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1JUJ

Human Thymidylate Synthase Bound to dUMP and LY231514, a Pyrrolo(2,3-d)pyrimidine-based Antifolate

Functional Information from GO Data
ChainGOidnamespacecontents
A0000900molecular_functionmRNA regulatory element binding translation repressor activity
A0004799molecular_functionthymidylate synthase activity
A0005515molecular_functionprotein binding
A0005542molecular_functionfolic acid binding
A0005634cellular_componentnucleus
A0005657cellular_componentreplication fork
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005743cellular_componentmitochondrial inner membrane
A0005759cellular_componentmitochondrial matrix
A0005829cellular_componentcytosol
A0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
A0006231biological_processdTMP biosynthetic process
A0006235biological_processdTTP biosynthetic process
A0006260biological_processDNA replication
A0016741molecular_functiontransferase activity, transferring one-carbon groups
A0017148biological_processnegative regulation of translation
A0035999biological_processtetrahydrofolate interconversion
A0071897biological_processDNA biosynthetic process
A1990825molecular_functionsequence-specific mRNA binding
B0000900molecular_functionmRNA regulatory element binding translation repressor activity
B0004799molecular_functionthymidylate synthase activity
B0005515molecular_functionprotein binding
B0005542molecular_functionfolic acid binding
B0005634cellular_componentnucleus
B0005657cellular_componentreplication fork
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005743cellular_componentmitochondrial inner membrane
B0005759cellular_componentmitochondrial matrix
B0005829cellular_componentcytosol
B0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
B0006231biological_processdTMP biosynthetic process
B0006235biological_processdTTP biosynthetic process
B0006260biological_processDNA replication
B0016741molecular_functiontransferase activity, transferring one-carbon groups
B0017148biological_processnegative regulation of translation
B0035999biological_processtetrahydrofolate interconversion
B0071897biological_processDNA biosynthetic process
B1990825molecular_functionsequence-specific mRNA binding
C0000900molecular_functionmRNA regulatory element binding translation repressor activity
C0004799molecular_functionthymidylate synthase activity
C0005515molecular_functionprotein binding
C0005542molecular_functionfolic acid binding
C0005634cellular_componentnucleus
C0005657cellular_componentreplication fork
C0005737cellular_componentcytoplasm
C0005739cellular_componentmitochondrion
C0005743cellular_componentmitochondrial inner membrane
C0005759cellular_componentmitochondrial matrix
C0005829cellular_componentcytosol
C0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
C0006231biological_processdTMP biosynthetic process
C0006235biological_processdTTP biosynthetic process
C0006260biological_processDNA replication
C0016741molecular_functiontransferase activity, transferring one-carbon groups
C0017148biological_processnegative regulation of translation
C0035999biological_processtetrahydrofolate interconversion
C0071897biological_processDNA biosynthetic process
C1990825molecular_functionsequence-specific mRNA binding
D0000900molecular_functionmRNA regulatory element binding translation repressor activity
D0004799molecular_functionthymidylate synthase activity
D0005515molecular_functionprotein binding
D0005542molecular_functionfolic acid binding
D0005634cellular_componentnucleus
D0005657cellular_componentreplication fork
D0005737cellular_componentcytoplasm
D0005739cellular_componentmitochondrion
D0005743cellular_componentmitochondrial inner membrane
D0005759cellular_componentmitochondrial matrix
D0005829cellular_componentcytosol
D0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
D0006231biological_processdTMP biosynthetic process
D0006235biological_processdTTP biosynthetic process
D0006260biological_processDNA replication
D0016741molecular_functiontransferase activity, transferring one-carbon groups
D0017148biological_processnegative regulation of translation
D0035999biological_processtetrahydrofolate interconversion
D0071897biological_processDNA biosynthetic process
D1990825molecular_functionsequence-specific mRNA binding
Functional Information from PDB Data
site_idAC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UMP A 314
ChainResidue
AARG50
ATYR258
ALYA315
BARG175
BARG176
ACYS195
AHIS196
AGLN214
AARG215
ASER216
AASP218
AASN226
AHIS256

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE LYA A 315
ChainResidue
ALYS77
APHE80
AASN112
AASP218
AGLY222
ATYR258
AILE307
AALA312
AUMP314

site_idAC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UMP B 314
ChainResidue
AARG175
AARG176
BARG50
BCYS195
BHIS196
BGLN214
BARG215
BSER216
BASP218
BASN226
BHIS256
BTYR258
BLYA315

site_idAC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE LYA B 315
ChainResidue
BLYS77
BPHE80
BASN112
BASP218
BGLY222
BTYR258
BILE307
BALA312
BUMP314

site_idAC5
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UMP C 314
ChainResidue
CARG50
CCYS195
CHIS196
CGLN214
CARG215
CSER216
CASP218
CASN226
CHIS256
CTYR258
CLYA315
DARG175
DARG176

site_idAC6
Number of Residues9
DetailsBINDING SITE FOR RESIDUE LYA C 315
ChainResidue
CLYS77
CPHE80
CASN112
CASP218
CGLY222
CTYR258
CILE307
CALA312
CUMP314

site_idAC7
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UMP D 314
ChainResidue
CARG175
CARG176
DARG50
DCYS195
DHIS196
DGLN214
DARG215
DSER216
DASP218
DASN226
DHIS256
DTYR258
DLYA315

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE LYA D 315
ChainResidue
DLYS77
DPHE80
DASN112
DASP218
DGLY222
DTYR258
DILE307
DALA312
DUMP314

Functional Information from PROSITE/UniProt
site_idPS00091
Number of Residues29
DetailsTHYMIDYLATE_SYNTHASE Thymidylate synthase active site. RriImcaWNprdlplma.....LpPCHalcQFyV
ChainResidueDetails
AARG175-VAL203

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsActive site: {"description":"Nucleophile","evidences":[{"source":"UniProtKB","id":"P0A884","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues8
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"UniProtKB","id":"P0A884","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"UniProtKB","id":"P45352","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues24
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"UniProtKB","id":"P45352","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues8
DetailsBinding site: {"evidences":[{"source":"UniProtKB","id":"P0A884","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues4
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"19690332","evidenceCode":"ECO:0007744"},{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues16
DetailsCross-link: {"description":"Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2)","evidences":[{"source":"PubMed","id":"28112733","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues6
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
AASP254
ASER216
ACYS195
AASP218
AGLU87
AHIS256

site_idCSA2
Number of Residues6
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
BASP254
BSER216
BCYS195
BASP218
BGLU87
BHIS256

site_idCSA3
Number of Residues6
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
CASP254
CSER216
CCYS195
CASP218
CGLU87
CHIS256

site_idCSA4
Number of Residues6
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
DASP254
DSER216
DCYS195
DASP218
DGLU87
DHIS256

site_idCSA5
Number of Residues3
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
AASN226
ASER229
ACYS195

site_idCSA6
Number of Residues3
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
BASN226
BSER229
BCYS195

site_idCSA7
Number of Residues3
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
CASN226
CSER229
CCYS195

site_idCSA8
Number of Residues3
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
DASN226
DSER229
DCYS195

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PDB entries from 2026-04-01

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