GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucP in Gallaecimonas xiamenensis 3-C-1

Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_008482148.1 B3C1_RS00390 sugar MFS transporter

Query= SwissProt::P11551
         (438 letters)



>NCBI__GCF_000299915.1:WP_008482148.1
          Length = 424

 Score =  232 bits (591), Expect = 2e-65
 Identities = 146/418 (34%), Positives = 217/418 (51%), Gaps = 9/418 (2%)

Query: 20  QSRSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPI 79
           + + Y      +  LFF+      LNDIL+P  +  F+L   QA LIQ  F+  YF++  
Sbjct: 15  EHQGYTFALTSMTFLFFMMGFITCLNDILIPHLKNVFSLNYTQAMLIQFCFFGAYFVVSY 74

Query: 80  PAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAAN 139
           PAG L ++L YK  ++  L + A+G  LF  AA    Y LFL  LFI+A+G+  L+ A N
Sbjct: 75  PAGALARRLGYKWALVISLVVSAIGCLLFITAASYRVYELFLGALFILASGVTTLQVAVN 134

Query: 140 PFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSA 199
           P+VTVLG   +   RL L Q FNS G  +A  FG  LIL             +S EQ++A
Sbjct: 135 PYVTVLGKPETASARLTLNQAFNSLGTTLAPTFGAMLILGAATAD----FTGLSQEQVTA 190

Query: 200 YKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRH 259
            + S   +V+ PY+++ +  L++A ++   K P ++  +++ A Q S   S     + RH
Sbjct: 191 LRLSEADAVKFPYLLLASTFLVLAAVLAYLKLPDMREQDNAAAAQASQGGS---AWQYRH 247

Query: 260 WRWAVLAQFCYVGAQTACWSYLIRYAVE-EIPGMTAGFAANYLTGTMVCFFIGRFTGTWL 318
                L  F YVGA+ +  S L+ +  E  I G+    AA+Y++       +GRF G+ +
Sbjct: 248 LVLGALGLFVYVGAEVSIGSLLVNFLGEANIAGLAEADAAHYVSYYWGGAMVGRFIGSAV 307

Query: 319 ISRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQ 378
           + +    KVLA  AL A+ L   +    G + + A+     F SI +PTIFSL +K LG 
Sbjct: 308 MRQVGAGKVLAFNALAAVLLLAAAVLGNGALAMWAVLAVGLFNSIMFPTIFSLAVKGLGH 367

Query: 379 DTKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIFARFRSQTA 436
            T  GS  + M I+GG IV  ++G  +D  G I  A  +P LC+  I  +    SQTA
Sbjct: 368 HTAQGSGILCMAIVGGAIVPLLVGVAADNLG-IQLAFALPILCYLYIAFYGLKGSQTA 424


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: 435
Number of extensions: 32
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: 438
Length of database: 424
Length adjustment: 32
Effective length of query: 406
Effective length of database: 392
Effective search space:   159152
Effective search space used:   159152
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 24 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