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UniProt P10721

Isoform 2 of Mast/stem cell growth factor receptor Kit (P10721)

Isoform 2 of Mast/stem cell growth factor receptor Kit (UniProt P10721), EC 2.7.10.1: 44 experimental structures and 1 predicted model on GenesisL1, 15 ligands bound, 24 pockets. Binding sites, druggability and experiment against…

UniProt
P10721
Protein
Isoform 2 of Mast/stem cell growth factor receptor Kit
EC
2.7.10.1
Experimental structures
44
Predicted models
1
Ligands
15
Pockets
24 · 3 records with a druggable one

Structures

45 records of P10721 in the MolNFT archive: 44 experimental, 1 predicted.

EntryTitleMethodChainsLigandsPockets
1PKGStructure of a c-Kit Kinase Product Complexx-ray diffractionA——
1PKGStructure of a C-kit kinase product complexx-ray diffractionA——
1T45Structural basis for the autoinhibition and sti-571 inhibition of C-kit tyrosine kinasex-ray diffractionA——
1T45Structural basis for the autoinhibition and sti-571 inhibition of C- kit tyrosine kinasex-ray diffractionA——
1T46Structural basis for the autoinhibition and sti-571 inhibition of C-kit tyrosine kinasex-ray diffractionA——
1T46Structural basis for the autoinhibition and sti-571 inhibition of C- kit tyrosine kinasex-ray diffractionA——
2E9WCrystal structure of the extracellular domain of Kit in complex with stem cell factor (SCF)x-ray diffractionA, B——
2E9WCrystal structure of the extracellular domain of kit in complex with stem cell factor (scf)x-ray diffractionA, B——
2EC8Crystal structure of the exctracellular domain of the receptor tyrosine kinase, Kitx-ray diffractionA——
2EC8Crystal structure of the exctracellular domain of the receptor tyrosine kinase, kitx-ray diffractionA——
2VIFCrystal structure of SOCS6 SH2 domain in complex with a c-KIT phosphopeptidex-ray diffractionP——
2VIFCrystal structure of SOCS6 SH2 domain in complex with a C-kit phosphopeptidex-ray diffractionP——
3G0EKIT kinase domain in complex with sunitinibx-ray diffractionA——
3G0EKit kinase domain in complex with sunitinibx-ray diffractionA——
3G0FKIT kinase domain mutant D816H in complex with sunitinibx-ray diffractionA, B——
3G0FKit kinase domain mutant D816H in complex with sunitinibx-ray diffractionA, B——
4HVSCrystal structure of KIT kinase domain with a small molecule inhibitor, PLX647x-ray diffractionA——
4HVSCrystal structure of kit kinase domain with a small molecule inhibitor, PLX647x-ray diffractionA——
4K94Crystal structure of KIT D4D5 fragment in complex with anti-Kit antibody Fab19x-ray diffractionC——
4K94Crystal structure of kit D4D5 fragment in complex with anti-kit antibody FAB19x-ray diffractionC——
4K9ECrystal structure of KIT D4D5 fragment in complex with anti-Kit antibodies Fab79Dx-ray diffractionC——
4K9ECrystal structure of kit D4D5 fragment in complex with anti-kit antibodies FAB79Dx-ray diffractionC——
4PGZStructural basis of KIT activation by oncogenic mutations in the extracellular region reveals a…x-ray diffractionC, A, B——
4PGZStructural basis of kit activation by oncogenic mutations in the extracellular region reveals a…x-ray diffractionC, A, B——
4U0ICrystal structure of KIT in complex with ponatinibx-ray diffractionA——
4U0ICrystal structure of kit in complex with ponatinibx-ray diffractionA——
6GQJCrystal structure of human c-KIT kinase domain in complex with AZD3229-analogue (compound 18)x-ray diffractionA, BF82—
6GQJCrystal structure of human C-kit kinase domain in complex with AZD3229-analogue (compound 18)x-ray diffractionA, BF82—
6GQKCrystal structure of human C-kit kinase domain in complex with AZD3229-analogue (compound 23)x-ray diffractionA, BF88—
6GQLCrystal structure of human C-kit kinase domain in complex with AZD3229-analogue (compound 35)x-ray diffractionA, BF8B—
6GQMCrystal structure of human c-KIT kinase domain in complex with a small molecule inhibitor, AZD3229x-ray diffractionA, BF8H, CL—
6GQMCrystal structure of human C-kit kinase domain in complex with a small molecule inhibitor, AZD3229x-ray diffractionA, BF8H, CL—
6HH1Structure of C-kit with allosteric inhibitor 3G8x-ray diffractionAPO4, G4E—
6ITTCrystal structure of unactivated C-kit in complex with compoundx-ray diffractionA, BAWO—
6ITVCrystal structure of activated C-kit in complex with compoundx-ray diffractionAAWO—
6KLACrystal structure of human C-kit kinase domain in complex with compound 15Ax-ray diffractionADJX—
6MOBCrystal structure of KIT1 in complex with DP2976 via co-crystallizationx-ray diffractionANO3, JWY—
6MOBCrystal structure of KIT1 in complex with DP2976 via co- crystallizationx-ray diffractionANO3, JWY—
6XV9Crystal structure of the kinase domain of human c-KIT in complex with a type-II inhibitorx-ray diffractionA, BO352 (best 0.83)
6XV9Crystal structure of the kinase domain of human C-kit in complex with a type-II inhibitorx-ray diffractionA, BO35—
6XVACrystal structure of the kinase domain of human C-kit in complex with a type-II inhibitor bearing…x-ray diffractionA, BO2K—
6XVBCrystal structure of the kinase domain of human C-kit with a cyclic imidate inhibitor covalently…x-ray diffractionA, BO2H—
8DFMEctodomain of full-length wild-type KIT-SCF dimerselectron microscopyA, BNAG8 (best 0.64)
8DFQEctodomain of full-length KIT(T417I,delta418-419)-SCF dimerselectron microscopyA, BNAG14 (best 0.64)
P10721AlphaFold monomer V2.0 prediction for MAST/STEM cell growth factor receptor kit (P10721)predictedA——

Ligands

  • AWO · N-(5-ethyl-1,2-oxazol-3-yl)-N'-[4-(2-{[6-(4-ethylpyrazin-1(4H)-yl)pyrimidin-4-yl]amino}-1,3-thiazol-5-yl)phenyl]urea · in 2 records
  • CL · Chloride ion · in 2 records
  • F82 · 2-[4-(6,7-dimethoxyquinazolin-4-yl)oxy-2-methoxy-phenyl]-~{N}-(1-propan-2-ylpyrazol-4-yl)ethanamide · in 2 records
  • F8H · ~{N}-[4-[[5-fluoranyl-7-(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yl-1,2,3-triazol-1-yl) ethanamide · in 2 records
  • JWY · N-{4-chloro-5-[1-ethyl-7-(methylamino)-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl]-2-fluorophenyl}-N'-phenylurea · in 2 records
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · in 2 records
  • NO3 · Nitrate ion · in 2 records
  • O35 · ~{N}-[3-[(dimethylamino)methyl]-5-methyl-phenyl]-2-[3-methoxy-5-(7-methoxyquinolin-4-yl)oxy-pyridin-2-yl]ethanamide · in 2 records
  • DJX · N-[6-(4-ethylpiperazin-1-yl)-2-methyl-pyrimidin-4-yl]-5-pyridin-4-yl-1,3-thiazol-2-amine · in 1 record
  • F88 · ~{N}-[4-(6,7-dimethoxyquinazolin-4-yl)oxyphenyl]-2-(1-ethylpyrazol-4-yl)ethanamide · in 1 record
  • F8B · ~{N}-[4-(6,7-dimethoxyquinazolin-4-yl)oxyphenyl]-2-(4-propan-2-yl-1,2,3-triazol-1-yl)ethanamide · in 1 record
  • G4E · ~{N}-(2,3-dimethylphenyl)-5-(4-pyridin-4-yloxyphenyl)-4~{H}-1,2,4-triazol-3-amine · in 1 record
  • O2H · ~{N}-(4,4-dimethyl-2-propyl-3,1-benzoxazin-6-yl)-2-[3-methoxy-5-(7-methoxyquinolin-4-yl)oxy-pyridin-2-yl]ethanamide · in 1 record
  • O2K · ~{N}-[[3-[2-[3-methoxy-5-(7-methoxyquinolin-4-yl)oxy-pyridin-2-yl]ethanoylamino]-5-methyl-phenyl]methyl]propanamide · in 1 record
  • PO4 · Phosphate ion · in 1 record

Experiment against prediction

Elsewhere

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