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6GOU

Development of Alkyl Glycerone Phosphate Synthase Inhibitors: Complex with Inhibitor 2I

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0005777cellular_componentperoxisome
A0005778cellular_componentperoxisomal membrane
A0006629biological_processlipid metabolic process
A0008609molecular_functionalkylglycerone-phosphate synthase activity
A0008610biological_processlipid biosynthetic process
A0008611biological_processether lipid biosynthetic process
A0016020cellular_componentmembrane
A0016740molecular_functiontransferase activity
A0050660molecular_functionflavin adenine dinucleotide binding
A0071949molecular_functionFAD binding
B0003824molecular_functioncatalytic activity
B0005777cellular_componentperoxisome
B0005778cellular_componentperoxisomal membrane
B0006629biological_processlipid metabolic process
B0008609molecular_functionalkylglycerone-phosphate synthase activity
B0008610biological_processlipid biosynthetic process
B0008611biological_processether lipid biosynthetic process
B0016020cellular_componentmembrane
B0016740molecular_functiontransferase activity
B0050660molecular_functionflavin adenine dinucleotide binding
B0071949molecular_functionFAD binding
C0003824molecular_functioncatalytic activity
C0005777cellular_componentperoxisome
C0005778cellular_componentperoxisomal membrane
C0006629biological_processlipid metabolic process
C0008609molecular_functionalkylglycerone-phosphate synthase activity
C0008610biological_processlipid biosynthetic process
C0008611biological_processether lipid biosynthetic process
C0016020cellular_componentmembrane
C0016740molecular_functiontransferase activity
C0050660molecular_functionflavin adenine dinucleotide binding
C0071949molecular_functionFAD binding
D0003824molecular_functioncatalytic activity
D0005777cellular_componentperoxisome
D0005778cellular_componentperoxisomal membrane
D0006629biological_processlipid metabolic process
D0008609molecular_functionalkylglycerone-phosphate synthase activity
D0008610biological_processlipid biosynthetic process
D0008611biological_processether lipid biosynthetic process
D0016020cellular_componentmembrane
D0016740molecular_functiontransferase activity
D0050660molecular_functionflavin adenine dinucleotide binding
D0071949molecular_functionFAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues30
Detailsbinding site for residue FAD D 701
ChainResidue
DTRP96
DLEU245
DPRO302
DASP303
DSER304
DSER308
DTHR309
DGLY312
DTRP313
DSER315
DTHR316
DPRO234
DALA318
DSER319
DGLU368
DGLY369
DGLY372
DVAL373
DILE374
DALA512
DHIS616
DASN656
DILE235
DF6T702
DGLY236
DGLY237
DGLY238
DTHR239
DSER240
DGLY244

site_idAC2
Number of Residues14
Detailsbinding site for residue F6T D 702
ChainResidue
DASP303
DILE511
DMET514
DARG515
DGLY525
DGLU526
DSER527
DTYR578
DTYR580
DPHE581
DALA582
DHIS616
DHIS617
DFAD701

site_idAC3
Number of Residues30
Detailsbinding site for residue FAD A 701
ChainResidue
ATRP96
APRO234
AILE235
AGLY236
AGLY237
AGLY238
ATHR239
ASER240
AGLY244
ALEU245
APRO302
AASP303
ASER304
ASER308
ATHR309
AGLY312
ATRP313
ASER315
ATHR316
AALA318
ASER319
AGLU368
AGLY369
AGLY372
AVAL373
AILE374
AALA512
AHIS616
AASN656
AF6T702

site_idAC4
Number of Residues12
Detailsbinding site for residue F6T A 702
ChainResidue
AASP303
AILE511
AMET514
AARG515
AGLU526
ASER527
ATYR578
ATYR580
AALA582
AHIS616
AHIS617
AFAD701

site_idAC5
Number of Residues31
Detailsbinding site for residue FAD B 701
ChainResidue
BSER308
BTHR309
BGLY312
BTRP313
BSER315
BTHR316
BALA318
BSER319
BGLU368
BGLY369
BGLY372
BVAL373
BILE374
BALA512
BHIS616
BASN654
BASN656
BF6T702
BTRP96
BPRO234
BILE235
BGLY236
BGLY237
BGLY238
BTHR239
BSER240
BGLY244
BLEU245
BPRO302
BASP303
BSER304

site_idAC6
Number of Residues11
Detailsbinding site for residue F6T B 702
ChainResidue
BASP303
BILE511
BARG515
BGLU526
BSER527
BTYR578
BTYR580
BALA582
BHIS616
BHIS617
BFAD701

site_idAC7
Number of Residues29
Detailsbinding site for residue FAD C 701
ChainResidue
CTRP96
CPRO234
CILE235
CGLY236
CGLY237
CGLY238
CTHR239
CSER240
CGLY244
CLEU245
CPRO302
CASP303
CSER304
CSER308
CTHR309
CGLY312
CTRP313
CSER315
CTHR316
CALA318
CSER319
CGLU368
CGLY369
CGLY372
CVAL373
CILE374
CALA512
CHIS616
CASN656

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor/acceptor => ECO:0000269|PubMed:23112191
ChainResidueDetails
DTYR578
ATYR578
BTYR578
CTYR578

site_idSWS_FT_FI2
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:23112191
ChainResidueDetails
DPRO234
AARG515
BPRO234
BASP303
BTHR316
BGLU368
BARG515
CPRO234
CASP303
CTHR316
CGLU368
DASP303
CARG515
DTHR316
DGLU368
DARG515
APRO234
AASP303
ATHR316
AGLU368

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: Important for enzyme activity => ECO:0000269|PubMed:10692424, ECO:0000269|PubMed:23112191
ChainResidueDetails
DARG419
AARG419
BARG419
CARG419

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:O00116
ChainResidueDetails
DSER65
ASER65
BSER65
CSER65

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphothreonine => ECO:0000250|UniProtKB:O00116
ChainResidueDetails
DTHR74
ATHR74
BTHR74
CTHR74

site_idSWS_FT_FI6
Number of Residues8
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:O00116
ChainResidueDetails
DLYS102
DLYS347
ALYS102
ALYS347
BLYS102
BLYS347
CLYS102
CLYS347

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PDB entries from 2024-07-17

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