Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

1TLS

THYMIDYLATE SYNTHASE TERNARY COMPLEX WITH FDUMP AND METHYLENETETRAHYDROFOLATE

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 UFP A 265
ChainResidue
ACYS168
AASP169
AASN177
AHIS207
ATYR209
AC2F266
AHOH283
BARG126
BARG127
AARG21
ATYR94
ACYS146
AHIS147
AGLN165
AARG166
ASER167

site_idAC2
Number of Residues18
DetailsBINDING SITE FOR RESIDUE C2F A 266
ChainResidue
AHIS51
ASER54
AILE79
ATRP80
ATRP83
ALEU143
AASP169
AGLY173
APHE176
ATYR209
AALA263
AUFP265
AHOH285
AHOH286
AHOH291
AHOH293
AHOH332
AHOH453

site_idAC3
Number of Residues17
DetailsBINDING SITE FOR RESIDUE UFP B 265
ChainResidue
AARG126
AARG127
BARG21
BTRP80
BTYR94
BCYS146
BHIS147
BGLN165
BARG166
BSER167
BCYS168
BASP169
BASN177
BHIS207
BTYR209
BC2F266
BHOH393

site_idAC4
Number of Residues21
DetailsBINDING SITE FOR RESIDUE C2F B 266
ChainResidue
BHIS51
BSER54
BILE79
BTRP80
BTRP83
BLEU143
BASP169
BLEU172
BGLY173
BPHE176
BVAL262
BALA263
BUFP265
BHOH346
BHOH347
BHOH348
BHOH354
BHOH361
BHOH410
BHOH428
BHOH459

site_idS1
Number of Residues1
DetailsCARBOXY MODIFICATION AT N1.
ChainResidue
ACXM1

site_idS2
Number of Residues1
DetailsCARBOXY MODIFICATION AT N1.
ChainResidue
BCXM1

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
BARG21
BARG166
BASN177
BHIS207
AARG21
AARG166
AASN177
AHIS207

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

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

221051

PDB entries from 2024-06-12

PDB statisticsPDBj update infoContact PDBjnumon