<p>The RCL sequence shows a high degree of variance even within closely related proteins. The numbering of residues in the RCL of SERPINs is commonly in relation to the normal cleavage site in AAT between P1 and P1′. Already known cleavage sites are shown with grey boxes. The new cleavage site in human CBG observed in the structure is depicted in green. Introduced mutations in rat CBG-RCL1 through RCL3 are marked by orange boxes. The variant marked with an asterix bears in addition two mutations in the top of β-sheet A deleting a salt-bridge by converting it to amino acids present in human CBG (D323N, R174K). The wild-type protein sequences are annotated in the Uniprot knowledgebase with the following accession codes: rat CBG, P31211; human...
<p><b>a</b> Chromatograms of direct cDNA sequencing of R767H, S885N and R1441H. <b>b</b> Restriction...
<p>Sequences of the RLS (or RLT) motif from six adaptor proteins are aligned. The corresponding hept...
(A) The Met358 (P1) and Ser359 (P1’) residues, critical for the anti-protease activity of AAT, are s...
<p><b>A.</b> Sequence alignment of the RFs of Cbl, Cbl-b and Cbl-c. Amino acids in red show the nine...
<p>RCL region is dotted underlined. The two amino acids important for the inhibitory AAT function ar...
<p><b>A</b>: Sample 45 had a 6 bp tandem duplication in CBL leading to the insertion of the amino ac...
<p>Alignment of bovine, pig, murine and human CCL28 sequences demonstrates high amino acid homology ...
(A) AU-content (top, purple) over the entire genome and major rejoin region (inset, purple) of the R...
<p>Alignment has been performed using ClustalW2. It is focused on residues considered to participate...
<p>Sequence alignment around the catalytic triad including Cys (the active-site), His, and Asp was s...
<p>Multiple sequence alignment demonstrating evolutionary conservation of the six biologically chara...
<p>Clade C (upper panel) and Clade B (lower panel) serpin RCLs from P15-P4′ were aligned. Residues f...
<p>(Top) Compound mutations are double mutants that arise in the same clone and are detected in trea...
Contains fulltext : 75403.pdf (publisher's version ) (Closed access)Correlated mut...
<p>Dashes indicate identities with respect to the germline antibody sequence. Numbering corresponds ...
<p><b>a</b> Chromatograms of direct cDNA sequencing of R767H, S885N and R1441H. <b>b</b> Restriction...
<p>Sequences of the RLS (or RLT) motif from six adaptor proteins are aligned. The corresponding hept...
(A) The Met358 (P1) and Ser359 (P1’) residues, critical for the anti-protease activity of AAT, are s...
<p><b>A.</b> Sequence alignment of the RFs of Cbl, Cbl-b and Cbl-c. Amino acids in red show the nine...
<p>RCL region is dotted underlined. The two amino acids important for the inhibitory AAT function ar...
<p><b>A</b>: Sample 45 had a 6 bp tandem duplication in CBL leading to the insertion of the amino ac...
<p>Alignment of bovine, pig, murine and human CCL28 sequences demonstrates high amino acid homology ...
(A) AU-content (top, purple) over the entire genome and major rejoin region (inset, purple) of the R...
<p>Alignment has been performed using ClustalW2. It is focused on residues considered to participate...
<p>Sequence alignment around the catalytic triad including Cys (the active-site), His, and Asp was s...
<p>Multiple sequence alignment demonstrating evolutionary conservation of the six biologically chara...
<p>Clade C (upper panel) and Clade B (lower panel) serpin RCLs from P15-P4′ were aligned. Residues f...
<p>(Top) Compound mutations are double mutants that arise in the same clone and are detected in trea...
Contains fulltext : 75403.pdf (publisher's version ) (Closed access)Correlated mut...
<p>Dashes indicate identities with respect to the germline antibody sequence. Numbering corresponds ...
<p><b>a</b> Chromatograms of direct cDNA sequencing of R767H, S885N and R1441H. <b>b</b> Restriction...
<p>Sequences of the RLS (or RLT) motif from six adaptor proteins are aligned. The corresponding hept...
(A) The Met358 (P1) and Ser359 (P1’) residues, critical for the anti-protease activity of AAT, are s...