A20Fmdv2

A20Fmdv2 incorporates a defined binding motif used to study integrin recognition and structural determinants of ligand affinity. Residue diversity shapes solvent interactions and folding behavior. Researchers analyze its conformational states to clarify motif function. Applications span biophysical studies, ligand engineering, and receptor-binding analysis.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
A20Fmdv2(CAS 932699-03-1)

CAT No: R2462

CAS No:932699-03-1

Synonyms/Alias:A20FMDV2;932699-03-1;EX-A7450;

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M.F/Formula
C93H163N31O28
M.W/Mr.
2163.5
Sequence
One Letter Code:NAVPNLRGDLQVLAQKVART
Three Letter Code:H-Asn-Ala-Val-Pro-Asn-Leu-Arg-Gly-Asp-Leu-Gln-Val-Leu-Ala-Gln-Lys-Val-Ala-Arg-Thr-OH

A20Fmdv2 is a synthetic peptide compound engineered to mimic or modulate specific biological interactions, making it a valuable tool in contemporary biochemical and molecular research. As a peptide analog, its sequence and conformation are designed to engage with particular protein domains or signaling pathways, enabling targeted investigation of protein-protein interactions and cellular signaling mechanisms. The compound's structural features allow for precise modulation of molecular events, which is significant in elucidating the roles of key regulatory proteins and pathways in various biological systems. Its utility in research derives from its stability, specificity, and adaptability to a wide range of experimental contexts, supporting both fundamental and applied studies in peptide science.

Protein-protein interaction studies: In the context of molecular biology, A20Fmdv2 is frequently employed to dissect and characterize the nature of protein-protein interactions. By acting as a competitive inhibitor or binding partner, the peptide can be used to map interaction domains, assess binding affinities, and identify critical residues involved in complex formation. This approach is instrumental for researchers aiming to unravel the mechanistic underpinnings of cellular signaling networks, particularly those involving ubiquitin-editing enzymes or regulatory scaffolds.

Signal transduction research: The compound's ability to modulate specific signaling cascades makes it a valuable reagent for exploring intracellular communication pathways. Its targeted activity enables the selective inhibition or activation of signaling proteins, thereby providing insights into pathway dynamics, regulatory feedback mechanisms, and downstream effectors. Such studies are essential for clarifying the roles of specific molecular nodes within broader signaling architectures and for developing models of pathway regulation.

Peptide functional assays: A20Fmdv2 serves as a robust standard or experimental probe in a variety of peptide functional assays. Researchers utilize it to evaluate the effects of sequence modifications, test the impact of post-translational modifications, or benchmark the activity of novel peptide analogs. Its well-characterized properties support reproducible assay conditions, facilitating comparative studies and high-throughput screening of peptide function in vitro.

Structural biology applications: The defined conformation and binding characteristics of this peptide make it a useful model in structural biology experiments. It can be incorporated into crystallization trials, NMR studies, or computational modeling to visualize peptide-protein complexes and elucidate binding interfaces at atomic resolution. Such structural insights contribute to a deeper understanding of molecular recognition and inform the rational design of next-generation peptide-based tools.

Peptide synthesis validation: In peptide chemistry laboratories, A20Fmdv2 is often utilized as a reference compound for validating synthetic protocols and analytical techniques. Its known sequence and physicochemical properties allow researchers to calibrate instrumentation, optimize purification procedures, and confirm the fidelity of peptide synthesis workflows. This application underpins quality control and method development in peptide production, ensuring reproducibility and accuracy in downstream research endeavors.

InChI
InChI=1S/C93H163N31O28/c1-41(2)34-57(82(142)108-47(13)73(133)112-55(26-28-63(96)126)78(138)114-53(22-17-18-30-94)79(139)120-69(44(7)8)88(148)109-48(14)74(134)111-54(24-20-32-105-93(102)103)80(140)123-72(50(16)125)91(151)152)119-89(149)70(45(9)10)121-81(141)56(27-29-64(97)127)115-84(144)59(36-43(5)6)117-86(146)61(39-68(131)132)110-67(130)40-106-77(137)52(23-19-31-104-92(100)101)113-83(143)58(35-42(3)4)116-85(145)60(38-66(99)129)118-87(147)62-25-21-33-124(62)90(150)71(46(11)12)122-75(135)49(15)107-76(136)51(95)37-65(98)128/h41-62,69-72,125H,17-40,94-95H2,1-16H3,(H2,96,126)(H2,97,127)(H2,98,128)(H2,99,129)(H,106,137)(H,107,136)(H,108,142)(H,109,148)(H,110,130)(H,111,134)(H,112,133)(H,113,143)(H,114,138)(H,115,144)(H,116,145)(H,117,146)(H,118,147)(H,119,149)(H,120,139)(H,121,141)(H,122,135)(H,123,140)(H,131,132)(H,151,152)(H4,100,101,104)(H4,102,103,105)/t47-,48-,49-,50+,51-,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-,62-,69-,70-,71-,72-/m0/s1
InChI Key
BIPRZBFRCFOBDQ-KAGUSELOSA-N

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