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6JWR

Crystal structure of Plasmodium falciparum HPPK-DHPS wild type with Pteroate

Functional Information from GO Data
ChainGOidnamespacecontents
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
A0016310biological_processphosphorylation
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
B0005740cellular_componentmitochondrial envelope
B0009396biological_processfolic acid-containing compound biosynthetic process
B0016301molecular_functionkinase activity
B0016310biological_processphosphorylation
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 Residues16
Detailsbinding site for residue PT1 A 801
ChainResidue
ASER436
APHE603
AGLY605
ALYS609
AARG610
AARG686
AHOH921
AHOH952
APRO438
AASP482
AASN502
AILE504
AMET529
AASP575
AGLY579
APHE580

site_idAC2
Number of Residues14
Detailsbinding site for residue AMP A 802
ChainResidue
ALEU181
AASP208
AILE211
AASN312
AILE313
APHE315
ALEU316
ASER317
AILE318
AHIS320
AMG804
APH2805
AHOH901
AHOH914

site_idAC3
Number of Residues5
Detailsbinding site for residue MG A 803
ChainResidue
AASP208
APH2805
AHOH950
AHOH979
AHOH1011

site_idAC4
Number of Residues6
Detailsbinding site for residue MG A 804
ChainResidue
AASP208
AASP210
AAMP802
APH2805
AHOH901
AHOH914

site_idAC5
Number of Residues12
Detailsbinding site for residue PH2 A 805
ChainResidue
ATHR57
AVAL58
AGLU60
APHE163
AASN165
AASP208
AARG326
AAMP802
AMG803
AMG804
AHOH914
AHOH950

site_idAC6
Number of Residues4
Detailsbinding site for residue CA A 806
ChainResidue
AGLU42
AGLY46
AGLU99
AHOH988

site_idAC7
Number of Residues4
Detailsbinding site for residue ACT A 807
ChainResidue
AASP335
AARG350
AARG374
AGLU599

site_idAC8
Number of Residues3
Detailsbinding site for residue ACT A 808
ChainResidue
AHIS530
AARG532
AASP550

site_idAC9
Number of Residues3
Detailsbinding site for residue ACT A 809
ChainResidue
AILE49
AASN560
AHOH959

site_idAD1
Number of Residues2
Detailsbinding site for residue ACT A 810
ChainResidue
AGLN586
AHOH943

site_idAD2
Number of Residues17
Detailsbinding site for residue PT1 B 801
ChainResidue
BSER436
BPRO438
BASP482
BASN502
BILE504
BMET529
BASP575
BGLY579
BPHE580
BPHE603
BGLY605
BLYS609
BARG610
BARG686
BACT807
BHOH904
BHOH938

site_idAD3
Number of Residues13
Detailsbinding site for residue AMP B 802
ChainResidue
BLEU181
BLYS185
BASP208
BASP210
BILE211
BASN312
BILE313
BGLU314
BPHE315
BLEU316
BSER317
BHIS320
BMG803

site_idAD4
Number of Residues3
Detailsbinding site for residue MG B 803
ChainResidue
BASP208
BASP210
BAMP802

site_idAD5
Number of Residues3
Detailsbinding site for residue CA B 804
ChainResidue
BGLU42
BGLY46
BGLU99

site_idAD6
Number of Residues7
Detailsbinding site for residue ACT B 805
ChainResidue
AASN510
AHOH936
BHIS530
BARG532
BTYR544
BHOH942
BHOH953

site_idAD7
Number of Residues6
Detailsbinding site for residue ACT B 806
ChainResidue
ASER95
AGLU98
AGLU99
AHOH964
BTYR486
BASN510

site_idAD8
Number of Residues5
Detailsbinding site for residue ACT B 807
ChainResidue
BARG686
BHIS688
BPT1801
BHOH907
BHOH909

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

225946

PDB entries from 2024-10-09

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