multiple sequence alignment tool praline Search Results


clustalw multiple sequence alignment algorithm  (Imgen Inc)
90
Imgen Inc clustalw multiple sequence alignment algorithm
Clustalw Multiple Sequence Alignment Algorithm, supplied by Imgen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/clustalw multiple sequence alignment algorithm/product/Imgen Inc
Average 90 stars, based on 1 article reviews
clustalw multiple sequence alignment algorithm - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
muscle multiple sequence alignment tools  (GSL Biotech)
90
GSL Biotech muscle multiple sequence alignment tools
Muscle Multiple Sequence Alignment Tools, supplied by GSL Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/muscle multiple sequence alignment tools/product/GSL Biotech
Average 90 stars, based on 1 article reviews
muscle multiple sequence alignment tools - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
kalign multiple protein sequence alignment tool  (Inserm Transfert)
86
Inserm Transfert kalign multiple protein sequence alignment tool
High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the <t>KALIGN</t> multiple <t>protein</t> <t>sequence</t> alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.
Kalign Multiple Protein Sequence Alignment Tool, supplied by Inserm Transfert, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/kalign multiple protein sequence alignment tool/product/Inserm Transfert
Average 86 stars, based on 1 article reviews
kalign multiple protein sequence alignment tool - by Bioz Stars, 2026-06
86/100 stars
  Buy from Supplier
multiple sequence alignment tool by clustal w ver 1.83  (PrimerDesign Inc)
90
PrimerDesign Inc multiple sequence alignment tool by clustal w ver 1.83
High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the <t>KALIGN</t> multiple <t>protein</t> <t>sequence</t> alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.
Multiple Sequence Alignment Tool By Clustal W Ver 1.83, supplied by PrimerDesign Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multiple sequence alignment tool by clustal w ver 1.83/product/PrimerDesign Inc
Average 90 stars, based on 1 article reviews
multiple sequence alignment tool by clustal w ver 1.83 - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
multiple sequence alignment tool in the genome analysis toolkit  (Broad Institute Inc)
90
Broad Institute Inc multiple sequence alignment tool in the genome analysis toolkit
High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the <t>KALIGN</t> multiple <t>protein</t> <t>sequence</t> alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.
Multiple Sequence Alignment Tool In The Genome Analysis Toolkit, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multiple sequence alignment tool in the genome analysis toolkit/product/Broad Institute Inc
Average 90 stars, based on 1 article reviews
multiple sequence alignment tool in the genome analysis toolkit - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
sequence alignment tool  (Chemical Computing Group)
86
Chemical Computing Group sequence alignment tool
High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the <t>KALIGN</t> multiple <t>protein</t> <t>sequence</t> alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.
Sequence Alignment Tool, supplied by Chemical Computing Group, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/sequence alignment tool/product/Chemical Computing Group
Average 86 stars, based on 1 article reviews
sequence alignment tool - by Bioz Stars, 2026-06
86/100 stars
  Buy from Supplier

Image Search Results


High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the KALIGN multiple protein sequence alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.

Journal: Biology

Article Title: Evolution of CEACAM1 N Domain Biologically Active Sites in Primates

doi: 10.3390/biology14121744

Figure Lengend Snippet: High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the KALIGN multiple protein sequence alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.

Article Snippet: Amino acid sequence alignments were performed using the KALIGN multiple protein sequence alignment tool ( https://npsa.lyon.inserm.fr/cgi-bin/npsa_automat.pl?page=/NPSA/npsa_kalign.html , accessed 17 April 2025).

Techniques: Sequencing, Activation Assay, Derivative Assay, Binding Assay, Western Blot