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BPSPP:TUBE

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Species (Taxon ID) Bacillus phage SPP1 (Bacteriophage SPP1). (10724)
Gene Name(s) 17.1
Protein Name(s) Tail tube protein gp17.1* (ECO:0000303 with PMID:17611601[1])

TTP (ECO:0000305) Gene product 17.1 (ECO:0000305) gp17.1 (ECO:0000305) Major tail protein (ECO:0000303 with PMID:18786146[2]) MTP (ECO:0000303 with PMID:18786146[2])

External Links
UniProt O48449
EMBL X97918
PIR T42289
RefSeq NP_690680.1
YP_710298.1
PDB 5A20
5A21
PDBsum 5A20
5A21
ProteinModelPortal O48449
SMR O48449
GeneID 4229189
955320
KEGG vg:4229189
vg:955320
OrthoDB VOG090000SU
Proteomes UP000002559
GO GO:0019012
GO:0098026
GO:0099001
CDD cd00063
Gene3D 2.60.40.10
InterPro IPR003961
IPR036116
IPR013783
IPR011855
Pfam PF00041
PF06199
SMART SM00060
SUPFAM SSF49265
TIGRFAMs TIGR02126
PROSITE PS50853

Annotations

Qualifier GO ID GO term name Reference ECO ID ECO term name with/from Aspect Extension Notes Status

part_of

GO:0098026

virus tail, tube

PMID:18786146[2]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

GO:0098026

virus tail, tube

PMID:25525268[3]

ECO:0000314

C

TTP, gp17.1 has been identified to be able to self assemble into long tubes in the absence of other phage proteins. In figure 6 there is a comparison done between gp17.1 and tails of SSP1 virions that show similar morphology. These samples were negatively stained and it was observed that both gp17.1 is hollow and the empty virion tails that have ejected their DNA after incubation in a SSP1 bacterial receptor. Aligned segments of gp17.1 were taken then calculation was performed for its diffraction pattern. This pattern revealed that tubes have a 6-fold symmetry which are made by stacks of hexameric rings. These rings form helical tubes that elongate.

complete
CACAO 13178

part_of

GO:0019012

virion

PMID:16899078[4]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

GO:0098005

viral head-tail joining

PMID:24443902[5]

ECO:0000314

P

An in-vitro complementation assay was used to study incorporation of gp17 during assembly of viral particles. Each extract was separately mixed with 4 different components; water, complete tails purified from SPP1sus31 with gp17, tails without gp17 purified from SPP1sus82, and purified gp17. After incubation, the titer of the progeny was calculated in Figure 7. The expected result was sus31 tails in both extracts allowed it to join to the capsids for virion assembly. When mixing SPP1sus82 tails without gp17 with SPP1sus45, virion particles assembled, suggesting endogenous gp17 was able to join head and tail. SPP1sus82 had a low titer, thus tails weren’t able to attach. Finally, purified gp17 mixed SPP1sus82 extracts was sufficient for tail to head stickage. This assay shows that gp17 is involved in binding to the tail and later attaching to the DNA-filled capsid.

complete
CACAO 13181

part_of

GO:0098026

virus tail, tube

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-1228

C

Seeded From UniProt

complete

involved_in

GO:0046718

viral entry into host cell

GO_REF:0000037
GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-1160
UniProtKB-KW:KW-1162

P

Seeded From UniProt

complete

involved_in

GO:0099001

viral genome ejection through host cell envelope, long flexible tail mechanism

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-1243

P

Seeded From UniProt

complete

part_of

GO:0019012

virion

GO_REF:0000037
GO_REF:0000039

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0946
UniProtKB-SubCell:SL-0274

C

Seeded From UniProt

complete

part_of

GO:0098015

virus tail

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-1227

C

Seeded From UniProt

complete

Notes

References

See Help:References for how to manage references in GONUTS.

  1. Plisson, C et al. (2007) Structure of bacteriophage SPP1 tail reveals trigger for DNA ejection. EMBO J. 26 3720-8 PubMed GONUTS page
  2. 2.0 2.1 2.2 Auzat, I et al. (2008) Origin and function of the two major tail proteins of bacteriophage SPP1. Mol. Microbiol. 70 557-69 PubMed GONUTS page
  3. Langlois, C et al. (2015) Bacteriophage SPP1 tail tube protein self-assembles into β-structure-rich tubes. J. Biol. Chem. 290 3836-49 PubMed GONUTS page
  4. Vinga, I et al. (2006) The minor capsid protein gp7 of bacteriophage SPP1 is required for efficient infection of Bacillus subtilis. Mol. Microbiol. 61 1609-21 PubMed GONUTS page
  5. Auzat, I et al. (2014) A touch of glue to complete bacteriophage assembly: the tail-to-head joining protein (THJP) family. Mol. Microbiol. 91 1164-78 PubMed GONUTS page