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Peptide·modified or textual

ATLPC0012630

ATLPC0012630

YGRKKRRQRRR-NH2

Routes
Compare in workbenchDownload releaseAPI JSON
  • Length
    12 aa
On this page
  • 01 Sequence & molecular identity
  • 02 Physicochemical profile
  • 03 Distribution / Barrier
  • 04 Evidence landscape
  • 05 Product context
  • 06 Identity & reference map
  • 07 Data access & reproducibility
Coveragecounts only · not riskATLPC0012630
  • Measurements
    12
  • Endpoints
    1
  • 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 · 12
Exposure / Absorption
No evidence
Distribution / Barrier
12 measurements
Metabolic & Proteolytic Stability
No evidence
Excretion / Persistence
No evidence
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 view

A peptidoform is one specific molecular form of the peptide — its sequence plus the modifications at given positions (HUPO-PSI term). This view preserves the reported terminal groups, residue modifications, and stereo markers from the source notation.

YGRKKRRQRRR-NH2
Identity summarySpecific molecular form represented
Identity status
Specific molecular form represented
Residues
12
Peptidoform features
1
Documented molecular forms
1
Representations
2
Documented molecular forms1 form linked to this peptide identity
FormTopologyModificationsConnectionsRepresentationsMeasurements
ATLPF0013826———Notation only—
Residue view
Residue display
12 residues
Y1G2R3K4K5R6R7Q8R9R10R11X12X
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 12
X

Reported token NH2 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.

modified or textual
Parent-residue sequence

Residue string used for positional interpretation when available.

YGRKKRRQRRRX
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

Distribution / Barrier

12 records

What is known about distribution, binding, permeability, or barrier crossing?

Evidence records
12
Complete canonical measurements and observations attached to this domain.
Endpoint scope
1
Formal ADMET endpoints represented for this peptide.
Matched-context analysis
7
Quantitative results that may be analysed only with scientifically compatible records.
Reported-result review
5
Qualitative, narrative, or review-first results interpreted in their source context.
Endpoints in scopeBBB penetration
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.
7
Interpret as reported
Qualitative, narrative, or review-first findings preserved in source context.
5
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.

·
BBB penetration12 records · 7 matched-context · 5 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

3.1 x 10^-7 cm/s

Eligible when experimental context matches

(Co)-culture · blood-brain barrier

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

Reference
2

83 %

Eligible when experimental context matches

(Co)-culture · blood-brain barrier

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

Reference
3

21.09 %

Eligible when experimental context matches

Capillary depletion · blood-brain barrier

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

Reference
4

78.91 %

Eligible when experimental context matches

Capillary depletion · blood-brain barrier

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

Reference
5

0.21 min^-1

Eligible when experimental context matches

Efflux study (ICV) · blood-brain barrier

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

Reference
6

0.00113 mL/g/min

Eligible when experimental context matches

Intravenous injection (multiple time regression) · blood-brain barrier

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

Reference
7

0.02736 mL/g

Eligible when experimental context matches

Intravenous injection (multiple time regression) · blood-brain barrier

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

Reference
8

23.05 %

Interpret as reported

Not specified

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

Reference
9

76.95 %

Interpret as reported

Not specified

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

Reference
10

0.02762 mL/g

Interpret as reported

NA · NA · blood-brain barrier

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

Reference
1–10 / 12
Barrier and permeability assay context

PAMPA, Caco-2, MDCK/RRCK, and BBB findings are assay/model contexts under Distribution / Barrier. They should not be read as interchangeable measurements.

PAMPA
0

artificial membrane

Caco-2
0

cell monolayer

MDCK
0

cell monolayer

RRCK
0

cell monolayer

BBB
12

barrier evidence

04

Evidence landscape

12 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
12 evidence records
7
5
0
0
Metabolic & Proteolytic Stability
0 evidence records
0
0
0
0
Excretion / Persistence
0 evidence records
0
0
0
0
Toxicity / Safety
0 evidence records
0
0
0
0
Endpoint distribution

Top evidence-bearing endpoint questions.

Blood Brain Barrier Penetration
12
Assay context

Broad context buckets, useful before comparing values.

Matrix / stability
6
In vivo / route
4
Unspecified
2
Traceability

Reference-link availability for measurement-level audit.

Linked reference
12
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
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.028 mL/g
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: Intravenous
Reference
Primary reference linked
2
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.05 min^-1
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: NA
Reference
Primary reference linked
3
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
23.05 %
Reported point valueInterpret as reportedNot specifiedNot specified
Reference
Primary reference linked
4
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.006 mL/g/min
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: Intravenous
Reference
Primary reference linked
5
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
76.95 %
Reported point valueInterpret as reportedNot specifiedNot specified
Reference
Primary reference linked
6
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
3.1 x 10^-7 cm/s
Reported point valueEligible when experimental context matches(Co)-culture · blood-brain barrierNot specified
Reference
Primary reference linked
7
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
78.91 %
Reported point valueEligible when experimental context matchesCapillary depletion · blood-brain barrierNot specified
Reference
Primary reference linked
8
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.21 min^-1
Reported point valueEligible when experimental context matchesEfflux study (ICV) · blood-brain barrierNot specified
Reference
Primary reference linked
9
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.027 mL/g
Reported point valueEligible when experimental context matchesIntravenous injection (multiple time regression) · blood-brain barrierNot specified
Reference
Primary reference linked
10
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.001 mL/g/min
Reported point valueEligible when experimental context matchesIntravenous injection (multiple time regression) · blood-brain barrierNot specified
Reference
Primary reference linked
1–10 / 12
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

12 sources

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

·
Summary3 reference groups
Identity type
reported modified sequence
Reported notation
0
Reference groups
3
Measurements
12
ATL peptide ID
ATLPC0012630
Identity concordance
Identity concordance
Exact reported notation

Reported sequence string matches the current peptide notation.

0 / 12
Parent-residue compatible

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

0 / 12
Different notation

Reported notation does not resolve to the current display sequence.

0 / 12
Source sequence not captured

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

12 / 12
Reported sequence notation

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

Current identity
YGRKKRRQRRR-NH2
Reported names
No distinct human-readable aliases are exposed.
Reference map3 reference groups
Reference map

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

ReferenceSupportsReported identityRecords
Reference
Open
Distribution
Blood Brain Barrier Penetration
No reported alias
10 identity
10 evidence
Reference
Open
Distribution
Blood Brain Barrier Penetration
No reported alias
1 identity
1 evidence
Reference
Open
Distribution
Blood Brain Barrier Penetration
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
ATLPC0012630
Identity type
reported modified sequence
ADMET endpoints
1
Evidence records
12
Reference groups
3
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/ATLPC0012630
open
curl -sS 'https://admetatlas.scbdd.com/api/v1/peptides/ATLPC0012630' \
  -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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