The differential sensitivity of human and rhesus macaque CCR5 to small-molecule inhibitors of human immunodeficiency virus type 1 entry is explained by a single amino acid difference and suggests a mechanism of action for these inhibitors (Q37092774)

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scientific article published on April 2004

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English	The differential sensitivity of human and rhesus macaque CCR5 to small-molecule inhibitors of human immunodeficiency virus type 1 entry is explained by a single amino acid difference and suggests a mechanism of action for these inhibitors	scientific article published on April 2004

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scholarly article

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Europe PubMed Central

PMC publication ID

18 August 2017

The differential sensitivity of human and rhesus macaque CCR5 to small-molecule inhibitors of human immunodeficiency virus type 1 entry is explained by a single amino acid difference and suggests a mechanism of action for these inhibitors (English)

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Europe PubMed Central

PMC publication ID

18 August 2017

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Alexandra Trkola

5

object named as

Alexandra Trkola

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Europe PubMed Central

PMC publication ID

18 August 2017

author name string

Erika Billick

1

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Europe PubMed Central

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18 August 2017

Christoph Seibert

2

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18 August 2017

Pavel Pugach

3

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Europe PubMed Central

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18 August 2017

Tom Ketas

4

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Europe PubMed Central

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18 August 2017

Michael J Endres

6

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Europe PubMed Central

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18 August 2017

Nicholas J Murgolo

7

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Europe PubMed Central

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18 August 2017

Elizabeth Coates

8

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18 August 2017

Gregory R Reyes

9

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18 August 2017

Bahige M Baroudy

10

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Europe PubMed Central

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18 August 2017

Thomas P Sakmar

11

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18 August 2017

John P Moore

12

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18 August 2017

Shawn E Kuhmann

13

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18 August 2017

language of work or name

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publication date

1 April 2004

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18 August 2017

Journal of Virology

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18 August 2017

78

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18 August 2017

8

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Europe PubMed Central

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18 August 2017

4134-4144

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Europe PubMed Central

PMC publication ID

18 August 2017

Interaction of small molecule inhibitors of HIV-1 entry with CCR5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

The entry of entry inhibitors: a fusion of science and medicine

1 reference

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29 September 2017

Inhibitors of the entry of HIV into host cells.

1 reference

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29 September 2017

Recent progress in discovery of small-molecule CCR5 chemokine receptor ligands as HIV-1 inhibitors

1 reference

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Novel therapies based on mechanisms of HIV-1 cell entry.

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29 September 2017

Analysis of the mechanism by which the small-molecule CCR5 antagonists SCH-351125 and SCH-350581 inhibit human immunodeficiency virus type 1 entry.

1 reference

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Alternative conformations of HIV-1 V3 loops mimic beta hairpins in chemokines, suggesting a mechanism for coreceptor selectivity

1 reference

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Piperazine-based CCR5 antagonists as HIV-1 inhibitors. III: synthesis, antiviral and pharmacokinetic profiles of symmetrical heteroaryl carboxamides

1 reference

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Structure modeling of the chemokine receptor CCR5: implications for ligand binding and selectivity

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29 September 2017

Evaluation of current approaches to inhibit HIV entry.

1 reference

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29 September 2017

Sensitivity of HIV-1 to entry inhibitors correlates with envelope/coreceptor affinity, receptor density, and fusion kinetics

1 reference

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29 September 2017

Seven-transmembrane receptors

1 reference

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29 September 2017

The crown and stem of the V3 loop play distinct roles in human immunodeficiency virus type 1 envelope glycoprotein interactions with the CCR5 coreceptor

1 reference

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Balanced polymorphism selected by genetic versus infectious human disease

1 reference

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Cell surface receptors, virus entry and tropism of primate lentiviruses

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New therapeutics that modulate chemokine networks

1 reference

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29 September 2017

Synthesis, SAR, and biological evaluation of oximino-piperidino-piperidine amides. 1. Orally bioavailable CCR5 receptor antagonists with potent anti-HIV activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

HIV-1 escape from a small molecule, CCR5-specific entry inhibitor does not involve CXCR4 use

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

Piperazine-based CCR5 antagonists as HIV-1 inhibitors. II. Discovery of 1-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4- methyl-4-[3(S)-methyl-4-[1(S)-[4-(trifluoromethyl)phenyl]ethyl]-1-piperazinyl]- piperidine N1-oxide (Sch-350634), an orally bioavailabl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

Discovery of 4-[(Z)-(4-bromophenyl)- (ethoxyimino)methyl]-1'-[(2,4-dimethyl-3- pyridinyl)carbonyl]-4'-methyl-1,4'- bipiperidine N-oxide (SCH 351125): an orally bioavailable human CCR5 antagonist for the treatment of HIV infection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

Piperazine-based CCR5 antagonists as HIV-1 inhibitors. I: 2(S)-methyl piperazine as a key pharmacophore element

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

An overview of the determinants of CCR5 and CXCR4 co-receptor function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

Structural determinants of CCR5 recognition and HIV-1 blockade in RANTES.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=374253

29 September 2017

New targets for inhibitors of HIV-1 replication

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29 September 2017

Mapping the determinants of the CCR5 amino-terminal sulfopeptide interaction with soluble human immunodeficiency virus type 1 gp120-CD4 complexes

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29 September 2017

Global survey of genetic variation in CCR5, RANTES, and MIP-1alpha: impact on the epidemiology of the HIV-1 pandemic.

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HIV chemotherapy

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Mucosal transmission and induction of simian AIDS by CCR5-specific simian/human immunodeficiency virus SHIV(SF162P3)

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The effect of genetic variation in chemokines and their receptors on HIV transmission and progression to AIDS.

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The BBXB motif of RANTES is the principal site for heparin binding and controls receptor selectivity

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Higher macrophage inflammatory protein (MIP)-1alpha and MIP-1beta levels from CD8+ T cells are associated with asymptomatic HIV-1 infection

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29 September 2017

Beyond receptor expression: the influence of receptor conformation, density, and affinity in HIV-1 infection

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29 September 2017

Multiple nonfunctional alleles of CCR5 are frequent in various human populations

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Crystal structure of rhodopsin: A G protein-coupled receptor

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Use of inhibitors to evaluate coreceptor usage by simian and simian/human immunodeficiency viruses and human immunodeficiency virus type 2 in primary cells

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29 September 2017

A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5

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29 September 2017

Race-specific HIV-1 disease-modifying effects associated with CCR5 haplotypes

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29 September 2017

Genetics of HIV-1 infection: chemokine receptor CCR5 polymorphism and its consequences.

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29 September 2017

Structure and function of the glycosaminoglycan binding site of chemokine macrophage-inflammatory protein-1 beta

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29 September 2017

Naturally occurring CCR5 extracellular and transmembrane domain variants affect HIV-1 Co-receptor and ligand binding function

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29 September 2017

A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity

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Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5

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Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function

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Genetic acceleration of AIDS progression by a promoter variant of CCR5.

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Genealogy of the CCR5 locus and chemokine system gene variants associated with altered rates of HIV-1 disease progression

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Alanine substitutions of polar and nonpolar residues in the amino-terminal domain of CCR5 differently impair entry of macrophage- and dualtropic isolates of human immunodeficiency virus type 1.

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Amino-Terminal Substitutions in the CCR5 Coreceptor Impair gp120 Binding and Human Immunodeficiency Virus Type 1 Entry

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CCR5 levels and expression pattern correlate with infectability by macrophage-tropic HIV-1, in vitro

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Coreceptors--Implications for HIV Pathogenesis and Therapy

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Failure of human immunodeficiency virus entry and infection in CD4-positive human brain and skin cells

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HIV-1-resistance phenotype conferred by combination of two separate inherited mutations of CCR5 gene.

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Fine definition of a conserved CCR5-binding region on the human immunodeficiency virus type 1 glycoprotein 120

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Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the CKR5 Structural Gene

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https://pubmed.ncbi.nlm.nih.gov/15047829

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based on heuristic

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Identification of a glycosaminoglycan-binding site in chemokine macrophage inflammatory protein-1alpha

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https://pubmed.ncbi.nlm.nih.gov/15047829

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based on heuristic

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The extent of genetic variation in the CCR5 gene

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Identifiers

10.1128/JVI.78.8.4134-4144.2004

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

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