Dietzia cinnamea: VYL96_16815
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Entry
VYL96_16815 CDS
T10417
Name
(GenBank) N-acetylmuramoyl-L-alanine amidase
KO
K01448
N-acetylmuramoyl-L-alanine amidase [EC:
3.5.1.28
]
Organism
dcd Dietzia cinnamea
Pathway
dcd01503
Cationic antimicrobial peptide (CAMP) resistance
Brite
KEGG Orthology (KO) [BR:
dcd00001
]
09160 Human Diseases
09175 Drug resistance: antimicrobial
01503 Cationic antimicrobial peptide (CAMP) resistance
VYL96_16815
09180 Brite Hierarchies
09181 Protein families: metabolism
01011 Peptidoglycan biosynthesis and degradation proteins [BR:
dcd01011
]
VYL96_16815
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
dcd03036
]
VYL96_16815
Enzymes [BR:
dcd01000
]
3. Hydrolases
3.5 Acting on carbon-nitrogen bonds, other than peptide bonds
3.5.1 In linear amides
3.5.1.28 N-acetylmuramoyl-L-alanine amidase
VYL96_16815
Peptidoglycan biosynthesis and degradation proteins [BR:
dcd01011
]
Peptidoglycan biosynthesis and degradation
Amidase
VYL96_16815
Chromosome and associated proteins [BR:
dcd03036
]
Prokaryotic type
Chromosome partitioning proteins
Divisome proteins
VYL96_16815
BRITE hierarchy
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Paralog
Gene cluster
GFIT
Motif
Pfam:
PG_binding_1
Amidase_3
PG_binding_3
PG_binding_2
Motif
Other DBs
NCBI-ProteinID:
WVF63514
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Position
3612965..3614155
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AA seq
396 aa
AA seq
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MAWRRGDRGPEVAAIRATLAGMGLLHNIDSVGVTEPETGSVLARTDAVFDADLETAVLAF
QQARGLISDGIVGPATQAALDDASHVLGTRDLSYIVSKPMAGDDVAQLQRRLGELGFYAG
LVDGTFGALTHAAVTDFQRDCALEADGVVGAETLDTINRFSTLFKGGDMASLVEKERART
SGPMLAGKRIVLDPGPSGSENPIRIETPNGTITDAELLWDITRRLSERMNQAGVEVFLSR
PEAMIPTDPERAEIANAFNADLVISLRLDRHPNPVGNGVATFYFGNSLGAESMLGEALSG
FIQREIVSRTELRDCRTHGRSWPLLRMTRMPSVQIYLGYAHNAGDLAILGDRDAQDTIID
SILVGVKRLYLLDEDDHPTGSMSLDDLIDYEQRQRS
NT seq
1191 nt
NT seq
+upstream
nt +downstream
nt
atggcgtggaggcgtggtgaccgcgggcccgaggtggccgcgatccgggccaccctcgct
gggatgggcctgcttcacaacatcgattcggtcggggtcaccgagccggagaccggttcg
gtcctcgcccggaccgacgcggtgttcgacgccgatctcgagacggccgttctggccttc
cagcaggcccgtgggctgatctccgacgggatcgtgggtccggcgacccaggccgccctc
gacgacgccagccacgtcctggggacgcgggatctgagctacatcgtctccaagcccatg
gccggggacgacgtcgcccagctccagcgccggctcggggagctcggtttctacgccggt
ctcgtcgacgggaccttcggcgccctcacccacgctgcggtcaccgacttccagcgggac
tgcgccctcgaggcggacggcgtcgtgggcgccgagaccctcgacaccatcaaccgcttc
tcgaccctcttcaagggcggcgacatggcgtccctcgtggagaaggagcgcgcccgcacc
tccggtccgatgctcgccggcaagcggatcgtgctcgatcccggccccagcgggtccgag
aacccgatccgcatcgagaccccgaacggaacgatcacggatgccgagctcctgtgggac
atcacccgccgactctccgagcggatgaaccaggccggcgtggaggtcttcctctcgcgg
cccgaggccatgatccccaccgatcccgaacgcgcggagatcgccaacgcgttcaacgcc
gacctcgtgatctccctgcggctcgaccggcatcccaatcccgtgggcaacggggtcgcg
accttctacttcggtaactcgctgggcgcggagtccatgctcggtgaggctctgtcggga
ttcatccagcgggagatcgtcagccgcaccgagctgcgggactgccgcacccacggccgc
agctggccactgctgcggatgacccgtatgccgtccgtgcagatctacctcgggtacgca
cacaacgccggcgacctcgccatcctgggggaccgcgacgcgcaggacacgatcatcgat
tcgatcctcgtgggcgtcaagcgcctctatctactcgacgaggacgaccatcccaccggg
tctatgtccctcgacgacctcatcgactacgagcagcgccagcgcagctga
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