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6JWT

Crystal structure of Plasmodium falciparum HPPK-DHPS S436F/A437G/A613T triple mutant with Pteroate

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 Residues16
Detailsbinding site for residue AMP A 801
ChainResidue
ALEU181
ASER317
AILE318
AHIS320
AMG802
AMG803
AHOH912
AHOH968
ALYS185
AASP210
AILE211
AASN312
AILE313
AGLU314
APHE315
ALEU316

site_idAC2
Number of Residues5
Detailsbinding site for residue MG A 802
ChainResidue
AASP208
AASP210
AAMP801
AMG803
AHOH912

site_idAC3
Number of Residues3
Detailsbinding site for residue MG A 803
ChainResidue
AAMP801
AMG802
AHOH968

site_idAC4
Number of Residues17
Detailsbinding site for residue PT1 A 804
ChainResidue
AGLY437
APRO438
AASP482
AASN502
AILE504
AMET529
AASP575
AGLY579
APHE580
APHE603
AGLY605
ALYS609
AARG610
AARG686
AACT807
AHOH925
AHOH956

site_idAC5
Number of Residues3
Detailsbinding site for residue CA A 805
ChainResidue
AGLU42
AGLY46
AGLU99

site_idAC6
Number of Residues4
Detailsbinding site for residue ACT A 806
ChainResidue
AHIS530
AARG532
AASP550
ATYR554

site_idAC7
Number of Residues3
Detailsbinding site for residue ACT A 807
ChainResidue
AARG686
AHIS688
APT1804

site_idAC8
Number of Residues11
Detailsbinding site for residue ATP B 801
ChainResidue
BLEU181
BASP208
BASP210
BILE211
BASN312
BPHE315
BLEU316
BSER317
BHIS320
BMG802
BHOH903

site_idAC9
Number of Residues4
Detailsbinding site for residue MG B 802
ChainResidue
BASP208
BASP210
BATP801
BHOH903

site_idAD1
Number of Residues17
Detailsbinding site for residue PT1 B 803
ChainResidue
BGLY437
BPRO438
BASP482
BASN502
BILE504
BMET529
BASP575
BGLY579
BPHE580
BPHE603
BGLY605
BLYS609
BARG610
BARG686
BACT806
BHOH908
BHOH938

site_idAD2
Number of Residues3
Detailsbinding site for residue CA B 804
ChainResidue
BGLU42
BGLY46
BGLU99

site_idAD3
Number of Residues6
Detailsbinding site for residue ACT B 805
ChainResidue
AASN487
AASN510
AHOH947
BHIS530
BARG532
BHOH933

site_idAD4
Number of Residues5
Detailsbinding site for residue ACT B 806
ChainResidue
BASN396
BARG686
BHIS688
BPT1803
BHOH929

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PDB entries from 2024-07-10

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