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-4 isoform 2
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)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Trypsin
NAD_binding_7
Motif
Other DBs
NCBI-GeneID:
9622
NCBI-ProteinID:
NP_001289890
OMIM:
603767
HGNC:
6365
UniProt:
Q9Y5K2
Q5BQA0
M0R1S9
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:complement(50906351..50911395)
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AA seq
159 aa
AA seq
DB search
MVEASLSVRHPEYNRPLLANDLMLIKLDESVSESDTIRSISIASQCPTAGNSCLVSGWGL
LANGRMPTVLQCVNVSVVSEEVCSKLYDPLYHPSMFCAGGGQDQKDSCNGDSGGPLICNG
YLQGLVSFGKAPCGQVGVPGVYTNLCKFTEWIEKTVQAS
NT seq
480 nt
NT seq
+upstream
nt +downstream
nt
atggtggaggccagcctctccgtacggcacccagagtacaacagacccttgctcgctaac
gacctcatgctcatcaagttggacgaatccgtgtccgagtctgacaccatccggagcatc
agcattgcttcgcagtgccctaccgcggggaactcttgcctcgtttctggctggggtctg
ctggcgaacggcagaatgcctaccgtgctgcagtgcgtgaacgtgtcggtggtgtctgag
gaggtctgcagtaagctctatgacccgctgtaccaccccagcatgttctgcgccggcgga
gggcaagaccagaaggactcctgcaacggtgactctggggggcccctgatctgcaacggg
tacttgcagggccttgtgtctttcggaaaagccccgtgtggccaagttggcgtgccaggt
gtctacaccaacctctgcaaattcactgagtggatagagaaaaccgtccaggccagttaa
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integrated database retrieval system
