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).
35 rows where measurement_class = "intrinsic" and sequence_status = "pending_manual_figure" sorted by kd_log10_molar
This data as json, CSV (advanced)
Suggested facets: target_name_canonical, target_uniprot, aptamer_name, source_origin, pi_provenance_flag, assay_temperature_k, assay_buffer, aptamer_chemistry, aptamer_modifications, source_pmid, doi, source_db
assay_method 4
- filter_binding 12
- SPR 7
- microcantilever 2
- ELISA 1
verification_level 2
target_type 2
- protein 30
- glycan/conjugate 5
tier 1
- Gold 35
sequence_status 1
- pending_manual_figure · 35 ✖
measurement_class 1
- intrinsic · 35 ✖
binding_constant_type 1
- Kd 35
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 143 | P-selectin | protein | Q14242 | PF377 | 14.0 pM | -10.854 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF377 | 14 | step2c_literal_v3 | ||||
| 147 | P-selectin | protein | Q14242 | PF377sl | 14.0 pM | -10.854 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 296.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF377sl | 14 | step2c_literal_v3 | ||||
| 142 | P-selectin | protein | Q14242 | PF377 | 16.0 pM | -10.796 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF377 | 16 | step2c_literal_v3 | ||||
| 144 | P-selectin | protein | Q14242 | PF377 | 18.0 pM | -10.745 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 277.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF377 | 18 | step2c_literal_v3 | ||||
| 146 | P-selectin | protein | Q14242 | PF377sl | 29.0 pM | -10.538 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF377sl | 29 | step2c_literal_v3 | ||||
| 145 | P-selectin | protein | Q14242 | PF377sl | 46.0 pM | -10.337 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF377sl | 46 | step2c_literal_v3 | ||||
| 148 | P-selectin | protein | Q14242 | PF373sl | 56.0 pM | -10.252 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF373sl | 56 | step2c_literal_v3 | ||||
| 152 | PDGF-BB | protein | P01127 | PDGF-B aptamer | 0.1 nM | -10.0 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | DNA | 2'-fluoro; 2'-O-methyl; hexaethylene glycol spacer; inverted 3'-3' thymidine cap; 40-kd PEG conjugated | 9916931 | 10.1016/S0002-9440(10)65263-7 | the binding affinity of the aptamer used in the experiments described below ( K d ≈ 0.1 nM) | step2c_literal_v3 | |||||||
| 149 | P-selectin | protein | Q14242 | PF398sl | 178.0 pM | -9.75 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF398sl | 178 | step2c_literal_v3 | ||||
| 50 | PDGF-BB | protein | P01127 | PDGF-specific aptamer | 5e-10 M | -9.301 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | microcantilever | 310.15 | 7.4 | PBSM buffer (10.1 mM Na2HPO4, 1.8 mM KH2PO4, 137 mM NaCl, 2.7 mM KCl, and 1 mM MgCl2, pH 7.4) | 1.0 | DNA | 3'-3'-linked thymidine nucleotide ([3'T]); thiolated 5'-end | 24723743 | 10.1016/j.snb.2012.02.045 | K d , as shown in Fig. 10, decreased from approximately 12 × 10 -10 M to 5 × 10 -10 M as the temperature changed from 19 to 37 ◦ C. | step2c_literal_v3 | |||
| 4 | sLe X -BSA | glycan/conjugate | Q9NSU2 | Clone 2 | 8e-10 M | -9.097 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | KEEP_seq_in_figure | SPR | 7.4 | RNA binding buffer [150 mM NaCl, 20 mM Hepes (pH 7.4), 1 mM CaCl2, 1 mM MgCl2] | 1.0 | RNA | 11178986 | 10.1006/bbrc.2001.4327 | Clone 2 | 9.8 3 10 5 | 7.3 3 10 2 5 | 1.2 3 10 9 | 8.0 3 10 2 10 | step2c_literal_v3 | ||||
| 150 | P-selectin | protein | Q14242 | PF422sl | 1000.0 pM | -9.0 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | PF422sl | 1 X 103 | step2c_literal_v3 | ||||
| 49 | PDGF-BB | protein | P01127 | PDGF-specific aptamer | 1.2e-09 M | -8.921 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | microcantilever | 292.15 | 7.4 | PBSM buffer (10.1 mM Na2HPO4, 1.8 mM KH2PO4, 137 mM NaCl, 2.7 mM KCl, and 1 mM MgCl2, pH 7.4) | 1.0 | DNA | 3'-3'-linked thymidine nucleotide ([3'T]); thiolated 5'-end | 24723743 | 10.1016/j.snb.2012.02.045 | K d , as shown in Fig. 10, decreased from approximately 12 × 10 -10 M to 5 × 10 -10 M as the temperature changed from 19 to 37 ◦ C. | step2c_literal_v3 | |||
| 31 | VWF A1-domain | protein | P04275 | ARC1779 | 2.0 nM | -8.699 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 298.15 | Dulbecco's PBS containing 0.1 mg mL-1 BSA | DNA/RNA | 2'-O-methyl; phosphorothioate; inverted deoxythymidine; 20-kDa PEG conjugation | 19422452 | 10.1111/j.1538-7836.2009.03459.x | This resulted in a final aptamer (ARC1779) that is a 40-nucleotide modified DNA/RNA oligonucleotide with a K D of 2 nM for the A1-domain. | step2c_literal_v3 | |||||
| 64 | von Willebrand factor | protein | P04275 | 42-nt DNA aptamer | 2.0 nM | -8.699 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | FLAG_cited_data | ELISA | PBS with 1% BSA | DNA | biotinylated | 31493779 | 10.1055/s-0039-1696713 | a biotinylated DNA aptamer was able to bind an antibody-captured VWF in a concentration-dependent manner with a dissociation constant ( KD ) of 2.0 nM 0.3. | step2c_literal_v3 | |||||
| 5 | sLe X -BSA | glycan/conjugate | Q9NSU2 | Clone 15 | 2.3e-09 M | -8.638 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | KEEP_seq_in_figure | SPR | 7.4 | RNA binding buffer [150 mM NaCl, 20 mM Hepes (pH 7.4), 1 mM CaCl2, 1 mM MgCl2] | 1.0 | RNA | 11178986 | 10.1006/bbrc.2001.4327 | Clone 15 | 3.5 3 10 5 | 8.1 3 10 2 4 | 4.3 3 10 8 | 2.3 3 10 2 9 | step2c_literal_v3 | ||||
| 702 | melatonin | protein | P48039 | MLT-A-2 | 2.4 nM | -8.62 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | text | 36925277 | 10.1016/j.aca.2023.340971 | K d = 2.4 ± 2.8 nM for MLT-A-2 | elsevier_step2c | |||||||||
| 705 | melatonin | protein | P48039 | MLT-A-2F | 2.4 nM | -8.62 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | abstract | 36925277 | 10.1016/j.aca.2023.340971 | MLT-A-2F K d = 2.4 ± 2.8 nM | elsevier_step2c | |||||||||
| 545 | Human Cardiac Troponin I | protein | P19429 | TnIApt 23 | 2.69 nM | -8.57 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | abstract | 26003883 | 10.1016/j.jbiotec.2015.05.002 | Finally TnIApt 23 showed beast affinity in nanomolar range (2.69 nM) toward the target protein. | elsevier_step2c | |||||||||
| 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 | |||||||||||
| 6 | sLe X -BSA | glycan/conjugate | Q9NSU2 | Clone 18 | 3.9e-09 M | -8.409 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | KEEP_seq_in_figure | SPR | 7.4 | RNA binding buffer [150 mM NaCl, 20 mM Hepes (pH 7.4), 1 mM CaCl2, 1 mM MgCl2] | 1.0 | RNA | 11178986 | 10.1006/bbrc.2001.4327 | Clone 18 | 5.1 3 10 5 | 2.0 3 10 2 3 | 2.5 3 10 8 | 3.9 3 10 2 9 | step2c_literal_v3 | ||||
| 7 | sLe X -BSA | glycan/conjugate | Q9NSU2 | Clone 4 | 7.4e-09 M | -8.131 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | KEEP_seq_in_figure | SPR | 7.4 | RNA binding buffer [150 mM NaCl, 20 mM Hepes (pH 7.4), 1 mM CaCl2, 1 mM MgCl2] | 1.0 | RNA | 11178986 | 10.1006/bbrc.2001.4327 | Clone 4 | 4.1 3 10 5 | 3.1 3 10 2 3 | 1.3 3 10 8 | 7.4 3 10 2 9 | step2c_literal_v3 | ||||
| 569 | MPT64 | protein | aptamer sequence (17) | 8.92 nM | -8.05 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | text | 28454652 | 10.1016/j.tube.2017.03.004 | KD (dissociation equilibrium constant) was 8.92 nM | elsevier_step2c | ||||||||||
| 8 | sLe X -BSA | glycan/conjugate | Q9NSU2 | Clone 9 | 1e-08 M | -8.0 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | KEEP_seq_in_figure | SPR | 7.4 | RNA binding buffer [150 mM NaCl, 20 mM Hepes (pH 7.4), 1 mM CaCl2, 1 mM MgCl2] | 1.0 | RNA | 11178986 | 10.1006/bbrc.2001.4327 | Clone 9 | 3.5 3 10 5 | 3.1 3 10 2 3 | 9.5 3 10 7 | 1.0 3 10 2 8 | step2c_literal_v3 | ||||
| 704 | N-acetyl-5-hydroxytryptamine | protein | P46597 | MLT-A-4F | 0.016 μM | -7.796 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | text | 36925277 | 10.1016/j.aca.2023.340971 | for NAT very low K d value was observed i.e., 0.016 μM | elsevier_step2c | |||||||||
| 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 | ||||||||||
| 703 | 5-Methoxytryptamine | protein | P48039 | MLT-C-1F | 0.274 μM | -6.562 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | text | 36925277 | 10.1016/j.aca.2023.340971 | For L-TRP and 5-MT very low K d were observed i.e., 0.324 μM and 0.274 μM respectively | elsevier_step2c | |||||||||
| 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 | ||||||||||
| 563 | Brevetoxin-2 | protein | Bap5 | 4.83 uM | -5.316 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_figure | text | 28058132 | 10.1155/2016/9241860 | The Kd value for the binding between the Bap5 aptamer and BTX-2 was 4.83 uM | elsevier_step2c | ||||||||||
| 151 | P-selectin | protein | Q14242 | NX244 | 9000000.0 pM | -5.046 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_figure | filter_binding | 310.15 | 7.4 | SHMCK buffer | 1.0 | 2'F-RNA | 9743465 | 10.1089/oli.1.1998.8.265 | NX244 | 9 X 106 | step2c_literal_v3 |
Advanced export
JSON shape: default, array, newline-delimited
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';