GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HP1174 in Sphingomonas koreensis DSMZ 15582

Align Glucose/galactose porter (characterized)
to candidate Ga0059261_3850 Ga0059261_3850 Fucose permease

Query= TCDB::P0C105
         (412 letters)



>FitnessBrowser__Korea:Ga0059261_3850
          Length = 423

 Score =  250 bits (638), Expect = 6e-71
 Identities = 152/386 (39%), Positives = 212/386 (54%), Gaps = 8/386 (2%)

Query: 24  ALTSLTLLFFMWGFITCLNDILIPHLKNVFQLNYTQSMLIQFCFFGAYFIVSLPAGQLVK 83
           A  ++  LFF WGF+   ND LI  +++VF+L++T+++L    FF A+  VSLPA  L+ 
Sbjct: 11  AFAAVAALFFAWGFVCANNDPLIAAVRHVFRLSWTEALLTHIVFFFAFATVSLPAAALLA 70

Query: 84  RISYKRGIVVGLIVAAIGCALFIPAASYRVYALFLGALFVLASGVTILQVAANPYVTILG 143
           R    R I++ L     GC +         + + LG LF+LA+GV  LQVAANP    LG
Sbjct: 71  RAGATRTILIALGSMLAGCLVIQAVRWVPAFGVVLGGLFLLAAGVATLQVAANPLAAALG 130

Query: 144 KPETAASRLTLTQAFNSLGTTVAPVFGAVLILSA-----ATDATVNAEADAVRFPYLLLA 198
            P     RLTL  + NSLG      FGA  +L+      A  A+  A A  +   +L++ 
Sbjct: 131 PPGQRHFRLTLAHSLNSLGMVCGAHFGAQFLLAEVNLTPAMPASRVAGAPTIAHAFLVIG 190

Query: 199 -LAFTVLAIIFAILKPPDVQEDEPALSDKKEGSAWQYRHLVLGAIGIFVYVGAEVSVGSF 257
            L F +  +  A+ +  +     PA      G A + R  + GA  I +YVGAEVS+GS 
Sbjct: 191 GLTFGLALLTLAVRRTIERAAPAPAPGGGL-GDALRSRWAIAGAAAIGLYVGAEVSIGSV 249

Query: 258 LVNFLSDPTVAGLSETDAAHHVA-YFWGGAMVGRFIGSAAMRYIDDGKALAFNAFVAIIL 316
           L+ FLS P   GL    A  +VA  +WGGA+ GRF+GS A+R+I   + LA  A  A  L
Sbjct: 250 LIPFLSSPDTLGLPAAVAGAYVANLYWGGALAGRFLGSWALRFIPAARLLALFAGSAAAL 309

Query: 317 LFITVATTGHIAMWSVLAIGLFNSIMFPTIFSLALHGLGSHTSQGSGILCLAIVGGAIVP 376
               +   G  A W VLAIGLFNSI+FPT+F L L   G   +  SG+LC+AI  GA++P
Sbjct: 310 CLAALVLPGPAAAWCVLAIGLFNSILFPTVFGLTLERSGVSEAATSGLLCVAIGAGAVLP 369

Query: 377 LIQGALADAIGIHLAFLMPIICYAYI 402
            + G +AD  G+   F++P+I Y YI
Sbjct: 370 FLVGRIADLAGLGWTFVIPMIGYVYI 395


Lambda     K      H
   0.328    0.141    0.420 

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: 543
Number of extensions: 26
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: 412
Length of database: 423
Length adjustment: 32
Effective length of query: 380
Effective length of database: 391
Effective search space:   148580
Effective search space used:   148580
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: 50 (23.9 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