COMPOUND: C00752
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Entry
C00752 Compound
Name
Thrombin;
Coagulation factor IIa
Sequence
(A chain)
TFGSGEADCG LRPLFEKKSL EDKTERELLE SYIDGR
(B chain)
VEGSDAEIG MSPWQVMLFR KSPQELLCGA SLISDRWVLT AAHCLLYPPW DKNFTENDLL
VRIGKHSRTR YERNIEKISM LEKIYIHPRY NWRENLDRDI ALMKLKKPVA FSDYIHPVCL
PDRETAASLL QAGYKGRVTG WGNLKETWTA NVGKGQPSVL QVVNLPIVER PVCKDSTRIR
ITDNMFCAGY KPDEGKRGDA CEGDSGGPFV MKSPFNNRWY QMGIVSWGEG CDRDGKYGFY
THVFRLKKWI QKVIDQFGE
(Disulfide bridge: A9-B119)
Organism
Homo sapiens [HSA:
2147
]
Type
Peptide
Remark
Same as:
D00090
Comment
active form [EC:
3.4.21.5
] of prothrombin [KO:
K01313
]
Pathway
map04610
Complement and coagulation cascades
Network
nt06171
SARS coronavirus 2 (SARS-CoV-2)
nt06514
Coagulation cascade
Brite
Anatomical Therapeutic Chemical (ATC) classification [BR:
br08303
]
B BLOOD AND BLOOD FORMING ORGANS
B02 ANTIHEMORRHAGICS
B02B VITAMIN K AND OTHER HEMOSTATICS
B02BC Local hemostatics
B02BC06 Thrombin
D00090 Thrombin (JP18/USP/INN) <JP/US>
B02BD Blood coagulation factors
B02BD30 Thrombin
D00090 Thrombin (JP18/USP/INN) <JP/US>
Therapeutic category of drugs in Japan [BR:
br08301
]
3 Agents affecting metabolism
33 Blood and body fluid agents
332 Hemostatics
3323 Hemostatics for organs
D00090 Thrombin (JP18/USP/INN)
Drug groups [BR:
br08330
]
Blood modifier agent
DG02016 Hemostatics
DG02014 Blood coagulation accelerant
DG00169 Thrombin
D00090 Thrombin
Drugs listed in the Japanese Pharmacopoeia [BR:
br08311
]
Chemicals
D00090 Thrombin
BRITE hierarchy
Other DBs
CAS:
9002-04-4
PubChem:
4014
NIKKAJI:
J247.643F
LinkDB
All DBs
» Japanese version
Homo sapiens (human): 7056
Help
Entry
7056 CDS
T01001
Symbol
THBD, AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM, TM
Name
(RefSeq) thrombomodulin
KO
K03907
thrombomodulin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04610
Complement and coagulation cascades
hsa04933
AGE-RAGE signaling pathway in diabetic complications
hsa05418
Fluid shear stress and atherosclerosis
Network
nt06514
Coagulation cascade
Element
N01515
Regulation of coagulation cascade, protein C system
Disease
H00223
Inherited thrombophilia
H01434
Atypical hemolytic uremic syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04610 Complement and coagulation cascades
7056 (THBD)
09160 Human Diseases
09166 Cardiovascular disease
05418 Fluid shear stress and atherosclerosis
7056 (THBD)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
7056 (THBD)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
7056 (THBD)
00535 Proteoglycans [BR:
hsa00535
]
7056 (THBD)
04091 Lectins [BR:
hsa04091
]
7056 (THBD)
CD molecules [BR:
hsa04090
]
Proteins
7056 (THBD)
Proteoglycans [BR:
hsa00535
]
Cell surface proteoglycans
Others
7056 (THBD)
Lectins [BR:
hsa04091
]
C-Type lectins
Others
7056 (THBD)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
THBD
FXa_inhibition
cEGF
EGF_Tme5
EGF_CA
EGF
Lectin_C
hEGF
EGF_LRP2
Motif
Other DBs
NCBI-GeneID:
7056
NCBI-ProteinID:
NP_000352
OMIM:
188040
HGNC:
11784
Ensembl:
ENSG00000178726
UniProt:
P07204
Structure
PDB
PDBj
LinkDB
All DBs
Position
20:complement(23045633..23049672)
Genome browser
AA seq
575 aa
AA seq
DB search
MLGVLVLGALALAGLGFPAPAEPQPGGSQCVEHDCFALYPGPATFLNASQICDGLRGHLM
TVRSSVAADVISLLLNGDGGVGRRRLWIGLQLPPGCGDPKRLGPLRGFQWVTGDNNTSYS
RWARLDLNGAPLCGPLCVAVSAAEATVPSEPIWEEQQCEVKADGFLCEFHFPATCRPLAV
EPGAAAAAVSITYGTPFAARGADFQALPVGSSAAVAPLGLQLMCTAPPGAVQGHWAREAP
GAWDCSVENGGCEHACNAIPGAPRCQCPAGAALQADGRSCTASATQSCNDLCEHFCVPNP
DQPGSYSCMCETGYRLAADQHRCEDVDDCILEPSPCPQRCVNTQGGFECHCYPNYDLVDG
ECVEPVDPCFRANCEYQCQPLNQTSYLCVCAEGFAPIPHEPHRCQMFCNQTACPADCDPN
TQASCECPEGYILDDGFICTDIDECENGGFCSGVCHNLPGTFECICGPDSALARHIGTDC
DSGKVDGGDSGSGEPPPSPTPGSTLTPPAVGLVHSGLLIGISIASLCLVVALLALLCHLR
KKQGAARAKMEYKCAAPSKEVVLQHVRTERTPQRL
NT seq
1728 nt
NT seq
+upstream
nt +downstream
nt
atgcttggggtcctggtccttggcgcgctggccctggccggcctggggttccccgcaccc
gcagagccgcagccgggtggcagccagtgcgtcgagcacgactgcttcgcgctctacccg
ggccccgcgaccttcctcaatgccagtcagatctgcgacggactgcggggccacctaatg
acagtgcgctcctcggtggctgccgatgtcatttccttgctactgaacggcgacggcggc
gttggccgccggcgcctctggatcggcctgcagctgccacccggctgcggcgaccccaag
cgcctcgggcccctgcgcggcttccagtgggttacgggagacaacaacaccagctatagc
aggtgggcacggctcgacctcaatggggctcccctctgcggcccgttgtgcgtcgctgtc
tccgctgctgaggccactgtgcccagcgagccgatctgggaggagcagcagtgcgaagtg
aaggccgatggcttcctctgcgagttccacttcccagccacctgcaggccactggctgtg
gagcccggcgccgcggctgccgccgtctcgatcacctacggcaccccgttcgcggcccgc
ggagcggacttccaggcgctgccggtgggcagctccgccgcggtggctcccctcggctta
cagctaatgtgcaccgcgccgcccggagcggtccaggggcactgggccagggaggcgccg
ggcgcttgggactgcagcgtggagaacggcggctgcgagcacgcgtgcaatgcgatccct
ggggctccccgctgccagtgcccagccggcgccgccctgcaggcagacgggcgctcctgc
accgcatccgcgacgcagtcctgcaacgacctctgcgagcacttctgcgttcccaacccc
gaccagccgggctcctactcgtgcatgtgcgagaccggctaccggctggcggccgaccaa
caccggtgcgaggacgtggatgactgcatactggagcccagtccgtgtccgcagcgctgt
gtcaacacacagggtggcttcgagtgccactgctaccctaactacgacctggtggacggc
gagtgtgtggagcccgtggacccgtgcttcagagccaactgcgagtaccagtgccagccc
ctgaaccaaactagctacctctgcgtctgcgccgagggcttcgcgcccattccccacgag
ccgcacaggtgccagatgttttgcaaccagactgcctgtccagccgactgcgaccccaac
acccaggctagctgtgagtgccctgaaggctacatcctggacgacggtttcatctgcacg
gacatcgacgagtgcgaaaacggcggcttctgctccggggtgtgccacaacctccccggt
accttcgagtgcatctgcgggcccgactcggcccttgcccgccacattggcaccgactgt
gactccggcaaggtggacggtggcgacagcggctctggcgagcccccgcccagcccgacg
cccggctccaccttgactcctccggccgtggggctcgtgcattcgggcttgctcataggc
atctccatcgcgagcctgtgcctggtggtggcgcttttggcgctcctctgccacctgcgc
aagaagcagggcgccgccagggccaagatggagtacaagtgcgcggccccttccaaggag
gtagtgctgcagcacgtgcggaccgagcggacgccgcagagactctga
Homo sapiens (human): 10544
Help
Entry
10544 CDS
T01001
Symbol
PROCR, CCCA, CCD41, EPCR
Name
(RefSeq) protein C receptor
KO
K06557
protein C receptor, endothelial (EPCR)
Organism
hsa
Homo sapiens (human)
Pathway
hsa04610
Complement and coagulation cascades
Network
nt06514
Coagulation cascade
Element
N01515
Regulation of coagulation cascade, protein C system
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04610 Complement and coagulation cascades
10544 (PROCR)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
10544 (PROCR)
CD molecules [BR:
hsa04090
]
Proteins
10544 (PROCR)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MHC_I_3
MHC_I
Motif
Other DBs
NCBI-GeneID:
10544
NCBI-ProteinID:
NP_006395
OMIM:
600646
HGNC:
9452
Ensembl:
ENSG00000101000
UniProt:
Q9UNN8
Structure
PDB
PDBj
LinkDB
All DBs
Position
20:35171096..35216259
Genome browser
AA seq
238 aa
AA seq
DB search
MLTTLLPILLLSGWAFCSQDASDGLQRLHMLQISYFRDPYHVWYQGNASLGGHLTHVLEG
PDTNTTIIQLQPLQEPESWARTQSGLQSYLLQFHGLVRLVHQERTLAFPLTIRCFLGCEL
PPEGSRAHVFFEVAVNGSSFVSFRPERALWQADTQVTSGVVTFTLQQLNAYNRTRYELRE
FLEDTCVQYVQKHISAENTKGSQTSRSYTSLVLGVLVGSFIIAGVAVGIFLCTGGRRC
NT seq
717 nt
NT seq
+upstream
nt +downstream
nt
atgttgacaacattgctgccgatactgctgctgtctggctgggccttttgtagccaagac
gcctcagatggcctccaaagacttcatatgctccagatctcctacttccgcgacccctat
cacgtgtggtaccagggcaacgcgtcgctggggggacacctaacgcacgtgctggaaggc
ccagacaccaacaccacgatcattcagctgcagcccttgcaggagcccgagagctgggcg
cgcacgcagagtggcctgcagtcctacctgctccagttccacggcctcgtgcgcctggtg
caccaggagcggaccttggcctttcctctgaccatccgctgcttcctgggctgtgagctg
cctcccgagggctctagagcccatgtcttcttcgaagtggctgtgaatgggagctccttt
gtgagtttccggccggagagagccttgtggcaggcagacacccaggtcacctccggagtg
gtcaccttcaccctgcagcagctcaatgcctacaaccgcactcggtatgaactgcgggaa
ttcctggaggacacctgtgtgcagtatgtgcagaaacatatttccgcggaaaacacgaaa
gggagccaaacaagccgctcctacacttcgctggtcctgggcgtcctggtgggcagtttc
atcattgctggtgtggctgtaggcatcttcctgtgcacaggtggacggcgatgttaa
DBGET
integrated database retrieval system