GapMind for catabolism of small carbon sources

 

Alignments 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)



>FitnessBrowser__Phaeo:GFF383
          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.

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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 (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). 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. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. 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:

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