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5UZ0

Crystal structure of AICARFT bound to an antifolate

Functional Information from GO Data
ChainGOidnamespacecontents
A0003360biological_processbrainstem development
A0003824molecular_functioncatalytic activity
A0003937molecular_functionIMP cyclohydrolase activity
A0004643molecular_functionphosphoribosylaminoimidazolecarboxamide formyltransferase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0005886cellular_componentplasma membrane
A0006139biological_processnucleobase-containing compound metabolic process
A0006164biological_processpurine nucleotide biosynthetic process
A0006177biological_processGMP biosynthetic process
A0006189biological_process'de novo' IMP biosynthetic process
A0010035biological_processobsolete response to inorganic substance
A0016020cellular_componentmembrane
A0016740molecular_functiontransferase activity
A0016787molecular_functionhydrolase activity
A0021549biological_processcerebellum development
A0021987biological_processcerebral cortex development
A0031100biological_processanimal organ regeneration
A0042803molecular_functionprotein homodimerization activity
A0044208biological_process'de novo' AMP biosynthetic process
A0045296molecular_functioncadherin binding
A0046452biological_processdihydrofolate metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0070062cellular_componentextracellular exosome
A0097294biological_process'de novo' XMP biosynthetic process
A0098761biological_processcellular response to interleukin-7
B0003360biological_processbrainstem development
B0003824molecular_functioncatalytic activity
B0003937molecular_functionIMP cyclohydrolase activity
B0004643molecular_functionphosphoribosylaminoimidazolecarboxamide formyltransferase activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0005886cellular_componentplasma membrane
B0006139biological_processnucleobase-containing compound metabolic process
B0006164biological_processpurine nucleotide biosynthetic process
B0006177biological_processGMP biosynthetic process
B0006189biological_process'de novo' IMP biosynthetic process
B0010035biological_processobsolete response to inorganic substance
B0016020cellular_componentmembrane
B0016740molecular_functiontransferase activity
B0016787molecular_functionhydrolase activity
B0021549biological_processcerebellum development
B0021987biological_processcerebral cortex development
B0031100biological_processanimal organ regeneration
B0042803molecular_functionprotein homodimerization activity
B0044208biological_process'de novo' AMP biosynthetic process
B0045296molecular_functioncadherin binding
B0046452biological_processdihydrofolate metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0070062cellular_componentextracellular exosome
B0097294biological_process'de novo' XMP biosynthetic process
B0098761biological_processcellular response to interleukin-7
C0003360biological_processbrainstem development
C0003824molecular_functioncatalytic activity
C0003937molecular_functionIMP cyclohydrolase activity
C0004643molecular_functionphosphoribosylaminoimidazolecarboxamide formyltransferase activity
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0005886cellular_componentplasma membrane
C0006139biological_processnucleobase-containing compound metabolic process
C0006164biological_processpurine nucleotide biosynthetic process
C0006177biological_processGMP biosynthetic process
C0006189biological_process'de novo' IMP biosynthetic process
C0010035biological_processobsolete response to inorganic substance
C0016020cellular_componentmembrane
C0016740molecular_functiontransferase activity
C0016787molecular_functionhydrolase activity
C0021549biological_processcerebellum development
C0021987biological_processcerebral cortex development
C0031100biological_processanimal organ regeneration
C0042803molecular_functionprotein homodimerization activity
C0044208biological_process'de novo' AMP biosynthetic process
C0045296molecular_functioncadherin binding
C0046452biological_processdihydrofolate metabolic process
C0046654biological_processtetrahydrofolate biosynthetic process
C0070062cellular_componentextracellular exosome
C0097294biological_process'de novo' XMP biosynthetic process
C0098761biological_processcellular response to interleukin-7
D0003360biological_processbrainstem development
D0003824molecular_functioncatalytic activity
D0003937molecular_functionIMP cyclohydrolase activity
D0004643molecular_functionphosphoribosylaminoimidazolecarboxamide formyltransferase activity
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0005886cellular_componentplasma membrane
D0006139biological_processnucleobase-containing compound metabolic process
D0006164biological_processpurine nucleotide biosynthetic process
D0006177biological_processGMP biosynthetic process
D0006189biological_process'de novo' IMP biosynthetic process
D0010035biological_processobsolete response to inorganic substance
D0016020cellular_componentmembrane
D0016740molecular_functiontransferase activity
D0016787molecular_functionhydrolase activity
D0021549biological_processcerebellum development
D0021987biological_processcerebral cortex development
D0031100biological_processanimal organ regeneration
D0042803molecular_functionprotein homodimerization activity
D0044208biological_process'de novo' AMP biosynthetic process
D0045296molecular_functioncadherin binding
D0046452biological_processdihydrofolate metabolic process
D0046654biological_processtetrahydrofolate biosynthetic process
D0070062cellular_componentextracellular exosome
D0097294biological_process'de novo' XMP biosynthetic process
D0098761biological_processcellular response to interleukin-7
Functional Information from PDB Data
site_idAC1
Number of Residues17
Detailsbinding site for residue AMZ A 601
ChainResidue
AASN431
BARG207
BTYR208
BILE238
BHIS267
BGLY316
BASP339
B8US601
BHOH759
AARG451
AALA540
APHE541
AARG588
APHE590
AHOH704
AHOH745
AHOH764

site_idAC2
Number of Residues16
Detailsbinding site for residue AMZ A 602
ChainResidue
ASER10
AVAL11
ASER12
ALYS14
ASER34
AGLY36
ATHR37
AARG64
ALYS66
ATHR67
ACYS101
AASN102
ATYR104
AASP125
AGLY127
AGLY128

site_idAC3
Number of Residues7
Detailsbinding site for residue MG A 603
ChainResidue
AVAL425
ATHR428
ASER430
ASER432
AASP539
ALEU589
AHIS591

site_idAC4
Number of Residues16
Detailsbinding site for residue 8US B 601
ChainResidue
AASN431
ASER450
AARG451
AILE452
APRO543
APHE544
AASP546
AASN547
AAMZ601
BLYS266
BMET312
BSER313
BPHE315
BGLY316
BASP339
BASN489

site_idAC5
Number of Residues16
Detailsbinding site for residue 8US B 602
ChainResidue
ALYS266
AMET312
ASER313
APHE315
AGLY316
AASP339
AASN489
BASN431
BSER450
BARG451
BILE452
BPRO543
BPHE544
BASP546
BASN547
BAMZ603

site_idAC6
Number of Residues18
Detailsbinding site for residue AMZ B 603
ChainResidue
AARG207
ATYR208
AILE238
ALYS266
AHIS267
AGLY316
AASP339
BASN431
BARG451
BALA540
BPHE541
BARG588
BPHE590
B8US602
BHOH714
BHOH739
BHOH740
BHOH775

site_idAC7
Number of Residues7
Detailsbinding site for residue MG B 604
ChainResidue
BVAL425
BTHR428
BSER430
BSER432
BASP539
BLEU589
BHIS591

site_idAC8
Number of Residues17
Detailsbinding site for residue AMZ C 601
ChainResidue
CALA540
CPHE541
CARG588
CPHE590
CHOH716
CHOH734
CHOH741
CHOH777
DARG207
DTYR208
DLYS266
DHIS267
DGLY316
DASP339
D8US601
CASN431
CARG451

site_idAC9
Number of Residues16
Detailsbinding site for residue AMZ C 602
ChainResidue
CSER10
CVAL11
CSER12
CLYS14
CSER34
CGLY36
CTHR37
CARG64
CLYS66
CTHR67
CCYS101
CASN102
CTYR104
CASP125
CGLY127
CGLY128

site_idAD1
Number of Residues6
Detailsbinding site for residue MG C 603
ChainResidue
CVAL425
CTHR428
CSER430
CSER432
CASP539
CLEU589

site_idAD2
Number of Residues16
Detailsbinding site for residue 8US D 601
ChainResidue
CASN431
CSER450
CARG451
CILE452
CPRO543
CPHE544
CASP546
CASN547
CAMZ601
DLYS266
DMET312
DSER313
DPHE315
DGLY316
DASP339
DASN489

site_idAD3
Number of Residues15
Detailsbinding site for residue 8US D 602
ChainResidue
CLYS266
CMET312
CSER313
CPHE315
CASP339
CASN489
DASN431
DSER450
DARG451
DILE452
DPRO543
DPHE544
DASP546
DASN547
DAMZ603

site_idAD4
Number of Residues18
Detailsbinding site for residue AMZ D 603
ChainResidue
CARG207
CTYR208
CILE238
CLYS266
CHIS267
CGLY316
CASP339
DASN431
DARG451
DALA540
DPHE541
DARG588
DPHE590
D8US602
DHOH705
DHOH716
DHOH727
DHOH754

site_idAD5
Number of Residues17
Detailsbinding site for residue AMZ D 604
ChainResidue
DSER10
DVAL11
DSER12
DLYS14
DSER34
DGLY36
DTHR37
DARG64
DVAL65
DLYS66
DTHR67
DCYS101
DASN102
DTYR104
DASP125
DGLY127
DGLY128

site_idAD6
Number of Residues7
Detailsbinding site for residue MG D 605
ChainResidue
DVAL425
DTHR428
DSER430
DSER432
DASP539
DLEU589
DHIS591

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor/acceptor; for FAICAR cyclization activity => ECO:0000305|PubMed:14756553
ChainResidueDetails
ALYS137
BLYS137
CLYS137
DLYS137

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton acceptor; for AICAR formyltransferase activity => ECO:0000305|PubMed:14966129
ChainResidueDetails
AHIS267
BHIS267
CHIS267
DHIS267

site_idSWS_FT_FI3
Number of Residues20
DetailsBINDING: BINDING => ECO:0000305|PubMed:14756553, ECO:0000305|PubMed:14966129, ECO:0007744|PDB:1P4R, ECO:0007744|PDB:1PKX, ECO:0007744|PDB:1PL0
ChainResidueDetails
ASER12
BASP125
CSER12
CSER34
CARG64
CCYS101
CASP125
DSER12
DSER34
DARG64
DCYS101
ASER34
DASP125
AARG64
ACYS101
AASP125
BSER12
BSER34
BARG64
BCYS101

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: in other chain => ECO:0000269|PubMed:14966129, ECO:0007744|PDB:1P4R, ECO:0007744|PDB:1PL0
ChainResidueDetails
AARG207
BARG207
CARG207
DARG207

site_idSWS_FT_FI5
Number of Residues12
DetailsBINDING: in other chain => ECO:0000269|PubMed:14966129, ECO:0000269|PubMed:29072452, ECO:0007744|PDB:1P4R, ECO:0007744|PDB:1PL0
ChainResidueDetails
AHIS267
DHIS267
DGLY316
DASP339
AGLY316
AASP339
BHIS267
BGLY316
BASP339
CHIS267
CGLY316
CASP339

site_idSWS_FT_FI6
Number of Residues16
DetailsBINDING: BINDING => ECO:0000269|PubMed:14966129, ECO:0000269|PubMed:29072452, ECO:0007744|PDB:1P4R, ECO:0007744|PDB:1PL0
ChainResidueDetails
AASN431
CARG451
CPHE541
CARG588
DASN431
DARG451
DPHE541
DARG588
AARG451
APHE541
AARG588
BASN431
BARG451
BPHE541
BARG588
CASN431

site_idSWS_FT_FI7
Number of Residues12
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P31335
ChainResidueDetails
AILE452
DILE452
DASP546
DSER565
AASP546
ASER565
BILE452
BASP546
BSER565
CILE452
CASP546
CSER565

site_idSWS_FT_FI8
Number of Residues4
DetailsSITE: Transition state stabilizer => ECO:0000305|PubMed:14966129
ChainResidueDetails
ALYS266
BLYS266
CLYS266
DLYS266

site_idSWS_FT_FI9
Number of Residues4
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS199
BLYS199
CLYS199
DLYS199

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 646
ChainResidueDetails
ALYS266electrostatic stabiliser, proton acceptor, proton donor, proton relay
AHIS267electrostatic stabiliser, proton acceptor, proton donor, proton relay
AASN431electrostatic stabiliser, modifies pKa
AHIS592electrostatic stabiliser, modifies pKa, proton acceptor, proton donor, proton relay

site_idMCSA2
Number of Residues4
DetailsM-CSA 646
ChainResidueDetails
BLYS266electrostatic stabiliser, proton acceptor, proton donor, proton relay
BHIS267electrostatic stabiliser, proton acceptor, proton donor, proton relay
BASN431electrostatic stabiliser, modifies pKa
BHIS592electrostatic stabiliser, modifies pKa, proton acceptor, proton donor, proton relay

site_idMCSA3
Number of Residues4
DetailsM-CSA 646
ChainResidueDetails
CLYS266electrostatic stabiliser, proton acceptor, proton donor, proton relay
CHIS267electrostatic stabiliser, proton acceptor, proton donor, proton relay
CASN431electrostatic stabiliser, modifies pKa
CHIS592electrostatic stabiliser, modifies pKa, proton acceptor, proton donor, proton relay

site_idMCSA4
Number of Residues4
DetailsM-CSA 646
ChainResidueDetails
DLYS266electrostatic stabiliser, proton acceptor, proton donor, proton relay
DHIS267electrostatic stabiliser, proton acceptor, proton donor, proton relay
DASN431electrostatic stabiliser, modifies pKa
DHIS592electrostatic stabiliser, modifies pKa, proton acceptor, proton donor, proton relay

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PDB entries from 2024-07-10

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