Homo sapiens (human): 11153
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Entry
11153 CDS
T01001
Symbol
FICD, HIP13, HYPE, SPG92, UNQ3041
Name
(RefSeq) FIC domain protein adenylyltransferase
KO
K04095
cell filamentation protein, protein adenylyltransferase [EC:
2.7.7.108
]
Organism
hsa
Homo sapiens (human)
Disease
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
11153 (FICD)
Enzymes [BR:
hsa01000
]
2. Transferases
2.7 Transferring phosphorus-containing groups
2.7.7 Nucleotidyltransferases
2.7.7.108 protein adenylyltransferase
11153 (FICD)
Chromosome and associated proteins [BR:
hsa03036
]
Prokaryotic type
Chromosome partitioning proteins
Other chromosome partitioning proteins
11153 (FICD)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Fic
TPR_2
TPR_17
TPR_8
TPR_14
TPR_12
T7SS_EccA1_N
Motif
Other DBs
NCBI-GeneID:
11153
NCBI-ProteinID:
NP_009007
OMIM:
620875
HGNC:
18416
Ensembl:
ENSG00000198855
UniProt:
Q9BVA6
Structure
PDB
PDBj
LinkDB
All DBs
Position
12:108515277..108521210
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AA seq
458 aa
AA seq
DB search
MMLIPMASVMAVTEPKWVSVWSRFLWVTLLSMVLGSLLALLLPLGAVEEQCLAVLKGLYL
LRSKPDRAQHAATKCTSPSTELSITSRGATLLVAKTKASPAGKLEARAALNQALEMKRQG
KREKAQKLFMHALKMDPDFVDALTEFGIFSEEDKDIIQADYLYTRALTISPYHEKALVNR
DRTLPLVEEIDQRYFSIIDSKVKKVMSIPKGNSALRRVMEETYYHHIYHTVAIEGNTLTL
SEIRHILETRYAVPGKSLEEQNEVIGMHAAMKYINTTLVSRIGSVTISDVLEIHRRVLGY
VDPVEAGRFRTTQVLVGHHIPPHPQDVEKQMQEFVQWLNSEEAMNLHPVEFAALAHYKLV
YIHPFIDGNGRTSRLLMNLILMQAGYPPITIRKEQRSDYYHVLEAANEGDVRPFIRFIAK
CTETTLDTLLFATTEYSVALPEAQPNHSGFKETLPVKP
NT seq
1377 nt
NT seq
+upstream
nt +downstream
nt
atgatgctcataccaatggcttcagtgatggcggtgactgaaccgaaatgggtctcggtc
tggagccgcttcctctgggtgacgctgctgagcatggtgctggggtccctgctggccctg
ctgctgccgctgggggctgtggaggagcagtgcttggctgtgctcaaaggcctctacctg
ctcaggagcaaaccggacagggcgcagcatgccgccaccaagtgcaccagcccgtccacg
gagctcagcatcacctccaggggcgcgacgctgctggtggccaagaccaaggcctctcca
gcgggtaagttggaagccagagctgccctgaaccaggccctggagatgaagcgccagggc
aagcgggaaaaagcccaaaagctcttcatgcacgccctcaagatggacccggacttcgtg
gacgcgctcaccgagtttggcatcttctcggaagaagacaaggacatcatccaggcggac
tacttgtacaccagagcattgaccatctcaccctaccatgagaaagcactggtcaaccgc
gatcggacactgcctcttgtggaagagatcgaccagaggtatttcagcatcatcgacagc
aaagtgaagaaggtcatgtccatccccaaggggaactcagctctgcgcagggtcatggag
gagacctactaccatcacatctaccacacagtggccatcgagggcaacaccctcaccctc
tcggaaatcaggcacatcctggagacccgctacgccgtgcccgggaagagcctggaggag
cagaacgaggtcataggcatgcatgcagccatgaagtacatcaacacgactctggtttcg
cgcatcggctccgtcaccatcagcgacgtgctggagatccacaggcgggtgctgggctac
gtggaccccgtggaagccggcaggtttcggacaacacaggtcctggtcggacaccacatc
cctccccatccgcaggatgtggaaaagcagatgcaggagtttgtacagtggctcaactcc
gaggaagccatgaacctgcacccagtggagtttgcagccttagcccattataaactcgtt
tacatccaccctttcattgatggcaacgggaggacctcccgtctgctcatgaacctcatc
ctcatgcaggcgggctacccgcccatcaccatccgcaaggagcagcggtccgactactac
cacgtgttggaagctgccaacgagggcgacgtgaggcctttcattcgcttcatcgccaag
tgtactgagaccaccctggacaccctgctttttgccacaactgagtactcggtggcactg
ccagaagcccaacccaaccactctgggttcaaggagacgcttcctgtgaagccctaa
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