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3QGT

Crystal structure of Wild-type PfDHFR-TS COMPLEXED WITH NADPH, dUMP AND PYRIMETHAMINE

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0003824molecular_functioncatalytic activity
A0004146molecular_functiondihydrofolate reductase activity
A0004799molecular_functionthymidylate synthase activity
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006231biological_processdTMP biosynthetic process
A0006730biological_processone-carbon metabolic process
A0008168molecular_functionmethyltransferase activity
A0009165biological_processnucleotide biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0016740molecular_functiontransferase activity
A0016741molecular_functiontransferase activity, transferring one-carbon groups
A0032259biological_processmethylation
A0046654biological_processtetrahydrofolate biosynthetic process
B0000166molecular_functionnucleotide binding
B0003824molecular_functioncatalytic activity
B0004146molecular_functiondihydrofolate reductase activity
B0004799molecular_functionthymidylate synthase activity
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006231biological_processdTMP biosynthetic process
B0006730biological_processone-carbon metabolic process
B0008168molecular_functionmethyltransferase activity
B0009165biological_processnucleotide biosynthetic process
B0016491molecular_functionoxidoreductase activity
B0016740molecular_functiontransferase activity
B0016741molecular_functiontransferase activity, transferring one-carbon groups
B0032259biological_processmethylation
B0046654biological_processtetrahydrofolate biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues12
DetailsBINDING SITE FOR RESIDUE CP6 A 609
ChainResidue
AILE14
ATHR185
ANDP610
AHOH1103
ACYS15
AASP54
APHE58
ASER108
ASER111
AILE112
AILE164
ATYR170

site_idAC2
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NDP A 610
ChainResidue
ACYS15
AALA16
ALEU40
AGLY41
AGLY44
AVAL45
ALEU46
AGLY105
AARG106
ATHR107
ASER108
ALEU127
ASER128
AARG129
ATHR130
AASN144
AILE164
AGLY165
AGLY166
ASER167
AVAL168
AVAL169
ATYR170
AGLU172
ACP6609
AHOH1105
AHOH1131
AHOH1133
AHOH1277

site_idAC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UMP A 611
ChainResidue
ACYS490
AHIS491
AGLN509
AARG510
ASER511
AASP513
AGLY517
AASN521
AHIS551
ATYR553
AHOH1303
BARG470
BARG471

site_idAC4
Number of Residues12
DetailsBINDING SITE FOR RESIDUE CP6 B 609
ChainResidue
BILE14
BCYS15
BALA16
BASP54
BPHE58
BSER108
BSER111
BILE112
BILE164
BTYR170
BTHR185
BNDP610

site_idAC5
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NDP B 610
ChainResidue
BCYS15
BALA16
BLEU40
BGLY44
BVAL45
BTRP48
BARG106
BTHR107
BSER108
BLYS115
BLEU127
BSER128
BARG129
BTHR130
BASN144
BLYS145
BILE164
BGLY165
BGLY166
BSER167
BVAL168
BVAL169
BTYR170
BGLU172
BCP6609
BHOH1096

site_idAC6
Number of Residues13
DetailsBINDING SITE FOR RESIDUE UMP B 611
ChainResidue
BASP513
BGLY517
BASN521
BHIS551
BTYR553
BHOH1216
AARG470
AARG471
BCYS490
BHIS491
BGLN509
BARG510
BSER511

Functional Information from PROSITE/UniProt
site_idPS00075
Number of Residues24
DetailsDHFR_1 Dihydrofolate reductase (DHFR) domain signature. GLGnkgvLPWkcnslDmkyFcavT
ChainResidueDetails
AGLY39-THR62

site_idPS00091
Number of Residues29
DetailsTHYMIDYLATE_SYNTHASE Thymidylate synthase active site. RriLlcaWNvkdldqma.....LpPCHilcQFyV
ChainResidueDetails
AARG470-VAL498

238268

PDB entries from 2025-07-02

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