KEGG   ORTHOLOGY: K15896
Entry
K15896                      KO                                     
Symbol
pseH
Name
UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase [EC:2.3.1.202]
Pathway
map00541  Biosynthesis of various nucleotide sugars
map01100  Metabolic pathways
map01250  Biosynthesis of nucleotide sugars
Module
M01007  CMP-Pse5Ac7Ac biosynthesis, UDP-GlcNAc => CMP-Pse5Ac7Ac
Reaction
R09842  acetyl-CoA:UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine 4-N-acetyltransferase
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09107 Glycan biosynthesis and metabolism
   00541 Biosynthesis of various nucleotide sugars
    K15896  pseH; UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase
Enzymes [BR:ko01000]
 2. Transferases
  2.3  Acyltransferases
   2.3.1  Transferring groups other than aminoacyl groups
    2.3.1.202  UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase
     K15896  pseH; UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase
Other DBs
COG: COG1670
Genes
PAR: Psyc_0658
MEIN: methR_P0377
FAD: CDH04_02735(pseH)
FMI: F0R74_04810(pseH)
ACAV: VI35_07450(pseH)
AEA: C2U39_08090(pseH)
ARV: C7N77_17155(pseH)
ASIM: FE240_05745(pseH)
PSE: NH8B_3547
CHIC: N8I74_00615(pseH)
HPY: HP_0327
HPJ: jhp_0310(flaG)
HPG: HPG27_309(flaG-1)
HPP: HPP12_0325(flaG-1)
HPO: HMPREF4655_20570(pseH)
HPQ: hp2017_0335(flaG)
HEF: HPF16_0335(flaG-1)
HPF: HPF30_0968(flaG-1)
HEQ: HPF32_0977(flaG-1)
HEX: HPF57_0380(flaG-1)
HPX: HMPREF0462_0385(pseH)
HPD: KHP_0320(flaG)
HPYO: HPOK113_0335(flaG-1)
HPYL: HPOK310_0332(flaG-1)
HPYR: K747_10310
HPYI: K750_03225
HPYU: K751_05810
HPYM: K749_04015
HEB: U063_0669
HEZ: U064_0671
HAC: Hac_0993(flaG)
HMS: HMU11710(flaG1_flmH)
HFE: HFELIS_15220(flaG1_flmH)
HCE: HCW_06080
HCM: HCD_02150
HAD: CDV25_00755(pseH) CDV25_00765(pseH)
HWI: A0Z60_06265(pseH)
HSH: NHP194022_15530(pseH)
HPUL: NCTC13154_01210(flaG1_flmH)
HAIL: ASB7_09370(pseH)
HFI: NHP21005_02360(pseH)
HGA: NHP190012_07650(pseH)
HGS: NHP190003_09920(pseH)
WSU: WS2108
SUA: Saut_0137
SULR: B649_00695
CJE: Cj1313(pseH)
CJB: BN148_1313(pseH)
CJI: CJSA_1251(pseH)
CJM: CJM1_1285(pseH) CJM1_1286
CJS: CJS3_1413(pseH)
CJEJ: N564_01331
CJEU: N565_01370
CJEN: N755_01366
CJEI: N135_01402
CJER: H730_07515
CJY: QZ67_01448(pseH)
CJQ: UC78_1262(pseH)
CJR: CJE1508
CFT: CFF04554_1636(pseH)
CFV: CFVI03293_1658(pseH)
CFX: CFV97608_1761(pseH)
CFZ: CSG_17680
CAMP: CFT03427_1586(pseH)
CCV: CCV52592_0564(pseH)
CLA: CLA_1321(pseH) CLA_1324
CLR: UPTC16701_1295(pseH)
CLM: UPTC16712_1317(pseH)
CLQ: UPTC4110_1301(pseH)
CLN: UPTC3659_1537(pseH)
CLL: CONCH_1276(pseH)
CCQ: N149_1276(pseH)
CCF: YSQ_02280
CCY: YSS_07135
CCOI: YSU_02295
CCOF: VC76_06605(pseH)
CCOO: ATE51_00938(pseH)
CIS: CINS_1277(pseH)
CVO: CVOL_1308
CPEL: CPEL_1427(pseH)
CHV: CHELV3228_1545(pseH)
CCUN: CCUN_1343(pseH)
CLX: CLAN_0193(pseH)
CAVI: CAV_1215(pseH)
CHW: A2J15_000500(pseH) A2J15_000505(pseH)
CAMZ: CVIC12175_0229(pseH)
CAMY: CSUIS_1216(pseH)
COJ: CORN_1398(pseH) CORN_1401
CUX: CUP3940_0286(pseH)
CRX: CRECT_0229(pseH)
CARM: CARM_1352(pseH)
CMUC: CMCT_0214(pseH)
CSHO: CSHOW_1836(pseH)
CINF: CINF_0427(pseH)
CNV: CNZW441b_1304(pseH)
CVU: CVULP_1346(pseH)
CDEV: CIGN_1520(pseH)
CCAQ: CCAL_1593(pseH)
CMOL: CMOL_0973(pseH1) CMOL_0974(pseH2)
SDL: Sdel_2212
SHAL: SHALO_2911
SULJ: SJPD1_2796
SULT: FA592_06790(pseH)
ATHR: ATH_1856(pseH1) ATH_1860(pseH2)
APOC: APORC_1982(pseH)
NAP: C3L23_08290(pseH)
CPAF: C6V80_09005(pseH)
BHF: C3V43_13565(pseH)
FBU: UJ101_00317(pseH)
HTH: HTH_1537
TSQ: D3A95_13210(pseH)
 » show all
Reference
  Authors
Schoenhofen IC, McNally DJ, Brisson JR, Logan SM
  Title
Elucidation of the CMP-pseudaminic acid pathway in Helicobacter pylori: synthesis from UDP-N-acetylglucosamine by a single enzymatic reaction.
  Journal
Glycobiology 16:8C-14C (2006)
DOI:10.1093/glycob/cwl010
  Sequence
[hpy:HP_0327]
Reference
  Authors
McNally DJ, Hui JP, Aubry AJ, Mui KK, Guerry P, Brisson JR, Logan SM, Soo EC
  Title
Functional characterization of the flagellar glycosylation locus in Campylobacter jejuni 81-176 using a focused metabolomics approach.
  Journal
J Biol Chem 281:18489-98 (2006)
DOI:10.1074/jbc.M603777200
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