GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Acidovorax sp. GW101-3H11

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate Ac3H11_1841 Ribose ABC transport system, ATP-binding protein RbsA (TC 3.A.1.2.1)

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1841
          Length = 892

 Score =  154 bits (390), Expect = 6e-42
 Identities = 106/327 (32%), Positives = 172/327 (52%), Gaps = 25/327 (7%)

Query: 11  TPKRRFRWPTGMPQLVALLLVLL----VDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPV 66
           TP     W + +   + LL VL     + S ++ +FW           + I I N    +
Sbjct: 575 TPSSASVWRSQLGTYLGLLAVLAGMVALFSSLSEYFWSAE--------TFITIANEIPAL 626

Query: 67  ALLAIGMTLVIATGGIDLSVGAVMAIAGATTAAMTVA-GFSLPIVLLSALGTGILAGLWN 125
           A++A+GMT V+   GIDLSVG+VMA+A AT+AA  +  G+++P     AL TG++ G   
Sbjct: 627 AVMAVGMTFVLIIAGIDLSVGSVMALAAATSAAAILQWGWTVPAAAALALATGLVCGTIT 686

Query: 126 GILVAILKIQPFVATLILMVAGRGVAQLITAGQIVTFNSPDLSW-----FGSGSLLFLPT 180
           G +    ++  F+ +L ++ A RG A ++T  +   +    +SW     FG  S  FL  
Sbjct: 687 GAISVAWRLPSFIVSLGMLEAVRGSAYVVTDSR-TQYVGDAISWLSAPFFGGISFAFLLA 745

Query: 181 PVIIAVLTLILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIA 240
            V++ V  L+L      +T  G  +  +G N  A + AGV+ R I ++ + ++GL A +A
Sbjct: 746 VVLVVVAQLVL-----SRTVFGRCVVGIGTNEEAMRLAGVDPRPIRVIVFAMTGLLAGLA 800

Query: 241 GIIVAADIRGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGIL 300
           G++ +A +  AD N AG  +EL  I AVVIGG SLMGGR +++ +  G LII  +  G+ 
Sbjct: 801 GLMQSARLEAADPN-AGTGMELQVIAAVVIGGTSLMGGRGSVVNTAFGVLIIAVLEAGLA 859

Query: 301 LSGFPPEMNQVVKAVVVLCVLIVQSQR 327
             G      +++   V++  +IV + R
Sbjct: 860 QVGASEPSKRIITGFVIVAAVIVDTLR 886


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: 639
Number of extensions: 30
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: 341
Length of database: 892
Length adjustment: 36
Effective length of query: 305
Effective length of database: 856
Effective search space:   261080
Effective search space used:   261080
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: 52 (24.6 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