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Peptide·plain sequence-like

ATLPC0031403

ATLPC0031403

SQEPPISLDLTFHLLREVLEMTKADQLAQQAHSNRKLLDIA

Compare in workbenchDownload releaseAPI JSON
  • Length
    41 aa
  • Monoisotopic mass
    4668.5 Da
  • Net charge @ pH 7.4
    -1.80
  • Isoelectric point
    5.52
  • GRAVY
    -0.322
On this page
  • 01 Sequence & molecular identity
  • 02 Physicochemical profile
  • 03 Excretion / Persistence
  • 04 Evidence landscape
  • 05 Product context
  • 06 Identity & reference map
  • 07 Data access & reproducibility
Coveragecounts only · not riskATLPC0031403
  • Measurements
    16
  • Endpoints
    1
  • Domains
    1/5
  • Products
    —
  • No matrix stability evidence
  • 16 clearance measurements
  • No immunogenicity context
  • 1 liability motif
Jump to domain

Open the matching evidence section below

All evidence index · 16
Exposure / Absorption
No evidence
Distribution / Barrier
No evidence
Metabolic & Proteolytic Stability
No evidence
Excretion / Persistence
16 measurements
Toxicity / Safety
No evidence
01

Sequence & molecular identity

1 forms

Reviewed sequence, peptidoform forms, chemical representation, 3D references, and covalent topology used to interpret this peptide identity.

Sequence & peptidoform

·
Identity summaryCanonical sequence only
Identity status
Canonical sequence only
Residues
41
Peptidoform features
0
Documented molecular forms
1
Representations
2
Documented molecular forms1 form linked to this peptide identity
FormTopologyModificationsConnectionsRepresentationsMeasurements
ATLPF0034115———Notation only16
Residue view
Residue display
41 residues
S1Q2E3P4P5I6S7L8D9L10T11F12H13L14L15R16E17V18L19E20M21T22K23A24D25Q26L27A28Q29Q30A31H32S33N34R35K36L37L38D39I40A41
Side-chain classNonpolarPolarBasic (+)Acidic (−)Modified

Soft tints mark standard side-chain classes for scanning. Primary emphasis is reserved for reported modifications, termini, secondary-structure tracks, and topology links.

Peptidoform features

Features are shown only when a reported notation or topology record supports them.

No terminal modification, residue-level marker, disulfide, staple, coordination, or other topology signal is currently available.

Structure & chemistry

·
Chemical representationsequence / HELM only
Representation class

How the current release can interpret this identity chemically.

plain sequence-like
Parent-residue sequence

Residue string used for positional interpretation when available.

SQEPPISLDLTFHLLREVLEMTKADQLAQQAHSNRKLLDIA
HELM

Polymer notation for modified peptide representation when available.

Not available
SMILES

Chemical graph string used for atom-level 2D depiction when available.

Not available
No atom-level graph

A reviewed SMILES is required before a 2D molecular depiction can be shown. Sequence and HELM remain useful for identity interpretation, but they do not replace a chemical graph.

3D structure referencesnone attached
3D structure not available

A 3D structure isn't available for this peptide in the current release. Chemistry and topology fields remain available when represented by sequence, HELM, or SMILES.

Covalent topology & modificationsnone
Exact topology not established

No reviewed form-level topology or residue-level connection annotation is attached to this peptide in the current release. This is not evidence that every molecular form is linear or unmodified.

02

Physicochemical profile

4 descriptors

Computed sequence-derived descriptors and any measured physicochemical evidence such as lipophilicity. Computed values are interpretation aids, not experimental ADMET measurements.

·
Core descriptors41 aa · pI 5.5 · GRAVY -0.32
Length
41 aa
Monoisotopic mass
4668.47 Da
Average mass
4671.35 Da
Net charge at pH 7.4
-1.80
Estimated pI
5.52
GRAVY
-0.322
KD-positive residues
41.5%
Aromatic residues
2.4%
Developability interpretation
Ionization context
pH 7.4 separated from pI
Hydrophobicity balance
Leans hydrophilic
Amphipathic moment (μH)
0.25
Computation boundary
Standard-sequence only
Charge & residue composition
pH charge context

Modeled net charge across common formulation and assay pH checkpoints.

pH 2
6.91
pH 5
0.53
pH 6
-0.42
pH 7.4
-1.83
pH 9
-2.74
pH 12
-5.36
Residue-class composition

Grouped composition is often more interpretable than a long amino-acid list.

Acidic (D,E)
6 · 14.6%
Basic (K,R,H)
6 · 14.6%
Polar uncharged (N,Q,S,T)
10 · 24.4%
Hydrophobic aliphatic (A,V,I,L,M)
16 · 39.0%
Aromatic (F,W,Y)
1 · 2.4%
Conformational / sulfur (G,P,C)
2 · 4.9%
Top residues
L819.5%A49.8%Q49.8%D37.3%E37.3%S37.3%R24.9%H24.9%
Hydropathy & amphipathic windows
Hydropathy windows

Seven-residue sliding windows expose local patches hidden by whole-sequence GRAVY.

Most hydrophobic window
6-12
ISLDLTF
GRAVY 1.414
Most hydrophilic window
30-36
QAHSNRK
GRAVY -2.514
35 local hydropathy windows scanned. A local patch is context for solubility, adsorption, and membrane interaction review, not a standalone endpoint.
Amphipathic-window scan

Top alpha-helix hydrophobic-moment windows across 12, 15, 18, and 21 residues.

12 aa window
9-20
DLTFHLLREVLE
μH 1.88 · charge -1.9
12 aa window
12-23
FHLLREVLEMTK
μH 1.85 · charge 0.1
12 aa window
13-24
HLLREVLEMTKA
μH 1.81 · charge 0.1
12 aa window
8-19
LDLTFHLLREVL
μH 1.78 · charge -0.9
12 aa window
11-22
TFHLLREVLEMT
μH 1.66 · charge -0.9
Sequence-liability cues
Sequence-liability notes

Motifs are review prompts for formulation or CMC interpretation; they are not degradation predictions.

Oxidation-sensitive residues
M · pos 21
Met, Trp, and Cys residues can merit formulation review for oxidation or covalent-state sensitivity.
Alpha-helix amphipathic projection
Helical wheel · Edmundson projection
μH = 0.25100°/residue · 41 aa
μH1: S (Ser) · Polar · K-D -0.8S12: Q (Gln) · Polar · K-D -3.5Q3: E (Glu) · Acidic − · K-D -3.5E4: P (Pro) · Special · K-D -1.6P5: P (Pro) · Special · K-D -1.6P56: I (Ile) · Hydrophobic · K-D 4.5I7: S (Ser) · Polar · K-D -0.8S8: L (Leu) · Hydrophobic · K-D 3.8L9: D (Asp) · Acidic − · K-D -3.5D10: L (Leu) · Hydrophobic · K-D 3.8L1011: T (Thr) · Polar · K-D -0.7T12: F (Phe) · Aromatic · K-D 2.8F13: H (His) · Basic + · K-D -3.2H14: L (Leu) · Hydrophobic · K-D 3.8L15: L (Leu) · Hydrophobic · K-D 3.8L1516: R (Arg) · Basic + · K-D -4.5R17: E (Glu) · Acidic − · K-D -3.5E18: V (Val) · Hydrophobic · K-D 4.2V19: L (Leu) · Hydrophobic · K-D 3.8L20: E (Glu) · Acidic − · K-D -3.5E2021: M (Met) · Hydrophobic · K-D 1.9M22: T (Thr) · Polar · K-D -0.7T23: K (Lys) · Basic + · K-D -3.9K24: A (Ala) · Hydrophobic · K-D 1.8A25: D (Asp) · Acidic − · K-D -3.5D2526: Q (Gln) · Polar · K-D -3.5Q27: L (Leu) · Hydrophobic · K-D 3.8L28: A (Ala) · Hydrophobic · K-D 1.8A29: Q (Gln) · Polar · K-D -3.5Q30: Q (Gln) · Polar · K-D -3.5Q3031: A (Ala) · Hydrophobic · K-D 1.8A32: H (His) · Basic + · K-D -3.2H33: S (Ser) · Polar · K-D -0.8S34: N (Asn) · Polar · K-D -3.5N35: R (Arg) · Basic + · K-D -4.5R3536: K (Lys) · Basic + · K-D -3.9K37: L (Leu) · Hydrophobic · K-D 3.8L38: L (Leu) · Hydrophobic · K-D 3.8L39: D (Asp) · Acidic − · K-D -3.5D40: I (Ile) · Hydrophobic · K-D 4.5I4041: A (Ala) · Hydrophobic · K-D 1.8A41
Hydrophobic moment0.25
Mean K-D hydropathy-0.32
Approx. net charge-2
Projection angle100° / residue
The pale sector marks the direction of the hydrophobic face inferred from μH. This is a projection assumption, not a measured fold.
HydrophobicAromaticPolarBasic +Acidic −Specialhydrophobic faceμH arrow → hydrophobic face

The projection assumes an α-helix conformation; a long μH arrow indicates an amphipathic helix, common in antimicrobial peptides.Sequence > 30 aa — only termini and every fifth position are numbered because later turns share earlier wheel angles.

Method notes

Charge model: side-chain pKa D 3.9, E 4.1, C 8.5, Y 10.1, H 6.5, K 10.8, R 12.5 with EMBOSS termini. pI is estimated by binary search on modeled net charge. Hydropathy uses Kyte-Doolittle values; hydrophobic moment follows the Eisenberg alpha-helix vector-sum convention. When the basis is a parent-residue sequence, modified chemistry is intentionally not inferred.

Computed developability descriptors

Deterministic descriptors computed from the reviewed sequence or chemical structure (RDKit), each anchored to a literature method. These are computed estimates for developability interpretation — not experimental measurements — and are validated against independent reference implementations.

Sequence-derived

Computed from the standard parent-residue sequence; protein-origin metrics defined at any length.

Aliphatic index
111.95
Instability index
34.0

At or below 40 — predicted stable in vitro.

Boman index
1.83 kcal/mol
Molar extinction coefficient (280 nm)
0 M⁻¹·cm⁻¹

A280 (1 g/L) ≈ 0.00

Structure-derived descriptors are not shown because this identity has no resolved chemical structure (SMILES). This is a known coverage gap for disulfide-rich and unresolved peptidoforms, not a computation error.

03

Excretion / Persistence

16 records

What evidence describes clearance or persistence?

Evidence records
16
Complete canonical measurements and observations attached to this domain.
Endpoint scope
1
Formal ADMET endpoints represented for this peptide.
Matched-context analysis
16
Quantitative results that may be analysed only with scientifically compatible records.
Reported-result review
0
Qualitative, narrative, or review-first results interpreted in their source context.
Endpoints in scopeHalf Life
Evidence interpretation

Result type, analysis use, and source-check status are kept separate so a numerical value is not mistaken for a universally comparable result.

Eligible for matched-context analysis
Quantitative results whose endpoint and context must still be matched before analysis.
16
Interpret as reported
Qualitative, narrative, or review-first findings preserved in source context.
0
Supporting context only
Reference, label, clinical, or supporting context for interpretation.
0
Review before analysis
Records whose present structure does not establish a safe analysis role.
0
Evidence by endpoint

Rows are grouped by endpoint so value, assay context, interpretation layer, and reference can be checked in place.

·
Half Life16 records · 16 matched-context · 0 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

terminal elimination phase half life: 1962.0000000000002 seconds

Eligible when experimental context matches

Radioimmunoassay · monkey · Rhesus monkey plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Time: Blood samples collected at 1-180 minutes after peptide injection · Rhesus monkey proteases · in vivo · Source: Primary reference linked

Reference
2

terminal elimination phase half life: 1740 seconds

Eligible when experimental context matches

Radioimmunoassay · monkey · Rhesus monkey plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Time: Blood samples collected at 1-180 minutes after peptide injection · Rhesus monkey proteases · in vivo · Source: Primary reference linked

Reference
3

distribution initial phase half life: 762 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 75 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
4

distribution initial phase half life: 744 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 75 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
5

terminal elimination phase half life: 5724 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 75 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
6

terminal elimination phase half life: 5448 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 75 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
7

terminal elimination phase half life: 4248 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 76 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
8

distribution initial phase half life: 972 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 76 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
9

distribution initial phase half life: 564 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 80 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
10

terminal elimination phase half life: 4380 seconds

Eligible when experimental context matches

Radioimmunoassay and HPLC analysis · human · Intravenous administration to human plasma

Result: Reported point value · Molecular form: ATLPF0034115 · Dose/window: 80 μg · Time: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Human blood plasma proteases · in vivo · Source: Primary reference linked

Reference
1–10 / 16
04

Evidence landscape

16 records

Cross-domain evidence distribution and measurement-level detail; the domain modules above show evidence in context, and every row remains available for audit here.

Evidence landscape

A cross-domain view of evidence volume, scientifically permitted analysis use, and source traceability.

ADMET domain
Eligible when context matches
Interpret as reported
Supporting context only
Review before analysis
Exposure / Absorption
0 evidence records
0
0
0
0
Distribution / Barrier
0 evidence records
0
0
0
0
Metabolic & Proteolytic Stability
0 evidence records
0
0
0
0
Excretion / Persistence
16 evidence records
16
0
0
0
Toxicity / Safety
0 evidence records
0
0
0
0
Endpoint distribution

Top evidence-bearing endpoint questions.

Half Life
16
Assay context

Broad context buckets, useful before comparing values.

In vivo / route
16
Traceability

Reference-link availability for measurement-level audit.

Linked reference
16
Not linked
0
All evidence index

Every evidence record remains available for audit and drilldown. Counts describe evidence volume, not confidence.

#ADMET domainEndpointReported valueResult typeAnalysis useAssay / modelConditionReference
1
Excretion / Persistence
Persistence
Half Life
762 seconds
Result metric: DISTRIBUTION_INITIAL_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 75 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
2
Excretion / Persistence
Persistence
Half Life
336 seconds
Result metric: DISTRIBUTION_INITIAL_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 90 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
3
Excretion / Persistence
Persistence
Half Life
4,248 seconds
Result metric: TERMINAL_ELIMINATION_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 76 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
4
Excretion / Persistence
Persistence
Half Life
798 seconds
Result metric: DISTRIBUTION_INITIAL_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 85 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
5
Excretion / Persistence
Persistence
Half Life
744 seconds
Result metric: DISTRIBUTION_INITIAL_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 75 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
6
Excretion / Persistence
Persistence
Half Life
1,962 seconds
Result metric: TERMINAL_ELIMINATION_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay · monkey · Rhesus monkey plasmaTime: Blood samples collected at 1-180 minutes after peptide injection · Protease: Rhesus monkey proteases · in vivo
Reference
Primary reference linked
7
Excretion / Persistence
Persistence
Half Life
564 seconds
Result metric: DISTRIBUTION_INITIAL_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 80 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
8
Excretion / Persistence
Persistence
Half Life
5,724 seconds
Result metric: TERMINAL_ELIMINATION_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 75 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
9
Excretion / Persistence
Persistence
Half Life
4,380 seconds
Result metric: TERMINAL_ELIMINATION_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 80 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
10
Excretion / Persistence
Persistence
Half Life
2,874 seconds
Result metric: TERMINAL_ELIMINATION_PHASE_HALF_LIFE
Reported point valueEligible when experimental context matchesRadioimmunoassay and HPLC analysis · human · Intravenous administration to human plasmaTime: 0, 2, 5, 7,10,15, 20, 25, 30, 45, 60, 90, 120, 150, and 180 min. · Dose/window: 90 μg · Protease: Human blood plasma proteases · in vivo
Reference
Primary reference linked
1–10 / 16
05

Product context

Product-level route, label, and clinical context that frames peptide-level evidence. A peptide-level summary only; product pages keep the full drilldown.

No product association in this release

This peptide is currently interpreted from sequence, structure, physicochemical, and ADMET evidence only.

Browse products
06

Identity & reference map

16 sources

Reference-level support for checking reported names, sequence notation, and peptide identity agreement.

·
Summary2 reference groups
Identity type
canonical sequence
Reported notation
0
Reference groups
2
Measurements
16
ATL peptide ID
ATLPC0031403
Identity concordance
Identity concordance
Exact reported notation

Reported sequence string matches the current peptide notation.

0 / 16
Parent-residue compatible

Reported notation differs, but resolves to the same parent-residue display.

0 / 16
Different notation

Reported notation does not resolve to the current display sequence.

0 / 16
Source sequence not captured

No source-specific sequence was captured for comparison; this is not interpreted as agreement or disagreement.

16 / 16
Reported sequence notation

No source-specific sequence notation has been captured in the current identity references.

Current identity
SQEPPISLDLTFHLLREVLEMTKADQLAQQAHSNRKLLDIA
Reported names
No distinct human-readable aliases are exposed.
Reference map2 reference groups
Reference map

Grouped by reference link, with endpoint scope and reported identity kept visible.

ReferenceSupportsReported identityRecords
Reference
Open
Persistence
Half Life
No reported alias
14 identity
14 evidence
Reference
Open
Persistence
Half Life
No reported alias
2 identity
2 evidence
07

Data access & reproducibility

Stable record access, analysis-ready files, and scripted retrieval for reproducing this profile view.

·
Record scopePublic release
ATL peptide ID
ATLPC0031403
Identity type
canonical sequence
ADMET endpoints
1
Evidence records
16
Reference groups
2
Release view
Public release
Data access

Structured peptide profile

JSON

Peptide-specific profile used by this page, including identity and evidence context.

Open JSON

Peptide catalogue

TSV

Complete frozen peptide table. Filter the ATL peptide ID column locally to isolate this record.

Download catalogue

Measurement catalogue

TSV

Complete frozen measurement table. Join or filter by ATL peptide ID for peptide-level analysis.

Download measurements
Programmatic access

The request returns the same structured peptide record used by this profile. The tabular downloads are complete frozen release tables and should be filtered locally by ATL peptide ID.

Open endpoint
GET /api/v1/peptides/ATLPC0031403
open
curl -sS 'https://admetatlas.scbdd.com/api/v1/peptides/ATLPC0031403' \
  -H 'accept: application/json' \
  -H 'X-Visibility: public_release'
ADMETatlas
peptide evidence atlas

ADMETatlas is an open, curated atlas of ADMET evidence for therapeutic peptides — spanning developability, membrane permeability and blood–brain-barrier transport, immune-recognition context, and approved-product context. Every measurement stays linked to its original source, with stable identifiers and transparent curation, so results can be traced, cited, and reproduced.

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