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  3. ATLPC0004174
Peptide·plain sequence-like

ATLPC0004174

ATLPC0004174

KALXKTMLKKLGTMAL

Compare in workbenchDownload releaseAPI JSON
  • Length
    16 aa
On this page
  • 01 Sequence & molecular identity
  • 02 Physicochemical profile
  • 03 Toxicity / Safety
  • 04 Evidence landscape
  • 05 Product context
  • 06 Identity & reference map
  • 07 Data access & reproducibility
Coveragecounts only · not riskATLPC0004174
  • Measurements
    5
  • Endpoints
    4
  • Domains
    1/5
  • Products
    —
  • No matrix stability evidence
  • No clearance evidence
  • No immunogenicity context
  • No sequence liability cues
Jump to domain

Open the matching evidence section below

All evidence index · 5
Exposure / Absorption
No evidence
Distribution / Barrier
No evidence
Metabolic & Proteolytic Stability
No evidence
Excretion / Persistence
No evidence
Toxicity / Safety
5 measurements
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 summarySpecific molecular form represented
Identity status
Specific molecular form represented
Residues
16
Peptidoform features
1
Documented molecular forms
1
Representations
2
Documented molecular forms1 form linked to this peptide identity
FormTopologyModificationsConnectionsRepresentationsMeasurements
ATLPF0004556—1—Notation only2
Residue view
Residue display
16 residues
K1A2L3X4XK5T6M7L8K9K10L11G12T13M14A15L16
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.

Non-standard residue tokenpos 4
X

Reported token X is not one of the 20 standard residue symbols in this display.

Reported sequence notation was converted to parent-residue display for visualization; the original notation remains shown below.

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.

KALXKTMLKKLGTMAL
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

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

Physicochemical descriptors unavailable

These descriptors require a standard parent-residue sequence. The module remains visible so modified or unresolved identities are not forced into unreliable computed values.

03

Toxicity / Safety

5 records

What safety, toxicity, or tolerability evidence is attached?

Evidence records
5
Complete canonical measurements and observations attached to this domain.
Endpoint scope
4
Formal ADMET endpoints represented for this peptide.
Matched-context analysis
5
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 scopeCytotoxicity metric% cytotoxicityHemolysis metric% hemolysis
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.
5
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.

·
% hemolysis1 record · 1 matched-context · 0 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

50 %

Eligible when experimental context matches

Human erythrocytes · Human erythrocytes · human · RBC

Result: Reported point value · Molecular form: not reported · Source: Primary reference linked

Source record
Hemolysis metric1 record · 1 matched-context · 0 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

hc50: 80 μM

Eligible when experimental context matches

human · human red cells

Result: Reported point value · Molecular form: ATLPF0004556 · Source: Primary reference linked

Reference
% cytotoxicity2 records · 2 matched-context · 0 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

50 %

Eligible when experimental context matches

Human embryonic kidney HEK293T cells · Human embryonic kidney HEK293T cells · human

Result: Reported point value · Molecular form: not reported · Source: Primary reference linked

Reference
2

50 %

Eligible when experimental context matches

Vero cells · Vero cells

Result: Reported point value · Molecular form: not reported · Source: Primary reference linked

Reference
Cytotoxicity metric1 record · 1 matched-context · 0 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

cc50: 50 μM

Eligible when experimental context matches

Vero cells

Result: Reported point value · Molecular form: ATLPF0004556 · Source: Primary reference linked

Reference
04

Evidence landscape

5 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
0 evidence records
0
0
0
0
Toxicity / Safety
5 evidence records
5
0
0
0
Endpoint distribution

Top evidence-bearing endpoint questions.

Cytotoxicity Percent Observation
2
Cytotoxicity Metric
1
Hemolysis Metric
1
Hemolysis Percent Observation
1
Assay context

Broad context buckets, useful before comparing values.

In vivo / route
3
Unspecified
2
Traceability

Reference-link availability for measurement-level audit.

Linked reference
5
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
Toxicity / Safety
Safety
Cytotoxicity Metric
50 μM
Result metric: CC50
Reported point valueEligible when experimental context matchesVero cellsNot specified
Reference
Primary reference linked
2
Toxicity / Safety
Safety
Cytotoxicity Percent Observation
50 %
Reported point valueEligible when experimental context matchesHuman embryonic kidney HEK293T cells · humanNot specified
Reference
Primary reference linked
3
Toxicity / Safety
Safety
Cytotoxicity Percent Observation
50 %
Reported point valueEligible when experimental context matchesVero cellsNot specified
Reference
Primary reference linked
4
Toxicity / Safety
Safety
Hemolysis Metric
80 μM
Result metric: HC50
Reported point valueEligible when experimental context matcheshuman · human red cellsNot specified
Reference
Primary reference linked
5
Toxicity / Safety
Safety
Hemolysis Percent Observation
50 %
Reported point valueEligible when experimental context matchesHuman erythrocytes · human · RBCNot specified
Source record
Primary reference linked
1–5 / 5
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

5 sources

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

·
Summary2 reference groups
Identity type
reported modified sequence
Reported notation
0
Reference groups
2
Measurements
5
ATL peptide ID
ATLPC0004174
Identity concordance
Identity concordance
Exact reported notation

Reported sequence string matches the current peptide notation.

0 / 5
Parent-residue compatible

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

0 / 5
Different notation

Reported notation does not resolve to the current display sequence.

0 / 5
Source sequence not captured

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

5 / 5
Reported sequence notation

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

Current identity
KALXKTMLKKLGTMAL
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
Safety
Cytotoxicity Metric, Cytotoxicity Percent Observation, Hemolysis Metric
No reported alias
4 identity
4 evidence
Source record
Open
Safety
Hemolysis Percent Observation
No reported alias
1 identity
1 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
ATLPC0004174
Identity type
reported modified sequence
ADMET endpoints
4
Evidence records
5
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/ATLPC0004174
open
curl -sS 'https://admetatlas.scbdd.com/api/v1/peptides/ATLPC0004174' \
  -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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