KEGG   ORTHOLOGY: K22466
Entry
K22466                      KO                                     
Symbol
bzaF
Name
5-hydroxybenzimidazole synthase [EC:4.1.99.23]
Pathway
map00860  Porphyrin metabolism
Reaction
R11919  5-amino-1-(5-phospho-beta-D-ribosyl)imidazole formate-lyase (5-hydroxybenzimidazole-forming)
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09108 Metabolism of cofactors and vitamins
   00860 Porphyrin metabolism
    K22466  bzaF; 5-hydroxybenzimidazole synthase
Enzymes [BR:ko01000]
 4. Lyases
  4.1  Carbon-carbon lyases
   4.1.99  Other carbon-carbon lyases
    4.1.99.23  5-hydroxybenzimidazole synthase
     K22466  bzaF; 5-hydroxybenzimidazole synthase
Genes
GSU: GSU3005(thiC-2)
GSK: KN400_2948(thiC-2)
GME: Gmet_0471(thiC-2)
GPI: GPICK_02630
GAO: A2G06_14140
GBZ: JZM60_08015(thiC)
GEM: GM21_3893
GEB: GM18_4239
GEF: FO488_14370(thiC)
GEV: GSVR_35330(thiC)
GEC: GEO60473_24280(thiC_2)
GUR: Gura_4183
GEO: Geob_0543(thiC-2)
GLO: Glov_3677
TAMM: GEAMG1_2108(bzaF)
GBM: Gbem_3809(thiC-2)
GBN: GEOBRER4_37000(thiC)
GER: KP004_18205(thiC)
GSUB: KP001_18030(thiC)
GNT: KP003_18225(thiC)
GPL: M1B72_01565(thiC)
GHC: L9S41_11450(thiC)
PPD: Ppro_2809
DEU: DBW_3101
DVE: DESUT3_08050(thiC)
DEP: AOP6_0798(thiC)
DES: DSOUD_0618(thiC-2)
DSF: UWK_02784
DBK: DGMP_09610(thiC_1)
DDU: GF1_11200(thiC)
ECOM: QTN59_15175(thiC)
EAJ: Q3M24_07245(thiC)
ELAX: KKHLCK_12900(thiC)
EAQ: LDFHOB_04700(thiC)
DAL: Dalk_0439
DAT: HRM2_06760(thiC)
DTO: TOL2_C39750(thiC2)
DWD: DSCW_64740(thiC)
DALK: DSCA_61910(thiC_2)
DML: Dmul_38190(thiC2)
DLI: dnl_04700(thiC2)
DEK: DSLASN_49290(thiC_2)
DBR: Deba_2032
DMP: FAK_24670(thiC)
TAV: G4V39_09730(thiC)
TMAI: FVE67_00935(thiC)
BROC: IPI25_07410(thiC)
BPIT: BPIT_18350
DTP: JZK55_23310(thiC_2)
DHR: LGS26_04000(thiC)
 » show all
Reference
  Authors
Mehta AP, Abdelwahed SH, Fenwick MK, Hazra AB, Taga ME, Zhang Y, Ealick SE, Begley TP
  Title
Anaerobic 5-Hydroxybenzimidazole Formation from Aminoimidazole Ribotide: An Unanticipated Intersection of Thiamin and Vitamin B(1)(2) Biosynthesis.
  Journal
J Am Chem Soc 137:10444-7 (2015)
DOI:10.1021/jacs.5b03576
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