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4AGW

Discovery of a small molecule type II inhibitor of wild-type and gatekeeper mutants of BCR-ABL, PDGFRalpha, Kit, and Src kinases

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0004713molecular_functionprotein tyrosine kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
B0004672molecular_functionprotein kinase activity
B0004713molecular_functionprotein tyrosine kinase activity
B0005524molecular_functionATP binding
B0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues23
DetailsBINDING SITE FOR RESIDUE NG7 A 1534
ChainResidue
ALEU273
ATYR340
AMET341
ASER342
ALYS343
AGLY344
AVAL383
AHIS384
AARG385
ALEU393
AVAL402
AALA293
AALA403
AASP404
AMES1535
AHOH2004
ALYS295
AVAL313
AMET314
ALEU317
ALEU322
ATHR338
AGLU339

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MES A 1535
ChainResidue
AMET380
AASN381
ATYR382
AVAL383
ANG71534

site_idAC3
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 1536
ChainResidue
ALYS427
AVAL461
ATYR463
APRO464
AGLY465
BGLU517
BASP518
BTHR521

site_idAC4
Number of Residues23
DetailsBINDING SITE FOR RESIDUE NG7 B 1534
ChainResidue
BLEU273
BALA293
BLYS295
BGLU310
BVAL313
BMET314
BLEU317
BLEU322
BTHR338
BGLU339
BTYR340
BMET341
BSER342
BGLY344
BVAL383
BHIS384
BARG385
BLEU393
BVAL402
BALA403
BASP404
BPHE405
BMES1535

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MES B 1535
ChainResidue
BMET380
BASN381
BTYR382
BVAL383
BNG71534

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues23
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGQGCFGEVWmGtwngttr...........VAIK
ChainResidueDetails
ALEU273-LYS295

site_idPS00109
Number of Residues13
DetailsPROTEIN_KINASE_TYR Tyrosine protein kinases specific active-site signature. YVHrDLRAANILV
ChainResidueDetails
ATYR382-VAL394

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000255|PROSITE-ProRule:PRU10028
ChainResidueDetails
AASP386
BASP386

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00159
ChainResidueDetails
ALEU273
BLEU273

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING:
ChainResidueDetails
ALYS295
BLYS295

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: Phosphotyrosine; by autocatalysis => ECO:0000269|PubMed:6273838, ECO:0000269|PubMed:8856081
ChainResidueDetails
ATYR416
BTYR416

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphotyrosine; by autocatalysis => ECO:0000269|PubMed:8856081
ChainResidueDetails
ATYR436
BTYR436

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: S-nitrosocysteine => ECO:0000269|PubMed:19948721
ChainResidueDetails
ACYS498
BCYS498

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: Phosphotyrosine; by CSK => ECO:0000269|PubMed:2420005
ChainResidueDetails
ATYR527
BTYR527

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PDB entries from 2024-07-24

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