UniProt:Q16832 DDR2

chain
  • signal peptide:1-21
  • chain:22-855
checksum 78662021BC53E1A0
comment
  • FUNCTION Tyrosine kinase involved in the regulation of tissues remodeling (PubMed:30449416). It functions as a cell surface receptor for fibrillar collagen and regulates cell differentiation, remodeling of the extracellular matrix, cell migration and cell proliferation. Required for normal bone development. Regulates osteoblast differentiation and chondrocyte maturation via a signaling pathway that involves MAP kinases and leads to the activation of the transcription factor RUNX2. Regulates remodeling of the extracellular matrix by up-regulation of the collagenases MMP1, MMP2 and MMP13, and thereby facilitates cell migration and tumor cell invasion. Promotes fibroblast migration and proliferation, and thereby contributes to cutaneous wound healing.CATALYTIC ACTIVITY L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H(+)ACTIVITY REGULATION Present in an inactive state in the absence of collagen binding and phosphorylation by SRC. Tyrosine phosphorylation enhances the affinity for ATP and the catalytic activity.SUBUNIT Binds hydroxyproline-rich sequence motifs in fibrillar, glycosylated collagen, such as the GQOGVMGFO motif, where O stands for hydroxyproline. Interacts with SRC. Interacts (tyrosine phosphorylated) with SHC1.INTERACTION Detected in osteocytes, osteoblastic cells in subchondral bone, bone lining cells, tibia and cartilage (at protein level). Detected at high levels in heart and lung, and at low levels in brain, placenta, liver, skeletal muscle, pancreas, and kidney.INDUCTION Up-regulated during osteoblast differentiation (in vitro). Up-regulated in cartilage from osteoarthritis patients.PTM N-glycosylated.PTM Tyrosine phosphorylated in response to collagen binding. Phosphorylated by SRC; this is required for activation and subsequent autophosphorylation on additional tyrosine residues.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.SIMILARITY Belongs to the protein kinase superfamily. Tyr protein kinase family. Insulin receptor subfamily.
crossReference
databaseName UniProt
dbId 53502
description
  • recommendedName: Discoidin domain-containing receptor 2 shortName: Discoidin domain receptor 2 ecNumber: 2.7.10.1 alternativeName: CD167 antigen-like family member B alternativeName: Discoidin domain-containing receptor tyrosine kinase 2 alternativeName: Neurotrophic tyrosine kinase, receptor-related 3 alternativeName: Receptor protein-tyrosine kinase TKT alternativeName: Tyrosine-protein kinase TYRO10 cdAntigenNameCD167b/cdAntigenName
displayName UniProt:Q16832 DDR2
geneName
  • DDR2
  • NTRKR3
  • TKT
  • TYRO10
identifier Q16832
isSequenceChanged false
keyword
  • 3D-structure
  • ATP-binding
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Dwarfism
  • Glycoprotein
  • Kinase
  • Membrane
  • Nucleotide-binding
  • Osteogenesis
  • Phosphoprotein
  • Proteomics identification
  • Receptor
  • Reference proteome
  • Signal
  • Transferase
  • Transmembrane
  • Transmembrane helix
  • Tyrosine-protein kinase
modified [InstanceEdit:9939033] Weiser, Joel, 2025-02-21
moleculeType Protein
name
  • DDR2
otherIdentifier
  • 11723859_a_at
  • 11744349_s_at
  • 11757788_s_at
  • 11759442_s_at
  • 11759547_s_at
  • 11760934_x_at
  • 1319_at
  • 16673075
  • 205168_PM_at
  • 205168_at
  • 225442_PM_at
  • 225442_at
  • 227561_PM_at
  • 227561_at
  • 235631_PM_at
  • 235631_at
  • 2364232
  • 2364233
  • 2364234
  • 2364235
  • 2364236
  • 2364243
  • 2364253
  • 2364257
  • 2364258
  • 2364259
  • 2364269
  • 2364270
  • 2364271
  • 2364272
  • 2364273
  • 2364274
  • 2364278
  • 2364279
  • 2364280
  • 2364281
  • 2364282
  • 2364283
  • 2364284
  • 2364285
  • 2364287
  • 2364288
  • 2364291
  • 2364292
  • 2364293
  • 2364294
  • 2364295
  • 2364296
  • 2364297
  • 2364299
  • 2364301
  • 2364302
  • 2364303
  • 2364304
  • 2364305
  • 2364306
  • 244075_PM_at
  • 244075_at
  • 3243265
  • 3243268
  • 3243270
  • 3243271
  • 3243272
  • 3243273
  • 45199_at
  • 48967_at
  • 4921
  • 68597_at
  • 7906878
  • 7906900
  • 82956_at
  • A_14_P114165
  • A_23_P452
  • A_32_P88965
  • A_33_P3276376
  • GE59995
  • GE861252
  • GO:0000166
  • GO:0001503
  • GO:0003416
  • GO:0003824
  • GO:0004672
  • GO:0004713
  • GO:0004714
  • GO:0005515
  • GO:0005518
  • GO:0005524
  • GO:0005856
  • GO:0005886
  • GO:0005925
  • GO:0006355
  • GO:0006468
  • GO:0007155
  • GO:0007165
  • GO:0007169
  • GO:0008284
  • GO:0010715
  • GO:0010763
  • GO:0010976
  • GO:0015629
  • GO:0016020
  • GO:0016301
  • GO:0016324
  • GO:0016740
  • GO:0018108
  • GO:0030198
  • GO:0030199
  • GO:0030500
  • GO:0031214
  • GO:0032967
  • GO:0034103
  • GO:0035988
  • GO:0035994
  • GO:0038062
  • GO:0038063
  • GO:0043066
  • GO:0043235
  • GO:0045669
  • GO:0045860
  • GO:0046777
  • GO:0048146
  • GO:0048856
  • GO:0051091
  • GO:0051897
  • GO:0070374
  • GO:0071456
  • GO:0071560
  • GO:0090091
  • GO:0090303
  • GO:0140096
  • GO:1900087
  • GO:1901299
  • GO:1904385
  • GO:1904707
  • GO:1904754
  • GO:1904899
  • GO:2000491
  • HMNXSV003008235
  • HMNXSV003047825
  • Hs.146299.0.A1_3p_at
  • Hs.15248.0.S1_3p_at
  • Hs.192152.0.A1_3p_at
  • Hs.42392.0.A1_3p_at
  • ILMN_1664398
  • ILMN_1675794
  • ILMN_2410523
  • PH_hs_0025814
  • PH_hs_0041097
  • TC01001423.hg
  • TC01001425.hg
  • TC01004802.hg
  • X74764_at
  • g5453813_3p_at
physicalEntity
referenceDatabase [ReferenceDatabase:2] UniProt
referenceGene
referenceTranscript
schemaClass ReferenceGeneProduct
secondaryIdentifier
  • DDR2_HUMAN
  • Q7Z730
sequenceLength 855
species [Species:48887] Homo sapiens
stId uniprot:Q16832
url http://purl.uniprot.org/uniprot/Q16832
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