GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01115 in Echinicola vietnamensis KMM 6221, DSM 17526

Align deoxynucleoside transporter, permease component 1 (characterized)
to candidate Echvi_1280 Echvi_1280 Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components

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



>FitnessBrowser__Cola:Echvi_1280
          Length = 318

 Score =  108 bits (270), Expect = 2e-28
 Identities = 90/304 (29%), Positives = 158/304 (51%), Gaps = 9/304 (2%)

Query: 20  LIVNVLVVLVATWLSRGQFVDIDNLQSMGGQLPELGLLALGIMLSMVSGNGGIDLSGVGL 79
           LI  +++ LV + LS  +F+ + N  ++  Q+     +++G+ L +++   GIDLS   +
Sbjct: 10  LIALIILCLVLSLLS-DRFLTLANGWNVMRQVSVNICISVGMTLVILTA--GIDLSVGSI 66

Query: 80  ANLSGMVAAMLVPR--LVNGDDSPVLYTSLFCAIVLMMGLLGGL--LNGVVIARLRLTPI 135
             L G V A L+     V G +  + +  L  A++L +GL  GL   NG  I R ++ P 
Sbjct: 67  LALCGAVTASLIKNGIAVEGLNLHIGFAPLG-AVILGVGLGFGLGWFNGWTITRFKVPPF 125

Query: 136 LCTLGTQLLFTGFAVVISNGASVHVDYVEPLSDIGNGTVLQVPIAFCIFLAAVIVLGWLL 195
           + TL    +  G  ++ + G  ++    E  + +G G  L +P+   I    V +   L 
Sbjct: 126 VATLAMLTIARGLTMLWTGGFPIN-GLGEDFAFLGTGWFLGIPMPVWITAVIVALAVLLT 184

Query: 196 KRSPFGLRLYLMGTNPKAAFYAGIPRARMLITTYAMCGVLASLAGLISATHTSSAKWDYG 255
           K++ FG  +Y +G N +AA  +GI  +R+ +T YA+ G LA++ G+I  +   SA+ + G
Sbjct: 185 KKTKFGRYVYAIGGNERAARLSGINISRVKMTVYAIAGGLAAVGGMIVTSRLDSAQPNAG 244

Query: 256 NSYLLIAILIAVMGGVNPAGGHGRIICVFFAATVLQFLSSLFNLLGVSQFFGDCAWGFLL 315
            SY L AI   V+GG + +GG G I+       ++  L++   LL VS F+     G ++
Sbjct: 245 ISYELDAIAAVVIGGTSLSGGKGTIMGAVLGGIIIGVLNNGLVLLNVSPFWQQVVKGAVI 304

Query: 316 LLSL 319
           LL++
Sbjct: 305 LLAV 308


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: 307
Number of extensions: 16
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: 357
Length of database: 318
Length adjustment: 28
Effective length of query: 329
Effective length of database: 290
Effective search space:    95410
Effective search space used:    95410
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