GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Shewanella halifaxensis HAW-EB4

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_012277104.1 SHAL_RS10460 sugar ABC transporter permease

Query= uniprot:D8IZC8
         (344 letters)



>NCBI__GCF_000019185.1:WP_012277104.1
          Length = 345

 Score =  221 bits (563), Expect = 2e-62
 Identities = 126/329 (38%), Positives = 201/329 (61%), Gaps = 24/329 (7%)

Query: 28  LLHRLGMLPVLVVLYLLFYGLTLYLSGD--------GTSNFASAENTMNILRQVAINLVL 79
           +LH+ G     +VL  LF   T+ + G+         ++ F +  N +++LRQV+IN +L
Sbjct: 21  VLHKYG-----IVLAFLFICATIAVLGELCIHNGMWDSNYFLTQANLLSVLRQVSINGIL 75

Query: 80  AAGMTFVILTAGIDLSVGSVLAVSAVLGMQVSLGAAP----GWAIPMF------IFSGLV 129
           A GMTFVI+ AG+DLSVGSVLA++ ++  +    ++     G+  P+       I  G +
Sbjct: 76  AVGMTFVIIVAGVDLSVGSVLALAGIVAARFVTNSSNMLIGGFDSPILLPLMVAICIGAI 135

Query: 130 MGMVNGAMVALLNINAFVVTLGTMTAFRGAAYLLADGTTVLNNDIPSFEWIGNGDFLHVP 189
            G +NG +++   + AF+VT+G ++  RG   L  DG  V + D   F  +GN     +P
Sbjct: 136 CGFLNGYIISKFRLQAFIVTMGMLSVARGMTMLTTDGNPVSSLD-RGFRALGNSYTFGIP 194

Query: 190 WLIWVAVAVVLLSWVILRKTVLGMHIYAIGGNLQAARLTGIRVGLVLLFVYSISGLFSGL 249
             + +   +   +W +L KTV G +++A+GGN ++A+ +GI V  V + VY++ G+ + +
Sbjct: 195 TPVVIFAVIFAAAWFLLNKTVFGRYVFAVGGNEKSAQTSGIDVHKVKVAVYTLCGVTAAI 254

Query: 250 AGAMSASRLYGANGNWGSGYELDAIAAVVLGGTSLMGGVGSIWGTVVGALIIGVMNNGLT 309
           AG +  +R   A  + G GYELDAIAAVV+GGTS+ GG+G++ GT+ G LIIGVMNNGL 
Sbjct: 255 AGLILTARTGSAQTSAGFGYELDAIAAVVIGGTSMAGGLGTLTGTLFGVLIIGVMNNGLD 314

Query: 310 ILGLSSFWQYVAKGAVIVLAVILDKWRQK 338
           +LG+ S++Q + KG +IV AV+LD  R++
Sbjct: 315 LLGVQSYYQQIIKGLLIVAAVMLDPSRKQ 343


Lambda     K      H
   0.324    0.138    0.417 

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: 301
Number of extensions: 17
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: 344
Length of database: 345
Length adjustment: 29
Effective length of query: 315
Effective length of database: 316
Effective search space:    99540
Effective search space used:    99540
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 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 24 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