HUT2 = HIP2 + HAPTIC3 + HEPTAD2 + SETH

HIP2: HAPTIC3/HEPTAD2 Input Preprocessor

Use HIP2 to prepare input sequence data for HAPTIC3 and HEPTAD2.

Minimum excluded hydrophobic residue (ACFILMV) run length:
Minimum excluded order-promoting residue (CFHILMNVWY) run length:
Strongly disorder-promoting (PKRED/end) residue fraction window width:
Strongly disorder-promoting (PKRED/end) residue fraction cutoff value:
Excluded amino-acid residue/s:
A (ALA) C (CYS) D (ASP) E (GLU) F (PHE)
G (GLY) H (HIS) I (ILE) K (LYS) L (LEU)
M (MET) N (ASN) P (PRO) Q (GLN) R (ARG)
S (SER) T (THR) V (VAL) W (TRP) Y (TYR)
Excluded amino-acid residue/s in sequence motifs:
Glycosylated N in NXS or NXT where X is any residue except P
Input peptidic sequence data (FASTA format):

Notes:

  1. Minimum excluded hydrophobic residue (ACFILMV) run length is the size of the smallest hydrophobic blob whose residues are deemed inaccessible for binding by paratopes.
  2. Minimum excluded order-promoting residue (CFHILMNVWY) run length is the size of the shortest ordered sequence segment whose residues are deemed inaccessible for binding by paratopes.
  3. Strongly disorder-promoting residues are proline (P) and/or bear formal charge/s (KRED and/or at N- or C-terminal/end position), so sequence segments of length equal to window width whose fraction of such residues is less than cutoff value are deemed inaccessible for binding by paratopes.
  4. Excluded amino-acid residues may be those deemed problematic in view of chemical reactivity (e.g., susceptibility to oxidative damage, as in the case of methionine).
  5. Canonical N-glycosylation of asparagine is expected only for surface and secreted protein antigens of eukaryotes (versus prokaryotes).
  6. HIP2 output represents excluded residues using lower-case single-letter codes (e.g., 'a' versus 'A'), which are neglected by HAPTIC3 and HEPTAD2 for generation of candidate epitopes.