GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucP in Sphingomonas koreensis DSMZ 15582

Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate Ga0059261_0767 Ga0059261_0767 glucose/galactose transporter

Query= SwissProt::P11551
         (438 letters)



>FitnessBrowser__Korea:Ga0059261_0767
          Length = 434

 Score =  217 bits (553), Expect = 5e-61
 Identities = 139/407 (34%), Positives = 218/407 (53%), Gaps = 23/407 (5%)

Query: 33  SLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPIPAGILMKKLSYKA 92
           +LFF++    +LND+++P+ ++ FTL   QA L+Q  F+  Y +I IP   L+KKL Y  
Sbjct: 32  ALFFIFGGITSLNDVIIPKLKELFTLNYTQAMLVQFCFFTAYLVIGIPGAKLVKKLGYMR 91

Query: 93  GIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAANPFVTVLGPESSGH 152
           G + GL    +G  LF PA++   Y +FL  LF++A+G+  ++  ANP +++LG   + H
Sbjct: 92  GAVAGLLTMMVGCLLFIPASQYATYGVFLFALFVLASGVVIVQVVANPLISLLGKPETAH 151

Query: 153 FRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSAYKHSLVLSVQTPY 212
            RL  AQ FNS G  +  + G  LIL ++   +    D++S   L AY+ +   ++   Y
Sbjct: 152 SRLTFAQAFNSLGTTVFPIVGSILILGSL---ATVTADQLSGPALEAYRVAESKAIMHGY 208

Query: 213 MIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRHWRWAVLAQFCYVG 272
           + I A + +VA ++ L +   L+ + H   +  +  A L  L R R + +  L  F YVG
Sbjct: 209 LGIAAALAVVAGVVWLFR-NRLKGERH---QASAGLAGLDLLGRPR-FGFGALCIFLYVG 263

Query: 273 AQTACWSYLIRYAV--------EEIPGMTAGFAANYLTGTMVCFFIGRFTGTWLISRFAP 324
           A+ +  S ++ Y +        E+  G   GF   Y  G MV    GRF G+ L+   +P
Sbjct: 264 AEVSIGSLIVNYLMQPGVMGLQEQAAGKLIGF---YWGGAMV----GRFIGSGLMRVISP 316

Query: 325 HKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQDTKYGS 384
            K+LA  A+ A+AL LIS    GHV   +L       SI +PTIFSL  + LG     GS
Sbjct: 317 GKLLAFVAVGAVALILISTNTTGHVAGYSLLAIGLMNSIMFPTIFSLASEKLGGRAADGS 376

Query: 385 SFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIFARF 431
             I + I GG +V    G ++DA G++  A ++PA+C+A+I  F  +
Sbjct: 377 GIINIAIFGGAVVPLATGALADATGSLGLALILPAICYAIIAGFGYY 423


Lambda     K      H
   0.329    0.140    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: 470
Number of extensions: 25
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: 438
Length of database: 434
Length adjustment: 32
Effective length of query: 406
Effective length of database: 402
Effective search space:   163212
Effective search space used:   163212
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: 51 (24.3 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