<result><Target><Item><Target_ID> 1451</Target_ID>
<Target_Name>The Domain III of the Japan Encephalitis Virus Envelope Protein, E DIII</Target_Name>
<Target_Type>Protein&gt;Others</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Japanese encephalitis virus:11072</Target_Source>
<Target_Structure>1PJW</Target_Structure>
<Comments>Japanese encephalitis virus (JEV) is a major cause of acute viral encephalitis in both humans and animals. Domain III of the virus envelope glycoprotein (E DIII) plays an important role in the interaction of viral particles with host cell receptors to facilitate viral entry. In addition, DIII has been proposed to act as the binding region for the cellular receptor.</Comments>
</Item><Item><Target_ID> 1452</Target_ID>
<Target_Name>BCR/ABL-expressing NIH3T3 mouse fibroblast cells</Target_Name>
<Target_Type>Cell</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Mus musculus (Mouse):10090</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1453</Target_ID>
<Target_Name>Amorphous Ni3B</Target_Name>
<Target_Type>Inorganic molecules or materials</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>None</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1454</Target_ID>
<Target_Name>Crystalline Ni3B</Target_Name>
<Target_Type>Inorganic molecules or materials</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>None</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1455</Target_ID>
<Target_Name>Fibroblast growth factor 1, FGF-1</Target_Name>
<Target_Type>Protein&gt;Others</Target_Type>
<Target_Sequence>P05230</Target_Sequence>
<Synonyms>Acidic fibroblast growth factor
aFGF
Endothelial cell growth factor
ECGF
Heparin-binding growth factor 1
HBGF-1</Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure>1AXM, 1DJS ,1DZC ,1DZD ,1E0O ,1EVT ,1HKN ,1JQZ ,1JT3 ,1JT4 ,1JT5 ,1JT7 ,1JTC ,1JY0 ,1K5U ,1K5V ,1M16 ,1NZK ,1P63 ,1PZZ ,1Q03 ,1Q04 ,1RG8 ,1RML ,1RY7 ,1YTO ,1Z2V ,1Z4S ,2AFG ,2AQZ ,2AXM ,2ERM ,2HW9 ,2HWA ,2HWM ,2HZ9 ,2K43 ,2K4A ,2K8R ,2KI4 ,2KI6 ,2LDN ,2NTD ,2Q9X ,2RQ9 ,3B9U ,3BA4 ,3BA5 ,3BA7 ,3BAD ,3BAG ,3BAH ,3BAO ,3BAQ ,3BAU ,3BAV ,3BB2 ,3CQA ,3CRG ,3CRH ,3CRI ,3CU1 ,3FGM ,3FJ8 ,3FJ9 ,3FJA ,3FJB ,3FJC ,3FJD ,3FJE ,3FJF ,3FJH ,3FJI ,3FJJ ,3FJK ,3HOM ,3JUT ,3K1X ,3O3Q ,3OJ2 ,3OJM ,3OJV ,3UD7 ,3UD8 ,3UD9 ,3UDA ,4J23</Target_Structure>
<Comments>Acidic fibroblast growth factor (aFGF) is a member of the fibroblast growth factor family, originally isolated as mitogens for fibroblasts from the brain and pituitary. AFGF executes its pleiotropic biological actions by binding, dimerizing, and activating cell surface FGF receptors (FGFRs). The extra-cellular ligand-binding portion of FGFRs is composed of three immunoglobulin-like (Ig-like) domains (D1-D3). The crystal structure of the ectodomain of the FGFR complex with FGF demonstrated that the ligand-binding domain of FGFR involves Ig-like domains II and III (D2 and D3, respectively), as well as the linker between D2 and D3.</Comments>
</Item><Item><Target_ID> 1456</Target_ID>
<Target_Name>Mixture of murine melanoma cell lines B16.F1 and B16.F10</Target_Name>
<Target_Type>Cell</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1457</Target_ID>
<Target_Name>Calcium silicate hydrate 0.66, C-S-H 0.66</Target_Name>
<Target_Type>Inorganic molecules or materials</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>None</Target_Source>
<Target_Structure></Target_Structure>
<Comments>C-S-H suspensions were prepared by reacting lime and silica in appropriate ratios in a stirred aqueous suspension. The name of the samples refers to the lime to silica ratio (Ca/Si) of the mix.</Comments>
</Item><Item><Target_ID> 1458</Target_ID>
<Target_Name>Calcium silicate hydrate 1.0, C-S-H 1.0</Target_Name>
<Target_Type>Inorganic molecules or materials</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>None</Target_Source>
<Target_Structure></Target_Structure>
<Comments>C-S-H suspensions were prepared by reacting lime and silica in appropriate ratios in a stirred aqueous suspension. The name of the samples refers to the lime to silica ratio (Ca/Si) of the mix.</Comments>
</Item><Item><Target_ID> 1459</Target_ID>
<Target_Name>Calcium silicate hydrate 1.5, C-S-H 1.5</Target_Name>
<Target_Type>Inorganic molecules or materials</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>None</Target_Source>
<Target_Structure></Target_Structure>
<Comments>C-S-H suspensions were prepared by reacting lime and silica in appropriate ratios in a stirred aqueous suspension. The name of the samples refers to the lime to silica ratio (Ca/Si) of the mix.</Comments>
</Item><Item><Target_ID> 1460</Target_ID>
<Target_Name>Calcium silicate hydrate 1.7, C-S-H 1.7</Target_Name>
<Target_Type>Inorganic molecules or materials</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>None</Target_Source>
<Target_Structure></Target_Structure>
<Comments>C-S-H suspensions were prepared by reacting lime and silica in appropriate ratios in a stirred aqueous suspension. The name of the samples refers to the lime to silica ratio (Ca/Si) of the mix.</Comments>
</Item><Item><Target_ID> 1461</Target_ID>
<Target_Name>Salivary  pellicle</Target_Name>
<Target_Type>Protein&gt;Others</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>In the oral cavity, the salivary proteins and peptides are selectively adsorbed to the enamel surface to form a us film called the acquired salivary pellicle. This pellicle is composed of peptides and (glycosylated) proteins, such as statherin, histatins, proline-rich proteins and mucins.</Comments>
</Item><Item><Target_ID> 1462</Target_ID>
<Target_Name>Human umbilical vein endothelial cells, HUVECs</Target_Name>
<Target_Type>Cell</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1463</Target_ID>
<Target_Name>IGVH1 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1464</Target_ID>
<Target_Name>IGVH3 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1465</Target_ID>
<Target_Name>IGVH4 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1466</Target_ID>
<Target_Name>IGVH6 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1467</Target_ID>
<Target_Name>IGVK1 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1468</Target_ID>
<Target_Name>IGVK2 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1469</Target_ID>
<Target_Name>IGVK3 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1470</Target_ID>
<Target_Name>IGVK4 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1471</Target_ID>
<Target_Name>IGVK5 template protein</Target_Name>
<Target_Type>Protein&gt;Polyclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1472</Target_ID>
<Target_Name>IGVK6 template protein</Target_Name>
<Target_Type>Protein&gt;Monoclonal antibody</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Homo sapiens (Human):9606</Target_Source>
<Target_Structure></Target_Structure>
<Comments>All consensus sequences from the 7 IGHV and 6 IGKV gene groups are found. The complementarity-determining region 3 gene derived from the pertuzumab (anti-HER2 humanized antibody) gene was used. Each gene was synthesized, and ligated using the overlapped PCR method. The designed Fv template was cloned into the pMALp4e (New England Biolabs Inc., Ipswich, MA) maltosebinding protein (MBP) fusion protein expression vector.</Comments>
</Item><Item><Target_ID> 1473</Target_ID>
<Target_Name>Ephrin type-A receptor 2</Target_Name>
<Target_Type>Protein&gt;Receptor</Target_Type>
<Target_Sequence>Q03145</Target_Sequence>
<Synonyms>EC=2.7.10.1
Epithelial cell kinase
Tyrosine-protein kinase receptor ECK
Tyrosine-protein kinase receptor MPK-5
Tyrosine-protein kinase receptor SEK-2</Synonyms>
<Target_Source>Mus musculus (Mouse):10090</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1474</Target_ID>
<Target_Name>Colonic adenomas</Target_Name>
<Target_Type>Organ and tissue</Target_Type>
<Target_Sequence></Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Mus musculus (Mouse):10090</Target_Source>
<Target_Structure></Target_Structure>
<Comments></Comments>
</Item><Item><Target_ID> 1475</Target_ID>
<Target_Name>Envelope glycoprotein E2</Target_Name>
<Target_Type>Protein&gt;Others</Target_Type>
<Target_Sequence>P27958 [384-661]</Target_Sequence>
<Synonyms></Synonyms>
<Target_Source>Hepatitis C virus genotype 1a (isolate H) (HCV):11108</Target_Source>
<Target_Structure>1A1R, 1A1V, 1CWX, 1HEI, 1JR6, 1N1L, 1ONB, 1R7C, 1R7D, 1R7E, 1R7F, 1R7G, 1RGQ, 2A4R, 2F9V, 2HD0, 2JXF, 2KDR, 2O8M, 2OBO, 2OBQ, 2OC0, 2OC1, 2OC7, 2OC8, 2OIN, 2P59, 2QV1, 2XI2, 2XI3, 2XNI, 4CL1, 4JZN, 4JZO, 4MWF</Target_Structure>
<Comments>Full-length E2 protein extends from amino acids 384 to 746 of the HCV polyprotein and contains regions of extreme variability. E2661 is the C-terminal truncation of E2 at residue 661 (E2661).</Comments>
</Item></Target></result>