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1PL0

Crystal structure of human ATIC in complex with folate-based inhibitor, BW2315U89UC

Functional Information from GO Data
ChainGOidnamespacecontents
A0003360biological_processbrainstem development
A0003824molecular_functioncatalytic activity
A0003937molecular_functionIMP cyclohydrolase activity
A0004643molecular_functionphosphoribosylaminoimidazolecarboxamide formyltransferase activity
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
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
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
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
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
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
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
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 Residues7
DetailsBINDING SITE FOR RESIDUE K A 1001
ChainResidue
AVAL425
ATHR428
ASER430
ASER432
AASP539
ALEU589
AHIS591

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE K B 1002
ChainResidue
BSER430
BSER432
BASP539
BLEU589
BHIS591
BVAL425
BTHR428

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE K C 1003
ChainResidue
CVAL425
CTHR428
CSER430
CSER432
CASP539
CLEU589
CHIS591

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE K D 1004
ChainResidue
DVAL425
DTHR428
DSER430
DSER432
DASP539
DLEU589
DHIS591

site_idAC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE AMZ B 702
ChainResidue
AARG207
ATYR208
AHIS267
AGLY316
AASP339
BASN431
BARG451
BALA540
BPHE541
BARG588
BPHE590
BBW2802
BHOH1004
BHOH1048

site_idAC6
Number of Residues16
DetailsBINDING SITE FOR RESIDUE AMZ D 703
ChainResidue
CASN431
CARG451
CALA540
CPHE541
CARG588
CPHE590
DARG207
DTYR208
DLYS266
DHIS267
DGLY316
DASP339
DHOH1021
DHOH1024
DHOH1041
DHOH1044

site_idAC7
Number of Residues15
DetailsBINDING SITE FOR RESIDUE AMZ D 704
ChainResidue
CARG207
CTYR208
CLYS266
CHIS267
CGLY316
CASP339
CHOH1029
DASN431
DARG451
DALA540
DPHE541
DARG588
DPHE590
DBW2804
DHOH1019

site_idAC8
Number of Residues14
DetailsBINDING SITE FOR RESIDUE BW2 B 802
ChainResidue
ALYS266
AMET312
APHE315
AASN489
BASN431
BGLN449
BARG451
BILE452
BPHE541
BPRO543
BPHE544
BASN547
BAMZ702
BHOH1079

site_idAC9
Number of Residues16
DetailsBINDING SITE FOR RESIDUE BW2 D 804
ChainResidue
DASP546
DASN547
DAMZ704
DHOH1071
CLYS266
CMET312
CPHE315
CASN489
DASN431
DGLN449
DSER450
DARG451
DILE452
DPHE541
DPRO543
DPHE544

site_idBC1
Number of Residues19
DetailsBINDING SITE FOR RESIDUE XMP A 901
ChainResidue
ASER10
AVAL11
ASER12
ALYS14
ASER34
AGLY36
ATHR37
AARG64
ALYS66
ATHR67
ALEU68
ACYS101
AASN102
ALEU103
ATYR104
AASP125
AILE126
AGLY127
AGLY128

site_idBC2
Number of Residues22
DetailsBINDING SITE FOR RESIDUE XMP C 903
ChainResidue
CSER10
CVAL11
CSER12
CLYS14
CSER34
CGLY35
CGLY36
CTHR37
CGLY63
CARG64
CLYS66
CTHR67
CLEU68
CCYS101
CASN102
CLEU103
CTYR104
CASP125
CILE126
CGLY127
CGLY128
CHOH1014

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues393
DetailsRegion: {"description":"AICAR formyltransferase","evidences":[{"source":"UniProtKB","id":"P31335","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues4
DetailsActive site: {"description":"Proton donor/acceptor; for FAICAR cyclization activity","evidences":[{"source":"PubMed","id":"14756553","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsActive site: {"description":"Proton acceptor; for AICAR formyltransferase activity","evidences":[{"source":"PubMed","id":"14966129","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues40
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"14756553","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"14966129","evidenceCode":"ECO:0000305"},{"source":"PDB","id":"1P4R","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1PKX","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1PL0","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues4
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"PubMed","id":"14966129","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1P4R","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1PL0","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues12
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"PubMed","id":"14966129","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"29072452","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1P4R","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1PL0","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues16
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"14966129","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"29072452","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1P4R","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1PL0","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues12
DetailsBinding site: {"evidences":[{"source":"UniProtKB","id":"P31335","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues4
DetailsSite: {"description":"Transition state stabilizer","evidences":[{"source":"PubMed","id":"14966129","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI10
Number of Residues4
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"19608861","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1p4r
ChainResidueDetails
AASN431
ALYS266
AHIS592
AHIS267

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1p4r
ChainResidueDetails
BASN431
BLYS266
BHIS592
BHIS267

site_idCSA3
Number of Residues4
DetailsAnnotated By Reference To The Literature 1p4r
ChainResidueDetails
CASN431
CLYS266
CHIS592
CHIS267

site_idCSA4
Number of Residues4
DetailsAnnotated By Reference To The Literature 1p4r
ChainResidueDetails
DASN431
DLYS266
DHIS592
DHIS267

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 2025-10-29

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