance between | residues that form native contacts in the folded prote |
n catalyzes the removal of 3 distinct mannose | residues from peptide-bound Man(9)-GlcNAc(2) oligosacc |
samples, especially when finely divided, and | residues from reactions can be pyrophoric, which can i |
nd their source can include slag, dross, flux | residues, and pieces of the mold. |
due range and known to contain eight cysteine | residues; and the ‘short chain neurotoxins' (SCN) with |
red, the alpha carbons of the eight cysteine | residues in green, and the disulfide bridges in yellow |
c activity due probably to the elimination of | residues involved in the transfer of the free radical |
regard to consumers intake of endosulfan from | residues on food, the Food and Agriculture Organizatio |
tion that can occur to, for example, tyrosine | residues. |
For example, cysteine | residues in the peptide may be temporarily blocked fro |
lic acid has been removed to expose galactose | residues. |
lmost completely homologous for the first ~36 | residues and similar in tertiary structure for the fir |
K is associated with the last five C-terminal | residues. |
tive dyes, as a specific reagent for tyrosine | residues in enzymes, and as a fluorinating agent. |
s that provide single dihedral values for all | residues in the π-helix are misleading. |
For two | residues i and j, the ij element of the matrix is 1 if |
as nucleotide sugars act as donors for sugar | residues in the glycosylation reactions that produce p |
The loop, formed by | residues 166 to 176, closes and forms a hydrogen bond |
domain is a helical-hairpin and is formed by | residues 232-317. |
ective method of destroying the foul smelling | residues is to use an excess of sodium hypochlorite (c |
Apiose is a branched-chain sugar found as | residues in galacturonans-type pectins; that occurs in |
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