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6T5J

Structure of NUDT15 in complex with inhibitor TH1760

Functional Information from GO Data
ChainGOidnamespacecontents
A0000278biological_processmitotic cell cycle
A0000302biological_processresponse to reactive oxygen species
A0005515molecular_functionprotein binding
A0005829cellular_componentcytosol
A0006195biological_processpurine nucleotide catabolic process
A0006203biological_processdGTP catabolic process
A0008413molecular_function8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity
A0009217biological_processpurine deoxyribonucleoside triphosphate catabolic process
A0016787molecular_functionhydrolase activity
A0035539molecular_function8-oxo-7,8-dihydrodeoxyguanosine triphosphate pyrophosphatase activity
A0042178biological_processxenobiotic catabolic process
A0042262biological_processDNA protection
A0044715molecular_function8-oxo-dGDP phosphatase activity
A0046872molecular_functionmetal ion binding
A0047429molecular_functionnucleoside triphosphate diphosphatase activity
A0055086biological_processnucleobase-containing small molecule metabolic process
A0061136biological_processregulation of proteasomal protein catabolic process
A1901292biological_processnucleoside phosphate catabolic process
B0000278biological_processmitotic cell cycle
B0000302biological_processresponse to reactive oxygen species
B0005515molecular_functionprotein binding
B0005829cellular_componentcytosol
B0006195biological_processpurine nucleotide catabolic process
B0006203biological_processdGTP catabolic process
B0008413molecular_function8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity
B0009217biological_processpurine deoxyribonucleoside triphosphate catabolic process
B0016787molecular_functionhydrolase activity
B0035539molecular_function8-oxo-7,8-dihydrodeoxyguanosine triphosphate pyrophosphatase activity
B0042178biological_processxenobiotic catabolic process
B0042262biological_processDNA protection
B0044715molecular_function8-oxo-dGDP phosphatase activity
B0046872molecular_functionmetal ion binding
B0047429molecular_functionnucleoside triphosphate diphosphatase activity
B0055086biological_processnucleobase-containing small molecule metabolic process
B0061136biological_processregulation of proteasomal protein catabolic process
B1901292biological_processnucleoside phosphate catabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue MKB A 201
ChainResidue
AGLY15
APHE135
AGLY137
ALEU138
AHOH363
AHOH376
BPRO26
BARG27
AVAL16
AARG34
AGLN44
ALEU45
AGLY48
ATYR90
ATYR92
ATHR94

site_idAC2
Number of Residues6
Detailsbinding site for residue MG A 202
ChainResidue
AGLU63
AGLU67
AHOH310
AHOH333
AHOH354
AHOH375

site_idAC3
Number of Residues6
Detailsbinding site for residue MG A 203
ChainResidue
AHOH330
AHOH337
AHOH366
AHOH414
AHOH490
BHOH507

site_idAC4
Number of Residues6
Detailsbinding site for residue CL A 204
ChainResidue
AARG34
ASER37
AVAL38
BARG27
BPHE149
BHOH450

site_idAC5
Number of Residues17
Detailsbinding site for residue MKB B 201
ChainResidue
AARG27
BGLY15
BVAL16
BARG34
BGLN44
BLEU45
BGLY48
BTYR90
BTYR92
BTHR94
BPHE135
BGLY137
BLEU138
BHOH366
BHOH374
BHOH381
BHOH490

site_idAC6
Number of Residues6
Detailsbinding site for residue MG B 202
ChainResidue
BGLU63
BGLU67
BHOH313
BHOH332
BHOH350
BHOH394

site_idAC7
Number of Residues6
Detailsbinding site for residue MG B 203
ChainResidue
BHOH302
BHOH318
BHOH327
BHOH351
BHOH491
BHOH512

site_idAC8
Number of Residues6
Detailsbinding site for residue CL B 204
ChainResidue
AARG27
APHE149
AHOH446
BARG34
BSER37
BVAL38

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: BINDING => ECO:0000250
ChainResidueDetails
AGLU63
AGLU67
BGLU63
BGLU67

223790

PDB entries from 2024-08-14

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