Thioflavicoccus mobilis: Thimo_1692
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Entry
Thimo_1692 CDS
T02397
Name
(GenBank) N-acetylmuramoyl-L-alanine amidase
KO
K01448
N-acetylmuramoyl-L-alanine amidase [EC:
3.5.1.28
]
Organism
tmb
Thioflavicoccus mobilis
Pathway
tmb01503
Cationic antimicrobial peptide (CAMP) resistance
Brite
KEGG Orthology (KO) [BR:
tmb00001
]
09160 Human Diseases
09175 Drug resistance: antimicrobial
01503 Cationic antimicrobial peptide (CAMP) resistance
Thimo_1692
09180 Brite Hierarchies
09181 Protein families: metabolism
01011 Peptidoglycan biosynthesis and degradation proteins [BR:
tmb01011
]
Thimo_1692
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
tmb03036
]
Thimo_1692
Enzymes [BR:
tmb01000
]
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
Thimo_1692
Peptidoglycan biosynthesis and degradation proteins [BR:
tmb01011
]
Peptidoglycan biosynthesis and degradation
Amidase
Thimo_1692
Chromosome and associated proteins [BR:
tmb03036
]
Prokaryotic type
Chromosome partitioning proteins
Divisome proteins
Thimo_1692
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Amidase_3
AMIN
LysM
LysM3_LYK4_5
Motif
Other DBs
NCBI-ProteinID:
AGA90469
UniProt:
L0GYU8
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All DBs
Position
complement(1870271..1871578)
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AA seq
435 aa
AA seq
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MKKLIAILLLTFSIPAICQQVDVRGTRVWTSPSQTRLVIDVSGPVTHRIVPLANPDRLMI
DISDAQLTGRLPRVETADPLLMRLRSGSPDGHSLRLVLDLKQRVRAKSFLMPPNERYGHR
LIIDLLPKTSQGTILAGDGIGVFTSSRGAMRDLIIAIDAGHGGEDPGAIGPGGTYEKDVT
LAIARRLATLVDQALGMRAVMIRDGDYYVGLRQRTLLAHKHHADLFLSIHADAFRDTRVS
GASVYTLSSRGASSEAAQWLAEHENNADRIGGIELYESDNDLNRVLFELALNGAVEHSQY
AAEQMIAKLGTIGPLHHDSVQQARFVVLNSPDVPSMLIETAFISNPHDEKRLRDPAHQQR
IARSIFDGIQAYFAQHPLPGTQLASAGTRHHLIHRGDTLIEIAKRYDVTVRSLQNVNSLT
TDRIRVGDVLTIPES
NT seq
1308 nt
NT seq
+upstream
nt +downstream
nt
atgaagaagcttatcgcgatcttgttgttgaccttctcgataccggcgatctgccaacag
gtcgatgtccgggggacgcgcgtctggacgtcgccgagccaaacccgtctggtcatcgac
gtcagcggtcctgtgacccatcggatcgtccccctagcgaacccggatcggctgatgatc
gacatctccgacgcgcagctcacggggcgtctgccacgtgtcgaaaccgccgatcccctg
ctcatgcgcctgcgcagcggctcccccgatgggcacagcctgcgcctcgtcctcgacctc
aaacagcgggtgcgggccaagagtttcctgatgccgcccaatgagcgctatggccaccgc
ctgatcatcgacctgctaccgaagaccagccagggcacgatcctcgccggtgacggcatc
ggggtcttcacatcatcgcgcggcgcgatgcgcgacctgatcatcgcgatcgacgctgga
cacggcggcgaagacccgggtgcgatcggaccggggggtacgtacgagaaggacgtaacg
ctcgcgatcgcgcgccgactggcgaccttggtcgatcaggcgttggggatgcgggcagtg
atgatccgcgacggcgactactacgtcggcctgcgccagcgcacccttctggcccataag
caccacgccgacctcttcctgtcgatccacgccgatgccttccgggacacgcgcgtgagc
ggcgcatccgtctacacgctctcgtcccgtggagcaagcagcgaggctgcgcagtggttg
gcggagcacgagaacaacgccgatcggatcggcggaatcgagctctacgagtcggacaat
gacctcaatcgcgtcctcttcgaactcgccctcaacggcgcggtggaacacagtcagtac
gcggcggagcagatgatcgcgaagctcggtacgatcggtccgttgcaccacgactccgtt
cagcaagcacgcttcgtggtcctgaattctcccgacgtgccctcgatgctgatcgagacc
gccttcatctccaatccgcacgacgagaagcggctgcgggacccggctcaccagcaacgc
atcgcccgatcgatcttcgacggcatccaggcctattttgcacagcatccgctgcccggc
acccagctggcatcggctggcacgcgccatcacctgatccaccgcggcgacaccctgatc
gagatcgctaaacgctacgacgtgacggtacgctcgctccagaacgtcaatagcctgacc
accgaccggatccgggtcggcgatgtcttgacgatcccggagagttga
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