On the public citation graph

Mutational analysis and molecular modeling of the N-terminal kringle-containing domain of hepatocyte growth factor identifies amino acid side chains important for interaction with the c-Metreceptor

https://doi.org/10.1093/protein/7.7.895
0 signed · 66 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4094539openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470515457.ch6openalex-snapshot
Domain Structure of Hepatocyte Growth Factor/Scatter Factor (HGF/SF)
inferred← citeshttps://doi.org/10.1002/9781119044116.ch2openalex-snapshot
Protein Chemical Synthesis by SEA Ligation
inferred← citeshttps://doi.org/10.1002/9781119300229.ch6openalex-snapshot
Targeting HGF with Antibodies as an Anti‐Cancer Therapeutic Strategy
inferred← citeshttps://doi.org/10.1002/ange.201105837openalex-snapshot
A One‐Pot Three‐Segment Ligation Strategy for Protein Chemical Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201105837openalex-snapshot
A One‐Pot Three‐Segment Ligation Strategy for Protein Chemical Synthesis
inferred← citeshttps://doi.org/10.1002/cbf.2898openalex-snapshot
Dissociation of c‐Met phosphotyrosine sites in human cells in response to mouse hepatocyte growth factor but not human hepatocyte growth factor: the possible roles of different amino acids in different species
inferred← citeshttps://doi.org/10.1006/bbrc.1998.9950openalex-snapshot
A Mutant of Deleted Variant of Hepatocyte Growth Factor (dHGF) with Alanine Substitution in the N-Terminal Basic Region Has Higher Activityin Vivo
inferred← citeshttps://doi.org/10.1007/978-3-319-11888-8_8openalex-snapshot
The MET Receptor Family
inferred← citeshttps://doi.org/10.1016/j.bbapap.2012.10.012openalex-snapshot
Structural basis of MET receptor dimerization by the bacterial invasion protein InlB and the HGF/SF splice variant NK1
inferred← citeshttps://doi.org/10.1016/j.bbrep.2022.101295openalex-snapshot
A pilot study on nitration/dysfunction of NK1 segment of myogenic stem cell activator HGF
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2006.12.022openalex-snapshot
A fusion protein of hepatocyte growth factor for immobilization to collagen
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.06.029openalex-snapshot
Targeted Disruption of Heparan Sulfate Interaction with Hepatocyte and Vascular Endothelial Growth Factors Blocks Normal and Oncogenic Signaling
inferred← citeshttps://doi.org/10.1016/j.ejca.2009.12.026openalex-snapshot
Recombinant kringle 5 from plasminogen antagonises hepatocyte growth factor-mediated signalling
inferred← citeshttps://doi.org/10.1016/j.ejcb.2010.11.014openalex-snapshot
Structural insights into Met receptor activation
inferred← citeshttps://doi.org/10.1016/j.jmb.2008.01.034openalex-snapshot
Engineering the NK1 Fragment of Hepatocyte Growth Factor/Scatter Factor as a MET Receptor Antagonist
inferred← citeshttps://doi.org/10.1016/j.jmb.2008.09.091openalex-snapshot
Noncompetitive Inhibition of Hepatocyte Growth Factor-dependent Met Signaling by a Phage-derived Peptide
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2015.04.007openalex-snapshot
Achieving high signal-to-noise in cell regulatory systems: Spatial organization of multiprotein transmembrane assemblies of FGFR and MET receptors
inferred← citeshttps://doi.org/10.1016/s0014-5793(98)00558-4openalex-snapshot
Insights into the structure of hepatocyte growth factor/scatter factor (HGF/SF) and implications for receptor activation
inferred← citeshttps://doi.org/10.1016/s0014-5793(98)00971-5openalex-snapshot
Analysis of deleted variant of hepatocyte growth factor by alanine scanning mutagenesis: identification of residues essential for its biological function and generation of mutants with enhanced mitogenic activity on rat hepatocytes
inferred← citeshttps://doi.org/10.1016/s0014-5793(99)01416-7openalex-snapshot
The PAN module: the N‐terminal domains of plasminogen and hepatocyte growth factor are homologous with the apple domains of the prekallikrein family and with a novel domain found in numerous nematode proteins
inferred← citeshttps://doi.org/10.1016/s0022-2836(02)00199-7openalex-snapshot
A New Crystal Form of the NK1 Splice Variant of HGF/SF Demonstrates Extensive Hinge Movement and Suggests That the NK1 Dimer Originates by Domain Swapping
inferred← citeshttps://doi.org/10.1016/s0168-8278(96)80157-7openalex-snapshot
Hepatocyte proliferation and serum hepatocyte growth factor levels in patients with alcoholic hepatitis
inferred← citeshttps://doi.org/10.1016/s0960-9822(98)70059-4openalex-snapshot
Engineered mutants of HGF/SF with reduced binding to heparan sulphate proteoglycans, decreased clearance and enhanced activity in vivo
inferred← citeshttps://doi.org/10.1016/s0969-2126(98)00012-4openalex-snapshot
The solution structure of the N-terminal domain of hepatocyte growth factor reveals a potential heparin-binding site
inferred← citeshttps://doi.org/10.1016/s0969-2126(98)00138-5openalex-snapshot
Crystal structure of the NK1 fragment of human hepatocyte growth factor at 2.0 å resolution
inferred← citeshttps://doi.org/10.1016/s1350-9462(00)00015-xopenalex-snapshot
Hepatocyte growth factor/Scatter factor in the eye
inferred← citeshttps://doi.org/10.1038/4947openalex-snapshot
Crystal structure of the NK1 fragment of HGF/SF suggests a novel mode for growth factor dimerization and receptor binding.
inferred← citeshttps://doi.org/10.1038/nchembio.1533openalex-snapshot
An allosteric switch for pro-HGF/Met signaling using zymogen activator peptides
inferred← citeshttps://doi.org/10.1038/nrm1261openalex-snapshot
Met, metastasis, motility and more
inferred← citeshttps://doi.org/10.1038/s41467-021-24367-3openalex-snapshot
Structural basis of the activation of c-MET receptor
inferred← citeshttps://doi.org/10.1039/c4sc03856hopenalex-snapshot
Semi-synthesis of a HGF/SF kringle one (K1) domain scaffold generates a potent in vivo MET receptor agonist
inferred← citeshttps://doi.org/10.1042/bj20141236openalex-snapshot
The solution structure of the MANEC-type domain from hepatocyte growth factor activator inhibitor-1 reveals an unexpected PAN/apple domain-type fold
inferred← citeshttps://doi.org/10.1042/bj3260763openalex-snapshot
Functional and biophysical characterization of recombinant human hepatocyte growth factor isoforms produced in Escherichia coli
inferred← citeshttps://doi.org/10.1042/bst0340414openalex-snapshot
Signalling by HGF/SF and Met: the role of heparan sulphate co-receptors
inferred← citeshttps://doi.org/10.1042/bst20200394openalex-snapshot
State of the structure address on MET receptor activation by HGF
inferred← citeshttps://doi.org/10.1046/j.1365-2613.2000.00138.xopenalex-snapshot
Hepatocyte growth factor/scatter factor‐induced intracellular signalling
inferred← citeshttps://doi.org/10.1046/j.1523-1755.2000.00987.xopenalex-snapshot
Hepatocyte growth factor in renal failure: Promise and reality
inferred← citeshttps://doi.org/10.1073/pnas.0509040103openalex-snapshot
Structural basis of hepatocyte growth factor/scatter factor and MET signalling
inferred← citeshttps://doi.org/10.1073/pnas.0704290104openalex-snapshot
A mechanistic basis for converting a receptor tyrosine kinase agonist to an antagonist
inferred← citeshttps://doi.org/10.1073/pnas.1005183107openalex-snapshot
Structural basis for agonism and antagonism of hepatocyte growth factor
inferred← citeshttps://doi.org/10.1073/pnas.1102561108openalex-snapshot
Engineering hepatocyte growth factor fragments with high stability and activity as Met receptor agonists and antagonists
inferred← citeshttps://doi.org/10.1074/jbc.270.28.16871openalex-snapshot
Sulfated Oligosaccharides Promote Hepatocyte Growth Factor Association and Govern Its Mitogenic Activity
inferred← citeshttps://doi.org/10.1074/jbc.271.40.24576openalex-snapshot
Mechanisms of Hepatocyte Growth Factor Stimulation of Keratinocyte Metalloproteinase Production
inferred← citeshttps://doi.org/10.1074/jbc.271.46.29461openalex-snapshot
Kringle Domains of Human Angiostatin
inferred← citeshttps://doi.org/10.1074/jbc.273.44.28805openalex-snapshot
Prothrombin Kringle-2 Domain Has a Growth Inhibitory Activity against Basic Fibroblast Growth Factor-stimulated Capillary Endothelial Cells
inferred← citeshttps://doi.org/10.1074/jbc.274.42.29937openalex-snapshot
Interaction of Macrophage-stimulating Protein with Its Receptor
inferred← citeshttps://doi.org/10.1074/jbc.m105486200openalex-snapshot
Dissociation of Heparan Sulfate and Receptor Binding Domains of Hepatocyte Growth Factor Reveals That Heparan Sulfate-c-Met Interaction Facilitates Signaling
inferred← citeshttps://doi.org/10.1074/jbc.m112196200openalex-snapshot
Differential Mitogenic Effects of Single Chain Hepatocyte Growth Factor (HGF)/Scatter Factor and HGF/NK1 following Cleavage by Factor Xa
inferred← citeshttps://doi.org/10.1074/jbc.m212768200openalex-snapshot
The N-terminal Domain of Hepatocyte Growth Factor Inhibits the Angiogenic Behavior of Endothelial Cells Independently from Binding to the c-met Receptor
inferred← citeshttps://doi.org/10.1074/jbc.m404795200openalex-snapshot
Structural and Functional Basis of the Serine Protease-like Hepatocyte Growth Factor β-Chain in Met Binding and Signaling
inferred← citeshttps://doi.org/10.1074/jbc.m405043200openalex-snapshot
Inhibition by Copper(II) Binding of Hepatocyte Growth Factor (HGF) Interaction with Its Receptor Met and Blockade of HGF/Met Function
inferred← citeshttps://doi.org/10.1093/jb/mvaa006openalex-snapshot
The constitutive high-affinity Met-binding site in the kringle domain is dispensable for the signalling activity of hepatocyte growth factor
inferred← citeshttps://doi.org/10.1096/fasebj.12.13.1267openalex-snapshot
Interactions between scatter factors and their receptors: hints for therapeutic applications
inferred← citeshttps://doi.org/10.1101/2020.07.20.212654openalex-snapshot
Dimerization of kringle 1 domain from hepatocyte growth factor/scatter factor provides a potent minimal MET receptor agonist
inferred← citeshttps://doi.org/10.1111/acel.14041openalex-snapshot
Age‐related nitration/dysfunction of myogenic stem cell activator HGF
inferred← citeshttps://doi.org/10.1111/dgd.12818openalex-snapshot
A novel agonist for the HGF receptor MET promotes differentiation of human pluripotent stem cells into hepatocyte‐like cells
inferred← citeshttps://doi.org/10.1111/j.1524-475x.2005.00081.xopenalex-snapshot
The molecular and clinical impact of hepatocyte growth factor, its receptor, activators, and inhibitors in wound healing
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2009.01004.xopenalex-snapshot
High efficacy and minimal peptide required for the anti‐angiogenic and anti‐hepatocarcinoma activities of plasminogen K5
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2012.01384.xopenalex-snapshot
Shedding‐Generated Met Receptor Fragments can be Routed to Either the Proteasomal or the Lysosomal Degradation Pathway
inferred← citeshttps://doi.org/10.1158/0008-5472.can-05-3329openalex-snapshot
Fully Human Monoclonal Antibodies to Hepatocyte Growth Factor with Therapeutic Potential against Hepatocyte Growth Factor/c-Met–Dependent Human Tumors
inferred← citeshttps://doi.org/10.1158/1535-7163.mct-09-0824openalex-snapshot
Biochemical Characterization of AMG 102: A Neutralizing, Fully Human Monoclonal Antibody to Human and Nonhuman Primate Hepatocyte Growth Factor
inferred← citeshttps://doi.org/10.1242/jcs.112.12.1999openalex-snapshot
Differential regulation of hepatocyte growth factor/scatter factor by cell surface proteoglycans and free glycosaminoglycan chains
inferred← citeshttps://doi.org/10.1517/13543784.17.7.997openalex-snapshot
Targeting the c-MET signaling pathway for cancer therapy
inferred← citeshttps://doi.org/10.26508/lsa.202201424openalex-snapshot
Dimerization of kringle 1 domain from hepatocyte growth factor/scatter factor provides a potent MET receptor agonist
inferred← citeshttps://doi.org/10.5772/22241openalex-snapshot
Significance, Mechanisms, and Progress of Anticancer Drugs Targeting HGF-Met
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.