GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Caulobacter crescentus NA1000

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate CCNA_00904 CCNA_00904 inositol ABC transport system, permease protein IatP

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__Caulo:CCNA_00904
          Length = 332

 Score =  152 bits (383), Expect = 2e-41
 Identities = 99/316 (31%), Positives = 158/316 (50%), Gaps = 3/316 (0%)

Query: 24  PASRGKRARSELARLRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLA 83
           P +  K     LA  R+   +  L LL+ +    +  FLT  N +++L   +   ++ + 
Sbjct: 9   PLATDKPRFDLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVG 68

Query: 84  ESLIVLTGKFDLSLESTVGIAPAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFI 143
            + ++L G  D+++ S +  A    A +V      G    W  A  LL   ++G   G++
Sbjct: 69  MTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDG-PATWLIA--LLVSTLIGLAGGYV 125

Query: 144 NGFLVVRLRLNAFIVTLAMLIVLRGMLVGATKGGTLFDMPTSFFALATTIVLGLPLSVWL 203
            G  V  L + AFIVTL  + V RG  +    GG +     ++    +  +L LP+ V +
Sbjct: 126 QGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWWGSGEILFLPVPVVI 185

Query: 204 AAAAFAIAAFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIV 263
            A   A     LRY R GR +YA+GGN EAAR +G+ V+ IT  V+ +   LA + G ++
Sbjct: 186 FALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLL 245

Query: 264 TGYVGAINANQGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVP 323
           +  +G+  A  G G    V A+ VIGG SL GG G + G + G LL+GV+ N L +  V 
Sbjct: 246 SARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVT 305

Query: 324 SFWIQAIYGAIILGSL 339
           S+  Q + G II+ ++
Sbjct: 306 SYVQQVVIGLIIVAAV 321


Lambda     K      H
   0.326    0.140    0.397 

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: 314
Number of extensions: 15
Number of successful extensions: 1
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: 351
Length of database: 332
Length adjustment: 29
Effective length of query: 322
Effective length of database: 303
Effective search space:    97566
Effective search space used:    97566
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: 49 (23.5 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