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Polymorphic residues in HLA-B that mediate HIV control distinctly modulate peptide interactions with both TCR and KIR molecules

Structure(2024)10.1016/j.str.2024.04.015Source: DataRank Database

Polymorphic residues in HLA-B that mediate HIV control distinctly modulate peptide interactions with both TCR and KIR molecules is a research paper published in Structure (2024). On theSindex it has a DataRank of 0. It has been cited 7 times.

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Open Access7 citations

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Enrichment:Funding (12 grants)Impact (FWCI 1.09)OA: hybridTopics (54)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (16)

Nishant K. Singh ORCID,Itai Muzhingi ORCID,Xiaolong Li ORCID,Michael V Mandanas,Clarety Kaseke ORCID

Live enrichment

PubMed:38733995 PMC:PMC11329236 OpenAlex:https://openalex.org/W4396796969

NIDA NIH HHS

Grant: DP1 DA058476

NIAID NIH HHS

Grant: DP2 AI154421

NCI NIH HHS

Grant: 75N91019D00024

NIDDK NIH HHS

Grant: P30 DK043351

NIAID NIH HHS

Grant: R01 AI176533

NIAID NIH HHS

Grant: UM1 AI144462

NIAID NIH HHS

Grant: UM1 AI164560

National Institutes of Health

Grant: 3UM1AI144462-02S1

Identification of neutralizing epitopes on SARS-CoV-2 spike for design of vaccines and small-molecule antivirals

National Institutes of Health

Grant: 5DP2AI154421-04

Exploiting Highly Networked CTL Epitopes to Achieve a Functional HIV Cure

National Institutes of Health

Grant: 1R01AI176533-01

Investigating the Protective Efficacy of SIV/HIV T and B cell Immunity Induced by RNA Replicons

National Institutes of Health

Grant: 1DP1DA058476-01

Harnessing Highly Networked HLA-E-Restricted CTL Epitopes to Achieve a Broadly Effective HIV Cure

National Institutes of Health

Grant: 5UM1AI164560-05

Delaney AIDS Research Enterprise to Cure HIV

FWCI

1.09

Citation Percentile

0.8%

Citation Trend

2024

2025

2026

hybridLicense: cc-by

journalhttps://doi.org/10.1016/j.str.2024.04.015

publisherhttps://api.elsevier.com/content/article/PII:S0969212624001412?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0969212624001412?httpAccept=text/plain

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38733995

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11329236

Fields of Study

Immune Cell Function and InteractionReproductive System and PregnancyHIV Research and Treatment0301 basic medicine03 medical and health sciences

MeSH Terms

Binding SitesHumansModels, MolecularPeptidesPolymorphism, GeneticProtein BindingReceptors, Antigen, T-CellHLA-B AntigensHIV-1HIV InfectionsCD8-Positive T-LymphocytesReceptors, KIR3DL1Protein Stability

Keywords

Human leukocyte antigenT-cell receptorHLA-BPeptideHuman immunodeficiency virus (HIV)BiologyHLA-B AntigensFunction (biology)GeneticsChemistryCell biologyImmunologyBiochemistryImmune systemAntigenT cellTCRHIVNK cellsHLAKirimmunogeneticsCd8(+) T cellsModels, MolecularBinding SitesPolymorphism, GeneticProtein StabilityReceptors, Antigen, T-CellReceptors, KIR3DL1HIV InfectionsCD8-Positive T-LymphocytesArticleHIV-1HumansPeptidesProtein Binding

Sustainable Development Goals

SDG 0: Good health and well-being

Polymorphic residues in HLA-B that mediate HIV control distinctly modulate peptide interactions with both TCR and KIR molecules

FAIR Checklist

Authors (16)

Funding (12 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)