GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Phaeobacter inhibens BS107

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate GFF2549 PGA1_c25900 putative iron ABC transport system, permease protein

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__Phaeo:GFF2549
          Length = 343

 Score =  184 bits (468), Expect = 2e-51
 Identities = 127/327 (38%), Positives = 176/327 (53%), Gaps = 9/327 (2%)

Query: 9   LLWGLPVAALIIIFWLSLFCYS--AIPVSGADATRALLPGHTPTLPEALVQNLRLPRSLV 66
           LLW    AAL+ +  LS    S  A   S A+    L           +V+N+RLPR + 
Sbjct: 19  LLW--LAAALLTLCLLSAAALSLGARATSWAEIWGGLTAYDPNNADHIVVRNMRLPRLIG 76

Query: 67  AVLIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTS-ALSPTPIAGYSLSFIA 125
           A L GA+L ++G L+Q +T NP+A P LLGIN GAAL + L    L  T  A +   ++A
Sbjct: 77  AGLAGAALGMSGALIQAMTRNPLADPGLLGINGGAALGVVLCILVLGVTDPAEFI--WVA 134

Query: 126 ACGGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDHAYGIFYWL 185
             GG  + +LV   GGG +    R  LILAG A+SA  + LTR  LL++        +W+
Sbjct: 135 LGGGLAASVLVFLLGGGSQANPLR--LILAGAAVSALFLALTRALLLVSRQTLDVYRFWV 192

Query: 186 AGGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINML 245
            GG        +  LLP ++    + ++    LN L L + TA  LGV     RL     
Sbjct: 193 LGGFDGILPATLQSLLPFLILGALLAIIAGFGLNALMLGEDTAKGLGVRTGLTRLTAGAA 252

Query: 246 VLLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALA 305
           ++LL GA V++AGP+AF GL+VPH+AR+ AG      L  S + GA L++ AD+L R   
Sbjct: 253 IVLLCGATVAMAGPIAFAGLIVPHMARWAAGPAIGWSLAFSAVFGALLLIAADLLGRLAL 312

Query: 306 FPGDLPAGAVLALIGSPCFVWLVRRRG 332
           F G++ AG + ALIG P  +WLVRR G
Sbjct: 313 FGGNMQAGVMTALIGGPVLIWLVRRNG 339


Lambda     K      H
   0.327    0.140    0.436 

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: 382
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: 332
Length of database: 343
Length adjustment: 28
Effective length of query: 304
Effective length of database: 315
Effective search space:    95760
Effective search space used:    95760
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