Modelled DT Structure
Method:homology modeling
Template PDB:3F1R_A; 3WIQ_A; 6EI3_A
Identity:63.636%;21.818%;23.952%
Minimized Score:-828.827 kcal/mol
Detail: Structure Info
General Information of DT | |||||
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DT ID | DTD0099 | ||||
Gene Name | SLC15A4 | ||||
Protein Name | Peptide transporter 4 | ||||
Gene ID | |||||
UniProt ID | |||||
TCDB ID | |||||
3D Structure |
Modelled DT Structure Method:homology modeling Template PDB:3F1R_A; 3WIQ_A; 6EI3_A Identity:63.636%;21.818%;23.952% Minimized Score:-828.827 kcal/mol Detail: Structure Info |
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Synonyms | FP12591; PHT1; PTR4; Peptide/histidine transporter 1; SLC15A4; Solute carrier family 15 member 4; hPHT1 | ||||
DT Family | Proton-Dependent Oligopeptide Transporter (POT/PTR) Family ; | ||||
Tissue Specificity | Highly expressed in skeletal muscle.Moderately expressed in kidney, liver, and heart. Weakly expressedin colon and brain. Expressed in low levels throughout thegastrointestinal tract and in Caco-2 cells. Expressed in retinalfragment epithelium (RPE) and neural retina. Expressed in smallintestine, stomach, duodenum, jejunum, ileum and colon. | ||||
Function | This proton oligopeptide cotransporter mediates the transport of free histidine and certain di- and tripeptides. | ||||
Endogenous Substrate(s) | Peptides; Histidine | ||||
Variability Data of This Drug Transporter (DT) | |||||
Regulatory Variability Data of This DT (VARIDT 4.0) |
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(α) Tissue Distribution Level of Peptide transporter 4 |
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(β) Cell Distribution Level of Peptide transporter 4 |
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(γ) Organelle Distribution Level of Peptide transporter 4 |
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Regulatory Variability Data of This DT |
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(β) Post-translational Modification of Peptide transporter 4 |
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(γ) Transcriptional Regulation of Peptide transporter 4 |
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(δ) Epigenetic Regulation of Peptide transporter 4 |
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(ε) Exogenous Modulation of Peptide transporter 4 |
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Structural Variability Data of This DT |
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(γ) Outward/inward-facing Conformation |
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General Variability Data of This DT |
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(α) Genetic Polymorphisms of Peptide transporter 4 |
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(β) Disease-specific Protein Abundances of Peptide transporter 4 |
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(γ) Species- and Tissue-specific DT Abundances |
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Molecular Transporting Profile of This DT | |||||
Full List of Drug(s) Transported by This DT |
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Clinical Trial Drug |
Click to Show/Hide the Full List of Drug: 1 Drugs in Total | ||||
Drug Name | Highest Status | Detail | Indication | ICD 11 | Ref |
L-histidine
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Phase 2/3 | Drug Info | HARS Syndrome | N.A. | [1] |
Drug-DT Affinity Assessed by Cell Line |
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Clinical Trial Drug |
Click to Show/Hide the Full List of Drug: 3 Drugs in Total | ||||
Drug Name | Highest Status | Detail | Cell Line | Affinity | Ref |
L-histidine | Phase 2/3 | Drug Info | Xenopus laevis oocytes-PTR4 | Km =16.3 microM | [1] |
L-histidine | Phase 2/3 | Drug Info | Xenopus laevis oocytes-PTR4 | Km =16.3 microM | [1] |
L-histidine | Phase 2/3 | Drug Info | Xenopus laevis oocytes-PTR4 | Km =16.3 microM | [1] |
Withdrawn, Discontinued or Preclinical Drug |
Click to Show/Hide the Full List of Drug: 1 Drugs in Total | ||||
Drug Name | Highest Status | Detail | Cell Line | Affinity | Ref |
Peptides | Investigative | Drug Info | Xenopus laevis oocytes-PTR4 | Km =1.69 microM | [1] |
References | |||||
1 | Functional Characterization of Human Peptide/Histidine Transporter 1 in Stably Transfected MDCK Cells. Mol Pharm. 2018 Feb 5;15(2):385-393. | ||||
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