GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01115 in Klebsiella michiganensis M5al

Align deoxynucleoside transporter, permease component 1 (characterized)
to candidate BWI76_RS00280 BWI76_RS00280 ribose ABC transporter permease

Query= reanno::Burk376:H281DRAFT_01115
         (357 letters)



>FitnessBrowser__Koxy:BWI76_RS00280
          Length = 321

 Score =  135 bits (339), Expect = 2e-36
 Identities = 97/304 (31%), Positives = 155/304 (50%), Gaps = 15/304 (4%)

Query: 19  LLIVNVLVVLVATWLSRGQFVDIDNLQSMGGQLPELGLLALGIMLSMVSGNGGIDLSGVG 78
           L+ + VL+ +V+T      F  ++NL ++  Q     ++A+G+ L +++   GIDLS   
Sbjct: 23  LIALLVLIAIVSTMSPN--FFTVNNLFNILQQTSVNAIMAVGMTLVILTS--GIDLSVGS 78

Query: 79  LANLSGMVAAMLVPRLVNGDDSPVLYTSLFCAIVLMMGLLGGLLNGVVIARLRLTPILCT 138
           L  L+G VAA +V   VN          +  A  L +G   G + GV++A+ R+   + T
Sbjct: 79  LLALTGAVAASIVGIEVNA--------LVAVAAALALGAAIGAVTGVIVAKGRVQAFIAT 130

Query: 139 LGTQLLFTGFAVVISNGASVHV---DYVEPLSDIGNGTVLQVPIAFCIFLAAVIVLGWLL 195
           L   LL  G  +V +NG+ V+    D  +     G G  L +P    I     +   ++L
Sbjct: 131 LVMMLLLRGVTMVYTNGSPVNTGFTDNADLFGWFGIGRPLGIPTPVWIMAIVFLAAWYML 190

Query: 196 KRSPFGLRLYLMGTNPKAAFYAGIPRARMLITTYAMCGVLASLAGLISATHTSSAKWDYG 255
             +  G  +Y +G N  A   +GI   ++ I  Y++CG+LASLAG+I     SSA+   G
Sbjct: 191 HHTRLGRYIYALGGNEAATRLSGISVNKVKIIVYSLCGMLASLAGIIEVARLSSAQPTAG 250

Query: 256 NSYLLIAILIAVMGGVNPAGGHGRIICVFFAATVLQFLSSLFNLLGVSQFFGDCAWGFLL 315
             Y L AI   V+GG + AGG GRI+     A +L FL++  NLLGVS ++       ++
Sbjct: 251 TGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQMIVKAVVI 310

Query: 316 LLSL 319
           LL++
Sbjct: 311 LLAV 314


Lambda     K      H
   0.327    0.143    0.429 

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: 277
Number of extensions: 18
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: 357
Length of database: 321
Length adjustment: 28
Effective length of query: 329
Effective length of database: 293
Effective search space:    96397
Effective search space used:    96397
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 (21.7 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, 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