Homo sapiens (human): 11012
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Entry
11012 CDS
T01001
Symbol
KLK11, IEKD, PRSS20, TLSP
Name
(RefSeq) kallikrein related peptidase 11
KO
K09620
kallikrein 11 [EC:3.4.21.-]
Organism
hsa
Homo sapiens (human)
Disease
H02781
Ichthyosis with erythrokeratoderma
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
11012 (KLK11)
Peptidases and inhibitors [BR:
hsa01002
]
Serine peptidases
Family S1: chymotrypsin family
11012 (KLK11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Trypsin
DUF1986
Trypsin_2
Motif
Other DBs
NCBI-GeneID:
11012
NCBI-ProteinID:
NP_659196
OMIM:
604434
HGNC:
6359
Ensembl:
ENSG00000167757
UniProt:
Q9UBX7
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All DBs
Position
19:complement(51022236..51027991)
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AA seq
282 aa
AA seq
DB search
MQRLRWLRDWKSSGRGLTAAKEPGARSSPLQAMRILQLILLALATGLVGGETRIIKGFEC
KPHSQPWQAALFEKTRLLCGATLIAPRWLLTAAHCLKPRYIVHLGQHNLQKEEGCEQTRT
ATESFPHPGFNNSLPNKDHRNDIMLVKMASPVSITWAVRPLTLSSRCVTAGTSCLISGWG
STSSPQLRLPHTLRCANITIIEHQKCENAYPGNITDTMVCASVQEGGKDSCQGDSGGPLV
CNQSLQGIISWGQDPCAITRKPGVYTKVCKYVDWIQETMKNN
NT seq
849 nt
NT seq
+upstream
nt +downstream
nt
atgcagaggttgaggtggctgcgggactggaagtcatcgggcagaggtctcacagcagcc
aaggaacctggggcccgctcctcccccctccaggccatgaggattctgcagttaatcctg
cttgctctggcaacagggcttgtagggggagagaccaggatcatcaaggggttcgagtgc
aagcctcactcccagccctggcaggcagccctgttcgagaagacgcggctactctgtggg
gcgacgctcatcgcccccagatggctcctgacagcagcccactgcctcaagccccgctac
atagttcacctggggcagcacaacctccagaaggaggagggctgtgagcagacccggaca
gccactgagtccttcccccaccccggcttcaacaacagcctccccaacaaagaccaccgc
aatgacatcatgctggtgaagatggcatcgccagtctccatcacctgggctgtgcgaccc
ctcaccctctcctcacgctgtgtcactgctggcaccagctgcctcatttccggctggggc
agcacgtccagcccccagttacgcctgcctcacaccttgcgatgcgccaacatcaccatc
attgagcaccagaagtgtgagaacgcctaccccggcaacatcacagacaccatggtgtgt
gccagcgtgcaggaagggggcaaggactcctgccagggtgactccgggggccctctggtc
tgtaaccagtctcttcaaggcattatctcctggggccaggatccgtgtgcgatcacccga
aagcctggtgtctacacgaaagtctgcaaatatgtggactggatccaggagacgatgaag
aacaattag
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