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).
207 rows where sequence_status = "pending_manual_supp" sorted by kd_log10_molar
This data as json, CSV (advanced)
Suggested facets: source_origin, assay_temperature_k, assay_ph, assay_cations, aptamer_chemistry, source_db
assay_method 13
- fluorescence 23
- BLI 12
- SPR 12
- flow_cytometry 12
- ELISA 8
- ITC 7
- dot_blot 4
- CE-LIF 3
- MST 3
- EMSA 2
- filter_binding 2
- DPV 1
- ELONA 1
measurement_class 4
verification_level 2
tier 1
- Gold 207
sequence_status 1
- pending_manual_supp · 207 ✖
binding_constant_type 1
- Kd 207
| 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 | |||||||
| 598 | human α-Thrombin | protein | P00734 | A1 | 2.0 pM | -11.699 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 31129134 | 10.1016/j.ab.2019.05.012 | Also for aptamer A1 we measured with MST KD values in the pico- and nanomolar range (2 pM and 52 nM). The lowest KD value is determined with MST (shown as bar) for aptamer A1, which is 2 pM. | elsevier_step2c | |||||||||
| 406 | SARS-CoV-2 spike protein (wild type) | protein | DSA1N5 | 3e-12 M | -11.523 | avidity_multivalent | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | dot_blot | undiluted wastewater | DNA | dimeric | 36926840 | 10.1021/acssensors.2c02655 | DSA1N5 also demonstrated high binding affinity in undiluted wastewater samples ( K d = 3.0 -3.9 pM for WTPV, Figure S1A,B). | step2c_acs_v1 | |||||||
| 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 | ||||||||
| 743 | SARS-CoV-2 spike protein (wild type) | protein | DSA1N5 | 3.9e-12 M | -11.409 | avidity_multivalent | Kd | Gold | ACS | multi_agent_verified | pending_manual_supp | dot_blot | undiluted wastewater | DNA | dimeric | 36926840 | 10.1021/acssensors.2c02655 | DSA1N5 also demonstrated high binding affinity in undiluted wastewater samples ( K d = 3.0 -3.9 pM for WTPV, Figure S1A,B). | step2c_acs_v1 | |||||||
| 404 | SARS-CoV-2 pseudotyped lentivirus (omicron variant) | protein | DSA1N5 | 4.8e-12 M | -11.319 | avidity_multivalent | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | dot_blot | deionized water | DNA | dimeric | 36926840 | 10.1021/acssensors.2c02655 | This study demonstrates that DSA1N5 has high affinity for recognizing OMPV with a K d value of 4.8 pM, which is in the same order of magnitude as that measured for the WTPV (2.1 pM) in deionized water (DI water) | step2c_acs_v1 | |||||||
| 405 | SARS-CoV-2 pseudotyped lentivirus (omicron variant) | protein | DSA1N5 | 5.1e-12 M | -11.292 | avidity_multivalent | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | dot_blot | wastewater (diluted 50% with binding buffer) | DNA | dimeric | 36926840 | 10.1021/acssensors.2c02655 | DSA1N5 preserves its binding affinity in 50% wastewater ( K d = 2.1 -4.1 pM for WTPV and 5.1 for OMPV in wastewater). | step2c_acs_v1 | |||||||
| 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 | |||||||
| 351 | thrombin | protein | P00734 | Supra-TBA15/29-GO | 1.9e-11 M | -10.721 | avidity_multivalent | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | DNA | Graphene Oxide immobilization; poly(adenine) anchor | 31157200 | 10.3389/fchem.2019.00280 | Supra-TBA15 / 29-GO prepared with GO (40 μ g mL -1 ) at 60 ◦ C exhibited much higher binding affinity toward thrombin ( K d = 1.9 × 10 -11 M, Figure S10 , Supporting Information). | step2c_acs_v1 | ||||||||
| 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 | ||||||||
| 56 | von Willebrand factor A1-domain | protein | P04275 | Rn-DsDsDs-53mh | 61.3 pM | -10.213 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | 310.15 | 1 × PBS supplemented with 0.05% (w/v) Nonidet P-40 | DNA | Ds (7-(2-thienyl)imidazo[4,5b]pyridine); mini-hairpin DNA | 27966933 | 10.1021/jacs.6b10767 | RnDsDsDs-53mh ( K D = 61.3 pM) | step2c_literal_v3 | |||||
| 542 | Myoglobin | protein | P02144 | anti-Mb aptamer | 65.0 pM | -10.187 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 25957831 | 10.1016/j.bios.2015.04.089 | The corresponding af fi nity, K D, values calculated from the ratio between dissociation ( k d) and association ( k a ) was found to be 65 pM. | elsevier_step2c | |||||||||
| 53 | von Willebrand factor A1-domain | protein | P04275 | Rn-DsDsDs-44 | 74.9 pM | -10.126 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | 310.15 | 1 × PBS supplemented with 0.05% (w/v) Nonidet P-40 | DNA | Ds (7-(2-thienyl)imidazo[4,5b]pyridine) | 27966933 | 10.1021/jacs.6b10767 | Rn-DsDsDs-44 ( K D = 74.9 pM) exhibited the highest a ffi nity | 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 | |||||
| 57 | von Willebrand factor A1-domain | protein | P04275 | Rn-DsDs-51mh2 | 182.0 pM | -9.74 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | 310.15 | 1 × PBS supplemented with 0.05% (w/v) Nonidet P-40 | DNA | Ds (7-(2-thienyl)imidazo[4,5b]pyridine); mini-hairpin DNA | 27966933 | 10.1021/jacs.6b10767 | Rn-DsDs-51mh2 ( K D = 182 pM) | step2c_literal_v3 | |||||
| 55 | von Willebrand factor A1-domain | protein | P04275 | ARC1172-41 | 326.0 pM | -9.487 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | 310.15 | 1 × PBS supplemented with 0.05% (w/v) Nonidet P-40 | DNA | 27966933 | 10.1021/jacs.6b10767 | ARC1172-41 ( K D = 326 pM) | step2c_literal_v3 | ||||||
| 478 | FLRPp (O serotype) | protein | FMD_1 | 3.46e-10 M | -9.461 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | SPR | DNA | 42010751 | 10.1021/acs.analchem.5c04748 | dissociation constants ( KD ) of 3.46 × 10 -10 M | step2c_acs_v1 | |||||||||
| 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 | |||||||||
| 550 | Thrombin | protein | P00734 | TBA29 | 5e-10 M | -9.301 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 26643617 | 10.1016/j.jconrel.2015.11.028 | and TBA29 (~5 × 10 -10 M) | elsevier_step2c | |||||||||
| 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 | ||||||||
| 536 | tetracycline | protein | Q14728 | TC aptamer | 770.0 pM | -9.114 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 25517161 | 10.1016/j.bpj.2014.11.001 | dissociation constant Kd of 770 pM ([Mg 2 þ ] 1⁄4 10 mM) | elsevier_step2c | |||||||||
| 459 | PSMA | protein | Q04609 | C3 | 8.000000000000001e-10 M | -9.097 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | EMSA | 5 mM Mg2+ | DNA | phenol-dT; naphthyl-dC; PSMA-617 bait | 41126016 | 10.1021/jacs.5c13307 | an exemplar shows very high affinity for PSMA ( K d ∼ 0.8 nM). | step2c_acs_v1 | ||||||
| 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 | |||||
| 458 | PSMA | protein | Q04609 | C3 (without fluorescein) | 1e-09 M | -9.0 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | EMSA | DNA | phenol-dT; naphthyl-dC; Cy5 label | 41126016 | 10.1021/jacs.5c13307 | EMSA data show that Cy5-labeled C3 without fluorescein binds PSMA just as strongly as the parent construct, with an apparent K d of ∼ 1 nM (Figure S9). | step2c_acs_v1 | |||||||
| 54 | von Willebrand factor A1-domain | protein | P04275 | Pr-DsDsDs-40 | 1.03 nM | -8.987 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | 310.15 | 1 × PBS supplemented with 0.05% (w/v) Nonidet P-40 | DNA | Ds (7-(2-thienyl)imidazo[4,5b]pyridine) | 27966933 | 10.1021/jacs.6b10767 | Pr-DsDsDs-40 ( K D = 1.03 nM) | step2c_literal_v3 | |||||
| 664 | PD-L1 | protein | Q9NZQ7 | 8-60 | 1.4 nM | -8.854 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 34711320 | 10.1016/j.aca.2021.339066 | 8 e 60, a representative aptamer with high af fi nity (KD 1⁄4 1.4 nM determined by SPR) | elsevier_step2c | |||||||||
| 108 | thrombin | protein | P00734 | T.7 | 1.5 nM | -8.824 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | binding buffer supplemented with 0.05% of Tween-20 | DNA | 37798416 | 10.1038/s41587-023-01973-8 | T.7 exhibited the strongest binding signal with a 1.5 nM K d | step2c_literal_v3 | |||||||
| 337 | human α-thrombin | protein | P00734 | LOOPER modified thrombin aptamer | 1.6000000000000003e-09 M | -8.796 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | SPR | DNA | diversely functionalized; heteromultivalent | 28938065 | 10.1021/jacs.7b07241 | Using single-cycle kinetics surface plasmon resonance (SPR), the LOOPER aptamer exhibited a Kd of 1.6 nM | step2c_acs_v1 | |||||||
| 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 | ||||||||
| 316 | CD44-HABD | protein | Motif 4 (ADDA adduct) | 2e-09 M | -8.699 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | 23057694 | 10.1021/bi300471d | motifs 2 and 4(ADDA adduct) have ~2 nM affinity to CD44-HABD | step2c_acs_v1 | |||||||||||
| 322 | S-adenosylmethionine | protein | P17707 | Bs SAM-I riboswitch | 3.0000000000000004e-09 M | -8.523 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | 23343213 | 10.1021/ja310742m | Both μ MSA values agree well with results from the in-line probing assays performed using identical buffer conditions: ... 3 nM K d , respectively | step2c_acs_v1 | ||||||||||
| 323 | S-adenosylmethionine | protein | P17707 | Pi SAM-I riboswitch | 3.0000000000000004e-09 M | -8.523 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | 23343213 | 10.1021/ja310742m | which is on the order of the 3 nM value measured using a conventional inline probing assay | step2c_acs_v1 | ||||||||||
| 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 | ||||||||
| 614 | human α-Thrombin | protein | P00734 | B1 | 3.4 nM | -8.469 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 31129134 | 10.1016/j.ab.2019.05.012 | for MST the B aptamers (B1: 3.4 nM, B2: 5 nM, B3: 7.6 nM) | elsevier_step2c | |||||||||
| 338 | human α-thrombin | protein | P00734 | LOOPER modified thrombin aptamer | 4e-09 M | -8.398 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | 28938065 | 10.1021/jacs.7b07241 | Preliminary binding analysis by label-free microscale thermophoresis showed a promising dissociation constant K d = 4 nM for thrombin | step2c_acs_v1 | ||||||||||
| 465 | SARS-CoV-2 spike RBD | protein | Aptx2-L | 4.900000000000001e-09 M | -8.31 | avidity_multivalent | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | flow_cytometry | 298.15 | 7.4 | PBS, pH 7.4, 0.55 mM MgCl2 | DNA | 41498844 | 10.1021/acsami.5c16490 | The Aptx2-L variant showed superior affinity with a dissociation constant ( K d) of 4.9 nM | step2c_acs_v1 | ||||||
| 615 | human α-Thrombin | protein | P00734 | B2 | 5.0 nM | -8.301 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 31129134 | 10.1016/j.ab.2019.05.012 | for MST the B aptamers (B1: 3.4 nM, B2: 5 nM, B3: 7.6 nM) | elsevier_step2c | |||||||||
| 710 | sST2 | protein | P30874 | sS9_P | 5.6 nM | -8.252 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 37992929 | 10.1016/j.ijbiomac.2023.128295 | in case of sS9, parent aptamer has outperformed its truncated counterpart in terms of affinity as it has shown higher affinity (Kd ~5.6 nM). | elsevier_step2c | |||||||||
| 603 | human α-Thrombin | protein | P00734 | A2 | 6.3 nM | -8.201 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 31129134 | 10.1016/j.ab.2019.05.012 | for SCORE (b-nd analysis) the best are A2 (6.3 nM) | elsevier_step2c | |||||||||
| 461 | Lipopolysaccharide from Klebsiella pneumoniae ATCC 15380 | protein | aptamer seq. 5 | 6.68e-09 M | -8.175 | intrinsic | Kd | Gold | v4 | multi_agent_verified | pending_manual_supp | DPV | 1 × PBS | DNA | biotin | 41323700 | 10.1039/d5ra06759f | The binding affinity of aptamer seq. 5 was 6.68 nM (Fig. 9C). | step2c_acs_v1 | |||||||
| 609 | human α-Thrombin | protein | P00734 | A3 | 6.9 nM | -8.161 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 31129134 | 10.1016/j.ab.2019.05.012 | for SCORE (b-nd analysis) the best are A2 (6.3 nM) and A3 (6.9 nM) | elsevier_step2c | |||||||||
| 139 | PTK7 | protein | Q13308 | 4AsF | 7.2 nM | -8.143 | intrinsic | Kd | Gold | v4 | extraction_verified | pending_manual_supp | SPR | 310.15 | 7.4 | 1 × DPBS | 5.0 | DNA | SF at positions A23, A24, A25, A26 | 41065179 | 10.1021/jacs.5c11823 | 4AsF, which exhibited a 10-fold reduction compared to 4APS (0.77 vs 7.20 nM) | step2c_literal_v3 | |||
| 556 | VEGF165 | protein | P15692 | cot-pega | 7.33 nM | -8.135 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 26956592 | 10.1016/j.jconrel.2016.03.006 | The K D of cot-pega for VEGF was 7.33 nM (Fig. 1b) | elsevier_step2c | |||||||||
| 616 | human α-Thrombin | protein | P00734 | B3 | 7.6 nM | -8.119 | intrinsic | Kd | Gold | elsevier | extraction_verified | pending_manual_supp | text | 31129134 | 10.1016/j.ab.2019.05.012 | for MST the B aptamers (B1: 3.4 nM, B2: 5 nM, B3: 7.6 nM) | elsevier_step2c |
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';