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

4GTD

T. Maritima FDTS (E144R mutant) with FAD and dUMP

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
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
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
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
D0032259biological_processmethylation
D0050660molecular_functionflavin adenine dinucleotide binding
D0050797molecular_functionthymidylate synthase (FAD) activity
D0070402molecular_functionNADPH binding
Functional Information from PDB Data
site_idAC1
Number of Residues11
DetailsBINDING SITE FOR RESIDUE UMP A 301
ChainResidue
AGLU86
DARG174
DFAD301
ASER88
AARG144
AARG147
AHOH416
AHOH437
AHOH499
DGLN75
DARG78

site_idAC2
Number of Residues27
DetailsBINDING SITE FOR RESIDUE FAD A 302
ChainResidue
AARG78
AHIS79
AARG80
AILE81
AASN169
ALEU173
AARG174
AHIS178
AHOH413
AHOH415
AHOH469
AHOH484
AHOH485
AHOH497
AHOH500
CTHR55
CGLU58
CILE81
CASN163
CARG165
CASN169
CFAD301
CHOH402
DSER83
DASN85
DGLU86
DUMP302

site_idAC3
Number of Residues12
DetailsBINDING SITE FOR RESIDUE UMP B 301
ChainResidue
BGLU86
BSER88
BARG144
BARG147
BHOH408
BHOH411
BHOH455
BHOH464
CGLN75
CARG78
CARG174
CFAD301

site_idAC4
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FAD B 302
ChainResidue
BARG78
BHIS79
BARG80
BILE81
BASN169
BLEU173
BARG174
BHIS178
BHOH418
BHOH427
BHOH434
BHOH474
CASN85
CGLU86
CSER88
CUMP302
DTHR55
DGLU58
DILE81
DASN163
DARG165
DFAD301
DHOH430

site_idAC5
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FAD C 301
ChainResidue
ATHR55
AGLU58
AILE81
AASN163
AARG165
AFAD302
BSER83
BASN85
BGLU86
BSER88
BUMP301
CARG78
CHIS79
CARG80
CILE81
CASN169
CLEU173
CARG174
CHIS178
CHOH404
CHOH406
CHOH420
CHOH447

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE UMP C 302
ChainResidue
BFAD302
CGLU86
CSER88
CARG144
CARG147
CHOH411
CHOH417
CHOH449
BGLN75
BARG78
BARG174

site_idAC7
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FAD D 301
ChainResidue
AASN85
AGLU86
ASER88
AUMP301
BTHR55
BGLU58
BILE81
BASN163
BARG165
BFAD302
BHOH475
DARG78
DHIS79
DARG80
DILE81
DASN169
DLEU173
DHIS178
DHOH407
DHOH410
DHOH424
DHOH458
DHOH459

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE UMP D 302
ChainResidue
AGLN75
AARG78
AARG174
AFAD302
AHOH407
DGLU86
DARG147
DHOH423
DHOH433

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

226262

PDB entries from 2024-10-16

PDB statisticsPDBj update infoContact PDBjnumon