Link type | Probability | Loop ranges | Chain A piercings | Chain B piercings | Chain C piercings | Chain D piercings | ||||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B | |||||||||
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Other | 39% | -A | -352D | -351A -352C -352D | -194A -351B |
Chain A Sequence |
SHMREIIERVKEKTTIPVYERTIENVLSAIQASGDVWRIVDLSEEPLPLVVAVVTALYELGYVAFENNQVILTRKGKELVEKYGIGPRADYTCSHCQGRTVEIDAFSELLEQFKEITRDRPEPAHQFDQAYVTPETTVARVALMHSRGDLENKEVFVLGDDDLTSVALMLSGLPKRIAVLDIDERLTKFIEKAADEIGYENIEIFTFDLRKPLPDYALHKFDTFITDPPETVEAIRAFVGRGIATLKGPGCAGYFGITRRESSLDKWREIQRVLLNEFGVVITDIIRNFNEYVNWGYVEETRAWRLLPIKVKPSYNWYKSYMFRIQTLEGSKGFEDEITVGQELYDDEESSTT |
Chain A Sequence |
GSHMREIIERVKEKTTIPVYERTIENVLSAIQASGDVWRIVDLSEEPLPLVVAVVTALYELGYVAFENNQVILTRKGKELVEKYGIGPRADYTCSHCQGRTVEIDAFSELLEQFKEITRDRPEPAHQFDQAYVTPETTVARVALMHSRGDLENKEVFVLGDDDLTSVALMLSGLPKRIAVLDIDERLTKFIEKAADEIGYENIEIFTFDLRKPLPDYALHKFDTFITDPPETVEAIRAFVGRGIATLKGPGCAGYFGITRRESSLDKWREIQRVLLNEFGVVITDIIRNFNEYVNWGYVEETRAWRLLPIKVKPSYNWYKSYMFRIQTLEGSKGFEDEITVGQELYDDEESSTT |
Chain A Sequence |
SHMREIIERVKEKTTIPVYERTIENVLSAIQASGDVWRIVDLSEEPLPLVVAVVTALYELGYVAFENNQVILTRKGKELVEKYGIGPRADYTCSHCQGRTVEIDAFSELLEQFKEITRDRPEPAHQFDQAYVTPETTVARVALMHSRGDLENKEVFVLGDDDLTSVALMLSGLPKRIAVLDIDERLTKFIEKAADEIGYENIEIFTFDLRKPLPDYALHKFDTFITDPPETVEAIRAFVGRGIATLKGPGCAGYFGITRRESSLDKWREIQRVLLNEFGVVITDIIRNFNEYVNWGYVEETRAWRLLPIKVKPSYNWYKSYMFRIQTLEGSKGFEDEITVGQELYDDEESSTT |
Chain A Sequence |
SHMREIIERVKEKTTIPVYERTIENVLSAIQASGDVWRIVDLSEEPLPLVVAVVTALYELGYVAFENNQVILTRKGKELVEKYGIGPRADYTCSHCQGRTVEIDAFSELLEQFKEITRDRPEPAHQFDQAYVTPETTVARVALMHSRGDLENKEVFVLGDDDLTSVALMLSGLPKRIAVLDIDERLTKFIEKAADEIGYENIEIFTFDLRKPLPDYALHKFDTFITDPPETVEAIRAFVGRGIATLKGPGCAGYFGITRRESSLDKWREIQRVLLNEFGVVITDIIRNFNEYVNWGYVEETRAWRLLPIKVKPSYNWYKSYMFRIQTLEGSKGFEDEITVGQELYDDEESSTT |
sequence length | 353,354,353,353 |
structure length | 353,354,353,353 |
publication title |
Active site geometry of a novel aminopropyltransferase for biosynthesis of hyperthermophile-specific branched-chain polyamine.
pubmed doi rcsb |
molecule tags | Transferase |
molecule keywords | N(4)-bis(aminopropyl)spermidine synthase |
source organism | Thermococcus kodakarensis (strain atcc baa-918 / jcm 12380 / kod1) |
pdb deposition date | 2017-05-22 |
LinkProt deposition date | 2018-08-17 |
#similar chains in the LinkProt database (?% sequence similarity) ...loading similar chains, please wait... #similar chains, but unlinked ...loading similar chains, please wait... #similar chains in the pdb database (?% sequence similarity) ...loading similar chains, please wait...