Homo sapiens (human): 6317
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Entry
6317 CDS
T01001
Symbol
SERPINB3, HsT1196, SCC, SCCA-1, SCCA-PD, SCCA1, SSCA1, T4-A
Name
(RefSeq) serpin family B member 3
KO
K13963
serpin B
Organism
hsa
Homo sapiens (human)
Pathway
hsa05146
Amoebiasis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09174 Infectious disease: parasitic
05146 Amoebiasis
6317 (SERPINB3)
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
6317 (SERPINB3)
Peptidases and inhibitors [BR:
hsa01002
]
Peptidase inhibitors
Family I4: serpin family
6317 (SERPINB3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Serpin
YgjP-like
TctC
Motif
Other DBs
NCBI-GeneID:
6317
NCBI-ProteinID:
NP_008850
OMIM:
600517
HGNC:
10569
Ensembl:
ENSG00000057149
UniProt:
P29508
Structure
PDB
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All DBs
Position
18:complement(63655197..63661893)
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AA seq
390 aa
AA seq
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MNSLSEANTKFMFDLFQQFRKSKENNIFYSPISITSALGMVLLGAKDNTAQQIKKVLHFD
QVTENTTGKAATYHVDRSGNVHHQFQKLLTEFNKSTDAYELKIANKLFGEKTYLFLQEYL
DAIKKFYQTSVESVDFANAPEESRKKINSWVESQTNEKIKNLIPEGNIGSNTTLVLVNAI
YFKGQWEKKFNKEDTKEEKFWPNKNTYKSIQMMRQYTSFHFASLEDVQAKVLEIPYKGKD
LSMIVLLPNEIDGLQKLEEKLTAEKLMEWTSLQNMRETRVDLHLPRFKVEESYDLKDTLR
TMGMVDIFNGDADLSGMTGSRGLVLSGVLHKAFVEVTEEGAEAAAATAVVGFGSSPTSTN
EEFHCNHPFLFFIRQNKTNSILFYGRFSSP
NT seq
1173 nt
NT seq
+upstream
nt +downstream
nt
atgaattcactcagtgaagccaacaccaagttcatgttcgacctgttccaacagttcaga
aaatcaaaagagaacaacatcttctattcccctatcagcatcacatcagcattagggatg
gtcctcttaggagccaaagacaacactgcacaacagattaagaaggttcttcactttgat
caagtcacagagaacaccacaggaaaagctgcaacatatcatgttgataggtcaggaaat
gttcatcaccagtttcaaaagcttctgactgaattcaacaaatccactgatgcatatgag
ctgaagatcgccaacaagctcttcggagaaaaaacgtatctatttttacaggaatattta
gatgccatcaagaaattttaccagaccagtgtggaatctgttgattttgcaaatgctcca
gaagaaagtcgaaagaagattaactcctgggtggaaagtcaaacgaatgaaaaaattaaa
aacctaattcctgaaggtaatattggcagcaataccacattggttcttgtgaacgcaatc
tatttcaaagggcagtgggagaagaaatttaataaagaagatactaaagaggaaaaattt
tggccaaacaagaatacatacaagtccatacagatgatgaggcaatacacatcttttcat
tttgcctcgctggaggatgtacaggccaaggtcctggaaataccatacaaaggcaaagat
ctaagcatgattgtgttgctgccaaatgaaatcgatggtctccagaagcttgaagagaaa
ctcactgctgagaaattgatggaatggacaagtttgcagaatatgagagagacacgtgtc
gatttacacttacctcggttcaaagtggaagagagctatgacctcaaggacacgttgaga
accatgggaatggtggatatcttcaatggggatgcagacctctcaggcatgaccgggagc
cgcggtctcgtgctatctggagtcctacacaaggcctttgtggaggttacagaggaggga
gcagaagctgcagctgccaccgctgtagtaggattcggatcatcacctacttcaactaat
gaagagttccattgtaatcaccctttcctattcttcataaggcaaaataagaccaacagc
atcctcttctatggcagattctcatccccgtag
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