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1O2A

Crystal structure of Thymidylate Synthase Complementing Protein (TM0449) from Thermotoga maritima with FAD at 1.8 A resolution

Functional Information from GO Data
ChainGOidnamespacecontents
A0004799molecular_functionthymidylate synthase activity
A0006231biological_processdTMP biosynthetic process
A0006235biological_processdTTP biosynthetic process
A0008168molecular_functionmethyltransferase activity
A0009165biological_processnucleotide biosynthetic process
A0016740molecular_functiontransferase activity
A0032259biological_processmethylation
A0050660molecular_functionflavin adenine dinucleotide binding
A0050797molecular_functionthymidylate synthase (FAD) activity
A0070402molecular_functionNADPH binding
B0004799molecular_functionthymidylate synthase activity
B0006231biological_processdTMP biosynthetic process
B0006235biological_processdTTP biosynthetic process
B0008168molecular_functionmethyltransferase activity
B0009165biological_processnucleotide biosynthetic process
B0016740molecular_functiontransferase activity
B0032259biological_processmethylation
B0050660molecular_functionflavin adenine dinucleotide binding
B0050797molecular_functionthymidylate synthase (FAD) activity
B0070402molecular_functionNADPH binding
C0004799molecular_functionthymidylate synthase activity
C0006231biological_processdTMP biosynthetic process
C0006235biological_processdTTP biosynthetic process
C0008168molecular_functionmethyltransferase activity
C0009165biological_processnucleotide biosynthetic process
C0016740molecular_functiontransferase activity
C0032259biological_processmethylation
C0050660molecular_functionflavin adenine dinucleotide binding
C0050797molecular_functionthymidylate synthase (FAD) activity
C0070402molecular_functionNADPH binding
D0004799molecular_functionthymidylate synthase activity
D0006231biological_processdTMP biosynthetic process
D0006235biological_processdTTP biosynthetic process
D0008168molecular_functionmethyltransferase activity
D0009165biological_processnucleotide biosynthetic process
D0016740molecular_functiontransferase activity
D0032259biological_processmethylation
D0050660molecular_functionflavin adenine dinucleotide binding
D0050797molecular_functionthymidylate synthase (FAD) activity
D0070402molecular_functionNADPH binding
Functional Information from PDB Data
site_idAC1
Number of Residues25
DetailsBINDING SITE FOR RESIDUE FAD D 700
ChainResidue
ASER83
BASN163
BARG165
BHOH567
BFAD710
DARG78
DHIS79
DARG80
DILE81
DASN169
DLEU173
AASN85
DARG174
DHIS178
DHOH339
DHOH455
DHOH498
DHOH589
AGLU86
ASER88
AARG90
AHOH341
BTHR55
BGLU58
BILE81

site_idAC2
Number of Residues19
DetailsBINDING SITE FOR RESIDUE FAD C 705
ChainResidue
AGLU58
AILE81
AASN163
AARG165
AFAD715
BSER83
BASN85
BGLU86
CARG78
CHIS79
CARG80
CILE81
CASN169
CLEU173
CARG174
CHIS178
CHOH320
CHOH334
CHOH354

site_idAC3
Number of Residues22
DetailsBINDING SITE FOR RESIDUE FAD B 710
ChainResidue
BARG78
BHIS79
BARG80
BILE81
BASN169
BLEU173
BARG174
BHIS178
BHOH317
BHOH342
CSER83
CASN85
CGLU86
CSER88
CARG90
DTHR55
DGLU58
DILE81
DASN163
DARG165
DHOH545
DFAD700

site_idAC4
Number of Residues24
DetailsBINDING SITE FOR RESIDUE FAD A 715
ChainResidue
AARG78
AHIS79
AARG80
AILE81
AASN169
ALEU173
AARG174
AHIS178
AHOH311
AHOH312
AHOH459
AHOH595
AHOH600
CTHR55
CGLU58
CILE81
CASN163
CARG165
CFAD705
DSER83
DASN85
DGLU86
DSER88
DARG90

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Involved in ionization of N3 of dUMP, leading to its activation => ECO:0000269|PubMed:27214228
ChainResidueDetails
AARG174
BARG174
CARG174
DARG174

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12791256, ECO:0000269|PubMed:19370033, ECO:0000269|PubMed:22477781, ECO:0000269|PubMed:23019356, ECO:0000269|PubMed:24563811, ECO:0000269|PubMed:27214228, ECO:0000269|PubMed:34315871, ECO:0007744|PDB:1O26, ECO:0007744|PDB:3G4A, ECO:0007744|PDB:3N0B, ECO:0007744|PDB:4GTD, ECO:0007744|PDB:4KAS, ECO:0007744|PDB:7NDW
ChainResidueDetails
ATHR55
BTHR55
CTHR55
DTHR55

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:12791256, ECO:0000269|PubMed:19370033, ECO:0000269|PubMed:22477781, ECO:0000269|PubMed:23019356, ECO:0000269|PubMed:24563811, ECO:0000269|PubMed:27214228, ECO:0007744|PDB:1O26, ECO:0007744|PDB:3G4A, ECO:0007744|PDB:3N0B, ECO:0007744|PDB:4GT9, ECO:0007744|PDB:4KAS
ChainResidueDetails
AGLN75
AARG174
BGLN75
BARG174
CGLN75
CARG174
DGLN75
DARG174

site_idSWS_FT_FI4
Number of Residues16
DetailsBINDING: BINDING => ECO:0000269|PubMed:12211025, ECO:0000269|PubMed:12791256, ECO:0000269|PubMed:19370033, ECO:0000269|PubMed:22477781, ECO:0000269|PubMed:23019356, ECO:0000269|PubMed:24563811, ECO:0000269|PubMed:27214228, ECO:0000269|PubMed:34315871, ECO:0007744|PDB:1KQ4, ECO:0007744|PDB:1O26, ECO:0007744|PDB:3G4A, ECO:0007744|PDB:3N0B, ECO:0007744|PDB:4GTD, ECO:0007744|PDB:4KAS, ECO:0007744|PDB:7NDW
ChainResidueDetails
AARG78
CGLU86
CASN163
CASN169
DARG78
DGLU86
DASN163
DASN169
AGLU86
AASN163
AASN169
BARG78
BGLU86
BASN163
BASN169
CARG78

site_idSWS_FT_FI5
Number of Residues4
DetailsBINDING: in other chain => ECO:0000269|PubMed:12791256, ECO:0000269|PubMed:19370033, ECO:0000269|PubMed:22477781, ECO:0000269|PubMed:23019356, ECO:0000269|PubMed:24563811, ECO:0000269|PubMed:27214228, ECO:0007744|PDB:1O26, ECO:0007744|PDB:3G4A, ECO:0007744|PDB:3N0B, ECO:0007744|PDB:4GT9, ECO:0007744|PDB:4KAS
ChainResidueDetails
AARG147
BARG147
CARG147
DARG147

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PDB entries from 2025-06-18

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