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).
31 rows where measurement_class = "non_intrinsic", sequence_status = "pending_manual_supp" and verification_level = "extraction_verified" sorted by kd_log10_molar
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Suggested facets: target_name_canonical, target_uniprot, aptamer_name, kd_reported, kd_log10_molar, assay_temperature_k, assay_ph, assay_buffer, assay_cations, aptamer_modifications, source_pmid, doi, verbatim_quote
assay_method 5
- flow_cytometry 9
- ELISA 5
- CE-LIF 3
- fluorescence 3
- filter_binding 2
verification_level 1
- extraction_verified · 31 ✖
tier 1
- Gold 31
sequence_status 1
- pending_manual_supp · 31 ✖
measurement_class 1
- non_intrinsic · 31 ✖
binding_constant_type 1
- Kd 31
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 188 | PDGF-BB | protein | P01127 | 36aApt | 0.036 pM | -13.444 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | ELISA | 298.0 | DNA | 28825469 | 10.1021/acscombsci.6b00163 | 36aApt | 0.036 ± 0.012 | - 18.33 | step2c_literal_v3 | |||||||
| 186 | PDGF-BB | protein | P01127 | 38aApt | 0.094 pM | -13.027 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | ELISA | 298.0 | DNA | 28825469 | 10.1021/acscombsci.6b00163 | 38aApt | 0.094 ± 0.008 | - 17.76 | step2c_literal_v3 | |||||||
| 208 | SW480 cells | cell/EV | Q16520 | Apt-nanovesicle | 3.66 pM | -11.437 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | cholesterol; multivalent | 32049531 | 10.1021/jacs.9b13782 | The dissociation constant ( K d ) value of Apt-nanovesicle against SW480 cells was found to be 3.66 ± 0.34 pM (Figure 2B) | step2c_literal_v3 | ||||||||
| 184 | PDGF-BB | protein | P01127 | FullApt | 5.33 pM | -11.273 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | ELISA | 298.0 | DNA | 28825469 | 10.1021/acscombsci.6b00163 | FullApt | 5.33 ± 2.36 | - 15.37 | step2c_literal_v3 | |||||||
| 185 | PDGF-BB | protein | P01127 | 40Apt | 5.92 pM | -11.228 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | ELISA | 298.0 | DNA | 28825469 | 10.1021/acscombsci.6b00163 | 40Apt | 5.92 ± 1.13 | - 15.31 | step2c_literal_v3 | |||||||
| 187 | PDGF-BB | protein | P01127 | 38bApt | 7.03 pM | -11.153 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | ELISA | 298.0 | DNA | 28825469 | 10.1021/acscombsci.6b00163 | 38bApt | 7.03 ± 1.28 | - 15.21 | step2c_literal_v3 | |||||||
| 269 | thrombin | protein | P00734 | HD1-12A-DAB | 13.1 pM | -10.883 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | filter_binding | selection buffer | DNA | 41053535 | 10.1002/advs.202509867 | HD1-12A-DAB EXACT inhibitor bound to thrombin and prothrombin with K D s of 13.1 pm | step2c_literal_v3 | |||||||
| 209 | SW480 cells | cell/EV | Q16520 | Fixed Apt-nanovesicle | 28.06 pM | -10.552 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | cholesterol; crosslinked | 32049531 | 10.1021/jacs.9b13782 | the K d value of fi xed Apt-nanovesicles to SW480 cells was increased to 28.06 ± 3.31 pM (Figure 2D) | step2c_literal_v3 | ||||||||
| 219 | CCRF-CEM cells | cell/EV | Q9NRR3 | CDN-sgc8 | 0.08 nM | -10.097 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | fluorescence | 1 × PBS, 5 mM MgCl2 | 5.0 | DNA | biotinylated | 35670775 | 10.1021/acs.analchem.2c01359 | Kd=0.08±0.01 nM | step2c_literal_v3 | |||||
| 218 | CCRF-CEM cells | cell/EV | Q9NRR3 | mono-CDN-sgc8 | 0.48 nM | -9.319 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | fluorescence | 1 × PBS, 5 mM MgCl2 | 5.0 | DNA | biotinylated | 35670775 | 10.1021/acs.analchem.2c01359 | Kd= 0.48 ± 0.04 nM | step2c_literal_v3 | |||||
| 205 | thrombin | protein | P00734 | TBA29 | 0.5 nM | -9.301 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | 31614078 | 10.1021/acs.analchem.9b03368 | The 29-nt TBA29 aptamer has a bimodular duplex-antiparallel G4 structure and binds to thrombin with a binding a ffi nity of 0.5 nM. 30 | step2c_literal_v3 | |||||||||
| 303 | EGFR | protein | P00533 | Anti-EGF receptor aptamer | 0.62 nM | -9.208 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | 3' end sulfhydryl group (-SH) | 41877526 | 10.1021/acs.molpharmaceut.5c01966 | Anti-EGF receptor aptamers ( K d : 0.62 nM, DNA aptamers) | step2c_literal_v3 | ||||||||
| 217 | CCRF-CEM cells | cell/EV | Q9NRR3 | individual sgc8 | 0.82 nM | -9.086 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | fluorescence | 1 × PBS, 5 mM MgCl2 | 5.0 | DNA | biotinylated | 35670775 | 10.1021/acs.analchem.2c01359 | Kd=0.82 ± 0.12 nM | step2c_literal_v3 | |||||
| 228 | CD8 | protein | P01732 | A3t | 2.0 nM | -8.699 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | 36149728 | 10.1021/acsami.2c11783 | A3t, a CD8 receptor-binding aptamer, which binds CD8-expressing cells with an equilibrium dissociation constant K D of 2 nM. | step2c_literal_v3 | |||||||||
| 232 | CD8 | protein | P01732 | rvCD8apt | 2.0 nM | -8.699 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | 8 nt toehold | 36149728 | 10.1021/acsami.2c11783 | apparent K D = 2 nM for CD8 + cells | step2c_literal_v3 | ||||||||
| 211 | K562 | protein | Q8WUY8 | PAM | 3.2 nM | -8.495 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | FAM | 32307868 | 10.1002/anie.202004206 | the K d value (3.2 nM) of PAM in binding the K562 cell is one order of magnitude lower than that of the aptamer alone (41 nM). | step2c_literal_v3 | ||||||||
| 267 | Thyroid-Stimulating Hormone Receptor (TSHR) 6X His tag | protein | ZMXLY-2a | 11.5 nM | -7.939 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | phosphate-buffered saline | DNA | FITC-labeled 5' primer used for synthesis | 40588369 | 10.1021/acs.analchem.5c02024 | As determined by flow cytometry, the K d of ZMXLY-2a was 11.5 ± 9.3 nM (Figure 2G) | step2c_literal_v3 | |||||||
| 183 | human immunoglobulin E | protein | Q96D42 | T40-AptIgE-3'-TMR | 15.0 nM | -7.824 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | CE-LIF | 298.15 | 7.5 | sample bu ff er containing 10 mM Tris-HCl (pH 7.5) and 1 mM MgCl2 | 1.0 | DNA | TMR label at 3'-end; polyT tail (40 T) at 5'-end | 28763192 | 10.1021/acs.analchem.7b02313 | The K d of T40-AptIgE-3 ′ -TMR was about 15 nM | step2c_literal_v3 | |||
| 212 | M2-like macrophage | protein | Q8IYS5 | A2 | 22.81 nM | -7.642 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | 277.15 | Wash Buffer (WB) supplemented with 10% FBS and 100 μg/mL tRNA | DNA | Cy5-label | 32589412 | 10.1021/acs.bioconjchem.0c00247 | apparent dissociation constants ( K d ) of 44.12 ± 8.0 and 22.81 ± 5.6 nM to M0- and M2-like macrophages, respectively | step2c_literal_v3 | |||||
| 210 | K562 | protein | Q8WUY8 | aptamer-FAM | 41.0 nM | -7.387 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | FAM | 32307868 | 10.1002/anie.202004206 | the K d value (3.2 nM) of PAM in binding the K562 cell is one order of magnitude lower than that of the aptamer alone (41 nM). | step2c_literal_v3 | ||||||||
| 257 | CD71 | protein | P02786 | XQ 2d | 42.34 nM | -7.373 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | PBS supplemented with 0.5 mM MgCl2 and 0.05% BSA (BB buffer) | 0.5 | DNA | FAM | 40156524 | 10.1021/acs.analchem.5c00711 | aptamers (HG1-9, K d = 43.23 ± 4.62 nM and XQ-2d, K d = 42.34 ± 5.15 nM)) | step2c_literal_v3 | |||||
| 258 | CD71 | protein | P02786 | HG1-9 | 43.23 nM | -7.364 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | PBS supplemented with 0.5 mM MgCl2 and 0.05% BSA (BB buffer) | 0.5 | DNA | FAM | 40156524 | 10.1021/acs.analchem.5c00711 | aptamers (HG1-9, K d = 43.23 ± 4.62 nM and XQ-2d, K d = 42.34 ± 5.15 nM)) | step2c_literal_v3 | |||||
| 213 | M0-like macrophage | protein | P01854 | A2 | 44.12 nM | -7.355 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | 277.15 | Wash Buffer (WB) supplemented with 10% FBS and 100 μg/mL tRNA | DNA | Cy5-label | 32589412 | 10.1021/acs.bioconjchem.0c00247 | apparent dissociation constants ( K d ) of 44.12 ± 8.0 and 22.81 ± 5.6 nM to M0- and M2-like macrophages, respectively | step2c_literal_v3 | |||||
| 214 | monocyte | protein | P13500 | A2 | 45.0 nM | -7.347 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | 277.15 | Wash Buffer (WB) supplemented with 10% FBS and 100 μg/mL tRNA | DNA | Cy5-label | 32589412 | 10.1021/acs.bioconjchem.0c00247 | aptamer A2 bound CD14 + cells (monocytes) with high speci fi city ( K d ∼ 45 ± 9.1 nM) | step2c_literal_v3 | |||||
| 300 | CD71 | protein | P02786 | ATL | 48.17 nM | -7.317 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | 277.15 | 6.5 | binding buffer | DNA | Cy5-labeled; Cy3-labeled; Triplex motif | 41412185 | 10.1021/acs.nanolett.5c04783 | K(pH 6.5) = 48.17 ± 2.70 nM | step2c_literal_v3 | ||||
| 182 | human immunoglobulin E | protein | Q96D42 | AptIgE-3'-TMR | 50.0 nM | -7.301 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | CE-LIF | 298.15 | 7.5 | sample bu ff er containing 10 mM Tris-HCl (pH 7.5) and 1 mM MgCl2 | 1.0 | DNA | TMR label at 3'-end | 28763192 | 10.1021/acs.analchem.7b02313 | The apparent K d of AptIgE-3 ′ -TMR was about 50 nM | step2c_literal_v3 | |||
| 268 | Thyroid-Stimulating Hormone Receptor (TSHR) | protein | P16473 | TSHRly-1c | 54.37 nM | -7.265 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | binding buffer | DNA | AlexaFluor 647-labeled | 40588369 | 10.1021/acs.analchem.5c02024 | As shown in Figure 4E, the apparent equilibrium dissociation constant ( K d) of TSHRly-1c was determined to be 54.37 ± 8.22 nM. | step2c_literal_v3 | ||||||
| 207 | SW480 cells | cell/EV | Q16520 | SYL3C | 142.5 nM | -6.846 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | DNA | cholesterol | 32049531 | 10.1021/jacs.9b13782 | monovalent SYL3C aptamer ( K d = 142.50 ± 20.55 nM, Figure 2A) | step2c_literal_v3 | ||||||||
| 179 | human α-thrombin | protein | P00734 | T25-Apt15-3'-TMR | 228.0 nM | -6.642 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | CE-LIF | 298.15 | 7.5 | sample bu ff er containing 10 mM Tris-HCl (pH 7.5) and 5 mM KCl | DNA | TMR label at 3'-end; polyT tail (25 T) at 5'-end | 28763192 | 10.1021/acs.analchem.7b02313 | The apparent K d values of T25-Apt15-3 ′ -TMR and 5 ′ -TMR-T25-Apt15 were estimated as 228 nM and 8.8 nM, respectively | step2c_literal_v3 | ||||
| 270 | prothrombin | protein | P00734 | HD1-12A-DAB | 296.0 nM | -6.529 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | filter_binding | selection buffer | DNA | 41053535 | 10.1002/advs.202509867 | and prothrombin with K D s of 13.1 pm and 296 nm | step2c_literal_v3 | |||||||
| 301 | CD71 | protein | P02786 | ATL | 696.7 nM | -6.157 | non_intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | flow_cytometry | 277.15 | 7.5 | binding buffer | DNA | Cy5-labeled; Cy3-labeled; Triplex motif | 41412185 | 10.1021/acs.nanolett.5c04783 | K(pH 7.5)= 696.7 ± 68.03 nM | step2c_literal_v3 |
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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';