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PDBsum entry 7nop

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protein Protein-protein interface(s) links
Viral protein PDB id
7nop

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
78 a.a.
217 a.a.
139 a.a.
PDB id:
7nop
Name: Viral protein
Title: Structure of the mature rsv ca lattice: group iv, hexamer-hexamer interface, class 5'beta
Structure: Capsid protein p27, alternate cleaved 1. Chain: a, b, c, d, e, f, g, h, i, j. Engineered: yes
Source: Rous sarcoma virus (strain praguE C). Rsv-prc. Organism_taxid: 11888. Strain: praguE C. Gene: gag. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008
Authors: M.Obr,C.L.Ricana,N.Nikulin,J.-P.R.Feathers,M.Klanschnig,A.Thader, M.C.Johnson,V.M.Vogt,F.K.M.Schur,R.A.Dick
Key ref: M.Obr et al. (2021). Structure of the mature Rous sarcoma virus lattice reveals a role for IP6 in the formation of the capsid hexamer. Nat Commun, 12, 3226. PubMed id: 34050170 DOI: 10.1107/S0907444909042073
Date:
25-Feb-21     Release date:   21-Apr-21    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
P03354  (POL_RSVP) -  Gag-Pol polyprotein from Rous sarcoma virus subgroup C (strain Prague)
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1603 a.a.
78 a.a.
Protein chains
Pfam   ArchSchema ?
P03354  (POL_RSVP) -  Gag-Pol polyprotein from Rous sarcoma virus subgroup C (strain Prague)
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1603 a.a.
217 a.a.
Protein chains
Pfam   ArchSchema ?
P03354  (POL_RSVP) -  Gag-Pol polyprotein from Rous sarcoma virus subgroup C (strain Prague)
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1603 a.a.
139 a.a.
Key:    PfamA domain  Secondary structure

 Enzyme reactions 
   Enzyme class 2: Chains A, B, C, D, E, F, G, H, I, J: E.C.2.7.7.-  - ?????
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
   Enzyme class 3: Chains A, B, C, D, E, F, G, H, I, J: E.C.2.7.7.49  - RNA-directed Dna polymerase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: DNA(n) + a 2'-deoxyribonucleoside 5'-triphosphate = DNA(n+1) + diphosphate
DNA(n)
+ 2'-deoxyribonucleoside 5'-triphosphate
= DNA(n+1)
+ diphosphate
   Enzyme class 4: Chains A, B, C, D, E, F, G, H, I, J: E.C.2.7.7.7  - DNA-directed Dna polymerase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: DNA(n) + a 2'-deoxyribonucleoside 5'-triphosphate = DNA(n+1) + diphosphate
DNA(n)
+ 2'-deoxyribonucleoside 5'-triphosphate
= DNA(n+1)
+ diphosphate
   Enzyme class 5: Chains A, B, C, D, E, F, G, H, I, J: E.C.3.1.-.-
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
   Enzyme class 6: Chains A, B, C, D, E, F, G, H, I, J: E.C.3.1.26.4  - ribonuclease H.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Endonucleolytic cleavage to 5'-phosphomonoester.
   Enzyme class 7: Chains A, B, C, D, E, F, G, H, I, J: E.C.3.4.23.-  - ?????
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
Note, where more than one E.C. class is given (as above), each may correspond to a different protein domain or, in the case of polyprotein precursors, to a different mature protein.
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
DOI no: 10.1107/S0907444909042073 Nat Commun 12:3226 (2021)
PubMed id: 34050170  
 
 
Structure of the mature Rous sarcoma virus lattice reveals a role for IP6 in the formation of the capsid hexamer.
M.Obr, C.L.Ricana, N.Nikulin, J.R.Feathers, M.Klanschnig, A.Thader, M.C.Johnson, V.M.Vogt, F.K.M.Schur, R.A.Dick.
 
  ABSTRACT  
 
Inositol hexakisphosphate (IP6) is an assembly cofactor for HIV-1. We report here that IP6 is also used for assembly of Rous sarcoma virus (RSV), a retrovirus from a different genus. IP6 is ~100-fold more potent at promoting RSV mature capsid protein (CA) assembly than observed for HIV-1 and removal of IP6 in cells reduces infectivity by 100-fold. Here, visualized by cryo-electron tomography and subtomogram averaging, mature capsid-like particles show an IP6-like density in the CA hexamer, coordinated by rings of six lysines and six arginines. Phosphate and IP6 have opposing effects on CA in vitro assembly, inducing formation of T = 1 icosahedrons and tubes, respectively, implying that phosphate promotes pentamer and IP6 hexamer formation. Subtomogram averaging and classification optimized for analysis of pleomorphic retrovirus particles reveal that the heterogeneity of mature RSV CA polyhedrons results from an unexpected, intrinsic CA hexamer flexibility. In contrast, the CA pentamer forms rigid units organizing the local architecture. These different features of hexamers and pentamers determine the structural mechanism to form CA polyhedrons of variable shape in mature RSV particles.
 

 

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