GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Sinorhizobium meliloti 1021

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate SM_b21343 SM_b21343 sugar uptake ABC transporter permease

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__Smeli:SM_b21343
          Length = 334

 Score =  199 bits (507), Expect = 6e-56
 Identities = 124/334 (37%), Positives = 187/334 (55%), Gaps = 21/334 (6%)

Query: 4   QSLPDTTTPKRRFRWPTGMPQLVALLLVLLVDSLV-APHFWQVVLQDGRLFGSPIDILNR 62
           Q+   T    +RF    G    VA  L L++ ++V  P+F  +   +  L         +
Sbjct: 7   QATAGTVPSGKRFFTLAGRYGTVAAFLALILFNVVFTPNFLSLQTLNVNL--------TQ 58

Query: 63  AAPVALLAIGMTLVIATGGIDLSVGAVMAIAGATTAAMTVAGFSLPI----------VLL 112
            A + ++AIGMTLVIATGGIDLSVG++MAI GA  A M   G   P+           +L
Sbjct: 59  VATIVIVAIGMTLVIATGGIDLSVGSLMAIGGAL-APMIFMGTLFPVSSMPVAVALAFVL 117

Query: 113 SALGTGILAGLWNGILVAILKIQPFVATLILMVAGRGVAQLITAGQIVTFNSPDLSWFGS 172
             + TG+L GL+NG+LV    IQP +ATL+L +AGRG+AQ++T G +  F +    +   
Sbjct: 118 PVVATGLL-GLFNGLLVTRFAIQPIIATLVLFIAGRGIAQVMTNGNLQVFRNEGFQFIAL 176

Query: 173 GSLLFLPTPVIIAVLTLILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVL 232
           G +  +P  VI+ +    + W   R T  G  + AVG N +A++  G+    + +L Y++
Sbjct: 177 GRVAGIPAQVILMIAIAAIAWAAIRYTVFGRQVIAVGGNEKASRLTGIPVHRVKLLVYMI 236

Query: 233 SGLCAAIAGIIVAADIRGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALII 292
           SG  A +AG+IV A    +DAN  GL +ELDAI AV +GG  L GGR N++ +V+GAL+I
Sbjct: 237 SGALAGVAGLIVVARNSASDANLVGLGMELDAIAAVAVGGTLLTGGRANIVGTVIGALVI 296

Query: 293 QGMNTGILLSGFPPEMNQVVKAVVVLCVLIVQSQ 326
           Q +   +L +G P     +VKA ++L  + +Q +
Sbjct: 297 QLVRYTLLANGVPDAAALIVKAALILLAVFIQQR 330


Lambda     K      H
   0.327    0.142    0.416 

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: 337
Number of extensions: 13
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: 341
Length of database: 334
Length adjustment: 28
Effective length of query: 313
Effective length of database: 306
Effective search space:    95778
Effective search space used:    95778
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