GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01115 in Sinorhizobium meliloti 1021

Align deoxynucleoside transporter, permease component 1 (characterized)
to candidate SMc02031 SMc02031 permease

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



>FitnessBrowser__Smeli:SMc02031
          Length = 349

 Score =  128 bits (322), Expect = 2e-34
 Identities = 91/307 (29%), Positives = 160/307 (52%), Gaps = 11/307 (3%)

Query: 24  VLVVLVATWLS--RGQFVDIDNLQSMGGQLPELGLLALGIMLSMVSGNGGIDLSGVGLAN 81
           + +VL+  +L+     F+ +DNL ++  Q   + +LA+G    +++G  GIDLS   +A 
Sbjct: 34  IALVLLMAYLAFATSNFLTLDNLSNVARQSAFVAILAVGQTFVILTG--GIDLSVAAIAA 91

Query: 82  LSGMVAAMLV--PRLVNGDDSPVLYTSLFCAIVLMMGLLGGLLNGVVIARLRLTPILCTL 139
           LS  + A+L+  P ++ G D   +   +   I +++G+  G LNG +I++ ++   + TL
Sbjct: 92  LSASITAVLLTQPLVLFGIDFGFVPPPVAILIGILIGMAAGALNGWLISKFKIPDFIATL 151

Query: 140 GTQLLFTGFAVVISNGASVHV-----DYVEPLSDIGNGTVLQVPIAFCIFLAAVIVLGWL 194
           GT   F G A+++++G  V          E L  +G G +  VP++  I L       ++
Sbjct: 152 GTMTAFRGAALLVTDGLPVPSFNAGRQLPESLIWVGGGQLFGVPVSALIALLCAAAGWYV 211

Query: 195 LKRSPFGLRLYLMGTNPKAAFYAGIPRARMLITTYAMCGVLASLAGLISATHTSSAKWDY 254
           L+ +  G  +Y +G N  AA  +GI  +R  I TYA+ G+LA++AG+I     +SA    
Sbjct: 212 LRYTALGRAIYAVGGNRAAAHSSGISISRTKIMTYAISGLLAAIAGIILVGRLNSANALM 271

Query: 255 GNSYLLIAILIAVMGGVNPAGGHGRIICVFFAATVLQFLSSLFNLLGVSQFFGDCAWGFL 314
            +   L +I   V+GG N  GG G +      A ++  L +  NLL VS F+   A G +
Sbjct: 272 ADGEELRSIASVVIGGTNLFGGEGGVWGSIIGAAIIGVLGNGLNLLDVSPFWQRIAQGVV 331

Query: 315 LLLSLAF 321
           +++ + F
Sbjct: 332 IVVVVIF 338


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: 339
Number of extensions: 17
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 357
Length of database: 349
Length adjustment: 29
Effective length of query: 328
Effective length of database: 320
Effective search space:   104960
Effective search space used:   104960
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