Homo sapiens (human): 836
Help
Entry
836 CDS
T01001
Symbol
CASP3, CPP32, CPP32B, SCA-1
Name
(RefSeq) caspase 3
KO
K02187
caspase 3 [EC:
3.4.22.56
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa01524
Platinum drug resistance
hsa04010
MAPK signaling pathway
hsa04115
p53 signaling pathway
hsa04148
Efferocytosis
hsa04210
Apoptosis
hsa04215
Apoptosis - multiple species
hsa04623
Cytosolic DNA-sensing pathway
hsa04650
Natural killer cell mediated cytotoxicity
hsa04657
IL-17 signaling pathway
hsa04668
TNF signaling pathway
hsa04726
Serotonergic synapse
hsa04932
Non-alcoholic fatty liver disease
hsa04933
AGE-RAGE signaling pathway in diabetic complications
hsa04936
Alcoholic liver disease
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05120
Epithelial cell signaling in Helicobacter pylori infection
hsa05130
Pathogenic Escherichia coli infection
hsa05132
Salmonella infection
hsa05133
Pertussis
hsa05134
Legionellosis
hsa05145
Toxoplasmosis
hsa05146
Amoebiasis
hsa05152
Tuberculosis
hsa05160
Hepatitis C
hsa05161
Hepatitis B
hsa05162
Measles
hsa05163
Human cytomegalovirus infection
hsa05164
Influenza A
hsa05165
Human papillomavirus infection
hsa05167
Kaposi sarcoma-associated herpesvirus infection
hsa05168
Herpes simplex virus 1 infection
hsa05169
Epstein-Barr virus infection
hsa05170
Human immunodeficiency virus 1 infection
hsa05200
Pathways in cancer
hsa05203
Viral carcinogenesis
hsa05205
Proteoglycans in cancer
hsa05206
MicroRNAs in cancer
hsa05210
Colorectal cancer
hsa05222
Small cell lung cancer
hsa05416
Viral myocarditis
hsa05417
Lipid and atherosclerosis
Network
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06162
Hepatitis B virus (HBV)
nt06163
Hepatitis C virus (HCV)
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06165
Epstein-Barr virus (EBV)
nt06166
Human papillomavirus (HPV)
nt06167
Human cytomegalovirus (HCMV)
nt06168
Herpes simplex virus 1 (HSV-1)
nt06170
Influenza A virus (IAV)
nt06231
Apoptosis (cancer)
nt06260
Colorectal cancer
nt06263
Hepatocellular carcinoma
nt06267
Small cell lung cancer
nt06460
Alzheimer disease
nt06461
Huntington disease
nt06462
Spinocerebellar ataxia
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06465
Prion disease
nt06466
Pathways of neurodegeneration
nt06516
TNF signaling
nt06524
Apoptosis
nt06528
Calcium signaling
nt06535
Efferocytosis
Element
N00098
Intrinsic apoptotic pathway
N00100
BCL2-overexpression to intrinsic apoptotic pathway
N00101
DCC-apoptotic pathway
N00102
Loss of DCC to DCC-apoptotic pathway
N00145
Extrinsic apoptotic pathway
N00146
Crosstalk between extrinsic and intrinsic apoptotic pathways
N00165
KSHV vIAP to crosstalk between extrinsic and intrinsic apoptotic pathways
N00449
HIV Tat/Nef to crosstalk between extrinsic and intrinsic apoptotic pathways
N00478
EBV BARF1 to intrinsic apoptotic pathway
N00580
HSV ICP0 to crosstalk between extrinsic and intrinsic apoptotic pathways
N00967
VGCC-Ca2+ -apoptotic pathway
N00983
Mutation-caused aberrant Htt to extrinsic apoptotic pathway
N00984
mGluR5-Ca2+ -apoptotic pathway
N00985
Mutation-caused aberrant Htt to mGluR5-Ca2+ -apoptotic pathway
N00987
Mutation-caused aberrant Htt to transport of calcium
N01002
Mutation-caused aberrant Abeta to mGluR5-Ca2+ -apoptotic pathway
N01005
Mutation-caused aberrant Abeta to crosstalk between extrinsic and intrinsic apoptotic pathways
N01007
Mutation-caused aberrant PSEN to mGluR5-Ca2+ -apoptotic pathway
N01031
Mutation-caused aberrant SNCA to VGCC-Ca2+ -apoptotic pathway
N01047
Mutation-activated LRRK2 to intrinsic apoptotic pathway
N01048
Mutation-inactivated PINK1 to intrinsic apoptotic pathway
N01049
Mutation-inactivated PRKN to intrinsic apoptotic pathway
N01050
Mutation-inactivated PINK1 to intrinsic apoptotic pathway
N01135
Mutation-caused aberrant SOD1 to intrinsic apoptotic pathway
N01199
Scrapie conformation PrPSc to mGluR5-Ca2+ -apoptotic pathway
N01200
Scrapie conformation PrPSc to transport of calcium
N01747
Find-me signal (nucleotide)
N01748
Find-me signal (LPC)
N01749
Find-me signal (CX3CL1)
N01750
Find-me signal (S1P)
N01754
Activation of XKR8
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
836 (CASP3)
04668 TNF signaling pathway
836 (CASP3)
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
836 (CASP3)
09143 Cell growth and death
04210 Apoptosis
836 (CASP3)
04215 Apoptosis - multiple species
836 (CASP3)
04115 p53 signaling pathway
836 (CASP3)
09150 Organismal Systems
09151 Immune system
04623 Cytosolic DNA-sensing pathway
836 (CASP3)
04650 Natural killer cell mediated cytotoxicity
836 (CASP3)
04657 IL-17 signaling pathway
836 (CASP3)
09156 Nervous system
04726 Serotonergic synapse
836 (CASP3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
836 (CASP3)
05206 MicroRNAs in cancer
836 (CASP3)
05205 Proteoglycans in cancer
836 (CASP3)
05203 Viral carcinogenesis
836 (CASP3)
09162 Cancer: specific types
05210 Colorectal cancer
836 (CASP3)
05222 Small cell lung cancer
836 (CASP3)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
836 (CASP3)
05161 Hepatitis B
836 (CASP3)
05160 Hepatitis C
836 (CASP3)
05164 Influenza A
836 (CASP3)
05162 Measles
836 (CASP3)
05168 Herpes simplex virus 1 infection
836 (CASP3)
05163 Human cytomegalovirus infection
836 (CASP3)
05167 Kaposi sarcoma-associated herpesvirus infection
836 (CASP3)
05169 Epstein-Barr virus infection
836 (CASP3)
05165 Human papillomavirus infection
836 (CASP3)
09171 Infectious disease: bacterial
05120 Epithelial cell signaling in Helicobacter pylori infection
836 (CASP3)
05130 Pathogenic Escherichia coli infection
836 (CASP3)
05132 Salmonella infection
836 (CASP3)
05133 Pertussis
836 (CASP3)
05134 Legionellosis
836 (CASP3)
05152 Tuberculosis
836 (CASP3)
09174 Infectious disease: parasitic
05146 Amoebiasis
836 (CASP3)
05145 Toxoplasmosis
836 (CASP3)
09164 Neurodegenerative disease
05010 Alzheimer disease
836 (CASP3)
05012 Parkinson disease
836 (CASP3)
05014 Amyotrophic lateral sclerosis
836 (CASP3)
05016 Huntington disease
836 (CASP3)
05020 Prion disease
836 (CASP3)
05022 Pathways of neurodegeneration - multiple diseases
836 (CASP3)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
836 (CASP3)
05416 Viral myocarditis
836 (CASP3)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
836 (CASP3)
04932 Non-alcoholic fatty liver disease
836 (CASP3)
04933 AGE-RAGE signaling pathway in diabetic complications
836 (CASP3)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
836 (CASP3)
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
836 (CASP3)
Enzymes [BR:
hsa01000
]
3. Hydrolases
3.4 Acting on peptide bonds (peptidases)
3.4.22 Cysteine endopeptidases
3.4.22.56 caspase-3
836 (CASP3)
Peptidases and inhibitors [BR:
hsa01002
]
Cysteine peptidases
Family C14: caspase family
836 (CASP3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Peptidase_C14
SICA_beta
Motif
Other DBs
NCBI-GeneID:
836
NCBI-ProteinID:
NP_004337
OMIM:
600636
HGNC:
1504
Ensembl:
ENSG00000164305
UniProt:
P42574
Structure
PDB
LinkDB
All DBs
Position
4:complement(184627696..184649447)
Genome browser
AA seq
277 aa
AA seq
DB search
MENTENSVDSKSIKNLEPKIIHGSESMDSGISLDNSYKMDYPEMGLCIIINNKNFHKSTG
MTSRSGTDVDAANLRETFRNLKYEVRNKNDLTREEIVELMRDVSKEDHSKRSSFVCVLLS
HGEEGIIFGTNGPVDLKKITNFFRGDRCRSLTGKPKLFIIQACRGTELDCGIETDSGVDD
DMACHKIPVEADFLYAYSTAPGYYSWRNSKDGSWFIQSLCAMLKQYADKLEFMHILTRVN
RKVATEFESFSFDATFHAKKQIPCIVSMLTKELYFYH
NT seq
834 nt
NT seq
+upstream
nt +downstream
nt
atggagaacactgaaaactcagtggattcaaaatccattaaaaatttggaaccaaagatc
atacatggaagcgaatcaatggactctggaatatccctggacaacagttataaaatggat
tatcctgagatgggtttatgtataataattaataataagaattttcataaaagcactgga
atgacatctcggtctggtacagatgtcgatgcagcaaacctcagggaaacattcagaaac
ttgaaatatgaagtcaggaataaaaatgatcttacacgtgaagaaattgtggaattgatg
cgtgatgtttctaaagaagatcacagcaaaaggagcagttttgtttgtgtgcttctgagc
catggtgaagaaggaataatttttggaacaaatggacctgttgacctgaaaaaaataaca
aactttttcagaggggatcgttgtagaagtctaactggaaaacccaaacttttcattatt
caggcctgccgtggtacagaactggactgtggcattgagacagacagtggtgttgatgat
gacatggcgtgtcataaaataccagtggaggccgacttcttgtatgcatactccacagca
cctggttattattcttggcgaaattcaaaggatggctcctggttcatccagtcgctttgt
gccatgctgaaacagtatgccgacaagcttgaatttatgcacattcttacccgggttaac
cgaaaggtggcaacagaatttgagtccttttcctttgacgctacttttcatgcaaagaaa
cagattccatgtattgtttccatgctcacaaaagaactctatttttatcactaa
Homo sapiens (human): 102
Help
Entry
102 CDS
T01001
Symbol
ADAM10, AD10, AD18, CD156c, CDw156, HsT18717, MADM, RAK, kuz
Name
(RefSeq) ADAM metallopeptidase domain 10
KO
K06704
disintegrin and metalloproteinase domain-containing protein 10 [EC:
3.4.24.81
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa04148
Efferocytosis
hsa05010
Alzheimer disease
hsa05120
Epithelial cell signaling in Helicobacter pylori infection
Network
nt06535
Efferocytosis
Element
N01749
Find-me signal (CX3CL1)
Disease
H00056
Alzheimer disease
H02665
Reticulate acropigmentation of Kitamura
Drug target
Aderbasib:
D09320
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
102 (ADAM10)
09160 Human Diseases
09171 Infectious disease: bacterial
05120 Epithelial cell signaling in Helicobacter pylori infection
102 (ADAM10)
09164 Neurodegenerative disease
05010 Alzheimer disease
102 (ADAM10)
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
102 (ADAM10)
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
102 (ADAM10)
Enzymes [BR:
hsa01000
]
3. Hydrolases
3.4 Acting on peptide bonds (peptidases)
3.4.24 Metalloendopeptidases
3.4.24.81 ADAM10 endopeptidase
102 (ADAM10)
Peptidases and inhibitors [BR:
hsa01002
]
Metallo peptidases
Family M12: astacin/adamalysin family
102 (ADAM10)
CD molecules [BR:
hsa04090
]
Proteins
102 (ADAM10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Reprolysin_2
Reprolysin_5
Reprolysin_3
ADAM10_Cys-rich
Reprolysin_4
Disintegrin
Pep_M12B_propep
Reprolysin
Peptidase_M66
Motif
Other DBs
NCBI-GeneID:
102
NCBI-ProteinID:
NP_001101
OMIM:
602192
HGNC:
188
Ensembl:
ENSG00000137845
UniProt:
O14672
Structure
PDB
LinkDB
All DBs
Position
15:complement(58588809..58749707)
Genome browser
AA seq
748 aa
AA seq
DB search
MVLLRVLILLLSWAAGMGGQYGNPLNKYIRHYEGLSYNVDSLHQKHQRAKRAVSHEDQFL
RLDFHAHGRHFNLRMKRDTSLFSDEFKVETSNKVLDYDTSHIYTGHIYGEEGSFSHGSVI
DGRFEGFIQTRGGTFYVEPAERYIKDRTLPFHSVIYHEDDINYPHKYGPQGGCADHSVFE
RMRKYQMTGVEEVTQIPQEEHAANGPELLRKKRTTSAEKNTCQLYIQTDHLFFKYYGTRE
AVIAQISSHVKAIDTIYQTTDFSGIRNISFMVKRIRINTTADEKDPTNPFRFPNIGVEKF
LELNSEQNHDDYCLAYVFTDRDFDDGVLGLAWVGAPSGSSGGICEKSKLYSDGKKKSLNT
GIITVQNYGSHVPPKVSHITFAHEVGHNFGSPHDSGTECTPGESKNLGQKENGNYIMYAR
ATSGDKLNNNKFSLCSIRNISQVLEKKRNNCFVESGQPICGNGMVEQGEECDCGYSDQCK
DECCFDANQPEGRKCKLKPGKQCSPSQGPCCTAQCAFKSKSEKCRDDSDCAREGICNGFT
ALCPASDPKPNFTDCNRHTQVCINGQCAGSICEKYGLEECTCASSDGKDDKELCHVCCMK
KMDPSTCASTGSVQWSRHFSGRTITLQPGSPCNDFRGYCDVFMRCRLVDADGPLARLKKA
IFSPELYENIAEWIVAHWWAVLLMGIALIMLMAGFIKICSVHTPSSNPKLPPPKPLPGTL
KRRRPPQPIQQPQRQRPRESYQMGHMRR
NT seq
2247 nt
NT seq
+upstream
nt +downstream
nt
atggtgttgctgagagtgttaattctgctcctctcctgggcggcggggatgggaggtcag
tatgggaatcctttaaataaatatatcagacattatgaaggattatcttacaatgtggat
tcattacaccaaaaacaccagcgtgccaaaagagcagtctcacatgaagaccaattttta
cgtctagatttccatgcccatggaagacatttcaacctacgaatgaagagggacacttcc
cttttcagtgatgaatttaaagtagaaacatcaaataaagtacttgattatgatacctct
catatttacactggacatatttatggtgaagaaggaagttttagccatgggtctgttatt
gatggaagatttgaaggattcatccagactcgtggtggcacattttatgttgagccagca
gagagatatattaaagaccgaactctgccatttcactctgtcatttatcatgaagatgat
attaactatccccataaatacggtcctcaggggggctgtgcagatcattcagtatttgaa
agaatgaggaaataccagatgactggtgtagaggaagtaacacagatacctcaagaagaa
catgctgctaatggtccagaacttctgaggaaaaaacgtacaacttcagctgaaaaaaat
acttgtcagctttatattcagactgatcatttgttctttaaatattacggaacacgagaa
gctgtgattgcccagatatccagtcatgttaaagcgattgatacaatttaccagaccaca
gacttctccggaatccgtaacatcagtttcatggtgaaacgcataagaatcaatacaact
gctgatgagaaggaccctacaaatcctttccgtttcccaaatattggtgtggagaagttt
ctggaattgaattctgagcagaatcatgatgactactgtttggcctatgtcttcacagac
cgagattttgatgatggcgtacttggtctggcttgggttggagcaccttcaggaagctct
ggaggaatatgtgaaaaaagtaaactctattcagatggtaagaagaagtccttaaacact
ggaattattactgttcagaactatgggtctcatgtacctcccaaagtctctcacattact
tttgctcacgaagttggacataactttggatccccacatgattctggaacagagtgcaca
ccaggagaatctaagaatttgggtcaaaaagaaaatggcaattacatcatgtatgcaaga
gcaacatctggggacaaacttaacaacaataaattctcactctgtagtattagaaatata
agccaagttcttgagaagaagagaaacaactgttttgttgaatctggccaacctatttgt
ggaaatggaatggtagaacaaggtgaagaatgtgattgtggctatagtgaccagtgtaaa
gatgaatgctgcttcgatgcaaatcaaccagagggaagaaaatgcaaactgaaacctggg
aaacagtgcagtccaagtcaaggtccttgttgtacagcacagtgtgcattcaagtcaaag
tctgagaagtgtcgggatgattcagactgtgcaagggaaggaatatgtaatggcttcaca
gctctctgcccagcatctgaccctaaaccaaacttcacagactgtaataggcatacacaa
gtgtgcattaatgggcaatgtgcaggttctatctgtgagaaatatggcttagaggagtgt
acgtgtgccagttctgatggcaaagatgataaagaattatgccatgtatgctgtatgaag
aaaatggacccatcaacttgtgccagtacagggtctgtgcagtggagtaggcacttcagt
ggtcgaaccatcaccctgcaacctggatccccttgcaacgattttagaggttactgtgat
gttttcatgcggtgcagattagtagatgctgatggtcctctagctaggcttaaaaaagca
atttttagtccagagctctatgaaaacattgctgaatggattgtggctcattggtgggca
gtattacttatgggaattgctctgatcatgctaatggctggatttattaagatatgcagt
gttcatactccaagtagtaatccaaagttgcctcctcctaaaccacttccaggcacttta
aagaggaggagacctccacagcccattcagcaaccccagcgtcagcggccccgagagagt
tatcaaatgggacacatgagacgctaa
Homo sapiens (human): 6868
Help
Entry
6868 CDS
T01001
Symbol
ADAM17, ADAM18, CD156B, CSVP, NISBD, NISBD1, TACE
Name
(RefSeq) ADAM metallopeptidase domain 17
KO
K06059
disintegrin and metalloproteinase domain-containing protein 17 [EC:
3.4.24.86
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa04148
Efferocytosis
hsa04330
Notch signaling pathway
hsa05010
Alzheimer disease
hsa05120
Epithelial cell signaling in Helicobacter pylori infection
hsa05171
Coronavirus disease - COVID-19
Network
nt06511
NOTCH signaling
nt06535
Efferocytosis
Element
N01478
Notch proteolytic activation
N01749
Find-me signal (CX3CL1)
Disease
H02467
Neonatal inflammatory skin and bowel disease
Drug target
Aderbasib:
D09320
Apratastat:
D08859
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04330 Notch signaling pathway
6868 (ADAM17)
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
6868 (ADAM17)
09160 Human Diseases
09172 Infectious disease: viral
05171 Coronavirus disease - COVID-19
6868 (ADAM17)
09171 Infectious disease: bacterial
05120 Epithelial cell signaling in Helicobacter pylori infection
6868 (ADAM17)
09164 Neurodegenerative disease
05010 Alzheimer disease
6868 (ADAM17)
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
6868 (ADAM17)
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
6868 (ADAM17)
Enzymes [BR:
hsa01000
]
3. Hydrolases
3.4 Acting on peptide bonds (peptidases)
3.4.24 Metalloendopeptidases
3.4.24.86 ADAM 17 endopeptidase
6868 (ADAM17)
Peptidases and inhibitors [BR:
hsa01002
]
Metallo peptidases
Family M12: astacin/adamalysin family
6868 (ADAM17)
CD molecules [BR:
hsa04090
]
Proteins
6868 (ADAM17)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Reprolysin_2
Reprolysin_5
ADAM17_MPD
Disintegrin
Reprolysin_3
Reprolysin
Reprolysin_4
Pep_M12B_propep
Motif
Other DBs
NCBI-GeneID:
6868
NCBI-ProteinID:
NP_003174
OMIM:
603639
HGNC:
195
Ensembl:
ENSG00000151694
UniProt:
P78536
B2RNB2
Structure
PDB
LinkDB
All DBs
Position
2:complement(9488486..9555830)
Genome browser
AA seq
824 aa
AA seq
DB search
MRQSLLFLTSVVPFVLAPRPPDDPGFGPHQRLEKLDSLLSDYDILSLSNIQQHSVRKRDL
QTSTHVETLLTFSALKRHFKLYLTSSTERFSQNFKVVVVDGKNESEYTVKWQDFFTGHVV
GEPDSRVLAHIRDDDVIIRINTDGAEYNIEPLWRFVNDTKDKRMLVYKSEDIKNVSRLQS
PKVCGYLKVDNEELLPKGLVDREPPEELVHRVKRRADPDPMKNTCKLLVVADHRFYRYMG
RGEESTTTNYLIELIDRVDDIYRNTSWDNAGFKGYGIQIEQIRILKSPQEVKPGEKHYNM
AKSYPNEEKDAWDVKMLLEQFSFDIAEEASKVCLAHLFTYQDFDMGTLGLAYVGSPRANS
HGGVCPKAYYSPVGKKNIYLNSGLTSTKNYGKTILTKEADLVTTHELGHNFGAEHDPDGL
AECAPNEDQGGKYVMYPIAVSGDHENNKMFSNCSKQSIYKTIESKAQECFQERSNKVCGN
SRVDEGEECDPGIMYLNNDTCCNSDCTLKEGVQCSDRNSPCCKNCQFETAQKKCQEAINA
TCKGVSYCTGNSSECPPPGNAEDDTVCLDLGKCKDGKCIPFCEREQQLESCACNETDNSC
KVCCRDLSGRCVPYVDAEQKNLFLRKGKPCTVGFCDMNGKCEKRVQDVIERFWDFIDQLS
INTFGKFLADNIVGSVLVFSLIFWIPFSILVHCVDKKLDKQYESLSLFHPSNVEMLSSMD
SASVRIIKPFPAPQTPGRLQPAPVIPSAPAAPKLDHQRMDTIQEDPSTDSHMDEDGFEKD
PFPNSSTAAKSFEDLTDHPVTRSEKAASFKLQRQNRVDSKETEC
NT seq
2475 nt
NT seq
+upstream
nt +downstream
nt
atgaggcagtctctcctattcctgaccagcgtggttcctttcgtgctggcgccgcgacct
ccggatgacccgggcttcggcccccaccagagactcgagaagcttgattctttgctctca
gactacgatattctctctttatctaatatccagcagcattcggtaagaaaaagagatcta
cagacttcaacacatgtagaaacactactaactttttcagctttgaaaaggcattttaaa
ttatacctgacatcaagtactgaacgtttttcacaaaatttcaaggtcgtggtggtggat
ggtaaaaacgaaagcgagtacactgtaaaatggcaggacttcttcactggacacgtggtt
ggtgagcctgactctagggttctagcccacataagagatgatgatgttataatcagaatc
aacacagatggggccgaatataacatagagccactttggagatttgttaatgataccaaa
gacaaaagaatgttagtttataaatctgaagatatcaagaatgtttcacgtttgcagtct
ccaaaagtgtgtggttatttaaaagtggataatgaagagttgctcccaaaagggttagta
gacagagaaccacctgaagagcttgttcatcgagtgaaaagaagagctgacccagatccc
atgaagaacacgtgtaaattattggtggtagcagatcatcgcttctacagatacatgggc
agaggggaagagagtacaactacaaattacttaatagagctaattgacagagttgatgac
atctatcggaacacttcatgggataatgcaggttttaaaggctatggaatacagatagag
cagattcgcattctcaagtctccacaagaggtaaaacctggtgaaaagcactacaacatg
gcaaaaagttacccaaatgaagaaaaggatgcttgggatgtgaagatgttgctagagcaa
tttagctttgatatagctgaggaagcatctaaagtttgcttggcacaccttttcacatac
caagattttgatatgggaactcttggattagcttatgttggctctcccagagcaaacagc
catggaggtgtttgtccaaaggcttattatagcccagttgggaagaaaaatatctatttg
aatagtggtttgacgagcacaaagaattatggtaaaaccatccttacaaaggaagctgac
ctggttacaactcatgaattgggacataattttggagcagaacatgatccggatggtcta
gcagaatgtgccccgaatgaggaccagggagggaaatatgtcatgtatcccatagctgtg
agtggcgatcacgagaacaataagatgttttcaaactgcagtaaacaatcaatctataag
accattgaaagtaaggcccaggagtgttttcaagaacgcagcaataaagtttgtgggaac
tcgagggtggatgaaggagaagagtgtgatcctggcatcatgtatctgaacaacgacacc
tgctgcaacagcgactgcacgttgaaggaaggtgtccagtgcagtgacaggaacagtcct
tgctgtaaaaactgtcagtttgagactgcccagaagaagtgccaggaggcgattaatgct
acttgcaaaggcgtgtcctactgcacaggtaatagcagtgagtgcccgcctccaggaaat
gctgaagatgacactgtttgcttggatcttggcaagtgtaaggatgggaaatgcatccct
ttctgcgagagggaacagcagctggagtcctgtgcatgtaatgaaactgacaactcctgc
aaggtgtgctgcagggacctttctggccgctgtgtgccctatgtcgatgctgaacaaaag
aacttatttttgaggaaaggaaagccctgtacagtaggattttgtgacatgaatggcaaa
tgtgagaaacgagtacaggatgtaattgaacgattttgggatttcattgaccagctgagc
atcaatacttttggaaagtttttagcagacaacatcgttgggtctgtcctggttttctcc
ttgatattttggattcctttcagcattcttgtccattgtgtggataagaaattggataaa
cagtatgaatctctgtctctgtttcaccccagtaacgtcgaaatgctgagcagcatggat
tctgcatcggttcgcattatcaaaccctttcctgcgccccagactccaggccgcctgcag
cctgcccctgtgatcccttcggcgccagcagctccaaaactggaccaccagagaatggac
accatccaggaagaccccagcacagactcacatatggacgaggatgggtttgagaaggac
cccttcccaaatagcagcacagctgccaagtcatttgaggatctcacggaccatccggtc
accagaagtgaaaaggctgcctcctttaaactgcagcgtcagaatcgtgttgacagcaaa
gaaacagagtgctaa
DBGET
integrated database retrieval system