GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Phaeobacter inhibens BS107

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate GFF3205 PGA1_c32580 high-affinity branched-chain amino acid transport permease protein

Query= uniprot:A0A165KER0
         (358 letters)



>FitnessBrowser__Phaeo:GFF3205
          Length = 358

 Score =  137 bits (344), Expect = 6e-37
 Identities = 117/363 (32%), Positives = 178/363 (49%), Gaps = 57/363 (15%)

Query: 8   WIIGAVALLVLPLILQSFGNAWVRIADLA-LLYVLLALGLNIVVGYAGLLDLGYVAFYAV 66
           +++ A+A LV+P ++  +   W     L  L+Y + A+GLNI+VGY G + LG   F AV
Sbjct: 30  YVVLALAFLVVPFVVNDY---WANAILLPFLIYSIAAIGLNILVGYCGQVSLGTGGFMAV 86

Query: 67  GAYL-FALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRG 125
           GAY  + LM +             FP     S++I + +A  + A      G P+L+++G
Sbjct: 87  GAYACYKLMTA-------------FPE---MSMFIHVLLAGGITALVCIGFGLPSLRIKG 130

Query: 126 DYLAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDI-- 183
            YLA+ TL      + FL  L + V         GQI + +          +VFG  I  
Sbjct: 131 FYLAVATLA----AQFFLVWLFNRVPWFYNYSASGQISAPE---------RDVFGIIITG 177

Query: 184 -NSVTLYYYLF-LVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAF 241
            N+     Y+F L+ +    ++   L    +GR+WMAIR+ +IAA+ +G+N    KL AF
Sbjct: 178 PNAPAWATYMFSLIFLAFCALVARNLTRGTVGRSWMAIRDMDIAAEIIGVNPLKAKLSAF 237

Query: 242 GMGASFGGVSGAM-FGAFQGFVS-PESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSA 299
           G+   F GVSGA+ F  + G V   E+F + +S +++ MV++GG+G I G   GA  L  
Sbjct: 238 GVSGFFIGVSGALFFSVYLGAVEVGEAFGINKSFLVLFMVIIGGLGSIFGSFAGAAFLVL 297

Query: 300 LPEVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLL-RPRG-------------LW 345
           LP VL+ V   +        D     QL+I  A+I+I L+  P G             LW
Sbjct: 298 LPVVLKVVGVDVLGWP---TDIVAHIQLVIVGALIVIFLIAEPHGIAQLWRVAKEKLRLW 354

Query: 346 PSP 348
           P P
Sbjct: 355 PFP 357


Lambda     K      H
   0.328    0.144    0.430 

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: 356
Number of extensions: 24
Number of successful extensions: 5
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: 358
Length of database: 358
Length adjustment: 29
Effective length of query: 329
Effective length of database: 329
Effective search space:   108241
Effective search space used:   108241
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