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6JWV

Crystal structure of Plasmodium falciparum HPPK-DHPS A437G with STZ-DHP

Functional Information from GO Data
ChainGOidnamespacecontents
A0003848molecular_function2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
A0004156molecular_functiondihydropteroate synthase activity
A0005524molecular_functionATP binding
A0009396biological_processfolic acid-containing compound biosynthetic process
A0016301molecular_functionkinase activity
A0042558biological_processpteridine-containing compound metabolic process
A0044237biological_processcellular metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0046656biological_processfolic acid biosynthetic process
A0046872molecular_functionmetal ion binding
B0003848molecular_function2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
B0004156molecular_functiondihydropteroate synthase activity
B0005524molecular_functionATP binding
B0009396biological_processfolic acid-containing compound biosynthetic process
B0016301molecular_functionkinase activity
B0042558biological_processpteridine-containing compound metabolic process
B0044237biological_processcellular metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0046656biological_processfolic acid biosynthetic process
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues14
Detailsbinding site for residue XTZ A 801
ChainResidue
AASP482
ALYS609
AARG610
AARG686
AGOL803
AHOH930
AASN502
AILE504
AMET529
AASP575
APHE580
APHE603
AGLY605
AARG608

site_idAC2
Number of Residues14
Detailsbinding site for residue PH2 A 802
ChainResidue
ATHR57
AVAL58
APRO59
AGLU60
ATYR61
APHE163
AASN165
AASP208
AARG326
ASER328
AATP804
AMG809
AHOH917
AHOH1002

site_idAC3
Number of Residues5
Detailsbinding site for residue GOL A 803
ChainResidue
AASN396
AARG686
AHIS688
AXTZ801
AHOH1013

site_idAC4
Number of Residues19
Detailsbinding site for residue ATP A 804
ChainResidue
ALEU181
ALYS185
AARG205
AASP208
AASP210
AILE211
AASN312
AILE313
AGLU314
APHE315
ALEU316
ASER317
AHIS320
ATYR322
AARG326
APH2802
AMG805
AMG809
AHOH949

site_idAC5
Number of Residues3
Detailsbinding site for residue MG A 805
ChainResidue
AASP208
AASP210
AATP804

site_idAC6
Number of Residues5
Detailsbinding site for residue CA A 806
ChainResidue
AGLU42
AGLY46
AGLU99
AHOH993
AHOH1073

site_idAC7
Number of Residues4
Detailsbinding site for residue ACT A 807
ChainResidue
AHIS530
AARG532
ATYR554
AHOH952

site_idAC8
Number of Residues2
Detailsbinding site for residue ACT A 808
ChainResidue
ALYS96
ATYR97

site_idAC9
Number of Residues6
Detailsbinding site for residue MG A 809
ChainResidue
AASP208
AASP210
APH2802
AATP804
AHOH1001
AHOH1002

site_idAD1
Number of Residues19
Detailsbinding site for residue XTZ B 801
ChainResidue
BASP482
BASN502
BILE504
BMET529
BPRO535
BMET538
BASP539
BASP575
BGLY579
BPHE580
BPHE603
BGLY605
BLYS609
BARG610
BARG686
BGOL802
BHOH906
BHOH934
BHOH938

site_idAD2
Number of Residues5
Detailsbinding site for residue GOL B 802
ChainResidue
BASN396
BARG686
BHIS688
BXTZ801
BHOH915

site_idAD3
Number of Residues3
Detailsbinding site for residue CA B 803
ChainResidue
BGLU42
BGLY46
BGLU99

site_idAD4
Number of Residues4
Detailsbinding site for residue ACT B 804
ChainResidue
AASN510
BHIS530
BARG532
BHOH939

site_idAD5
Number of Residues5
Detailsbinding site for residue ACT B 805
ChainResidue
ASER95
AGLU98
AGLU99
BASN510
BGLU512

site_idAD6
Number of Residues3
Detailsbinding site for residue MG B 806
ChainResidue
BASP208
BASP210
BHOH950

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

223166

PDB entries from 2024-07-31

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