On the public citation graph
Correlation between Protein Function and Ligand Binding Profiles
0 signed · 50 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527612178.ch2openalex-snapshot
Examples of Active Areas of Structure Based‐Design
inferredcites →https://doi.org/10.1002/pro.62openalex-snapshot
Structure and function of Pseudomonas aeruginosa protein PA1324 (21–170)
inferredcites →https://doi.org/10.1002/prot.22840openalex-snapshot
Solution structure and function of YndB, an AHSA1 protein fromBacillus subtilis
inferredcites →https://doi.org/10.1006/jmra.1995.1047openalex-snapshot
Water Suppression That Works. Excitation Sculpting Using Arbitrary Wave-Forms and Pulsed-Field Gradients
inferredcites →https://doi.org/10.1007/112_2007_0703openalex-snapshot
Assigning functions to genes—the main challenge of the post-genomics era
inferredcites →https://doi.org/10.1007/978-1-60761-931-4_1openalex-snapshot
Historical Overview of Chemical Library Design
inferredcites →https://doi.org/10.1007/s00018-003-3114-8openalex-snapshot
Automatic prediction of protein function
inferredcites →https://doi.org/10.1007/s10822-005-8694-yopenalex-snapshot
Virtual Computational Chemistry Laboratory – Design and Description
inferredcites →https://doi.org/10.1007/s10822-009-9280-5openalex-snapshot
Lessons for fragment library design: analysis of output from multiple screening campaigns
inferredcites →https://doi.org/10.1016/j.drudis.2007.11.001openalex-snapshot
The application of FAST-NMR for the identification of novel drug discovery targets
inferredcites →https://doi.org/10.1016/j.ijms.2004.09.004openalex-snapshot
The study of protein–ligand interactions by mass spectrometry—a personal view
inferredcites →https://doi.org/10.1016/j.tibtech.2009.01.002openalex-snapshot
Protein function prediction – the power of multiplicity
inferredcites →https://doi.org/10.1016/s0169-409x(00)00129-0openalex-snapshot
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings 1PII of original article: S0169-409X(96)00423-1. The article was originally published in Advanced Drug Delivery Reviews 23 (1997) 3–25. 1
inferredcites →https://doi.org/10.1016/s0169-409x(96)00423-1openalex-snapshot
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
inferredcites →https://doi.org/10.1016/s1359-6446(05)03477-xopenalex-snapshot
Kinomics: characterizing the therapeutically validated kinase space
inferredcites →https://doi.org/10.1021/cc800122mopenalex-snapshot
Estimating Protein−Ligand Binding Affinity Using High-Throughput Screening by NMR
inferredcites →https://doi.org/10.1021/ci100010vopenalex-snapshot
When is Chemical Similarity Significant? The Statistical Distribution of Chemical Similarity Scores and Its Extreme Values
inferredcites →https://doi.org/10.1021/ci800289yopenalex-snapshot
Binding Site Similarity Analysis for the Functional Classification of the Protein Kinase Family
inferredcites →https://doi.org/10.1021/ja0651759openalex-snapshot
FAST-NMR: Functional Annotation Screening Technology Using NMR Spectroscopy
inferredcites →https://doi.org/10.1021/jm049131ropenalex-snapshot
Druggability Indices for Protein Targets Derived from NMR-Based Screening Data
inferredcites →https://doi.org/10.1021/jm8011036openalex-snapshot
Assessment of Chemical Coverage of Kinome Space and Its Implications for Kinase Drug Discovery
inferredcites →https://doi.org/10.1021/jp952516oopenalex-snapshot
An Experimental Approach to Mapping the Binding Surfaces of Crystalline Proteins
inferredcites →https://doi.org/10.1038/75556openalex-snapshot
Gene Ontology: tool for the unification of biology
inferredcites →https://doi.org/10.1038/nbt0397-264openalex-snapshot
Organic solvents identify specific ligand binding sites on protein surfaces
inferredcites →https://doi.org/10.1038/nbt1228openalex-snapshot
Global mapping of pharmacological space
inferredcites →https://doi.org/10.1038/nbt1284openalex-snapshot
Relating protein pharmacology by ligand chemistry
inferredcites →https://doi.org/10.1038/nrd2220openalex-snapshot
A decade of fragment-based drug design: strategic advances and lessons learned
inferredcites →https://doi.org/10.1073/pnas.87.6.2264openalex-snapshot
Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes.
inferredcites →https://doi.org/10.1093/bib/bbp017openalex-snapshot
FINDSITE: a combined evolution/structure-based approach to protein function prediction
inferredcites →https://doi.org/10.1093/nar/gkm806openalex-snapshot
FunSimMat: a comprehensive functional similarity database
inferredcites →https://doi.org/10.1093/nar/gkm839openalex-snapshot
LigASite a database of biologically relevant binding sites in proteins with known apo-structures
inferredcites →https://doi.org/10.1093/protein/14.1.47openalex-snapshot
Experimental and computational mapping of the binding surface of a crystalline protein
inferredcites →https://doi.org/10.1126/science.275.5298.343openalex-snapshot
An Information-Intensive Approach to the Molecular Pharmacology of Cancer
inferredcites →https://doi.org/10.1186/1471-2105-6-194openalex-snapshot
Functional annotation by identification of local surface similarities: a novel tool for structural genomics
inferredcites →https://doi.org/10.1371/journal.pcbi.1000387openalex-snapshot
Drug Discovery Using Chemical Systems Biology: Identification of the Protein-Ligand Binding Network To Explain the Side Effects of CETP Inhibitors
inferredcites →https://doi.org/10.1371/journal.pone.0007442openalex-snapshot
Structural and Functional Similarity between the Bacterial Type III Secretion System Needle Protein PrgI and the Eukaryotic Apoptosis Bcl-2 Proteins
inferredcites →https://doi.org/10.2174/138620706777935342openalex-snapshot
Design and Characterization of a Functional Library for NMR Screening Against Novel Protein Targets
inferredcites →https://doi.org/10.2174/138620709787581738openalex-snapshot
A Multi-Step NMR Screen for the Identification and Evaluation of Chemical Leads for Drug Discovery
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s00726-023-03347-5openalex-snapshot
Serum albumin acted as an effective carrier to improve the stability of bioactive flavonoid
inferred← citeshttps://doi.org/10.1016/j.bpc.2019.106268openalex-snapshot
Formation of a bovine serum albumin diligand complex with rutin and single-walled carbon nanotubes for the reduction of cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.bpc.2020.106327openalex-snapshot
Formation of a bovine serum albumin diligand complex with rutin for the suppression of heme toxicity
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b01291openalex-snapshot
Systematic Identification of Protein–Metabolite Interactions in Complex Metabolite Mixtures by Ligand-Detected Nuclear Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.biochem.6b00954openalex-snapshot
Fragment Profiling Approach to Inhibitors of the Orphan M. tuberculosis P450 CYP144A1
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.0c00537openalex-snapshot
Generation of a Bovine Serum Albumin–Diligand Complex for the Protection of Bioactive Quercetin and Suppression of Heme Toxicity
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.2c00001openalex-snapshot
Bovine Serum Albumin as a Potential Carrier for the Protection of Bioactive Quercetin and Inhibition of Cu(II) Toxicity
inferred← citeshttps://doi.org/10.1021/acs.jafc.7b00326openalex-snapshot
Formation of a Multiligand Complex of Bovine Serum Albumin with Retinol, Resveratrol, and (−)-Epigallocatechin-3-gallate for the Protection of Bioactive Components
inferred← citeshttps://doi.org/10.1021/acs.jafc.8b02327openalex-snapshot
Generation of a Diligand Complex of Bovine Serum Albumin with Quercetin and Carbon Nanotubes for the Protection of Bioactive Quercetin and Reduction of Cytotoxicity
inferred← citeshttps://doi.org/10.1021/acs.jcim.2c01115openalex-snapshot
Practical Guidance for Consensus Scoring and Force Field Selection in Protein–Ligand Binding Free Energy Simulations
inferred← citeshttps://doi.org/10.1021/cb200507fopenalex-snapshot
The International Chemical Biology Community Synthesizes a New Society
inferred← citeshttps://doi.org/10.3390/ijms24076795openalex-snapshot
Molecular Docking and Dynamics Simulation Studies Predict Potential Anti-ADAR2 Inhibitors: Implications for the Treatment of Cancer, Neurological, Immunological and Infectious Diseases
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.