Piliocolobus tephrosceles (Ugandan red Colobus): 111520772
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Entry
111520772 CDS
T07491
Symbol
SLC46A1
Name
(RefSeq) proton-coupled folate transporter isoform X1
KO
K14613
MFS transporter, PCFT/HCP family, solute carrier family 46 (folate transporter), member 1
Organism
pteh
Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh01523
Antifolate resistance
pteh04977
Vitamin digestion and absorption
pteh04978
Mineral absorption
pteh04981
Folate transport and metabolism
pteh05215
Prostate cancer
Brite
KEGG Orthology (KO) [BR:
pteh00001
]
09150 Organismal Systems
09154 Digestive system
04977 Vitamin digestion and absorption
111520772 (SLC46A1)
04981 Folate transport and metabolism
111520772 (SLC46A1)
04978 Mineral absorption
111520772 (SLC46A1)
09160 Human Diseases
09162 Cancer: specific types
05215 Prostate cancer
111520772 (SLC46A1)
09176 Drug resistance: antineoplastic
01523 Antifolate resistance
111520772 (SLC46A1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
pteh02000
]
111520772 (SLC46A1)
Transporters [BR:
pteh02000
]
Solute carrier family (SLC)
SLC46: Folate transporter
111520772 (SLC46A1)
Major facilitator superfamily (MFS)
Organic acid transporters
Proton coupled folate transporter/heme carrier protein (PCFT/HCP) family [TC:
2.A.1.50
]
111520772 (SLC46A1)
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SSDB
Ortholog
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Gene cluster
GFIT
Motif
Pfam:
MFS_1
Sugar_tr
Motif
Other DBs
NCBI-GeneID:
111520772
NCBI-ProteinID:
XP_023039589
Ensembl:
ENSPTEG00000030528
UniProt:
A0A8C9I9U4
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Position
16:complement(22914919..22925730)
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AA seq
459 aa
AA seq
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MEGRASPPDKPRVRPAAAVLCRGPVEPLVFLANFALVLQGPLTTQYLWHRFSADLGYNGT
RQRGDCSNRSADPTMQEVETLTSHWTLYMNVGGFLVGLFSSTLLGAWSDGVGRRPLLVLA
SLGLLLQALVSVFVVQLQLHVGYFVLGRILCALLGDFGGLLAASFASVADVSSSRSRTFR
MALLEASIGVAGMLASLLGGHWLRAQGYANPFWLALALLIAMTLYAAFCFGETLKDPKST
RLFTFRHHRSIVQLYVAPAPEKSRKHLALYSLAIFVVITVHFGAQDILTLYELSTPLCWD
SKLIGYGSAAQHLPYLTSLLVLKLLQHCLADAWVAEIGLAFNILGMVVFAFATITPLMFT
GYGLLFLSLVITPVIRAKLSKLVRETEQGALFSAVACVNNLAMLTASGIFNSLYPATLNF
MKGFPFLLGAGLLLIPAVLIGMLEKAVSHPEFQQFPQSP
NT seq
1380 nt
NT seq
+upstream
nt +downstream
nt
atggagggaagggcgagtcccccggacaagccccgcgtccgtcccgcggctgctgtgctg
tgccggggcccggtagagccgctggtcttcctggccaactttgccttggtcctgcagggc
ccgctcaccacgcagtatctgtggcaccgcttcagtgccgacctcggctacaatggcacc
cgccaaaggggggactgcagcaaccgcagcgcggaccccaccatgcaggaagtggagacc
cttacttcccactggaccctctacatgaacgtgggcggcttcctggtggggcttttctcg
tccaccctgctgggagcttggagcgacggtgtgggccgccgcccgctgctagtgctggcc
tcgctgggcctgctgctccaggccctagtgtccgtctttgtggtgcagctacagctccac
gtcggctactttgtgttgggtcgcatcctttgtgccctcctcggcgacttcggtggcctt
ctggctgctagctttgcgtccgtggcagatgtcagctccagccgcagccgcaccttccgg
atggccctgctggaagccagcatcggggtggctgggatgctggcaagcctcctcgggggc
cactggctccgggcccagggttatgccaaccccttctggctggccttagccttgctgata
gccatgacactctatgcagctttctgctttggtgagaccttaaaggacccaaagtccacc
cggctcttcacgttccgtcaccaccgatccattgtccagctctatgtggctccagcccca
gagaagtccaggaagcatttagccctgtactcactggccatcttcgtggtgatcactgtg
cactttggggcccaggacatcttgaccctgtatgaactgagcacacccctctgctgggat
tccaaactaatcggctatggttctgcagctcagcatctcccctacctcaccagcctgctg
gtcctgaagctcctgcagcactgcctggccgacgcctgggtggctgagatcggcctggcc
ttcaacatcctggggatggtggtctttgcctttgccaccatcacacctctcatgttcaca
ggatatgggttgctcttcctgtcattagtcatcacacctgtcatccgggctaaactctcc
aagctggtgagagagacagagcagggtgctctcttttctgctgtggcctgtgtgaataac
ctggccatgctgacggcctccggcatcttcaactcactctacccagccactctgaacttt
atgaaggggttccccttcctcctgggagctggcctcctgctcatcccggccgttctgatt
gggatgctggaaaaggctgtttctcaccctgagttccagcagtttccccagagcccctga
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