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HOMO
SAPIENS
WITH MUS MUSCULUS
MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLMLSPDDIEQWFTEDPGP
MEE QSD S+E PLSQETFS LWKLLP ++L P P MDDL+L P D+E++F
GP
MEESQSDISLELPLSQETFSGLWKLLPPEDIL-PSP-HCMDDLLL-PQDVEEFFE---GP
DEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAK
EA R+ A P P P APAPA
WPLSS VPSQKTYQG+YGF LGFL SGTAK
SEALRVSGAPAAQDPVTETPGPVAPAPATPWPLSSFVPSQKTYQGNYGFHLGFLQSGTAK
SVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHE
SV CTYSP LNK+FCQLAKTCPVQLWV +TPP G+RVRAMAIYK+SQHMTEVVRRCPHHE
SVMCTYSPPLNKLFCQLAKTCPVQLWVSATPPAGSRVRAMAIYKKSQHMTEVVRRCPHHE
RCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNS
RCSD DGLAPPQHLIRVEGNL EYL+DR TFRHSVVVPYEPPE GS+ TTIHY YMCNS
RCSDGDGLAPPQHLIRVEGNLYPEYLEDRQTFRHSVVVPYEPPEAGSEYTTIHYKYMCNS
SCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELP
SCMGGMNRRPILTIITLEDSSGNLLGR+SFEVRVCACPGRDRRTEEEN RKK ELP
SCMGGMNRRPILTIITLEDSSGNLLGRDSFEVRVCACPGRDRRTEEENFRKKEVLCPELP
PGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPG
PGS KRALP TS+SP KKKPLDGEYFTL+IRGR+RFEMFRELNEALELKDA A +E
G
PGSAKRALPTCTSASPPQKKKPLDGEYFTLKIRGRKRFEMFRELNEALELKDAHATEESG
GSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD
SRAHSS+LK+KKGQSTSRHKK M K GPDSD
DSRAHSSYLKTKKGQSTSRHKKTMVKKVGPDSD
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HOMO
SAPIENS
WITH RATTUS NORVEGICUS
MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPS---QAMDDLMLSPDDIEQWFTED
ME+ QSD S+E PLSQETFS LWKLLP +++L + +M+DL
L P D+ +
MEDSQSDMSIELPLSQETFSCLWKLLPPDDILPTTATGSPNSMEDLFL-PQDVAELLE--
PGPDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSG
GP+EA ++ A A
A + P WPLSSSVPSQKTYQG+YGF LGFL SG
-GPEEALQVSAPAAQEPGTEAPAPVAPASATP-WPLSSSVPSQKTYQGNYGFHLGFLQSG
TAKSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCP
TAKSV CTYS +LNK+FCQLAKTCPVQLWV STPPPGTRVRAMAIYK+SQHMTEVVRR P
TAKSVMCTYSISLNKLFCQLAKTCPVQLWVTSTPPPGTRVRAMAIYKKSQHMTEVVRRWP
HHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYM
HHERCSD DGLAPPQHLIRVEGN EYLDDR TFRHSVVVPYEPPEVGSD TTIHY
YM
HHERCSDGDGLAPPQHLIRVEGNPYAEYLDDRQTFRHSVVVPYEPPEVGSDYTTIHYKYM
CNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHH
CNSSCMGGMNRRPILTIITLEDSSGNLLGR+SFEVRVCACPGRDRRTEEEN RKK E
CNSSCMGGMNRRPILTIITLEDSSGNLLGRDSFEVRVCACPGRDRRTEEENFRKKEEHCP
ELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGK
ELPPGS KRALP +TSSSPQ KKKPLDGEYFTL+IRGRERFEMFRELNEALELKDA+A +
ELPPGSAKRALPTSTSSSPQQKKKPLDGEYFTLKIRGRERFEMFRELNEALELKDARAAE
EPGGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD
E G SRAHSS+ K+KKGQSTSRHKK M K GPDSD
ESGDSRAHSSYPKTKKGQSTSRHKKPMIKKVGPDSD
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HOMO
SAPIENS
WITH CANIS FAMILIARIS
MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLMLSPDDIEQWFTEDPGP
MEE QS+ +++PPLSQETFS+LW LLPENNVLS A+D+L+L
P+ + W ED
MEESQSELNIDPPLSQETFSELWNLLPENNVLSSELCPAVDELLL-PESVVNWLDEDSDD
DEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAK
PA
P AP PAPSWPLSSSVPS KTY G+YGFRLGFLHSGTAK
------------APRMPATSAPTAPGPAPSWPLSSSVPSPKTYPGTYGFRLGFLHSGTAK
SVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHE
SVT TYSP LNK+FCQLAKTCPVQLWV S PPP T VRAMAIYK+S+ +TEVVRRCPHHE
SVTWTYSPLLNKLFCQLAKTCPVQLWVSSPPPPNTCVRAMAIYKKSEFVTEVVRRCPHHE
RCSDS-DGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCN
RCSDS DGLAPPQHLIRVEGNLR +YLDDRNTFRHSVVVPYEPPEVGSD TTIHYNYMCN
RCSDSSDGLAPPQHLIRVEGNLRAKYLDDRNTFRHSVVVPYEPPEVGSDYTTIHYNYMCN
SSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHEL
SSCMGGMNRRPILTIITLEDSSGN+LGRNSFEVRVCACPGRDRRTEEEN KKGEP E
SSCMGGMNRRPILTIITLEDSSGNVLGRNSFEVRVCACPGRDRRTEEENFHKKGEPCPEP
PPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEP
PPGSTKRALP +TSSSP KKKPLDGEYFTLQIRGRER+EMFR LNEALELKDAQ+GKEP
PPGSTKRALPPSTSSSPPQKKKPLDGEYFTLQIRGRERYEMFRNLNEALELKDAQSGKEP
GGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD
GGSRAHSSHLK+KKGQSTSRHKKLMFK EG DSD
GGSRAHSSHLKAKKGQSTSRHKKLMFKREGLDSD
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HOMO
SAPIENS
WITH SUS SCROFA
MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSP-LPSQAMDDLMLSPDDIEQWFTEDPG
MEE QS+ VEPPLSQETFSDLWKLLPENN+LS L A++DL+LSP
+ W E+P
MEESQSELGVEPPLSQETFSDLWKLLPENNLLSSELSLAAVNDLLLSP--VTNWLDENPD
PDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTA
P AA APA AP
SWPLSS VPSQKTY GSY
FRLGFLHSGTA
DASRVPAPPAATAPAPAAPAPAT-------SWPLSSFVPSQKTYPGSYDFRLGFLHSGTA
KSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHH
KSVTCTYSPALNK+FCQLAKTCPVQLWV S PPPGTRVRAMAIYK+S++MTEVVRRCPHH
KSVTCTYSPALNKLFCQLAKTCPVQLWVSSPPPPGTRVRAMAIYKKSEYMTEVVRRCPHH
ERCSD-SDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMC
ER SD SDGLAPPQHLIRVEGNLR EYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYN+MC
ERSSDYSDGLAPPQHLIRVEGNLRAEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNFMC
NSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHE
NSSCMGGMNRRPILTIITLED+SGNLLGRNSFEVRVCACPGRDRRTEEEN KKG+ E
NSSCMGGMNRRPILTIITLEDASGNLLGRNSFEVRVCACPGRDRRTEEENFLKKGQSCPE
LPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKE
PPGSTKRALP +TSSSP KKKPLDGEYFTLQIRGRERFEMFRELN+ALELKDAQ
+E
PPPGSTKRALPTSTSSSPVQKKKPLDGEYFTLQIRGRERFEMFRELNDALELKDAQTARE
PGGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD
G +RAHSSHLKSKKGQS SRHKK MFK EGPDSD
SGENRAHSSHLKSKKGQSPSRHKKPMFKREGPDSD
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HOMO
SAPIENS
WITH BOS TAURUS
MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLMLSPDDIEQWFTEDPGP
MEE Q++ +VEPPLSQETFSDLW LLPENN+LS S +DDL L D+
W E P
MEESQAELNVEPPLSQETFSDLWNLLPENNLLSSELSAPVDDL-LPYTDVATWLDECPNE
DEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAK
P
APAAP PA PAPA SWPLSS VPSQKTY G+YGFRLGFL SGTAK
-------APQMPEPSAPAAPPPATPAPATSWPLSSFVPSQKTYPGNYGFRLGFLQSGTAK
SVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHE
SVTCTYSP+LNK+FCQLAKTCPVQLWVDS PPPGTRVRAMAIYK+ +HMTEVVRRCPHHE
SVTCTYSPSLNKLFCQLAKTCPVQLWVDSPPPPGTRVRAMAIYKKLEHMTEVVRRCPHHE
RCSD-SDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCN
R SD SDGLAPPQHLIRVEGNLR EYLDDRNTFRHSVVVPYE PE+ S+CTTIHYN+MCN
RSSDYSDGLAPPQHLIRVEGNLRAEYLDDRNTFRHSVVVPYESPEIDSECTTIHYNFMCN
SSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHEL
SSCMGGMNRRPILTIITLEDS GNLLGRNSFEVRVCACPGRDRRTEEENLRKKG+ E
SSCMGGMNRRPILTIITLEDSCGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGQSCPEP
PPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEP
PP STKRALP NTSSSPQPKKKPLDGEYFTLQIRG +R+EMFRELN+ALELKDA G+EP
PPRSTKRALPTNTSSSPQPKKKPLDGEYFTLQIRGFKRYEMFRELNDALELKDALDGREP
GGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD
G SRAHSSHLKSKK S S HKK M K EGPDSD
GESRAHSSHLKSKKRPSPSCHKKPMLKREGPDSD
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HOMO
SAPIENS
WITH PAN TROGLODYTES
MFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQ
MFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQ
MFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQ
HLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPIL
HLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPIL HLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPIL
TIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNT
TIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNT TIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNT
SSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSK
SSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSK SSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSK
KGQSTSRHKKLMFKTEGPDSD
KGQSTSRHKKLMFKTEGPDSD
KGQSTSRHKKLMFKTEGPDSD
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N-TERMINAL
TRANSCRIPTION ACTIVATION DOMAIN
The binding of this protein by regulatory proteins regulates p53
transcription activation. his entry is comprised of a single amphipathic
alpha helix and contains a highly conserved motif. It present on
the 5 to 29 position in the protien. In the analysis we found that
there is some mutations in diffrent organisms but these mutations
did not affect the function of this protein.In this alignment this
domain shows in blue colour.
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DNA
BINDING DOMAIN
This domain is found in p53 transcription factor, where it is responsible
for DNA-binding. These transcription factors play diverse roles
in the regulation of cellular functions: the p53 tumour suppressor
upregulates the expression of genes involved in cell cycle arrest
and apoptosis he DNA-binding domain acts to clamp, or in the case
of TonEBP, encircle the DNA target in order to stabilize the protein-DNA
complex. Protein interactions may also serve to stabilize the protein-DNA
complex, for example in the STAT-1 dimer the SH2 (Src homology 2)
domain in each monomer is coupled to the DNA-binding domain to increase
stability The DNA-binding domain consists of a beta-sandwich formed
of 9 strands in 2 sheets with a Greek-key topology. This structure
is found in many transcription factors, often within the DNA-binding
domain.we analyse that there are very less mutation in these organism
so that the function of this protien did not changed in these organisms.In
this alignment this domain shows in pink
colour.
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Crystal
Structure of Core Domain
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PROLINE
RICH DOMAIN
This
Domain is responsible for the apoptotic activity of the protein.
These regions are often mosiacs of a small number of amino acids.
These regions have been shown to be functioanlly important in some
proteins. this domain present at the 60 to 89 position in the protein.In
this alignment this domain shows in green
colour.
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TETRAMERISATION
DOMAIN
The p53 protein is a tetrameric transcription factor that plays
a central role in the prevention of neoplastic transformation. Oligomerization
appears to be essential for the tumour suppressing activity of p53.
p53 can be divided into different functional domains: an N-terminal
transactivation domain, a proline-rich domain, a DNA-binding domain
(), a tetramerisation domain and a C-terminal regulatory region.
The tetramerisation domain of human p53 extends from residues 325
to 356, and has a 4-helical bundle fold. The tetramerisation domain
is essential for DNA binding, protein-protein interactions, post-translational
modifications, and p53 degradation.this domain is same in all seven
organism so the function of protein did not changed. In this alignment
this domain shows in red colour.
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