Structure of PDB 6dep Chain A Binding Site BS05
Receptor Information
>6dep Chain A (length=598) Species:
237561
(Candida albicans SC5314) [
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KEQLMDDSFIGLTGGEIFHEMMLRHKVDTVFGYAGGAILPVFDAIYNSDK
FKFVLPRHEQGAGHMAEGYARASGKPGVVLVTSGPGATNVITPMADALMD
GVPLVVFSGQVPTTAIGTDAFQEADIVGISRSCTKWNVMVKNVAELPRRI
NEAFEIATTGRPGPVLVDLPKDVTASILRESIPINTTLPSAVSEFTSEAI
KRAANILNKAKKPIIYAGAGILNNEQGPKLLKELADKANIPVTTTLQGLG
AFDQRDPKSLDMLGMHGSAAANTAIQNADCIIALGARFDDRVTGNISKFA
PEAKLAASEGRGGILHFEISPKNINKVVEATEAIEGDVTANLQSFIPLVD
SIENRPEWFNKINEWKKKYPYSYQLETPGSLIKPQTLIKEISDQAQTYNK
EVIVTTGVGQHQMWAAQHFTWTQPRTMITSGGLGTMGYGLPAAIGAQVAK
PDAIVIDIDGDASFNMTLTELSSAVQAGAPIKVCVLNNEEQGMVTQWQSL
FYEHRYSHTHQSNPDFMKLAESMNVKGIRITNQQELKSGVKEFLDATEPV
LLEVIVEKKVPVLPMVPAGKALDDFILWDAEVEKQQNDLRKERTGGKY
Ligand information
Ligand ID
TP9
InChI
InChI=1S/C11H20N4O7P2S/c1-7(13-5-9-6-14-8(2)15-11(9)12)10(25)3-4-21-24(19,20)22-23(16,17)18/h6,13,25H,3-5H2,1-2H3,(H,19,20)(H2,12,14,15)(H2,16,17,18)/p-2/b10-7-
InChIKey
WTQDUFKDQLXDPH-YFHOEESVSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
Cc1ncc(c(n1)N)CN/C(=C(/CCO[P@](=O)([O-])O[P@@](=O)(O)[O-])\S)/C
CACTVS 3.341
CC(NCc1cnc(C)nc1N)=C(S)CCO[P]([O-])(=O)O[P](O)([O-])=O
CACTVS 3.341
CC(/NCc1cnc(C)nc1N)=C(/S)CCO[P]([O-])(=O)O[P](O)([O-])=O
OpenEye OEToolkits 1.5.0
Cc1ncc(c(n1)N)CNC(=C(CCOP(=O)([O-])OP(=O)(O)[O-])S)C
Formula
C11 H18 N4 O7 P2 S
Name
(3Z)-4-{[(4-AMINO-2-METHYLPYRIMIDIN-5-YL)METHYL]AMINO}-3-MERCAPTOPENT-3-EN-1-YL TRIHYDROGEN DIPHOSPHATE
ChEMBL
DrugBank
ZINC
PDB chain
6dep Chain A Residue 706 [
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Receptor-Ligand Complex Structure
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PDB
6dep
Commercial AHAS-inhibiting herbicides are promising drug leads for the treatment of human fungal pathogenic infections.
Resolution
2.149 Å
Binding residue
(original residue number in PDB)
V493 G494 Q495 H496 G519 M521 G545 D546 A547 S548 M551 N573 E575 Q576 G577 M578 V579
Binding residue
(residue number reindexed from 1)
V408 G409 Q410 H411 G434 M436 G460 D461 A462 S463 M466 N488 E490 Q491 G492 M493 V494
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y109 G111 G112 A113 I114 E135 T158 F197 Q198 E199 K247 K314 M350 V377 V493 L518 G519 M521 D546 N573 E575 Q576 M578 V579 W582 L604 N609 V610
Catalytic site (residue number reindexed from 1)
Y33 G35 G36 A37 I38 E59 T82 F121 Q122 E123 K171 K229 M265 V292 V408 L433 G434 M436 D461 N488 E490 Q491 M493 V494 W497 L519 N524 V525
Enzyme Commision number
2.2.1.6
: acetolactate synthase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003984
acetolactate synthase activity
GO:0016740
transferase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0000463
maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)
GO:0006412
translation
GO:0008652
amino acid biosynthetic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009097
isoleucine biosynthetic process
GO:0009099
L-valine biosynthetic process
GO:0030150
protein import into mitochondrial matrix
Cellular Component
GO:0005948
acetolactate synthase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6dep
,
PDBe:6dep
,
PDBj:6dep
PDBsum
6dep
PubMed
30249642
UniProt
A0A1D8PJF9
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