GapMind for catabolism of small carbon sources

 

Aligments for a candidate for deoxyribonate-transport in Herbaspirillum seropedicae SmR1

Align 2-deoxy-D-ribonate transporter 1 (characterized)
to candidate HSERO_RS22270 HSERO_RS22270 MFS transporter

Query= reanno::WCS417:GFF1429
         (438 letters)



>FitnessBrowser__HerbieS:HSERO_RS22270
          Length = 445

 Score =  299 bits (766), Expect = 1e-85
 Identities = 167/417 (40%), Positives = 246/417 (58%), Gaps = 3/417 (0%)

Query: 6   SARTPQALNKLMFVKLMPLLIIAYILSFLDRTNIALAKHHLDVDLGISAAAYGLGAGLFF 65
           +A +  A  K +  +L+P +++ Y++S+LDR N+  A   ++ DLG++ + +GLGAGLFF
Sbjct: 16  AAVSEDATMKKVMRRLIPFILLCYVVSYLDRINVGFAALTMNKDLGLTPSQFGLGAGLFF 75

Query: 66  LTYALSEIPSNLIMHKVGARFWIARIMVTWGLISAAMAFVQGETSFYVLRLLLGIAEAGL 125
           + Y   EIPSNL +H+ GAR WI+RIM++WGLIS A AFV G  SF + R LLG+AEAG 
Sbjct: 76  IGYFFFEIPSNLALHRFGARMWISRIMISWGLISMATAFVVGPKSFALARFLLGMAEAGF 135

Query: 126 FPGVMLYLTYWFNREQRARATGYFLLGVCFANIIGGPVGAALMRMDGMLGWHGWQWMFML 185
            PG+ LY T WF    R +AT +FL+G+  ANIIG P+  ALM + GM G+ GWQ + +L
Sbjct: 136 TPGIYLYFTQWFPGAWRGKATAFFLIGIPVANIIGSPLSGALMELHGMWGFKGWQVLLLL 195

Query: 186 EGLPAVAFAWVVWRKLPDRPSKAPWLSAEEARGIEQRIAQETEEGAGEGGHSLKNWLTPQ 245
           E LPAV    +    LPDRP+KA WLSA+E + +E  ++ E    A   G+ LK+  T  
Sbjct: 196 EALPAVLLGVMCLFLLPDRPAKAKWLSADEKQWLENELSTEQNVLAARHGNKLKDAFTNW 255

Query: 246 ILLAIF-VYFCHQITIYTVIFFLPSIISKYGELSTMSVGLLTSLPWIAAALGALLIPRFA 304
            + A+    FC  I   ++  +LP II ++G L +  VGL+ ++P++  A+   L  R A
Sbjct: 256 RVFALAGANFCGIIGSLSIGLWLPQIIREFG-LPSHQVGLVAAIPYLVGAVAMTLWARLA 314

Query: 305 TTPGRCRRLLVTGLLTMALGLGI-ASVSGPVFSLLGFCLSAVMFFVVQSIIFLYPASRLK 363
               R    +   ++  AL LGI A +  P+  +L   ++       Q+  +  P+  L 
Sbjct: 315 NRSERRLFFVAGAIVLAALSLGISAFLHTPLLKMLAITVAVASILSFQATFWAIPSGFLT 374

Query: 364 GVALAGGLGFVNACGLLGGFVGPSVMGVIEQSTGNAMNGLKVIALVLVVAALAALRL 420
           G A AGGL  + + G LGGFVGPSV+G I ++T      L  +A  L++ A+  L L
Sbjct: 375 GRAAAGGLALIVSIGNLGGFVGPSVIGFIREATQGFTYPLIFVAGALLLGAVITLAL 431


Lambda     K      H
   0.327    0.141    0.438 

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: 581
Number of extensions: 33
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: 438
Length of database: 445
Length adjustment: 32
Effective length of query: 406
Effective length of database: 413
Effective search space:   167678
Effective search space used:   167678
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: 51 (24.3 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