Protein:DDR1 |
Protein Summary |
 Gene summary |
| Gene name: DDR1 | ASpdb.0 ID: 780 | Gene | Gene symbol | DDR1 | Gene ID | 780 |
| Gene name | discoidin domain receptor tyrosine kinase 1 |
| Synonyms | CAK|CD167|DDR|EDDR1|HGK2|MCK10|NEP|NTRK4|PTK3|PTK3A|RTK6|TRKE |
| Cytomap | 6p21.33 |
| Type of gene | protein-coding |
| Description | epithelial discoidin domain-containing receptor 1CD167 antigen-like family member APTK3A protein tyrosine kinase 3Acell adhesion kinasemammary carcinoma kinase 10neuroepithelial tyrosine kinaseneurotrophic tyrosine kinase, receptor, type 4protein-t |
| Modification date | 20240411 |
| UniProtAcc | Q08345 |
| Gene ontology of this gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Gene | DDR1 | GO:0005518 | collagen binding | 9659899 |
| Gene | DDR1 | GO:0038062 | protein tyrosine kinase collagen receptor activity | 9659899|21044884 |
| Gene | DDR1 | GO:0038063 | collagen-activated tyrosine kinase receptor signaling pathway | 9659899|21044884 |
| Gene | DDR1 | GO:0038083 | peptidyl-tyrosine autophosphorylation | 21044884 |
| Gene | DDR1 | GO:0043235 | receptor complex | 23382219 |
| Gene | DDR1 | GO:0046777 | protein autophosphorylation | 9659899 |
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 |
| Q08345-1 | Q08345-1_6y23_C.pdb | 6Y23 | X-ray | 2.58 | C | 574 | 911 |
| 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 |
| Q08345 | DDR1 | Q08345-1 | Q08345-2 | 913 | 876 | 506 | 542 | Deletion | none | none | 505 | 505 |
| Q08345 | DDR1 | Q08345-1 | Q08345-4 | 913 | 243 | 190 | 243 | Substitution | GLLSYTAPVGQTMYLSEAVYLNDSTYDGHTVGGLQYGGLGQLADGVVGLDDFRK | CSMGVWASWQMVWWGWMTLGRVRSCGSGQAMTMWDGATTASPVAMWRWSLSLTG | 190 | 243 |
| Q08345 | DDR1 | Q08345-1 | Q08345-4 | 913 | 243 | 244 | 913 | Deletion | none | none | 243 | 243 |
| Q08345 | DDR1 | Q08345-1 | Q08345-5 | 913 | 919 | 665 | 665 | Substitution | A | ASFSLFS | 665 | 671 |
| Q08345 | DDR1 | Q08345-1 | Q08345-6 | 913 | 894 | 1 | 1 | Substitution | M | MSLPRCCPHPLRPEGSGAM | 1 | 19 |
| Q08345 | DDR1 | Q08345-1 | Q08345-6 | 913 | 894 | 506 | 542 | Deletion | none | none | 523 | 523 |
| Multiple sequence alignment of our canonical and alternatively spliced DDR1 |
| Matched gene isoform IDs with Ensembl and RefSeq of our canonical and alternative spliced genes of DDR1 |
| UniProt-id | ENSG | ENST | ENSP |
| Q08345-1 | ENSG00000204580.14 | ENST00000324771.12 | ENSP00000318217.8 |
| Q08345-1 | ENSG00000204580.14 | ENST00000376568.8 | ENSP00000365752.3 |
| Q08345-1 | ENSG00000137332.19 | ENST00000383377.6 | ENSP00000372868.2 |
| Q08345-1 | ENSG00000137332.19 | ENST00000400414.5 | ENSP00000383265.1 |
| Q08345-1 | ENSG00000215522.11 | ENST00000400491.5 | ENSP00000383338.1 |
| Q08345-1 | ENSG00000215522.11 | ENST00000400492.5 | ENSP00000383339.1 |
| Q08345-1 | ENSG00000230456.10 | ENST00000412329.5 | ENSP00000391805.1 |
| Q08345-1 | ENSG00000234078.10 | ENST00000429699.5 | ENSP00000401397.1 |
| Q08345-1 | ENSG00000234078.10 | ENST00000430933.5 | ENSP00000397769.1 |
| Q08345-1 | ENSG00000230456.10 | ENST00000449518.5 | ENSP00000414285.1 |
| Q08345-1 | ENSG00000204580.14 | ENST00000452441.5 | ENSP00000405039.1 |
| Q08345-1 | ENSG00000230456.10 | ENST00000548133.4 | ENSP00000449611.2 |
| Q08345-1 | ENSG00000215522.11 | ENST00000550395.5 | ENSP00000449255.2 |
| Q08345-1 | ENSG00000234078.10 | ENST00000552068.5 | ENSP00000449190.2 |
| Q08345-1 | ENSG00000137332.19 | ENST00000553015.5 | ENSP00000448377.2 |
| Q08345-2 | ENSG00000137332.19 | ENST00000259875.11 | ENSP00000259875.7 |
| Q08345-2 | ENSG00000204580.14 | ENST00000376567.6 | ENSP00000365751.2 |
| Q08345-2 | ENSG00000204580.14 | ENST00000376569.7 | ENSP00000365753.3 |
| Q08345-2 | ENSG00000204580.14 | ENST00000376570.8 | ENSP00000365754.4 |
| Q08345-2 | ENSG00000137332.19 | ENST00000400410.5 | ENSP00000383261.1 |
| Q08345-2 | ENSG00000137332.19 | ENST00000400411.5 | ENSP00000383262.1 |
| Q08345-2 | ENSG00000215522.11 | ENST00000400486.5 | ENSP00000383334.1 |
| Q08345-2 | ENSG00000215522.11 | ENST00000400488.5 | ENSP00000383336.1 |
| Q08345-2 | ENSG00000215522.11 | ENST00000400489.7 | ENSP00000383337.3 |
| Q08345-2 | ENSG00000230456.10 | ENST00000415092.5 | ENSP00000405540.1 |
| Q08345-2 | ENSG00000204580.14 | ENST00000418800.6 | ENSP00000407699.2 |
| Q08345-2 | ENSG00000234078.10 | ENST00000419412.5 | ENSP00000416183.1 |
| Q08345-2 | ENSG00000234078.10 | ENST00000421229.6 | ENSP00000415730.2 |
| Q08345-2 | ENSG00000230456.10 | ENST00000427053.6 | ENSP00000416145.2 |
| Q08345-2 | ENSG00000230456.10 | ENST00000453510.5 | ENSP00000401208.1 |
| Q08345-2 | ENSG00000204580.14 | ENST00000454612.6 | ENSP00000406091.2 |
| Q08345-2 | ENSG00000234078.10 | ENST00000454774.5 | ENSP00000400393.1 |
| Q08345-4 | ENSG00000204580.14 | ENST00000376575.7 | ENSP00000365759.4 |
| Q08345-4 | ENSG00000204580.14 | ENST00000482873.6 | ENSP00000421978.1 |
| Q08345-4 | ENSG00000215522.11 | ENST00000617572.3 | ENSP00000479195.1 |
| Q08345-4 | ENSG00000234078.10 | ENST00000618059.2 | ENSP00000479204.1 |
| Q08345-4 | ENSG00000137332.19 | ENST00000620318.4 | ENSP00000484588.1 |
| Q08345-4 | ENSG00000230456.10 | ENST00000621544.4 | ENSP00000484013.1 |
| Q08345-5 | ENSG00000204580.14 | ENST00000513240.5 | ENSP00000427552.1 |
| Q08345-6 | ENSG00000204580.14 | ENST00000508312.5 | ENSP00000422442.1 |
| Q08345-6 | ENSG00000230456.10 | ENST00000548962.5 | ENSP00000448115.2 |
| Q08345-6 | ENSG00000215522.11 | ENST00000549026.3 | ENSP00000449238.2 |
| Q08345-6 | ENSG00000234078.10 | ENST00000550384.5 | ENSP00000447474.2 |
| Q08345-6 | ENSG00000137332.19 | ENST00000552721.4 | ENSP00000449307.2 |
| UniProt-id | NM ID | NP ID |
| Q08345-1 | NM_001297654.1 | NP_001284583.1 |
| Q08345-1 | NM_013993.2 | NP_054699.2 |
| Q08345-2 | NM_001202523.1 | NP_001189452.1 |
| Q08345-2 | NM_001297652.1 | NP_001284581.1 |
| Q08345-2 | NM_001297653.1 | NP_001284582.1 |
| Q08345-2 | NM_001954.4 | NP_001945.3 |
| Q08345-5 | NM_013994.2 | NP_054700.2 |
| Q08345-5 | XM_011514884.1 | XP_011513186.1 |
| Q08345-5 | XM_011514887.1 | XP_011513189.1 |
| Q08345-5 | XM_017011268.1 | XP_016866757.1 |
| Amino acid sequences of our canonical and alternatively spliced DDR1 |
| accession_id | Protein sequence |
| Q08345-1 | MGPEALSSLLLLLLVASGDADMKGHFDPAKCRYALGMQDRTIPDSDISASSSWSDSTAARHSRLESSDGDGAWCPAGSVFPKEEEYLQVD LQRLHLVALVGTQGRHAGGLGKEFSRSYRLRYSRDGRRWMGWKDRWGQEVISGNEDPEGVVLKDLGPPMVARLVRFYPRADRVMSVCLRV ELYGCLWRDGLLSYTAPVGQTMYLSEAVYLNDSTYDGHTVGGLQYGGLGQLADGVVGLDDFRKSQELRVWPGYDYVGWSNHSFSSGYVEM EFEFDRLRAFQAMQVHCNNMHTLGARLPGGVECRFRRGPAMAWEGEPMRHNLGGNLGDPRARAVSVPLGGRVARFLQCRFLFAGPWLLFS EISFISDVVNNSSPALGGTFPPAPWWPPGPPPTNFSSLELEPRGQQPVAKAEGSPTAILIGCLVAIILLLLLIIALMLWRLHWRRLLSKA ERRVLEEELTVHLSVPGDTILINNRPGPREPPPYQEPRPRGNPPHSAPCVPNGSALLLSNPAYRLLLATYARPPRGPGPPTPAWAKPTNT QAYSGDYMEPEKPGAPLLPPPPQNSVPHYAEADIVTLQGVTGGNTYAVPALPPGAVGDGPPRVDFPRSRLRFKEKLGEGQFGEVHLCEVD SPQDLVSLDFPLNVRKGHPLLVAVKILRPDATKNARNDFLKEVKIMSRLKDPNIIRLLGVCVQDDPLCMITDYMENGDLNQFLSAHQLED KAAEGAPGDGQAAQGPTISYPMLLHVAAQIASGMRYLATLNFVHRDLATRNCLVGENFTIKIADFGMSRNLYAGDYYRVQGRAVLPIRWM AWECILMGKFTTASDVWAFGVTLWEVLMLCRAQPFGQLTDEQVIENAGEFFRDQGRQVYLSRPPACPQGLYELMLRCWSRESEQRPPFSQ |
| Q08345-2 | MGPEALSSLLLLLLVASGDADMKGHFDPAKCRYALGMQDRTIPDSDISASSSWSDSTAARHSRLESSDGDGAWCPAGSVFPKEEEYLQVD LQRLHLVALVGTQGRHAGGLGKEFSRSYRLRYSRDGRRWMGWKDRWGQEVISGNEDPEGVVLKDLGPPMVARLVRFYPRADRVMSVCLRV ELYGCLWRDGLLSYTAPVGQTMYLSEAVYLNDSTYDGHTVGGLQYGGLGQLADGVVGLDDFRKSQELRVWPGYDYVGWSNHSFSSGYVEM EFEFDRLRAFQAMQVHCNNMHTLGARLPGGVECRFRRGPAMAWEGEPMRHNLGGNLGDPRARAVSVPLGGRVARFLQCRFLFAGPWLLFS EISFISDVVNNSSPALGGTFPPAPWWPPGPPPTNFSSLELEPRGQQPVAKAEGSPTAILIGCLVAIILLLLLIIALMLWRLHWRRLLSKA ERRVLEEELTVHLSVPGDTILINNRPGPREPPPYQEPRPRGNPPHSAPCVPNGSAYSGDYMEPEKPGAPLLPPPPQNSVPHYAEADIVTL QGVTGGNTYAVPALPPGAVGDGPPRVDFPRSRLRFKEKLGEGQFGEVHLCEVDSPQDLVSLDFPLNVRKGHPLLVAVKILRPDATKNARN DFLKEVKIMSRLKDPNIIRLLGVCVQDDPLCMITDYMENGDLNQFLSAHQLEDKAAEGAPGDGQAAQGPTISYPMLLHVAAQIASGMRYL ATLNFVHRDLATRNCLVGENFTIKIADFGMSRNLYAGDYYRVQGRAVLPIRWMAWECILMGKFTTASDVWAFGVTLWEVLMLCRAQPFGQ |
| Q08345-4 | MGPEALSSLLLLLLVASGDADMKGHFDPAKCRYALGMQDRTIPDSDISASSSWSDSTAARHSRLESSDGDGAWCPAGSVFPKEEEYLQVD LQRLHLVALVGTQGRHAGGLGKEFSRSYRLRYSRDGRRWMGWKDRWGQEVISGNEDPEGVVLKDLGPPMVARLVRFYPRADRVMSVCLRV |
| Q08345-5 | MGPEALSSLLLLLLVASGDADMKGHFDPAKCRYALGMQDRTIPDSDISASSSWSDSTAARHSRLESSDGDGAWCPAGSVFPKEEEYLQVD LQRLHLVALVGTQGRHAGGLGKEFSRSYRLRYSRDGRRWMGWKDRWGQEVISGNEDPEGVVLKDLGPPMVARLVRFYPRADRVMSVCLRV ELYGCLWRDGLLSYTAPVGQTMYLSEAVYLNDSTYDGHTVGGLQYGGLGQLADGVVGLDDFRKSQELRVWPGYDYVGWSNHSFSSGYVEM EFEFDRLRAFQAMQVHCNNMHTLGARLPGGVECRFRRGPAMAWEGEPMRHNLGGNLGDPRARAVSVPLGGRVARFLQCRFLFAGPWLLFS EISFISDVVNNSSPALGGTFPPAPWWPPGPPPTNFSSLELEPRGQQPVAKAEGSPTAILIGCLVAIILLLLLIIALMLWRLHWRRLLSKA ERRVLEEELTVHLSVPGDTILINNRPGPREPPPYQEPRPRGNPPHSAPCVPNGSALLLSNPAYRLLLATYARPPRGPGPPTPAWAKPTNT QAYSGDYMEPEKPGAPLLPPPPQNSVPHYAEADIVTLQGVTGGNTYAVPALPPGAVGDGPPRVDFPRSRLRFKEKLGEGQFGEVHLCEVD SPQDLVSLDFPLNVRKGHPLLVAVKILRPDATKNASFSLFSRNDFLKEVKIMSRLKDPNIIRLLGVCVQDDPLCMITDYMENGDLNQFLS AHQLEDKAAEGAPGDGQAAQGPTISYPMLLHVAAQIASGMRYLATLNFVHRDLATRNCLVGENFTIKIADFGMSRNLYAGDYYRVQGRAV LPIRWMAWECILMGKFTTASDVWAFGVTLWEVLMLCRAQPFGQLTDEQVIENAGEFFRDQGRQVYLSRPPACPQGLYELMLRCWSRESEQ |
| Q08345-6 | MSLPRCCPHPLRPEGSGAMGPEALSSLLLLLLVASGDADMKGHFDPAKCRYALGMQDRTIPDSDISASSSWSDSTAARHSRLESSDGDGA WCPAGSVFPKEEEYLQVDLQRLHLVALVGTQGRHAGGLGKEFSRSYRLRYSRDGRRWMGWKDRWGQEVISGNEDPEGVVLKDLGPPMVAR LVRFYPRADRVMSVCLRVELYGCLWRDGLLSYTAPVGQTMYLSEAVYLNDSTYDGHTVGGLQYGGLGQLADGVVGLDDFRKSQELRVWPG YDYVGWSNHSFSSGYVEMEFEFDRLRAFQAMQVHCNNMHTLGARLPGGVECRFRRGPAMAWEGEPMRHNLGGNLGDPRARAVSVPLGGRV ARFLQCRFLFAGPWLLFSEISFISDVVNNSSPALGGTFPPAPWWPPGPPPTNFSSLELEPRGQQPVAKAEGSPTAILIGCLVAIILLLLL IIALMLWRLHWRRLLSKAERRVLEEELTVHLSVPGDTILINNRPGPREPPPYQEPRPRGNPPHSAPCVPNGSAYSGDYMEPEKPGAPLLP PPPQNSVPHYAEADIVTLQGVTGGNTYAVPALPPGAVGDGPPRVDFPRSRLRFKEKLGEGQFGEVHLCEVDSPQDLVSLDFPLNVRKGHP LLVAVKILRPDATKNARNDFLKEVKIMSRLKDPNIIRLLGVCVQDDPLCMITDYMENGDLNQFLSAHQLEDKAAEGAPGDGQAAQGPTIS YPMLLHVAAQIASGMRYLATLNFVHRDLATRNCLVGENFTIKIADFGMSRNLYAGDYYRVQGRAVLPIRWMAWECILMGKFTTASDVWAF |
Protein Functional Features |
| Main function of this protein. (from UniProt) |
| DDR1 (go to UniProt):Q08345 |
| 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 |
| Q08345 | Topological domain | 21 | 417 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Substitution;Start=190;End=243 |
| Q08345 | Topological domain | 21 | 417 | Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=244;End=913 |
| Q08345 | Transmembrane | 418 | 438 | Note=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=244;End=913 |
| Q08345 | Topological domain | 439 | 913 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=506;End=542 |
| Q08345 | Topological domain | 439 | 913 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=244;End=913 |
| Q08345 | Topological domain | 439 | 913 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Substitution;Start=665;End=665 |
| Q08345 | Topological domain | 439 | 913 | Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 | Type=Deletion;Start=506;End=542 |
| Q08345 | Domain | 610 | 905 | Note=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159 | Type=Deletion;Start=244;End=913 |
| Q08345 | Domain | 610 | 905 | Note=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159 | Type=Substitution;Start=665;End=665 |
| Q08345 | Region | 192 | 367 | Note=DS-like domain | Type=Substitution;Start=190;End=243 |
| Q08345 | Region | 192 | 367 | Note=DS-like domain | Type=Deletion;Start=244;End=913 |
| Q08345 | Region | 470 | 499 | Note=Disordered;Ontology_term=ECO:0000256;evidence=ECO:0000256|SAM:MobiDB-lite | Type=Deletion;Start=244;End=913 |
| Q08345 | Motif | 481 | 484 | Note=PPxY motif | Type=Deletion;Start=244;End=913 |
| Q08345 | Compositional bias | 476 | 496 | Note=Pro residues;Ontology_term=ECO:0000256;evidence=ECO:0000256|SAM:MobiDB-lite | Type=Deletion;Start=244;End=913 |
Gene Isoform Structures and Expression Levels for DDR1 |
| Gene structures of our canonical and alternative spliced genes of DDR1 * 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 Q08345-1 |
| 3D view using mol* of Q08345-2 |
| 3D view using mol* of Q08345-4 |
| 3D view using mol* of Q08345-5 |
| 3D view using mol* of Q08345-6 |
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 Q08345-1 |
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| pLDDT distribution across the protein length of Q08345-2 |
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| pLDDT distribution across the protein length of Q08345-4 |
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| pLDDT distribution across the protein length of Q08345-5 |
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| pLDDT distribution across the protein length of Q08345-6 |
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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 Q08345-1 |
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| Ramachandran plot of Q08345-5 |
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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 |
| Q08345-1 | 1.063 | 91 | 1.108 | 219.863 | 0.48 | 0.759 | 0.97 | 1.487 | 0.749 | 1.987 | 1.09 | 616,617,618,624,653,685,701,702,703,704,707,708,71 1,770,771,773,783,785,787,788,791,792 |
| Q08345-2 | 1.055 | 107 | 1.093 | 189.336 | 0.493 | 0.735 | 1.047 | 0.458 | 0.885 | 0.517 | 1.585 | 96,122,124,130,131,132,133,134,135,137,157,158,159 ,160,213,214,215,216,228,229,232,233,253 |
| Q08345-4 | 1.056 | 247 | 1.105 | 779.982 | 0.554 | 0.716 | 0.98 | 0.959 | 0.812 | 1.181 | 0.741 | 22,24,25,26,27,28,30,31,96,122,124,128,130,131,132 ,133,134,157,158,159,160,185,186,187,188,190,210,2 11,212,213,214,215,216,217,218,219,220,221,222,223 ,224,225 |
| Q08345-5 | 1.075 | 100 | 1.11 | 195.853 | 0.479 | 0.766 | 1.109 | 0.692 | 0.888 | 0.778 | 1.919 | 122,124,130,131,132,133,134,135,137,157,158,159,16 0,213,214,215,216,217,219,228,229,232,233,250,253 |
| Q08345-6 | 1.036 | 120 | 1.065 | 279.545 | 0.588 | 0.727 | 1.062 | 0.534 | 0.953 | 0.56 | 1.369 | 101,136,137,139,140,142,146,148,149,150,151,152,15 3,155,157,175,176,177,178,185,187,231,232,233,234, 235,246,247,250,251,268 |
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 Q08345-1_Q08345-1_6y23_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 Q08345-1_6y23_C_Q08345-2.pdb |
| 3D view using mol* of Q08345-1_6y23_C_Q08345-4.pdb |
| 3D view using mol* of Q08345-1_6y23_C_Q08345-5.pdb |
| 3D view using mol* of Q08345-1_6y23_C_Q08345-6.pdb |
| Protein Structure Comparision Visualization with mol*. between Canonical predicted structure (AF2)(orange) vs Alternative predicted structure (AF2)(green) |
| 3D view using mol* of Q08345-1_Q08345-2.pdb |
| 3D view using mol* of Q08345-1_Q08345-4.pdb |
| 3D view using mol* of Q08345-1_Q08345-5.pdb |
| 3D view using mol* of Q08345-1_Q08345-6.pdb |
| Protein Feature Comparison of the protein sequendary structures among the protiens. |
| ./stats/secondary_structure/figure/Q08345-1_vs_Q08345-2.png |
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| ./stats/secondary_structure/figure/Q08345-1_vs_Q08345-4.png |
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| ./stats/secondary_structure/figure/Q08345-1_vs_Q08345-5.png |
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| ./stats/secondary_structure/figure/Q08345-1_vs_Q08345-6.png |
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| Protein Feature Comparison of the relative accessible surface area (ASA) among the protiens. |
| ./stats/relative_asa/Q08345-1_vs_Q08345-2.png |
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| ./stats/relative_asa/Q08345-1_vs_Q08345-4.png |
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| ./stats/relative_asa/Q08345-1_vs_Q08345-5.png |
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| ./stats/relative_asa/Q08345-1_vs_Q08345-6.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 DDR1 |
| Drugs targeting this gene/protein. (DrugBank) |
| UniProt accession | Gene name | DrugBank ID | Drug name | Drug group | Actions |
| Q08345 | DDR1 | DB12010 | Fostamatinib | approved, investigational | inhibitor |
| Q08345 | DDR1 | DB00619 | Imatinib | approved | antagonist |
| Q08345 | DDR1 | DB15822 | Pralsetinib | approved, investigational | inhibitor |
Related Diseases to DDR1 |
| Previous studies relating to the alternative splicing of DDR1 and disease information from the MeSH term (PubMed) |
| Gene | PMID | Title | Abstract | MeSH ID | MeSH term |
| DDR1 | 9659899 | The discoidin domain receptor tyrosine kinases are activated by collagen. | Two mammalian receptor tyrosine kinases (DDR1 and DDR2) have extracellular domains closely related to a D. discoideum lectin, discoidin, required for cell aggregation. Here, we show that the mammalian DDR receptors bind and are activated by specific types of collagen. Stimulation of DDR receptor tyrosine kinase activity requires the native triple-helical structure of collagen and occurs over an extended period of time. Collagen activation of DDR1 induces phosphorylation of a docking site for the Shc phosphotyrosine binding domain, whose presence is controlled by alternative splicing. Activation of DDR2 by collagen results in the up-regulation of matrix metalloproteinase-1 expression. These results suggest that the discoidin-related DDR tyrosine kinases are novel collagen receptors with the potential to control cellular responses to the extracellular matrix. | D001943 | Breast Neoplasms |
| DDR1 | 9659899 | The discoidin domain receptor tyrosine kinases are activated by collagen. | Two mammalian receptor tyrosine kinases (DDR1 and DDR2) have extracellular domains closely related to a D. discoideum lectin, discoidin, required for cell aggregation. Here, we show that the mammalian DDR receptors bind and are activated by specific types of collagen. Stimulation of DDR receptor tyrosine kinase activity requires the native triple-helical structure of collagen and occurs over an extended period of time. Collagen activation of DDR1 induces phosphorylation of a docking site for the Shc phosphotyrosine binding domain, whose presence is controlled by alternative splicing. Activation of DDR2 by collagen results in the up-regulation of matrix metalloproteinase-1 expression. These results suggest that the discoidin-related DDR tyrosine kinases are novel collagen receptors with the potential to control cellular responses to the extracellular matrix. | D005354 | Fibrosarcoma |
| DDR1 | 18593464 | Novel splice variants derived from the receptor tyrosine kinase superfamily are potential therapeutics for rheumatoid arthritis. | Despite the advent of biological therapies for the treatment of rheumatoid arthritis, there is a compelling need to develop alternative therapeutic targets for nonresponders to existing treatments. Soluble receptors occur naturally in vivo, such as the splice variant of the cell surface receptor for vascular endothelial growth factor (VEGF)--a key regulator of angiogenesis in rheumatoid arthritis. Bioinformatics analyses predict that the majority of human genes undergo alternative splicing, generating proteins--many of which may have regulatory functions. The objective of the present study was to identify alternative splice variants (ASV) from cell surface receptor genes, and to determine whether the novel proteins encoded exert therapeutic activity in an in vivo model of arthritis. | D001172 | Arthritis, Rheumatoid |
| DDR1 | 18593464 | Novel splice variants derived from the receptor tyrosine kinase superfamily are potential therapeutics for rheumatoid arthritis. | Despite the advent of biological therapies for the treatment of rheumatoid arthritis, there is a compelling need to develop alternative therapeutic targets for nonresponders to existing treatments. Soluble receptors occur naturally in vivo, such as the splice variant of the cell surface receptor for vascular endothelial growth factor (VEGF)--a key regulator of angiogenesis in rheumatoid arthritis. Bioinformatics analyses predict that the majority of human genes undergo alternative splicing, generating proteins--many of which may have regulatory functions. The objective of the present study was to identify alternative splice variants (ASV) from cell surface receptor genes, and to determine whether the novel proteins encoded exert therapeutic activity in an in vivo model of arthritis. | D004195 | Disease Models, Animal |
Clinically important variants in DDR1 |
| (ClinVar, 04/20/2024) |
| accession_id | uniprot_id | gene_name | Type | Variant | Clinical_significance |
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