Homo sapiens (human): 9622
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Entry
9622 CDS
T01001
Symbol
KLK4, AI2A1, ARM1, EMSP, EMSP1, KLK-L1, PRSS17, PSTS, kallikrein
Name
(RefSeq) kallikrein related peptidase 4
KO
K08666
kallikrein 4 [EC:3.4.21.-]
Organism
hsa
Homo sapiens (human)
Disease
H00615
Amelogenesis imperfecta
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
9622 (KLK4)
Peptidases and inhibitors [BR:
hsa01002
]
Serine peptidases
Family S1: chymotrypsin family
9622 (KLK4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Trypsin
Trypsin_2
DUF1986
NAD_binding_7
Motif
Other DBs
NCBI-GeneID:
9622
NCBI-ProteinID:
NP_004908
OMIM:
603767
HGNC:
6365
Ensembl:
ENSG00000167749
UniProt:
Q9Y5K2
A0A0C4DFQ5
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:complement(50906351..50911395)
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AA seq
254 aa
AA seq
DB search
MATAGNPWGWFLGYLILGVAGSLVSGSCSQIINGEDCSPHSQPWQAALVMENELFCSGVL
VHPQWVLSAAHCFQNSYTIGLGLHSLEADQEPGSQMVEASLSVRHPEYNRPLLANDLMLI
KLDESVSESDTIRSISIASQCPTAGNSCLVSGWGLLANGRMPTVLQCVNVSVVSEEVCSK
LYDPLYHPSMFCAGGGQDQKDSCNGDSGGPLICNGYLQGLVSFGKAPCGQVGVPGVYTNL
CKFTEWIEKTVQAS
NT seq
765 nt
NT seq
+upstream
nt +downstream
nt
atggccacagcaggaaatccctggggctggttcctggggtacctcatccttggtgtcgca
ggatcgctcgtctctggtagctgcagccaaatcataaacggcgaggactgcagcccgcac
tcgcagccctggcaggcggcactggtcatggaaaacgaattgttctgctcgggcgtcctg
gtgcatccgcagtgggtgctgtcagccgcacactgtttccagaactcctacaccatcggg
ctgggcctgcacagtcttgaggccgaccaagagccagggagccagatggtggaggccagc
ctctccgtacggcacccagagtacaacagacccttgctcgctaacgacctcatgctcatc
aagttggacgaatccgtgtccgagtctgacaccatccggagcatcagcattgcttcgcag
tgccctaccgcggggaactcttgcctcgtttctggctggggtctgctggcgaacggcaga
atgcctaccgtgctgcagtgcgtgaacgtgtcggtggtgtctgaggaggtctgcagtaag
ctctatgacccgctgtaccaccccagcatgttctgcgccggcggagggcaagaccagaag
gactcctgcaacggtgactctggggggcccctgatctgcaacgggtacttgcagggcctt
gtgtctttcggaaaagccccgtgtggccaagttggcgtgccaggtgtctacaccaacctc
tgcaaattcactgagtggatagagaaaaccgtccaggccagttaa
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