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3JSU

Quadruple mutant(N51I+C59R+S108N+I164L) plasmodium falciparum dihydrofolate reductase-thymidylate synthase(PFDHFR-TS) complexed with QN254, NADPH, and dUMP

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0004146molecular_functiondihydrofolate reductase activity
A0004799molecular_functionthymidylate synthase activity
A0006231biological_processdTMP biosynthetic process
A0006730biological_processone-carbon metabolic process
A0008168molecular_functionmethyltransferase activity
A0009165biological_processnucleotide biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0016741molecular_functiontransferase activity, transferring one-carbon groups
A0032259biological_processmethylation
A0046654biological_processtetrahydrofolate biosynthetic process
B0000166molecular_functionnucleotide binding
B0004146molecular_functiondihydrofolate reductase activity
B0004799molecular_functionthymidylate synthase activity
B0006231biological_processdTMP biosynthetic process
B0006730biological_processone-carbon metabolic process
B0008168molecular_functionmethyltransferase activity
B0009165biological_processnucleotide biosynthetic process
B0016491molecular_functionoxidoreductase activity
B0016741molecular_functiontransferase activity, transferring one-carbon groups
B0032259biological_processmethylation
B0046654biological_processtetrahydrofolate biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues14
DetailsBINDING SITE FOR RESIDUE KA5 A 609
ChainResidue
AILE14
ALEU119
ALEU164
ATYR170
ATHR185
ANDP610
ACYS15
AALA16
ALEU46
AASP54
AMET55
APHE58
ASER111
APHE116

site_idAC2
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NDP A 610
ChainResidue
ACYS15
AALA16
ALEU40
AGLY44
AVAL45
ALEU46
AGLY105
AARG106
ATHR107
AASN108
ALEU127
ASER128
AARG129
ATHR130
AASN144
AVAL146
ALEU164
AGLY166
ASER167
AVAL168
AVAL169
AGLU172
AKA5609
AHOH1089
AHOH1103
AHOH1182

site_idAC3
Number of Residues14
DetailsBINDING SITE FOR RESIDUE UMP A 611
ChainResidue
AARG345
ACYS490
AHIS491
AGLN509
AARG510
ASER511
AASP513
AGLY517
AASN521
AHIS551
ATYR553
AHOH1019
BARG470
BARG471

site_idAC4
Number of Residues13
DetailsBINDING SITE FOR RESIDUE KA5 B 609
ChainResidue
BILE14
BCYS15
BASP54
BMET55
BPHE58
BASN108
BSER111
BILE112
BPHE116
BLEU119
BLEU164
BTYR170
BNDP610

site_idAC5
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NDP B 610
ChainResidue
BCYS15
BALA16
BLEU40
BGLY44
BVAL45
BGLY105
BARG106
BTHR107
BASN108
BLEU127
BSER128
BARG129
BTHR130
BASN144
BLYS145
BVAL146
BLEU164
BGLY165
BGLY166
BSER167
BVAL168
BVAL169
BTYR170
BGLU172
BVAL195
BKA5609

site_idAC6
Number of Residues14
DetailsBINDING SITE FOR RESIDUE UMP B 611
ChainResidue
BARG510
BSER511
BASP513
BGLY517
BASN521
BHIS551
BTYR553
BHOH1087
AARG470
AARG471
BARG345
BCYS490
BHIS491
BGLN509

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

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

223166

PDB entries from 2024-07-31

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