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6ATO

Crystal structure of hGSTA1-1 complexed with GSH and MPD in each subunit

Functional Information from GO Data
ChainGOidnamespacecontents
A0004364molecular_functionglutathione transferase activity
A0004601molecular_functionperoxidase activity
A0004602molecular_functionglutathione peroxidase activity
A0004769molecular_functionsteroid delta-isomerase activity
A0005504molecular_functionfatty acid binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006629biological_processlipid metabolic process
A0006693biological_processprostaglandin metabolic process
A0006749biological_processglutathione metabolic process
A0006805biological_processxenobiotic metabolic process
A0016740molecular_functiontransferase activity
A0016853molecular_functionisomerase activity
A0030855biological_processepithelial cell differentiation
A0043651biological_processlinoleic acid metabolic process
A0070062cellular_componentextracellular exosome
A0098869biological_processcellular oxidant detoxification
A1901687biological_processglutathione derivative biosynthetic process
B0004364molecular_functionglutathione transferase activity
B0004601molecular_functionperoxidase activity
B0004602molecular_functionglutathione peroxidase activity
B0004769molecular_functionsteroid delta-isomerase activity
B0005504molecular_functionfatty acid binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006629biological_processlipid metabolic process
B0006693biological_processprostaglandin metabolic process
B0006749biological_processglutathione metabolic process
B0006805biological_processxenobiotic metabolic process
B0016740molecular_functiontransferase activity
B0016853molecular_functionisomerase activity
B0030855biological_processepithelial cell differentiation
B0043651biological_processlinoleic acid metabolic process
B0070062cellular_componentextracellular exosome
B0098869biological_processcellular oxidant detoxification
B1901687biological_processglutathione derivative biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue GSH A 301
ChainResidue
ATYR9
AHOH417
AHOH482
AHOH500
AHOH545
AHOH588
BASP101
BARG131
AARG15
AARG45
AGLN54
AVAL55
AGLN67
ATHR68
APHE220
AMPD302

site_idAC2
Number of Residues4
Detailsbinding site for residue MPD A 302
ChainResidue
ATYR9
AARG15
AGSH301
AHOH415

site_idAC3
Number of Residues6
Detailsbinding site for residue MPD A 303
ChainResidue
AMET63
ALYS64
ALYS141
ASER142
AHOH420
BMET94

site_idAC4
Number of Residues3
Detailsbinding site for residue MPD A 304
ChainResidue
AARG45
AGLN53
AHOH561

site_idAC5
Number of Residues4
Detailsbinding site for residue MPD A 305
ChainResidue
ATYR49
AGLU59
AHOH416
AHOH419

site_idAC6
Number of Residues16
Detailsbinding site for residue GSH B 301
ChainResidue
AASP101
AARG131
AHOH431
BTYR9
BARG15
BARG45
BGLN54
BVAL55
BGLN67
BTHR68
BPHE220
BMPD302
BHOH407
BHOH500
BHOH572
BHOH578

site_idAC7
Number of Residues2
Detailsbinding site for residue MPD B 302
ChainResidue
BTYR9
BGSH301

site_idAC8
Number of Residues7
Detailsbinding site for residue MPD B 303
ChainResidue
BSER18
BARG69
BLEU72
BGLU97
BALA100
BHIS159
BHOH630

site_idAC9
Number of Residues8
Detailsbinding site for residue MPD B 304
ChainResidue
BARG13
BILE106
BTYR166
BGLU169
BPRO207
BHOH439
BHOH459
BHOH481

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:16421451, ECO:0000269|PubMed:19618965
ChainResidueDetails
BTYR9
BARG45
BGLN54
BGLN67
ATYR9
AARG45
AGLN54
AGLN67

site_idSWS_FT_FI2
Number of Residues2
DetailsMOD_RES: N-acetylalanine; in Glutathione S-transferase A1, N-terminally processed => ECO:0000250|UniProtKB:P30115
ChainResidueDetails
AALA2
BALA2

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:P30115
ChainResidueDetails
ALYS4
BLYS4

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PDB entries from 2024-06-12

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