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BPP22:NEEDL

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Species (Taxon ID) Enterobacteria phage P22 (Bacteriophage P22). (10754)
Gene Name(s) 26
Protein Name(s) Tail needle protein gp26

Head completion protein Packaged DNA stabilization protein Tail accessory factor gp26

External Links
UniProt P35837
EMBL L14810
AF217253
AF527608
PIR S34956
PDB 2POH
3C9I
4LIN
4ZKP
4ZKU
4ZXQ
PDBsum 2POH
3C9I
4LIN
4ZKP
4ZKU
4ZXQ
ProteinModelPortal P35837
SMR P35837
DIP DIP-60502N
TCDB 1.K.4.1.1
EvolutionaryTrace P35837
Proteomes UP000001796
UP000007960
GO GO:0019012
GO:0044694

Annotations

Qualifier GO ID GO term name Reference ECO ID ECO term name with/from Aspect Extension Notes Status
GO:0019073

viral DNA genome packaging

PMID:6363718[1]

ECO:0000315

P

Fro. I. Dependence of phage formation in vitro on the concentration of the capsid donor extract. Infected cell[ extracts containing incomplete capsids were freshly thawed and lysed as described in Materials and Methods. Diluted .samples were mixed with concentrated protein donor extract {5-) and incubated for I h at 23°C, at which time the reactions were stopped by further dilution and titered for viable phage. The background of the protein donor extract was 102 phage/mi. The background of the • at mo.~l, Conc-entrated calmid donor extracts were (0) 3.3× 10 (4- extract), (t) 2:5 × l0 T (10- extract) and (at) 2 x 103 (26-extract).

Dependence of in vitro assembly on the concentration of the 4", lO ÷ and 26* activities. (a)

Complementation of 10- extracts (O), 26- extracts (11) and 4- extracts (~lk) with protein donor extract. The capsid extracts were diluted 25-fold, to a final infected cell conventration of about 2 x 10 ° c~lls/ml. Samples were mixed with serial dilutions of the 5- protein donor. The maximum slo|~s determined from these curve,a were: 4+ activity, 5 to 6; 26 + activity. I to 2; 10 + activity, 4 to 5. The background of the undiluted extracts were protein donor 10a; 4- extract < 10s; 10- extracts, 5 x 10~; 26- extract, 2 x l0 a. (b) Variation of the ratio of cap`aid,a to protein; complemcntation of 4- capsids with cap,aid donor cell concentration: (O) 5x lO 9 cell,a/ml; (A) 2 x l0 s cell,a/ml; (m) 4 x 10 v (~lls/ml. The protein donor extract was from the same batch a.s used in (a).

complete
CACAO 12034

involved_in

GO:0099002

viral genome ejection through host cell envelope, short tail mechanism

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-1244

P

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

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-1162
UniProtKB-KW:KW-1160

P

Seeded From UniProt

complete

involved_in

GO:0044694

pore-mediated entry of viral genome into host cell

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-1172

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

Notes

References

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

  1. Strauss, H & King, J (1984) Steps in the stabilization of newly packaged DNA during phage P22 morphogenesis. J. Mol. Biol. 172 523-43 PubMed GONUTS page