GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07310 in Paraburkholderia bryophila 376MFSha3.1

Align Inositol transport system permease protein (characterized)
to candidate H281DRAFT_01120 H281DRAFT_01120 monosaccharide ABC transporter membrane protein, CUT2 family

Query= reanno::Phaeo:GFF716
         (373 letters)



>FitnessBrowser__Burk376:H281DRAFT_01120
          Length = 333

 Score =  144 bits (363), Expect = 3e-39
 Identities = 102/325 (31%), Positives = 155/325 (47%), Gaps = 37/325 (11%)

Query: 36  ITVFAMFLIFAGDSGMFNS-QGVMNWSQISAQFMIIAVGACLLMIAGEFDLSVGSMIGFA 94
           I    + ++F+  S  F S    +N  + +A   IIA+G   ++IA + DLSVGS +  +
Sbjct: 40  IAFAVLLVVFSFASPWFLSIDNFLNIGRQTALVSIIAIGMTFVIIARQIDLSVGSSLALS 99

Query: 95  GMLIAIFSVTLGWPVWLAILVTFAIATAIGALNGFIVVRTGLPSFIVTLAFLFILRGFAI 154
           GM  A+    +G    +  +        +G +NG +  R  +PSF+VTL  L   RG A+
Sbjct: 100 GMSAALAMAYIGDHWLIGAVAGIGTGALVGVINGLVTTRLNIPSFLVTLGSLSAARGLAL 159

Query: 155 YLPQTIERKTIIGGVADAAEGDWLAALFGGKILTGLFQWFGDNGWIAVFERGTRKGQPVV 214
            +  T   K +I                             ++ +IA+F      G+  +
Sbjct: 160 LVTTT---KPVI---------------------------ITNDSFIAIF------GEGDI 183

Query: 215 EGLPMLIVWAILLVIIGHVILTKTRFGNWIFAAGGDAEAARNSGVPVNRVKILMFMFTAF 274
            G+P+ I+W +L VI G ++L  + FG  ++AAGG+  AAR SG+ + RV  L F+ T  
Sbjct: 184 AGVPVPIIWTVLAVIAGILLLHYSVFGRQVYAAGGNPTAARYSGIDIRRVTTLAFILTGV 243

Query: 275 CATVFATCQVMEFGGAGSDRGLLKEFEAIIAVVIGGALLTGGYGSVLGAALGALIFGVVQ 334
            A + A         A  D     E + I +V +GG  L GG G VLG  LG+LI G + 
Sbjct: 244 LAGLAALVLSARSHAARPDVVQGLELDVIASVTLGGCSLFGGRGFVLGTLLGSLIIGTLN 303

Query: 335 QGLFFAGVESSLFRVFLGLILLFAV 359
            GL   GV SSL  V  G+I++ AV
Sbjct: 304 NGLVLLGVSSSLQLVIKGIIIVAAV 328


Lambda     K      H
   0.330    0.145    0.443 

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: 400
Number of extensions: 27
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: 373
Length of database: 333
Length adjustment: 29
Effective length of query: 344
Effective length of database: 304
Effective search space:   104576
Effective search space used:   104576
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 (21.8 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