GapMind for catabolism of small carbon sources

 

Aligments for a candidate for nupC' in Phaeobacter inhibens BS107

Align Purine/cytidine ABC transporter permease protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate GFF383 PGA1_c03940 putative permease protein

Query= TCDB::A2RKA5
         (317 letters)



>lcl|FitnessBrowser__Phaeo:GFF383 PGA1_c03940 putative permease
           protein
          Length = 278

 Score =  181 bits (460), Expect = 1e-50
 Identities = 106/284 (37%), Positives = 158/284 (55%), Gaps = 17/284 (5%)

Query: 45  MTIGAFSSVVFNLTTAGMFGSMTPWLSILFGALIGALFSSLHAVATVNLRADHIVSGTVL 104
           M + AF S     TT  +      WL +L G     + S LH +A++  R + ++SG  +
Sbjct: 1   MLMAAFFSAAVAATTGNV------WLGLLAGIASSLVLSGLHGLASITFRGNQLISGVAI 54

Query: 105 NLMAPALGVFLLQVFYQQGQININ-------EQIGYWNVPLLSNIPVIGKIF---FTQTS 154
           N +A  + V + Q ++QQG    +       E I       L+N+PV+G I+    +  S
Sbjct: 55  NFLAAGMTVLIAQDWFQQGGRTPSLFSGGRFEPINLPFADALANVPVLGPIYSELLSGHS 114

Query: 155 LPGFLAIVVAILAWYVLFKTRFGLRLRSVGENPQAADTLGINVYAYRWAGVLLSGVLGGV 214
           +  +LA +      +VLF TRFGLRLR+VGENP A DT G++V   R+A V++ G+L G+
Sbjct: 115 VLVYLAFLAVPATAWVLFGTRFGLRLRAVGENPAAVDTAGVSVVGLRYAAVMICGLLCGI 174

Query: 215 GGAIYAQAISGNFSVSTIAGQGFISLAAMIFGKWNPIGAMLSSLLFGLFTSLAVVGGQIP 274
            GA  A A+   F     AG+GFI+LAA+IF KW P  A+ + LLFGL  ++A+    I 
Sbjct: 175 AGAYLATALQAGFVKDMTAGRGFIALAALIFAKWRPWHALGACLLFGLLQAVALRFQNIE 234

Query: 275 -GIKEIPSSFLQMAPYVFTIIVLALFLGKAIAPKADGVNYIKSK 317
            G   IP   +   PY+ T+++LA F+GKA+ PKA G  Y+K +
Sbjct: 235 IGTFVIPVQMMDALPYILTVVILAGFVGKAVPPKAGGEPYVKER 278


Lambda     K      H
   0.326    0.142    0.419 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 229
Number of extensions: 12
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 317
Length of database: 278
Length adjustment: 26
Effective length of query: 291
Effective length of database: 252
Effective search space:    73332
Effective search space used:    73332
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, or view the source code.

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory