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6JWX

Crystal structure of Plasmodium falciparum HPPK-DHPS wild type with SDX-DHP

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0003824molecular_functioncatalytic activity
A0003848molecular_function2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
A0004156molecular_functiondihydropteroate synthase activity
A0005524molecular_functionATP binding
A0005740cellular_componentmitochondrial envelope
A0009396biological_processfolic acid-containing compound biosynthetic process
A0016301molecular_functionkinase activity
A0016740molecular_functiontransferase activity
A0042558biological_processpteridine-containing compound metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0046656biological_processfolic acid biosynthetic process
A0046872molecular_functionmetal ion binding
B0000166molecular_functionnucleotide binding
B0003824molecular_functioncatalytic activity
B0003848molecular_function2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
B0004156molecular_functiondihydropteroate synthase activity
B0005524molecular_functionATP binding
B0005740cellular_componentmitochondrial envelope
B0009396biological_processfolic acid-containing compound biosynthetic process
B0016301molecular_functionkinase activity
B0016740molecular_functiontransferase activity
B0042558biological_processpteridine-containing compound metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0046656biological_processfolic acid biosynthetic process
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue CKL A 801
ChainResidue
AASP482
AGLY605
ALYS609
AARG610
AARG686
AACT806
AHOH903
AHOH927
AASN502
AILE504
AMET529
AASP539
AASP575
AGLY579
APHE580
APHE603

site_idAC2
Number of Residues12
Detailsbinding site for residue PH2 A 802
ChainResidue
ATHR57
AVAL58
APRO59
AGLU60
ATYR61
APHE163
AASN165
AASP208
AARG326
ASER328
AHOH921
AHOH942

site_idAC3
Number of Residues17
Detailsbinding site for residue AMP A 803
ChainResidue
ALEU181
ALYS185
AASP208
AASP210
AILE211
AASN312
AILE313
AGLU314
APHE315
ALEU316
ASER317
AILE318
AHIS320
AMG804
AHOH986
AHOH1013
AHOH1037

site_idAC4
Number of Residues5
Detailsbinding site for residue MG A 804
ChainResidue
AASP208
AASP210
AAMP803
AHOH951
AHOH993

site_idAC5
Number of Residues5
Detailsbinding site for residue ACT A 805
ChainResidue
AHIS530
AARG532
AASP550
ATYR554
AHOH962

site_idAC6
Number of Residues5
Detailsbinding site for residue ACT A 806
ChainResidue
AASN396
AARG686
AHIS688
ACKL801
AHOH968

site_idAC7
Number of Residues5
Detailsbinding site for residue CA A 807
ChainResidue
AGLU42
AGLY46
AGLU99
AHOH1041
AHOH1056

site_idAC8
Number of Residues16
Detailsbinding site for residue CKL B 801
ChainResidue
BASP482
BASN502
BILE504
BMET529
BPRO535
BASP575
BGLY579
BPHE580
BPHE603
BGLY605
BLYS609
BARG610
BARG686
BACT806
BHOH931
BHOH940

site_idAC9
Number of Residues15
Detailsbinding site for residue AMP B 802
ChainResidue
BLYS185
BASP208
BASP210
BILE211
BASN312
BILE313
BGLU314
BPHE315
BLEU316
BSER317
BILE318
BHIS320
BMG803
BHOH929
BHOH951

site_idAD1
Number of Residues5
Detailsbinding site for residue MG B 803
ChainResidue
BHOH912
BHOH929
BASP208
BASP210
BAMP802

site_idAD2
Number of Residues9
Detailsbinding site for residue ACT B 804
ChainResidue
AASN487
AASN510
AHOH977
BHIS530
BARG532
BTYR544
BTYR554
BHOH933
BHOH976

site_idAD3
Number of Residues6
Detailsbinding site for residue ACT B 805
ChainResidue
AGLU94
ATYR97
AGLU98
AGLU99
BTYR486
BASN510

site_idAD4
Number of Residues4
Detailsbinding site for residue ACT B 806
ChainResidue
BASN396
BARG686
BHIS688
BCKL801

site_idAD5
Number of Residues3
Detailsbinding site for residue CA B 807
ChainResidue
BGLU42
BGLY46
BGLU99

Functional Information from PROSITE/UniProt
site_idPS00793
Number of Residues14
DetailsDHPS_2 Dihydropteroate synthase signature 2. GAsVIDIGGesSaP
ChainResidueDetails
AGLY425-PRO438

246905

PDB entries from 2025-12-31

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