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1AXW

E. COLI THYMIDYLATE SYNTHASE IN COMPLEX WITH METHOTREXATE (MTX) AND 2'-DEOXYURIDINE 5'-MONOPHOSPHATE (DUMP)

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0003723molecular_functionRNA binding
A0004799molecular_functionthymidylate synthase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006231biological_processdTMP biosynthetic process
A0006235biological_processdTTP biosynthetic process
A0006417biological_processregulation of translation
A0008168molecular_functionmethyltransferase activity
A0009165biological_processnucleotide biosynthetic process
A0009314biological_processresponse to radiation
A0016741molecular_functiontransferase activity, transferring one-carbon groups
A0032259biological_processmethylation
A0042803molecular_functionprotein homodimerization activity
B0000287molecular_functionmagnesium ion binding
B0003723molecular_functionRNA binding
B0004799molecular_functionthymidylate synthase activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006231biological_processdTMP biosynthetic process
B0006235biological_processdTTP biosynthetic process
B0006417biological_processregulation of translation
B0008168molecular_functionmethyltransferase activity
B0009165biological_processnucleotide biosynthetic process
B0009314biological_processresponse to radiation
B0016741molecular_functiontransferase activity, transferring one-carbon groups
B0032259biological_processmethylation
B0042803molecular_functionprotein homodimerization activity
Functional Information from PDB Data
site_idAC1
Number of Residues16
DetailsBINDING SITE FOR RESIDUE UMP A 603
ChainResidue
AASP169
AASN177
AHIS207
ATYR209
AMTX732
AHOH786
AHOH815
BARG126
BARG127
AARG21
ACYS146
AHIS147
AGLN165
AARG166
ASER167
ACYS168

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE MTX A 732
ChainResidue
ALYS48
AHIS51
AILE79
ATRP83
ALEU143
AASP169
ALEU172
AGLY173
APHE176
ATYR209
AVAL262
AALA263
AUMP603

site_idAC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE UMP B 604
ChainResidue
AARG126
AARG127
BARG21
BCYS146
BHIS147
BGLN165
BARG166
BSER167
BCYS168
BASP169
BASN177
BHIS207
BTYR209
BMTX733
BHOH738

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE MTX B 733
ChainResidue
BLYS48
BHIS51
BTRP83
BASP169
BPHE171
BLEU172
BGLY173
BTYR209
BILE258
BALA263
BUMP604

site_idCAA
Number of Residues1
DetailsCATALYTIC CYSTEINE.
ChainResidue
ACYS146

site_idCAB
Number of Residues1
DetailsCATALYTIC CYSTEINE.
ChainResidue
BCYS146

Functional Information from PROSITE/UniProt
site_idPS00091
Number of Residues29
DetailsTHYMIDYLATE_SYNTHASE Thymidylate synthase active site. RriIvsaWNvgeldkma.....LaPCHaffQFyV
ChainResidueDetails
AARG126-VAL154

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000255|HAMAP-Rule:MF_00008, ECO:0000269|PubMed:2223754, ECO:0000269|PubMed:8973201, ECO:0000269|PubMed:9416600
ChainResidueDetails
ACYS146
BCYS146

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: in other chain => ECO:0000269|PubMed:2223754, ECO:0000269|PubMed:8973201, ECO:0007744|PDB:1KCE, ECO:0007744|PDB:2TSC
ChainResidueDetails
AARG21
AARG166
AASN177
AHIS207
BARG21
BARG166
BASN177
BHIS207

site_idSWS_FT_FI3
Number of Residues6
DetailsBINDING: BINDING => ECO:0000305|PubMed:8312270, ECO:0007744|PDB:1TYS
ChainResidueDetails
AHIS51
AASP169
AALA263
BHIS51
BASP169
BALA263

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:2223754, ECO:0000269|PubMed:8973201, ECO:0007744|PDB:1KCE, ECO:0007744|PDB:2TSC
ChainResidueDetails
AARG126
BARG126

Catalytic Information from CSA
site_idCSA1
Number of Residues6
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
AHIS207
AGLU58
AASP169
ASER167
ACYS146
AASP205

site_idCSA2
Number of Residues6
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
BHIS207
BGLU58
BASP169
BSER167
BCYS146
BASP205

site_idCSA3
Number of Residues3
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
ASER180
AASN177
ACYS146

site_idCSA4
Number of Residues3
DetailsAnnotated By Reference To The Literature 1b02
ChainResidueDetails
BSER180
BASN177
BCYS146

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PDB entries from 2024-11-06

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