GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01115 in Paraburkholderia bryophila 376MFSha3.1

Align deoxynucleoside transporter, permease component 1 (characterized)
to candidate H281DRAFT_01221 H281DRAFT_01221 monosaccharide ABC transporter membrane protein, CUT2 family

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



>FitnessBrowser__Burk376:H281DRAFT_01221
          Length = 338

 Score =  125 bits (313), Expect = 2e-33
 Identities = 96/303 (31%), Positives = 156/303 (51%), Gaps = 14/303 (4%)

Query: 19  LLIVNVLVVLVATWLSRGQFVDIDNLQSMGGQLPELGLLALGIMLSMVSGNGGIDLSGVG 78
           L+IV +L + +   LS   F+   NL ++   L E+ L+AL + L +V+    IDLS   
Sbjct: 23  LVIVLILSIALGRVLSP-VFLTGANLSNVLADLTEIALMALPMTLIIVAAE--IDLS--- 76

Query: 79  LANLSGMVAAMLVPRLVNGDDSPVLYTSLFCAIVLMMGLLGGLLNGVVIARLRLTPILCT 138
           +A++ G  +A++      G   PV+      A+VL+ G L GLLNG+VI +L L  +  T
Sbjct: 77  VASVLGASSALMGVLWHMGLPMPVVI-----ALVLVAGALAGLLNGLVIVKLNLPSLAVT 131

Query: 139 LGTQLLFTGFAVVISNGASVHVDYVEPLSDIGNGTV--LQVPIAFCIFLAAVIVLGWLLK 196
           +GT  LF G A V+    +V  D+    +  G  T+    VP+ F I +   ++   LL+
Sbjct: 132 IGTLALFRGLAYVLLGDQAV-ADFPPAYTAFGMDTLGGTFVPLPFAIVMVGAVLFTVLLQ 190

Query: 197 RSPFGLRLYLMGTNPKAAFYAGIPRARMLITTYAMCGVLASLAGLISATHTSSAKWDYGN 256
            + FG  LY +G NP AA ++GI   ++ +  + + G++ +LAG++     +SA+ D G 
Sbjct: 191 STAFGRSLYAIGANPTAAAFSGIEVTKIRLRLFVLSGLMGALAGVVYTLRFTSARGDNGE 250

Query: 257 SYLLIAILIAVMGGVNPAGGHGRIICVFFAATVLQFLSSLFNLLGVSQFFGDCAWGFLLL 316
            + L  I   + GGV+  GG G +I V  +  ++  L +   L  VS        G LLL
Sbjct: 251 GFELSVIAAVLFGGVSIFGGRGSMIGVLLSLLIIGVLKNALTLDDVSSETLTIVTGVLLL 310

Query: 317 LSL 319
            S+
Sbjct: 311 ASV 313


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: 295
Number of extensions: 26
Number of successful extensions: 2
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: 338
Length adjustment: 29
Effective length of query: 328
Effective length of database: 309
Effective search space:   101352
Effective search space used:   101352
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:

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