Binding affinities (Kd) — source-verified (view)
Data license: CC BY 4.0 · Data source: apt-scout automated curation pipeline (E. Dohi, NCNP) — values harvested from public databases; raw source stored per target
- target_name_canonical
- Target as named in the source paper.
- target_type
- protein / cell-line+EV / glycan-conjugate. Filter to 'protein' for molecular targets.
- target_uniprot
- UniProt accession when a human protein (sparse for now; links to apt-scout target).
- aptamer_name
- Aptamer identifier as reported.
- kd_reported
- Kd value AS REPORTED in the paper (value + unit). Units are MIXED — do NOT compare this column directly.
- kd_log10_molar
- log10(Kd in molar). THE column to sort / compare / learn on (lower = tighter).
- measurement_class
- intrinsic = equilibrium vs purified target; non_intrinsic = apparent/cellular or avidity (NOT comparable to intrinsic).
- binding_constant_type
- Kd / apparent-Kd etc. as reported.
- assay_method
- SPR / filter binding / flow cytometry / ITC / BLI …
- assay_temperature_k
- Assay temperature (K) — a reason the same pair can have several rows.
- source_pmid
- PubMed ID of the source paper (links out).
- verbatim_quote
- The exact sentence the value was taken from.
- verification_level
- QC status (honest, growing): human_verified / human_corrected = a logged human verdict from the stratified-random sample; multi_agent_verified = passed independent multi-agent (L2) check; extraction_verified = extraction-pipeline verified; automated. Human verification is in progress: as of this release 0 records carry a logged human verdict — the published set is multi-agent-/extraction-verified, and human spot-checking is being added post-publication (version-tracked). No record is labelled human_verified without a logged human review.
- sequence_status
- Aptamer-sequence provenance: verified_in_text_or_SI = sequence verbatim-verified against the source text/SI (shown); pending_manual_supp / pending_supp_oa / pending_manual_figure = sequence reported only in a (often paywalled) SI or a figure, being curated post-submission; no_single_sequence_pool = a pool/library/primer, no single sequence exists.
- pi_provenance_flag
- PI manual-review flag: KEEP_seq_in_figure = valid record, sequence is in a 3D-structure figure; FLAG_cited_data = Kd may be a value cited from elsewhere, re-verify. (EXCLUDE rows are hidden from this view.)
- seq_source
- original (already in source DB) / backfill_text_verified (recovered from paper or SI text).
9 rows where sequence_status = "pending_manual_figure", tier = "Gold" and verification_level = "multi_agent_verified" sorted by kd_log10_molar
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Suggested facets: target_name_canonical, target_uniprot, aptamer_name, source_pmid, doi
measurement_class 2
verification_level 1
- multi_agent_verified · 9 ✖
tier 1
- Gold · 9 ✖
target_type 1
- protein 9
sequence_status 1
- pending_manual_figure · 9 ✖
binding_constant_type 1
- Kd 9
assay_method 1
- SPR 2
| id | target_name_canonical | target_type | target_uniprot | aptamer_name | aptamer_seq | kd_reported | kd_log10_molar ▼ | measurement_class | binding_constant_type | tier | source_origin | verification_level | sequence_status | seq_source | pi_provenance_flag | assay_method | assay_temperature_k | assay_ph | assay_buffer | assay_cations | aptamer_chemistry | aptamer_modifications | source_pmid | doi | verbatim_quote | source_db |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 378 | dT70 | protein | DCC-SSB | 3.0000000000000004e-09 M | -8.523 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 34085169 | 10.1007/s12010-021-03585-x | At a low concentration ( ∼ 2.5 nM), the titration with dT70 gave an approximate assessment of affinity ( K d ∼ 3 nM). | step2c_acs_v1 | |||||||||||
| 336 | VEGF-165 | protein | P15692 | bivalent construct for VEGF-165 (no linker) | 1.7e-08 M | -7.77 | avidity_multivalent | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 27043498 | 10.3390/molecules21040421 | this bivalent construct had about 28-fold higher binding affinity ( K D = 17 nM) | step2c_acs_v1 | ||||||||||
| 377 | dT35 | protein | DCC-SSB | 2.9e-08 M | -7.538 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 34085169 | 10.1007/s12010-021-03585-x | The second stage was fitted to a hyperbola to give a K d value of 29 nM. | step2c_acs_v1 | |||||||||||
| 346 | Ciprofloxacin | protein | Q86VL8 | R10K6 | 3.1e-08 M | -7.509 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 30609709 | 10.3390/bios9010007 | a dissociation constant (KD) for the RNA-ligand complex of 31 nM was determined. | step2c_acs_v1 | ||||||||||
| 347 | Ciprofloxacin | protein | Q86VL8 | R10K6_V11 | 3.6000000000000005e-08 M | -7.444 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 30609709 | 10.3390/bios9010007 | The determined dissociation constant of 36 nM for V11 is similar to the original full-length aptamer R10K6 (31 nM). | step2c_acs_v1 | ||||||||||
| 370 | ODAM | protein | A1E959 | OD64 | 4.771e-08 M | -7.321 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | SPR | DNA | 33455205 | 10.1021/acsbiomaterials.0c01203 | the obtained OD64 and OD35 (aptamer cognate pair) presented high a ffi nity and excellent speci fi city, along with dissociation constants ( K d ) of 47.71 nM (OD64) | step2c_acs_v1 | ||||||||
| 371 | ODAM | protein | A1E959 | OD35 | 5.1360000000000005e-08 M | -7.289 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | SPR | DNA | 33455205 | 10.1021/acsbiomaterials.0c01203 | the obtained OD64 and OD35 (aptamer cognate pair) presented high a ffi nity and excellent speci fi city, along with dissociation constants ( K d ) of 47.71 nM (OD64) and 51.36 nM (OD35). | step2c_acs_v1 | ||||||||
| 379 | dT20 | protein | DCC-SSB | 2.4000000000000003e-07 M | -6.62 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 293.15 | 34085169 | 10.1007/s12010-021-03585-x | Titrations of dT 27 and dT20 at low concentrations of DCCSSB gave smaller fluorescence changes, and the data were fit to give single K d values of 43 and 240 nM, respectively | step2c_acs_v1 | ||||||||||
| 380 | dT20 | protein | DCC-SSB | 3.96e-07 M | -6.402 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_figure | 293.15 | 34085169 | 10.1007/s12010-021-03585-x | With dT20, the intercept suggests a dissociation rate constant of 49 s -1 , producing a value of 396 nM for the equilibrium dissociation constant | step2c_acs_v1 |
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CREATE VIEW v_kd AS
SELECT k.id,
target_name_canonical,
CASE
WHEN target_name_canonical LIKE '%cell%' OR target_name_canonical LIKE '%vesicle%' OR target_name_canonical LIKE '%exosome%' THEN 'cell/EV'
WHEN target_name_canonical LIKE '%BSA%' OR target_name_canonical LIKE '%sLe%' OR target_name_canonical LIKE '%glycan%' OR target_name_canonical LIKE '% Le %' THEN 'glycan/conjugate'
ELSE 'protein'
END AS target_type,
target_uniprot, aptamer_name, aptamer_seq,
(COALESCE(kd_value,'') || CASE WHEN COALESCE(kd_unit,'')!='' THEN ' '||kd_unit ELSE '' END) AS kd_reported,
CAST(NULLIF(kd_log10_molar,'') AS REAL) AS kd_log10_molar,
measurement_class, binding_constant_type, 'Gold' AS tier, k.tier AS source_origin,
CASE
WHEN vh.verdict='confirmed' THEN 'human_verified'
WHEN vh.verdict='corrected' THEN 'human_corrected'
WHEN vh.verdict='rejected' THEN 'human_rejected'
WHEN k.verification_status='agent_verified_L2' THEN 'multi_agent_verified'
WHEN k.verification_status IN ('verified','CONFIRM') THEN 'extraction_verified'
ELSE 'automated'
END AS verification_level,
sequence_status, seq_source, pi_provenance_flag,
assay_method,
CAST(NULLIF(assay_temperature_k,'') AS REAL) AS assay_temperature_k,
CAST(NULLIF(assay_ph,'') AS REAL) AS assay_ph,
assay_buffer, assay_cations, aptamer_chemistry, aptamer_modifications,
source_pmid, doi, verbatim_quote, source_db
FROM kd_measurements k LEFT JOIN verification_human vh ON vh.row_id=k.source_record_id
WHERE LOWER(COALESCE(k.include_in_gold,''))='true';