Thioflavicoccus mobilis: Thimo_2781
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Entry
Thimo_2781 CDS
T02397
Name
(GenBank) penicillin-binding protein 2
KO
K05515
penicillin-binding protein 2 [EC:
3.4.16.4
]
Organism
tmb
Thioflavicoccus mobilis
Pathway
tmb00550
Peptidoglycan biosynthesis
tmb01100
Metabolic pathways
tmb01501
beta-Lactam resistance
Brite
KEGG Orthology (KO) [BR:
tmb00001
]
09100 Metabolism
09107 Glycan biosynthesis and metabolism
00550 Peptidoglycan biosynthesis
Thimo_2781
09160 Human Diseases
09175 Drug resistance: antimicrobial
01501 beta-Lactam resistance
Thimo_2781
09180 Brite Hierarchies
09181 Protein families: metabolism
01011 Peptidoglycan biosynthesis and degradation proteins [BR:
tmb01011
]
Thimo_2781
Enzymes [BR:
tmb01000
]
3. Hydrolases
3.4 Acting on peptide bonds (peptidases)
3.4.16 Serine-type carboxypeptidases
3.4.16.4 serine-type D-Ala-D-Ala carboxypeptidase
Thimo_2781
Peptidoglycan biosynthesis and degradation proteins [BR:
tmb01011
]
Peptidoglycan biosynthesis and degradation
DD-Transpeptidase (Class B PBP)
Thimo_2781
BRITE hierarchy
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Ortholog
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Gene cluster
GFIT
Motif
Pfam:
Transpeptidase
PBP_dimer
Motif
Other DBs
NCBI-ProteinID:
AGA91489
UniProt:
L0H1P7
LinkDB
All DBs
Position
complement(3066938..3068821)
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AA seq
627 aa
AA seq
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MAVSPEKIRFKDRSFEQRLVTRRIAVAAGVVLVALMVLVARLSYLQVTNHAHYSTLSEDN
RVRIEPLPPSRGLIYDASGVLLADNYPTYSLEMVLDKVTDPPATIAALSQILTIDDGDRR
RYERLSRQRRRYEGVPIRLNLTQEEIARFAVDAHHFPGVDVQAELVRYYPYGQYTAHVLG
YVGRINEAEQQRVDKSAYAGTHFIGKGGLEKAYEGVLHGRVGYQQVEVNARGRVQRVLTS
HLPEPGRDLHLFLDIDLQKEAAVALGDRRGAVVAIDPRSGGVLALVSEPSFDPNLFVEGI
SQADYDALIGSPDKPLFNRAVRGQYPPGSTVKPFVGLGGLAAGAVTFEKSTWCPGYYTLP
GHTHKFRDWKRGGHGWMTMGQAIEQSCDVYFYHLADQLGIDRLHDSLAEFGFGASTGIDV
AGELGGLLPSRTWKRATRGQVWYPGETLILGIGQGYFLATPLQLAAATAAVAARGHYRVP
RVVRATHAPGAEGLEATPATGHRITLVRPADWEKVIEAMANVIEGRRGTARHIRNEAYRI
AGKTGTSQVFSLGQTERYRADEIAERLRDHALFVAFAPIAEPRIAVAVIVENGGGGGSVA
APVAAQVVDAYLSRPQVLKAAGGDYDR
NT seq
1884 nt
NT seq
+upstream
nt +downstream
nt
atggccgtgtcacccgagaagatacggttcaaggaccgatccttcgagcagcgcctcgta
acccgccgcatcgccgtagcggctggtgtcgtcttggtcgcgctgatggtcctggtggcg
cggctgtcctatttgcaggtcaccaaccatgcgcattactcgaccctctcggaggacaat
cgggtacgtatcgagccgctgccgccgagtcgcggcctcatctacgatgccagcggtgtc
ctgctagcggataactatccgacctactcccttgagatggtcctggacaaggtgaccgac
ccgccggcgactatcgccgcgttgtcgcagatcctgaccatcgatgatggcgatcggcgg
cgctacgagcggttgagtcgccagcgtcggcgctacgagggggtgccgattcggctcaat
ctcactcaggaggagatcgcccgctttgccgtggacgcccatcacttccccggcgtcgac
gtgcaggcggaactggtgcgctactatccctacggtcagtacacggcccacgtgctcggc
tatgtcggacggatcaacgaggccgagcagcagcgtgtcgacaaatcggcctacgccggg
acccacttcatcggcaagggtggcctcgagaaggcttacgagggtgttctccacggccgc
gtcggctatcaacaggtggaggtgaacgcccgaggtcgggtgcagcgggtattgaccagc
cacctgcccgagcccgggcgcgatctgcacctctttctcgacatcgatctccagaaggag
gcagccgtagcgctcggagatcgccgcggggccgtggttgcgatcgatccccgtagcggc
ggcgtcctggcgctcgtcagcgagccgagtttcgatcccaaccttttcgtcgagggcatc
agtcaagccgactacgatgccctgatcggttcgccagacaagccgctcttcaatcgggct
gtccgcggccaatacccgcccggctcgacggtcaaacccttcgtcgggctgggcggcctc
gccgcgggtgccgtgaccttcgagaaatcgacctggtgtcctggctattacacactgccg
ggccatacccacaagtttcgcgactggaagcgcggggggcacggttggatgacgatggga
caggcgatcgagcagtcttgcgacgtctatttctatcacctggcggatcagctcggaatc
gatcgactacacgactcgctcgcggaattcggcttcggcgcgtcgaccggtatcgatgtt
gccggggagctgggtgggttgctgccgtcgcgcacgtggaagcgcgcgacacgagggcag
gtctggtatccgggcgagaccctgatcctcgggatcggccagggctattttctggcgacc
cctctgcagctcgcagcggcgacggccgccgtcgcggcgcgggggcattatcgggtgccg
cgggtcgtgcgggcgacccatgcgccgggggccgaggggttggaggcgacaccggccacc
ggtcaccggatcaccctggtacgcccggcggattgggagaaggtgatcgaggccatggcc
aacgtgatcgagggcaggcgggggacggcgcgccacatccgcaatgaggcctaccgtatc
gccggcaagaccggcacttcgcaggtcttctcgctcggtcagacggagcgctaccgggct
gatgagatcgccgagcggctgcgcgaccacgccctgttcgtcgctttcgccccgatcgcg
gagccgcgcatcgcggtggccgtgatcgtcgagaacggtggtggcggtggctcggtcgcg
gccccggtcgccgcccaagtggtcgacgcctatctgagtcggccgcaggtgttgaaggcc
gcggggggagactatgacaggtag
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