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
map00520  Amino sugar and nucleotide sugar metabolism
map00541  O-Antigen nucleotide sugar biosynthesis
map01100  Metabolic pathways
map01250  Biosynthesis of nucleotide sugars
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09101 Carbohydrate metabolism
   00520 Amino sugar and nucleotide sugar metabolism
    K15896  pseH; UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase
  09107 Glycan biosynthesis and metabolism
   00541 O-Antigen nucleotide sugar biosynthesis
    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
RN: R09842
COG: COG1670
Genes
PALL: UYA_15075
PAR: Psyc_0658
PSPG: AK823_00660
PAT: Patl_3074
AMAG: I533_04900
ALT: ambt_13345
ASP: AOR13_2471
ASQ: AVL57_11030
AAW: AVL56_10170
ALE: AV939_10050
GPS: C427_3687
AGZ: M0C34_07855(pseH)
FAD: CDH04_02735(pseH)
FMI: F0R74_04810(pseH)
RHH: E0Z06_10265(pseH)
ACAV: VI35_07450(pseH)
AEA: C2U39_08090(pseH)
ARV: C7N77_17155(pseH)
ASIM: FE240_05745(pseH)
PSE: NH8B_3547
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
HHE: HH_0907
HAC: Hac_0993(flaG)
HMS: HMU11710(flaG1_flmH)
HFE: HFELIS_15220(flaG1_flmH)
HCE: HCW_06080
HCM: HCD_02150
HCP: HCN_1784
HAD: CDV25_00755(pseH) CDV25_00765(pseH)
HWI: A0Z60_06265(pseH)
HSH: NHP194022_15530(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)
SDL: Sdel_2212
SHAL: SHALO_2911
SULJ: SJPD1_2796
SULT: FA592_06790(pseH)
APOC: APORC_1982(pseH)
ATHR: ATH_1856(pseH1) ATH_1860(pseH2)
NAP: C3L23_08290(pseH)
CPAF: C6V80_09005(pseH)
BHF: C3V43_13565(pseH)
FBU: UJ101_00317(pseH)
HTH: HTH_1537
 » 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
LinkDB

KEGG   ENZYME: 2.3.1.202
Entry
EC 2.3.1.202                Enzyme                                 
Name
UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase;
PseH
Class
Transferases;
Acyltransferases;
Transferring groups other than aminoacyl groups
Sysname
acetyl-CoA:UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase
Reaction(IUBMB)
acetyl-CoA + UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine = CoA + UDP-2,4-diacetamido-2,4,6-trideoxy-beta-L-altropyranose [RN:R09842]
Reaction(KEGG)
R09842
Substrate
acetyl-CoA [CPD:C00024];
UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine [CPD:C19961]
Product
CoA [CPD:C00010];
UDP-2,4-diacetamido-2,4,6-trideoxy-beta-L-altropyranose
Comment
Isolated from Helicobacter pylori. The enzyme is involved in the biosynthesis of pseudaminic acid.
History
EC 2.3.1.202 created 2012
Pathway
ec00520  Amino sugar and nucleotide sugar metabolism
ec00541  O-Antigen nucleotide sugar biosynthesis
ec01100  Metabolic pathways
Orthology
K15896  UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase
Genes
PALLUYA_15075
PARPsyc_0658
PSPGAK823_00660
PATPatl_3074
AMAGI533_04900
ALTambt_13345
ASPAOR13_2471
ASQAVL57_11030
AAWAVL56_10170
ALEAV939_10050
ALZAV940_09820
GAGGlaag_1260
GPSC427_3687
PMESFX988_03839
LALAT746_12890
AGZM0C34_07855(pseH)
MEINmethR_P0377
FADCDH04_02735(pseH)
FMIF0R74_04810(pseH)
RHHE0Z06_10265(pseH)
ACAVVI35_07450(pseH)
AEAC2U39_08090(pseH)
ARVC7N77_17155(pseH)
ASIMFE240_05745(pseH)
PSENH8B_3547
HPYHP_0327
HEOC694_01655
HPJjhp_0310(flaG)
HPAHPAG1_0331
HPSHPSH_01700
HHPHPSH112_01935
HHQHPSH169_01820
HHRHPSH417_01640
HPGHPG27_309(flaG-1)
HPPHPP12_0325(flaG-1)
HPBHELPY_0331
HPCHPPC_01660
HCAHPPC18_01655
HPMHPSJM_01755
HPEHPELS_05110
HPOHMPREF4655_20570(pseH)
HPIhp908_0343
HPQhp2017_0335(flaG)
HPWhp2018_0337
HPUHPCU_01965
HEFHPF16_0335(flaG-1)
HPFHPF30_0968(flaG-1)
HEQHPF32_0977(flaG-1)
HEXHPF57_0380(flaG-1)
HPTHPSAT_01635
HPVHPV225_0346
HPXHMPREF0462_0385(pseH)
HENHPSNT_01815
HPHHPLT_01680
HEGHPGAM_01820
HPNHPIN_01495
HEPHPPN120_01665
HEUHPPN135_01675
HESHPSA_01665
HCNHPB14_01610
HPDKHP_0320(flaG)
HERC695_01655
HEIC730_01655
HPYAHPAKL117_01620
HPYKHPAKL86_03500
HPYOHPOK113_0335(flaG-1)
HPYLHPOK310_0332(flaG-1)
HPYBHPOKI102_01950
HPYCHPOKI112_01935
HPYDHPOKI128_01750
HPYEHPOKI154_01765
HPYFHPOKI422_01940
HPYGHPOKI673_01755
HPYHHPOKI828_01750
HPYJHPOKI898_01950
HPYRK747_10310
HPYIK750_03225
HPYUK751_05810
HPYMK749_04015
HEMK748_02440
HEBU063_0669
HEZU064_0671
HHEHH_0907
HACHac_0993(flaG)
HMSHMU11710(flaG1_flmH)
HFEHFELIS_15220(flaG1_flmH)
HBIHBZC1_10960
HCEHCW_06080
HCMHCD_02150
HCPHCN_1784
HCBHCBAA847_2067
HHMBN341_3130
HTYBN2458_PEG0382
HBLXJ32_08280
HADCDV25_00755(pseH) CDV25_00765(pseH)
HWIA0Z60_06265(pseH)
HSHNHP194022_15530(pseH)
WSUWS2108
SUASaut_0137
SKUSulku_0154
SULRB649_00695
CJECj1313(pseH)
CJBBN148_1313(pseH)
CJJCJJ81176_1330
CJUC8J_1246 C8J_1247
CJNICDCCJ07001_1259
CJICJSA_1251(pseH)
CJMCJM1_1285(pseH) CJM1_1286
CJSCJS3_1413(pseH)
CJPA911_06385
CJEJN564_01331
CJEUN565_01370
CJENN755_01366
CJEIN135_01402
CJERH730_07515
CJVMTVDSCj20_1308(pseH) MTVDSCj20_1309
CJYQZ67_01448(pseH)
CJQUC78_1262(pseH)
CJLPJ17_06955
CJWPJ18_06760
CJRCJE1508
CJDJJD26997_0400
CJZM635_02255
CJXBN867_13020
CFFCFF8240_1634
CFTCFF04554_1636(pseH)
CFVCFVI03293_1658(pseH)
CFXCFV97608_1761(pseH)
CFZCSG_17680
CAMPCFT03427_1586(pseH)
CFPCR44_08060
CCVCCV52592_0564(pseH)
CLACLA_1321(pseH) CLA_1324
CLRUPTC16701_1295(pseH)
CLMUPTC16712_1317(pseH)
CLQUPTC4110_1301(pseH)
CLNUPTC3659_1537(pseH)
CLLCONCH_1276(pseH)
CCOLBN865_08230c
CCCG157_02240
CCQN149_1276(pseH)
CCFYSQ_02280
CCYYSS_07135
CCOIYSU_02295
CCOFVC76_06605(pseH)
CCOOATE51_00938(pseH)
CISCINS_1277(pseH)
CVOCVOL_1308
CPELCPEL_1427(pseH)
CAMRCAQ16704_1327(pseH) CAQ16704_1330
CSMCSUB8521_1504(pseH) CSUB8521_1507
CSFCSUB8523_1600(pseH) CSUB8523_1603
CHVCHELV3228_1545(pseH)
CCUNCCUN_1343(pseH)
CLXCLAN_0193(pseH)
CAVICAV_1215(pseH)
CHWA2J15_000500(pseH) A2J15_000505(pseH)
CAMZCVIC12175_0229(pseH)
CAMYCSUIS_1216(pseH)
COJCORN_1398(pseH) CORN_1401
CUXCUP3940_0286(pseH)
CRXCRECT_0229(pseH)
CARMCARM_1352(pseH)
CMUCCMCT_0214(pseH)
CSHOCSHOW_1836(pseH)
CINFCINF_0427(pseH)
CNVCNZW441b_1304(pseH)
SDLSdel_2212
SBASulba_2446
SHALSHALO_2911
SULJSJPD1_2796
SULTFA592_06790(pseH)
APOCAPORC_1982(pseH)
ATHRATH_1856(pseH1) ATH_1860(pseH2)
NAPC3L23_08290(pseH)
CPAFC6V80_09005(pseH)
BHFC3V43_13565(pseH)
BEGINE88_04057
BHUMJXR92_011955
FBUUJ101_00317(pseH)
HTHHTH_1537
HTEHydth_1525
CNICalni_0722
MEQMSWHS_1970
 » show all
Reference
1  [PMID:16751642]
  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]
Other DBs
ExplorEnz - The Enzyme Database: 2.3.1.202
IUBMB Enzyme Nomenclature: 2.3.1.202
ExPASy - ENZYME nomenclature database: 2.3.1.202
BRENDA, the Enzyme Database: 2.3.1.202
LinkDB

KEGG   REACTION: R09842
Entry
R09842                      Reaction                               
Name
acetyl-CoA:UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine 4-N-acetyltransferase
Definition
UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine + Acetyl-CoA <=> UDP-2,4-bis(acetamido)-2,4,6-trideoxy-beta-L-altropyranose + CoA
Equation
Reaction class
RC00004  C00010_C00024
RC00166  C19961_C19971
Enzyme
Pathway
rn00520  Amino sugar and nucleotide sugar metabolism
rn00541  O-Antigen nucleotide sugar biosynthesis
rn01100  Metabolic pathways
rn01250  Biosynthesis of nucleotide sugars
Orthology
K15896  UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine N-acetyltransferase [EC:2.3.1.202]
Other DBs
RHEA: 34158
LinkDB

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