Homo sapiens (human): 51651
Help
Entry
51651 CDS
T01001
Symbol
PTRH2, BIT1, CFAP37, CGI-147, IMNEPD, PTH, PTH_2, PTH2
Name
(RefSeq) peptidyl-tRNA hydrolase 2
KO
K04794
peptidyl-tRNA hydrolase, PTH2 family [EC:
3.1.1.29
]
Organism
hsa
Homo sapiens (human)
Disease
H02391
Infantile-onset multisystem neurologic, endocrine, and pancreatic disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03012 Translation factors [BR:
hsa03012
]
51651 (PTRH2)
Enzymes [BR:
hsa01000
]
3. Hydrolases
3.1 Acting on ester bonds
3.1.1 Carboxylic-ester hydrolases
3.1.1.29 peptidyl-tRNA hydrolase
51651 (PTRH2)
Translation factors [BR:
hsa03012
]
Eukaryotic type
Release factors
51651 (PTRH2)
Prokaryotic type
51651 (PTRH2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PTH2
Motif
Other DBs
NCBI-GeneID:
51651
NCBI-ProteinID:
NP_057161
OMIM:
608625
HGNC:
24265
Ensembl:
ENSG00000141378
UniProt:
Q9Y3E5
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:complement(59697308..59707430)
Genome browser
AA seq
179 aa
AA seq
DB search
MPSKSLVMEYLAHPSTLGLAVGVACGMCLGWSLRVCFGMLPKSKTSKTHTDTESEASILG
DSGEYKMILVVRNDLKMGKGKVAAQCSHAAVSAYKQIQRRNPEMLKQWEYCGQPKVVVKA
PDEETLIALLAHAKMLGLTVSLIQDAGRTQIAPGSQTVLGIGPGPADLIDKVTGHLKLY
NT seq
540 nt
NT seq
+upstream
nt +downstream
nt
atgccctccaaatccttggttatggaatatttggctcatcccagtacactcggcttggct
gttggagttgcttgtggcatgtgcctgggctggagccttcgagtatgctttgggatgctc
cccaaaagcaagacgagcaagacacacacagatactgaaagtgaagcaagcatcttggga
gacagcggggagtacaagatgattcttgtggttcgaaatgacttaaagatgggaaaaggg
aaagtggctgcccagtgctctcatgctgctgtttcagcctacaagcagattcaaagaaga
aatcctgaaatgctcaaacaatgggaatactgtggccagcccaaggtggtggtcaaagct
cctgatgaagaaaccctgattgcattattggcccatgcaaaaatgctgggactgactgta
agtttaattcaagatgctggacgtactcagattgcaccaggctctcaaactgtcctaggg
attgggccaggaccagcagacctaattgacaaagtcactggtcacctaaaactttactag
DBGET
integrated database retrieval system
