GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gluP in Dyella japonica UNC79MFTsu3.2

Align D-mannitol and D-mannose transporter (MFS superfamily) (characterized)
to candidate N515DRAFT_0592 N515DRAFT_0592 glucose/galactose transporter

Query= reanno::SB2B:6936374
         (413 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0592
          Length = 430

 Score =  181 bits (459), Expect = 4e-50
 Identities = 136/398 (34%), Positives = 199/398 (50%), Gaps = 35/398 (8%)

Query: 31  LFFIWGFITALNDILIPHLKGIFDLSYTQAMLVQFCFFGAYFLVSPLAGVLIARIGYLRG 90
           LFFI+GF+T LN  LI  +K  F L    A LV   F+ +YF ++  +  ++ R G  +G
Sbjct: 27  LFFIFGFVTWLNGPLITFVKLAFSLDDVNAFLVPMVFYCSYFFLALPSSAVLKRTGMKKG 86

Query: 91  IIFGLSTMATGCLLFYPASSLEQYALFLLALFVLASGITILQVSANPFVARLGPERTAAS 150
           +  GL  MA G +LF    S+  Y   L  LFV+ +G+ +LQ ++NP+++ LGP  +AA 
Sbjct: 87  MALGLFVMAIGAVLFGQFVSMRVYGGALAGLFVIGAGLALLQTASNPYISILGPIDSAAQ 146

Query: 151 RLNLAQALNSLGHTLGP-LFGSLLIFG--------AAAGTHEA-----------VQLPYL 190
           R+      N +   L P +FG L++ G         AA T EA           V +PYL
Sbjct: 147 RIAFMGICNKVAGALAPFVFGWLVLSGIDTFDQQVKAAPTPEAREALLNTFAAKVHMPYL 206

Query: 191 LLAAVIGIIAVGF-------IFLGGKVKHADMGVDHRHKGSLLSHKRLLLGALAIFLYVG 243
            +A ++ ++AV         I   G    A++G     KG+LLS   L LG L +FLYVG
Sbjct: 207 AMAGLLVLLAVWVLRSPLPEIKPSGANSEAEIG---HAKGNLLSFPHLWLGVLCLFLYVG 263

Query: 244 AEVSIGSFLVNYFAEPSIGGLDEKSAAELVSWYWGGAMIGRFAGAALTRR-FNPAMVLAA 302
            EV  G  +  Y       GL   +     S+     ++G  AG  L  +  +    LA 
Sbjct: 264 VEVMAGDAIGTYGQGL---GLPLDATKHFTSFTLFAMLLGYLAGLVLIPKIISQQSYLAV 320

Query: 303 NAVFANLLLMLTIVSSGELALVAVLAVGFFNSIMFPTIFTLAIEGLGELTSRGSGLLCQA 362
           +AV      +    ++G  ++  V A+GF N++M+P IF LAI+GLG  T  GS LL  A
Sbjct: 321 SAVLGVAFTVGAWATTGYTSVGFVAALGFANAMMWPAIFPLAIKGLGRWTEAGSALLIMA 380

Query: 363 IVGGALLPVIQGVVADNVGVQLSF-IVPTFCYFYICWY 399
           IVGGAL+P     +  +   QL F ++   CY YI +Y
Sbjct: 381 IVGGALVPQAFVHLKQHYDFQLVFMLLMVPCYLYILFY 418


Lambda     K      H
   0.329    0.142    0.425 

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: 468
Number of extensions: 31
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: 413
Length of database: 430
Length adjustment: 32
Effective length of query: 381
Effective length of database: 398
Effective search space:   151638
Effective search space used:   151638
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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