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BPP22:NEEDL
Contents
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 |
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 | |||||
involved_in |
GO:0099002 |
viral genome ejection through host cell envelope, short tail mechanism |
ECO:0000322 |
imported manually asserted information used in automatic assertion |
P |
Seeded From UniProt |
complete | |||
part_of |
GO:0098015 |
virus tail |
ECO:0000322 |
imported manually asserted information used in automatic assertion |
C |
Seeded From UniProt |
complete | |||
involved_in |
GO:0046718 |
viral entry into host cell |
ECO:0000322 |
imported manually asserted information used in automatic assertion |
P |
Seeded From UniProt |
complete | |||
involved_in |
GO:0044694 |
pore-mediated entry of viral genome into host cell |
ECO:0000322 |
imported manually asserted information used in automatic assertion |
P |
Seeded From UniProt |
complete | |||
part_of |
GO:0019012 |
virion |
ECO:0000322 |
imported manually asserted information used in automatic assertion |
C |
Seeded From UniProt |
complete | |||
Notes
References
See Help:References for how to manage references in GONUTS.
- ↑ 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