Structure of PDB 6vvb Chain A

Receptor sequence
>6vvbA (length=160) Species: 83332 (Mycobacterium tuberculosis H37Rv) [Search protein sequence]
TMVGLIWAQATSGVIGRGGDIPWRLPEDQAHFREITMGHTIVMGRRTWDS
LPAKVRPLPGRRNVVLSRQADFMASGAEVVGSLEEALTSPETWVIGGGQV
YALALPYATRCEVTEVDIGLPREAGDALAPVLDETWRGETGEWRFSRSGL
RYRLYSYHRS
3D structure
PDB6vvb Using a Fragment-Based Approach to Identify Alternative Chemical Scaffolds Targeting Dihydrofolate Reductase fromMycobacterium tuberculosis.
ChainA
Resolution1.45 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) I5 I20 W22 D27 Q28 F31 L57 T91 T113
Catalytic site (residue number reindexed from 1) I6 I21 W23 D28 Q29 F32 L58 T92 T114
Enzyme Commision number 1.5.1.3: dihydrofolate reductase.
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 RQ4 A Q28 F31 R32 L50 P51 K53 V54 L57 R60 Q29 F32 R33 L51 P52 K54 V55 L58 R61 MOAD: Kd=0.095mM
BS02 NAP A W6 A7 I14 G15 D19 I20 G43 R44 R45 T46 L65 S66 R67 I94 G96 G97 Q98 V99 W7 A8 I15 G16 D20 I21 G44 R45 R46 T47 L66 S67 R68 I95 G97 G98 Q99 V100
Gene Ontology
Molecular Function
GO:0004146 dihydrofolate reductase activity
GO:0016491 oxidoreductase activity
GO:0050661 NADP binding
GO:0070401 NADP+ binding
Biological Process
GO:0006730 one-carbon metabolic process
GO:0046452 dihydrofolate metabolic process
GO:0046654 tetrahydrofolate biosynthetic process
GO:0046655 folic acid metabolic process
Cellular Component
GO:0005829 cytosol

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:6vvb, PDBe:6vvb, PDBj:6vvb
PDBsum6vvb
PubMed32603583
UniProtP9WNX1|DYR_MYCTU Dihydrofolate reductase (Gene Name=folA)

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