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Peptide·map backed

ATLPC0026640

ATLPC0026640

MKKKIISAILMSTVILSAAAPLSGVYALDISSTCDADLIWKLLVKAQEKFGRGKPSKRVKKMRRQWQACKSSHHHHHH

Compare in workbenchDownload releaseAPI JSON
  • Length
    78 aa
  • Monoisotopic mass
    8798.8 Da
  • Net charge @ pH 7.4
    11.60
  • Isoelectric point
    11.04
  • GRAVY
    -0.287
On this page
  • 01 Sequence & molecular identity
  • 02 Physicochemical profile
  • 03 Evidence landscape
  • 04 Product context
  • 05 Identity & reference map
  • 06 Data access & reproducibility
Coveragecounts only · not riskATLPC0026640
  • Measurements
    0
  • Endpoints
    0
  • Domains
    0/5
  • Products
    —
  • No matrix stability evidence
  • No clearance evidence
  • No immunogenicity context
  • 2 liability motifs
Jump to domain

Open the matching evidence section below

All evidence index
Exposure / Absorption
No evidence
Distribution / Barrier
No evidence
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 summarySpecific molecular form represented
Identity status
Specific molecular form represented
Residues
78
Peptidoform features
0
Documented molecular forms
1
Representations
4
Documented molecular forms1 form linked to this peptide identity
FormTopologyModificationsConnectionsRepresentationsMeasurements
ATLPF0028970—1—1—
Residue view
Residue display
78 residues
M1K2K3K4I5I6S7A8I9L10M11S12T13V14I15L16S17A18A19A20P21L22S23G24V25Y26A27L28D29I30S31S32T33C34D35A36D37L38I39W40K41L42L43V44K45A46Q47E48K49F50G51R52G53K54P55S56K57R58V59K60K61M62R63R64Q65W66Q67A68C69K70S71S72H73H74H75H76H77H78
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 representationSMILES available
2D structure·RDKit.js
rendering molecule…
Canonical SMILES
CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCSC)[C@@H](C)CC)[C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)O)C(C)C)C(C)C)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(C)C)[C@@H](C)CC)C(C)C)[C@@H](C)O
Representation class

How the current release can interpret this identity chemically.

map backed
Parent-residue sequence

Residue string used for positional interpretation when available.

MKKKIISAILMSTVILSAAAPLSGVYALDISSTCDADLIWKLLVKAQEKFGRGKPSKRVKKMRRQWQACKSSHHHHHH
HELM

Polymer notation for modified peptide representation when available.

MKKKIISAILMSTVILSAAAPLSGVYALDISSTCDADLIWKLLVKAQEKFGRGKPSKRVKKMRRQWQACKSSHHHHHH{ct:His-tag}
SMILES

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

CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCSC)[C@@H](C)CC)[C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)O)C(C)C)C(C)C)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(C)C)[C@@H](C)CC)C(C)C)[C@@H](C)O
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 & modifications1 signal
FeaturePositionsInterpretationLink
Form-level topologyATLPF0028970Open-chain form. Residue-level connection endpoints are shown separately when available.Not linked
02

Physicochemical profile

10 descriptors

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

·
Core descriptors78 aa · pI 11.0 · GRAVY -0.29
Length
78 aa
Monoisotopic mass
8798.76 Da
Average mass
8804.47 Da
Net charge at pH 7.4
11.60
Estimated pI
11.04
GRAVY
-0.287
KD-positive residues
39.7%
Aromatic residues
5.1%
Developability interpretation
Ionization context
pH 7.4 separated from pI
Hydrophobicity balance
Leans hydrophilic
Amphipathic moment (μH)
0.13
Computation boundary
Standard-sequence only
Charge & residue composition
pH charge context

Modeled net charge across common formulation and assay pH checkpoints.

pH 2
21.93
pH 5
17.19
pH 6
15.59
pH 7.4
11.46
pH 9
8.54
pH 12
-4.29
Residue-class composition

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

Acidic (D,E)
4 · 5.1%
Basic (K,R,H)
21 · 26.9%
Polar uncharged (N,Q,S,T)
14 · 17.9%
Hydrophobic aliphatic (A,V,I,L,M)
28 · 35.9%
Aromatic (F,W,Y)
4 · 5.1%
Conformational / sulfur (G,P,C)
7 · 9.0%
Top residues
K1114.1%S911.5%A810.3%L79.0%H67.7%I67.7%R45.1%V45.1%
Hydropathy & amphipathic windows
Hydropathy windows

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

Most hydrophobic window
5-11
IISAILM
GRAVY 2.886
Most hydrophilic window
72-78
SHHHHHH
GRAVY -2.857
72 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
41-52
KLLVKAQEKFGR
μH 1.67 · charge 3.0
12 aa window
39-50
IWKLLVKAQEKF
μH 1.62 · charge 2.0
12 aa window
37-48
DLIWKLLVKAQE
μH 1.61 · charge 0.0
15 aa window
39-53
IWKLLVKAQEKFGRG
μH 1.57 · charge 3.0
15 aa window
36-50
ADLIWKLLVKAQEKF
μH 1.48 · charge 1.0
Sequence-liability cues
Sequence-liability notes

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

Oxidation-sensitive residues
M, W, C · pos 1, 11, 34, 40, 62, 66 +1
Met, Trp, and Cys residues can merit formulation review for oxidation or covalent-state sensitivity.
Cys covalent complexity
C · pos 34, 69
Multiple cysteines can indicate disulfide or free-thiol interpretation requirements.
Alpha-helix amphipathic projection
Helical wheel · Edmundson projection
μH = 0.13100°/residue · 78 aa
μH1: M (Met) · Hydrophobic · K-D 1.9M12: K (Lys) · Basic + · K-D -3.9K3: K (Lys) · Basic + · K-D -3.9K4: K (Lys) · Basic + · K-D -3.9K5: I (Ile) · Hydrophobic · K-D 4.5I56: I (Ile) · Hydrophobic · K-D 4.5I7: S (Ser) · Polar · K-D -0.8S8: A (Ala) · Hydrophobic · K-D 1.8A9: I (Ile) · Hydrophobic · K-D 4.5I10: L (Leu) · Hydrophobic · K-D 3.8L1011: M (Met) · Hydrophobic · K-D 1.9M12: S (Ser) · Polar · K-D -0.8S13: T (Thr) · Polar · K-D -0.7T14: V (Val) · Hydrophobic · K-D 4.2V15: I (Ile) · Hydrophobic · K-D 4.5I1516: L (Leu) · Hydrophobic · K-D 3.8L17: S (Ser) · Polar · K-D -0.8S18: A (Ala) · Hydrophobic · K-D 1.8A19: A (Ala) · Hydrophobic · K-D 1.8A20: A (Ala) · Hydrophobic · K-D 1.8A2021: P (Pro) · Special · K-D -1.6P22: L (Leu) · Hydrophobic · K-D 3.8L23: S (Ser) · Polar · K-D -0.8S24: G (Gly) · Special · K-D -0.4G25: V (Val) · Hydrophobic · K-D 4.2V2526: Y (Tyr) · Aromatic · K-D -1.3Y27: A (Ala) · Hydrophobic · K-D 1.8A28: L (Leu) · Hydrophobic · K-D 3.8L29: D (Asp) · Acidic − · K-D -3.5D30: I (Ile) · Hydrophobic · K-D 4.5I3031: S (Ser) · Polar · K-D -0.8S32: S (Ser) · Polar · K-D -0.8S33: T (Thr) · Polar · K-D -0.7T34: C (Cys) · Special · K-D 2.5C35: D (Asp) · Acidic − · K-D -3.5D3536: A (Ala) · Hydrophobic · K-D 1.8A37: D (Asp) · Acidic − · K-D -3.5D38: L (Leu) · Hydrophobic · K-D 3.8L39: I (Ile) · Hydrophobic · K-D 4.5I40: W (Trp) · Aromatic · K-D -0.9W4041: K (Lys) · Basic + · K-D -3.9K42: L (Leu) · Hydrophobic · K-D 3.8L43: L (Leu) · Hydrophobic · K-D 3.8L44: V (Val) · Hydrophobic · K-D 4.2V45: K (Lys) · Basic + · K-D -3.9K4546: A (Ala) · Hydrophobic · K-D 1.8A47: Q (Gln) · Polar · K-D -3.5Q48: E (Glu) · Acidic − · K-D -3.5E49: K (Lys) · Basic + · K-D -3.9K50: F (Phe) · Aromatic · K-D 2.8F5051: G (Gly) · Special · K-D -0.4G52: R (Arg) · Basic + · K-D -4.5R53: G (Gly) · Special · K-D -0.4G54: K (Lys) · Basic + · K-D -3.9K55: P (Pro) · Special · K-D -1.6P5556: S (Ser) · Polar · K-D -0.8S57: K (Lys) · Basic + · K-D -3.9K58: R (Arg) · Basic + · K-D -4.5R59: V (Val) · Hydrophobic · K-D 4.2V60: K (Lys) · Basic + · K-D -3.9K6061: K (Lys) · Basic + · K-D -3.9K62: M (Met) · Hydrophobic · K-D 1.9M63: R (Arg) · Basic + · K-D -4.5R64: R (Arg) · Basic + · K-D -4.5R65: Q (Gln) · Polar · K-D -3.5Q6566: W (Trp) · Aromatic · K-D -0.9W67: Q (Gln) · Polar · K-D -3.5Q68: A (Ala) · Hydrophobic · K-D 1.8A69: C (Cys) · Special · K-D 2.5C70: K (Lys) · Basic + · K-D -3.9K7071: S (Ser) · Polar · K-D -0.8S72: S (Ser) · Polar · K-D -0.8S73: H (His) · Basic + · K-D -3.2H74: H (His) · Basic + · K-D -3.2H75: H (His) · Basic + · K-D -3.2H7576: H (His) · Basic + · K-D -3.2H77: H (His) · Basic + · K-D -3.2H78: H (His) · Basic + · K-D -3.2H78
Hydrophobic moment0.13
Mean K-D hydropathy-0.29
Approx. net charge+11
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
90.13
Instability index
53.0

Above 40 — predicted unstable in vitro.

Boman index
1.53 kcal/mol
Molar extinction coefficient (280 nm)
12,490 M⁻¹·cm⁻¹

A280 (1 g/L) ≈ 1.42 · 12,615 M⁻¹·cm⁻¹ with 1 disulfide

Structure-derived (developability)

Computed from the representative peptidoform's chemical structure. Rule-of-5 / beyond-Ro5 framing per Lipinski/Doak.

Topological polar surface area
3545.2 Ų
Computed logP (Crippen)
-32.18

Computed logP — distinct from the measured logD endpoint.

Hydrogen-bond donors
129
Hydrogen-bond acceptors
124
Rotatable bonds
303
Rule-of-5 / beyond-Ro5 flags
Beyond bRo5

3 Ro5 violations · MW 8,804.54 Da

03

Evidence landscape

Cross-domain evidence distribution and measurement-level detail. No assay-level evidence is available for this peptide in the current release.

No endpoint-level measurements returned

No ADMET endpoint evidence is attached to this peptide yet.

/evidence/drilldown
04

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
05

Identity & reference map

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

No identity references available

No reported identity references are available for this peptide in the current release.

06

Data access & reproducibility

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

·
Record scopePublic release
ATL peptide ID
ATLPC0026640
Identity type
canonical sequence
ADMET endpoints
0
Evidence records
0
Reference groups
1
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/ATLPC0026640
open
curl -sS 'https://admetatlas.scbdd.com/api/v1/peptides/ATLPC0026640' \
  -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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