Protein:TSHR |
Protein Summary |
 Gene summary |
| Gene name: TSHR | ASpdb.0 ID: 7253 | Gene | Gene symbol | TSHR | Gene ID | 7253 |
| Gene name | thyroid stimulating hormone receptor |
| Synonyms | CHNG1|LGR3|hTSHR-I |
| Cytomap | 14q31.1 |
| Type of gene | protein-coding |
| Description | thyrotropin receptorTSH receptorseven transmembrane helix receptorthyrotropin receptor-I, hTSHR-I |
| Modification date | 20240407 |
| UniProtAcc | P16473 |
| Gene ontology of this gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Gene | TSHR | GO:0005886 | plasma membrane | 11847099 |
| Gene | TSHR | GO:0016323 | basolateral plasma membrane | 11847099 |
| Gene | TSHR | GO:0043235 | receptor complex | 23382219 |
| Gene | TSHR | GO:0044877 | protein-containing complex binding | 12045258 |
AS Summary |
| Information of the canonical protein with experimentally identified structure from PDB (2023). |
| UniProt Acc | File name | PDB ID | Method | Resolution | Chain | Start | End |
| P16473-1 | P16473-1_2xwt_C.pdb | 2XWT | X-ray | 1.9 | C | 24 | 257 |
| ASpdb's canonical and alternatively spliced isoform information. |
| accession_id | gene_name | canonical_id | alternative_id | canonical_length | alternative_length | canonical_start | canonical_end | type | originalSEQ | variationSEQ | alternative_start | alternative_end |
| P16473 | TSHR | P16473-1 | P16473-2 | 764 | 253 | 232 | 253 | Substitution | DVSQTSVTALPSKGLEHLKELI | LPLGRKSLSFETQKAPRSSMPS | 232 | 253 |
| P16473 | TSHR | P16473-1 | P16473-2 | 764 | 253 | 254 | 764 | Deletion | none | none | 253 | 253 |
| P16473 | TSHR | P16473-1 | P16473-3 | 764 | 274 | 232 | 274 | Substitution | DVSQTSVTALPSKGLEHLKELIARNTWTLKKLPLSLSFLHLTR | VENVAVSGKGFCKSLFSWLYRLPLGRKSLSFETQKAPRSSMPS | 232 | 274 |
| P16473 | TSHR | P16473-1 | P16473-3 | 764 | 274 | 275 | 764 | Deletion | none | none | 274 | 274 |
| Multiple sequence alignment of our canonical and alternatively spliced TSHR |
| Matched gene isoform IDs with Ensembl and RefSeq of our canonical and alternative spliced genes of TSHR |
| UniProt-id | ENSG | ENST | ENSP |
| P16473-2 | ENSG00000165409.18 | ENST00000342443.10 | ENSP00000340113.6 |
| P16473-3 | ENSG00000165409.18 | ENST00000554435.1 | ENSP00000450549.1 |
| UniProt-id | NM ID | NP ID |
| P16473-2 | NM_001018036.2 | NP_001018046.1 |
| P16473-3 | NM_001142626.2 | NP_001136098.1 |
| Amino acid sequences of our canonical and alternatively spliced TSHR |
| accession_id | Protein sequence |
| P16473-1 | MRPADLLQLVLLLDLPRDLGGMGCSSPPCECHQEEDFRVTCKDIQRIPSLPPSTQTLKLIETHLRTIPSHAFSNLPNISRIYVSIDVTLQ QLESHSFYNLSKVTHIEIRNTRNLTYIDPDALKELPLLKFLGIFNTGLKMFPDLTKVYSTDIFFILEITDNPYMTSIPVNAFQGLCNETL TLKLYNNGFTSVQGYAFNGTKLDAVYLNKNKYLTVIDKDAFGGVYSGPSLLDVSQTSVTALPSKGLEHLKELIARNTWTLKKLPLSLSFL HLTRADLSYPSHCCAFKNQKKIRGILESLMCNESSMQSLRQRKSVNALNSPLHQEYEENLGDSIVGYKEKSKFQDTHNNAHYYVFFEEQE DEIIGFGQELKNPQEETLQAFDSHYDYTICGDSEDMVCTPKSDEFNPCEDIMGYKFLRIVVWFVSLLALLGNVFVLLILLTSHYKLNVPR FLMCNLAFADFCMGMYLLLIASVDLYTHSEYYNHAIDWQTGPGCNTAGFFTVFASELSVYTLTVITLERWYAITFAMRLDRKIRLRHACA IMVGGWVCCFLLALLPLVGISSYAKVSICLPMDTETPLALAYIVFVLTLNIVAFVIVCCCYVKIYITVRNPQYNPGDKDTKIAKRMAVLI FTDFICMAPISFYALSAILNKPLITVSNSKILLVLFYPLNSCANPFLYAIFTKAFQRDVFILLSKFGICKRQAQAYRGQRVPPKNSTDIQ |
| P16473-2 | MRPADLLQLVLLLDLPRDLGGMGCSSPPCECHQEEDFRVTCKDIQRIPSLPPSTQTLKLIETHLRTIPSHAFSNLPNISRIYVSIDVTLQ QLESHSFYNLSKVTHIEIRNTRNLTYIDPDALKELPLLKFLGIFNTGLKMFPDLTKVYSTDIFFILEITDNPYMTSIPVNAFQGLCNETL |
| P16473-3 | MRPADLLQLVLLLDLPRDLGGMGCSSPPCECHQEEDFRVTCKDIQRIPSLPPSTQTLKLIETHLRTIPSHAFSNLPNISRIYVSIDVTLQ QLESHSFYNLSKVTHIEIRNTRNLTYIDPDALKELPLLKFLGIFNTGLKMFPDLTKVYSTDIFFILEITDNPYMTSIPVNAFQGLCNETL TLKLYNNGFTSVQGYAFNGTKLDAVYLNKNKYLTVIDKDAFGGVYSGPSLLVENVAVSGKGFCKSLFSWLYRLPLGRKSLSFETQKAPRS |
Protein Functional Features |
| Main function of this protein. (from UniProt) |
| TSHR (go to UniProt):P16473 |
| Retention analysis result of protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * Minus value of BPloci means that the break pointn is located before the CDS. |
| - Retained protein feature among the 13 regional features. |
| Accession_id | Subsection | Start | End | Funcitonal feature | Splicing information |
| P16473 | Topological domain | 21 | 413 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Substitution;Start=232;End=253 |
| P16473 | Topological domain | 21 | 413 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 21 | 413 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Substitution;Start=232;End=274 |
| P16473 | Topological domain | 21 | 413 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 414 | 441 | Note=Helical%3B Name%3D1;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 414 | 441 | Note=Helical%3B Name%3D1;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 442 | 450 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 442 | 450 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 451 | 473 | Note=Helical%3B Name%3D2;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 451 | 473 | Note=Helical%3B Name%3D2;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 474 | 494 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 474 | 494 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 495 | 517 | Note=Helical%3B Name%3D3;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 495 | 517 | Note=Helical%3B Name%3D3;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 518 | 537 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 518 | 537 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 538 | 560 | Note=Helical%3B Name%3D4;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 538 | 560 | Note=Helical%3B Name%3D4;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 561 | 580 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 561 | 580 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 581 | 602 | Note=Helical%3B Name%3D5;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 581 | 602 | Note=Helical%3B Name%3D5;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 603 | 625 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 603 | 625 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 626 | 649 | Note=Helical%3B Name%3D6;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 626 | 649 | Note=Helical%3B Name%3D6;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 650 | 660 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 650 | 660 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Transmembrane | 661 | 682 | Note=Helical%3B Name%3D7;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Transmembrane | 661 | 682 | Note=Helical%3B Name%3D7;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Topological domain | 683 | 764 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=254;End=764 |
| P16473 | Topological domain | 683 | 764 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=275;End=764 |
| P16473 | Repeat | 227 | 248 | Note=LRR 6 | Type=Substitution;Start=232;End=253 |
| P16473 | Repeat | 227 | 248 | Note=LRR 6 | Type=Substitution;Start=232;End=274 |
| P16473 | Repeat | 250 | 271 | Note=LRR 7 | Type=Substitution;Start=232;End=253 |
| P16473 | Repeat | 250 | 271 | Note=LRR 7 | Type=Deletion;Start=254;End=764 |
| P16473 | Repeat | 250 | 271 | Note=LRR 7 | Type=Substitution;Start=232;End=274 |
| P16473 | Motif | 762 | 764 | Note=PDZ-binding | Type=Deletion;Start=254;End=764 |
| P16473 | Motif | 762 | 764 | Note=PDZ-binding | Type=Deletion;Start=275;End=764 |
Gene Isoform Structures and Expression Levels for TSHR |
| Gene structures of our canonical and alternative spliced genes of TSHR * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| Expression levels of gene isoforms across GTEx. |
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| Expression levels of gene isoforms across TCGA. |
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Protein Structures |
| PDB and CIF files of the predicted protein structures * Here we show the 3D structure of the proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format. |
| 3D view using mol* of P16473-1 |
| 3D view using mol* of P16473-2 |
| 3D view using mol* of P16473-3 |
pLDDT Score Distribution |
| pLDDT score distribution of the predicted protein structures from AlphaFold2 * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
| pLDDT distribution across the protein length of P16473-1 |
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| pLDDT distribution across the protein length of P16473-2 |
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| pLDDT distribution across the protein length of P16473-3 |
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Ramachandran Plot of Protein Structures |
| Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this protein peptide. |
| Ramachandran plot of P16473-1 |
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| Ramachandran plot of P16473-2 |
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Potential Active Site Information |
| The potential binding sites of these proteins were identified using SiteMap, a module of the Schrodinger suite. |
| UniProt-id | Site score | Size | D score | Volume | Exposure | Enclosure | Contact | Phobic | Philic | Balance | Don/Acc | Residues |
| P16473-1 | 1.31 | 114 | 1.407 | 193.795 | 0.305 | 0.956 | 1.123 | 3.577 | 0.325 | 11.004 | 3.128 | 501,502,505,506,509,570,571,572,582,583,586,587,59 0,594,634,637,640,641,643,644,663,667 |
| P16473-2 | 0.996 | 121 | 1.038 | 253.134 | 0.554 | 0.652 | 0.91 | 0.805 | 0.899 | 0.895 | 1.169 | 216,217,218,219,220,221,222,223,224,226,227,228,22 9,230,231,239,240,241,242,243,244,245,246,247 |
| P16473-3 | 0.73 | 41 | 0.727 | 105.644 | 0.762 | 0.592 | 0.686 | 0.641 | 0.706 | 0.907 | 0.906 | 115,116,117,118,119,138,139,140,141,142,143,144,14 5,168,169,170,171 |
Protein Structure and Feature Comparision |
| Protein Structure Comparision Using Template Modeling Scores (TM-score). |
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| Protein Structure Comparision Visualization with mol*. between Canonical predicted structure (AF2)(orange) vs Canonical validated structure (PDB)(green) |
| 3D view using mol* of P16473-1_P16473-1_2xwt_C.pdb |
| Protein Structure Comparision Visualization with mol*. between Canonical validated structure (PDB)(orange) vs Alternative predicted structure (AF2)(green) |
| 3D view using mol* of P16473-1_2xwt_C_P16473-2.pdb |
| 3D view using mol* of P16473-1_2xwt_C_P16473-3.pdb |
| Protein Structure Comparision Visualization with mol*. between Canonical predicted structure (AF2)(orange) vs Alternative predicted structure (AF2)(green) |
| 3D view using mol* of P16473-1_P16473-2.pdb |
| 3D view using mol* of P16473-1_P16473-3.pdb |
| Protein Feature Comparison of the protein sequendary structures among the protiens. |
| ./stats/secondary_structure/figure/P16473-1_vs_P16473-2.png |
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| ./stats/secondary_structure/figure/P16473-1_vs_P16473-3.png |
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| Protein Feature Comparison of the relative accessible surface area (ASA) among the protiens. |
| ./stats/relative_asa/P16473-1_vs_P16473-2.png |
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| ./stats/relative_asa/P16473-1_vs_P16473-3.png |
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Protein-Protein Interaction |
| Interactors from UniProt. |
| Accession_id | Subsection | Start | End | Funcitonal feature | Splicing information |
| Interactors from STRING. |
| Gene name | Interactors |
Related Drugs to TSHR |
| Drugs targeting this gene/protein. (DrugBank) |
| UniProt accession | Gene name | DrugBank ID | Drug name | Drug group | Actions |
| P16473 | TSHR | DB00024 | Thyrotropin alfa | approved, vet_approved | agonist |
Related Diseases to TSHR |
| Previous studies relating to the alternative splicing of TSHR and disease information from the MeSH term (PubMed) |
| Gene | PMID | Title | Abstract | MeSH ID | MeSH term |
| TSHR | 2610690 | Cloning, sequencing and expression of the human thyrotropin (TSH) receptor: evidence for binding of autoantibodies. | A human thyroid cDNA library was screened by hybridization with a dog thyrotropin receptor (TSHr) cDNA. Sequencing of the resulting clones identified a 2292 residue open reading frame encoding a 744 amino acid mature polypeptide presenting 90.3% similarity with the dog TSHr. Two major transcripts (4.6 and 4.4 kilobases) were identified in the human thyroid which suggests that alternative splicing could generate multiple forms of human TSHr. Transfection of the coding sequence in COS-7 cells conferred to a membrane preparation of these cells the ability to bind specifically TSH. TSH binding was completely displaced by immunoglobulin preparations from patients with idiopathic myxoedema. | D006111 | Graves Disease |
| TSHR | 2610690 | Cloning, sequencing and expression of the human thyrotropin (TSH) receptor: evidence for binding of autoantibodies. | A human thyroid cDNA library was screened by hybridization with a dog thyrotropin receptor (TSHr) cDNA. Sequencing of the resulting clones identified a 2292 residue open reading frame encoding a 744 amino acid mature polypeptide presenting 90.3% similarity with the dog TSHr. Two major transcripts (4.6 and 4.4 kilobases) were identified in the human thyroid which suggests that alternative splicing could generate multiple forms of human TSHr. Transfection of the coding sequence in COS-7 cells conferred to a membrane preparation of these cells the ability to bind specifically TSH. TSH binding was completely displaced by immunoglobulin preparations from patients with idiopathic myxoedema. | D009230 | Myxedema |
Clinically important variants in TSHR |
| (ClinVar, 04/20/2024) |
| accession_id | uniprot_id | gene_name | Type | Variant | Clinical_significance |
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