KEGG   ORTHOLOGY: K21721
Entry
K21721                      KO                                     
Symbol
sbnB
Name
N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate dehydrogenase [EC:1.5.1.51]
Pathway
map00997  Biosynthesis of various other secondary metabolites
map00998  Biosynthesis of various antibiotics
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
Module
M00875  Staphyloferrin B biosynthesis, L-serine => staphyloferrin B
Reaction
R11655  N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate:NAD+ dehydrogenase (L-2,3-diaminopropanoate-forming)
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09110 Biosynthesis of other secondary metabolites
   00998 Biosynthesis of various antibiotics
    K21721  sbnB; N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate dehydrogenase
   00997 Biosynthesis of various other secondary metabolites
    K21721  sbnB; N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate dehydrogenase
Enzymes [BR:ko01000]
 1. Oxidoreductases
  1.5  Acting on the CH-NH group of donors
   1.5.1  With NAD+ or NADP+ as acceptor
    1.5.1.51  N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate dehydrogenase
     K21721  sbnB; N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate dehydrogenase
Other DBs
COG: COG2423
Genes
ACC: BDGL_001498(ocd2)
ANO: RR32_07480
ACAL: BUM88_11500
ASEI: I8T81_07365(sbnB)
ACD: AOLE_07115
ACW: A0J50_07100
AGU: AS4_16160
SDN: Sden_0589
TACT: SG35_003595(sbnB)
CEK: D0B88_14055(sbnB)
CEG: D0C16_05385(sbnB)
RSO: RSp0418
RSE: F504_3906
RPU: CDC45_19720
RNC: GO999_24060(sbnB)
RSL: RPSI07_mp0379
RSN: RSPO_m01410
RSM: CMR15_mp10431
RSY: RSUY_34860(rapL_2)
RSG: JK151_14180(sbnB)
CNC: CNE_2c14840(ocd)
CUH: BJN34_08320
RME: Rmet_1116(ocd)
CUK: KB879_12560(sbnB)
BPLA: bpln_2g05020
NLC: EBAPG3_006455
NIZ: NNRS527_01549
ALEG: CFBP4996_27385(sbnB)
MNO: Mnod_6949
MAQU: Maq22A_c25430
MIWA: SS37A_35540(ocd2_1) SS37A_39060(ocd2_2)
SBD: ATN00_04615
DBK: DGMP_24730
BTHT: H175_328p223
BBAD: K7T73_21445(sbnB)
BARD: QRY57_11940(sbnB)
PCAL: BV455_03923
LMAC: I6G82_02105(sbnB)
SCIA: HUG15_04755
SAU: SA0113(sbnB)
SAV: SAV0117
SAW: SAHV_0116
SAH: SaurJH1_0108
SAJ: SaurJH9_0104
SAM: MW0090(sbnB)
SAS: SAS0091
SAR: SAR0120
SAC: SACOL0101
SAX: USA300HOU_0128(ocd)
SAA: SAUSA300_0119
SAO: SAOUHSC_00076
SAE: NWMN_0061(sbnB)
SAD: SAAV_0085
SUU: M013TW_0107(sbnB)
SUV: SAVC_00325
SUE: SAOV_0064
SUJ: SAA6159_00100(sbnB)
SUK: SAA6008_00095
SUC: ECTR2_73
SUT: SAT0131_00103
SUQ: HMPREF0772_10380
SUZ: MS7_0109
SUD: ST398NM01_0128
SUX: SAEMRSA15_00830(sbnB)
SUW: SATW20_01290(sbnB)
SUG: SAPIG0128
SUF: SARLGA251_00920(sbnB)
SAUA: SAAG_00601
SAUE: RSAU_000071
SAUN: SAKOR_00091
SAUS: SA40_0084(sbnB)
SAUU: SA957_0099(sbnB)
SAUG: SA268_0096(sbnB)
SAUZ: SAZ172_0128(sbnB)
SAUT: SAI1T1_2000730
SAUJ: SAI2T2_1000730
SAUK: SAI3T3_1000730
SAUQ: SAI4T8_1000730
SAUV: SAI7S6_1000730
SAUW: SAI5S5_1000730
SAUX: SAI6T6_1000730
SAUY: SAI8T7_1000730
SAUF: X998_0096
SAB: SAB0056
SUY: SA2981_0118(sbnB)
SAUB: C248_0105
SAUM: BN843_1190
SAUC: CA347_128
SAUR: SABB_01723(sbnB)
SAUI: AZ30_00610
SAUD: CH52_05135
SAMS: NI36_00505
SUH: SAMSHR1132_00930
SSD: SPSINT_0335
SDT: SPSE_2123(sbnB)
SDP: NCTC12225_02340(sbnB)
SHU: SHYC_00360(sbnB)
SSCH: LH95_00360
SSCZ: RN70_00580
SAGQ: EP23_09765(sbnB)
SEQO: SE1039_25100
SLZ: B5P37_07595
SARL: SAP2_02040
SSH: NCTC13712_00070
SRAI: LN051_00235(sbnB)
SROT: ML435_00405(sbnB)
STAP: AOB58_1874
SFF: FOB90_07430(sbnB)
BLR: BRLA_c008320
BAGR: BA6348_15350
BRW: GOP56_19910(sbnB)
BBOR: RFB14_00530(sbnB)
PMAH: PTQ21_17790(sbnB)
PPAB: KET34_14030(sbnB)
ANX: ACH33_02520
ATHE: K3F53_05635 K3F53_16430(sbnB)
SACA: FFV09_03655(sbnB)
TUM: CBW65_11390
TAB: CIG75_16790
LFB: C1X05_04235
KPUL: GXN76_14220(sbnB)
PABS: JIR001_05100(sbnB)
BACG: D2962_02975
SHAU: K9S39_08615(sbnB)
SACG: FDZ84_26435(sbnB)
PMAD: BAY61_28575
UME: RM788_51380
AFLO: HEQ12_15470(sbnB)
AMIZ: RBH88_00230
PPIO: CE91St28_22640(ocd2)
PYY: RAH42_12000
 » show all
Reference
PMID:24485762
  Authors
Kobylarz MJ, Grigg JC, Takayama SJ, Rai DK, Heinrichs DE, Murphy ME
  Title
Synthesis of L-2,3-diaminopropionic acid, a siderophore and antibiotic precursor.
  Journal
Chem Biol 21:379-88 (2014)
DOI:10.1016/j.chembiol.2013.12.011
  Sequence
[sae:NWMN_0061]
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