GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Pseudovibrio axinellae Ad2

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate WP_068009573.1 PsAD2_RS19075 iron ABC transporter permease

Query= SwissProt::P15030
         (332 letters)



>NCBI__GCF_001623255.1:WP_068009573.1
          Length = 332

 Score =  162 bits (411), Expect = 8e-45
 Identities = 104/326 (31%), Positives = 167/326 (51%), Gaps = 8/326 (2%)

Query: 8   VLLWGLPVAALIIIFWLSLFCYSAIPVSGADATRALLPGHTPTLPEALVQNLRLPRSLVA 67
           VL+W L +    + F  SL   +A          AL    TP     ++  +R+PR+L+ 
Sbjct: 8   VLIWALSIITATL-FLASLMLGAADLSLPQLINAALSTQDTPV--STVLWEIRVPRALLG 64

Query: 68  VLIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALSPTPIAGYSLSFIAAC 127
           V+ GA+L L+G +LQ L  NP+A P L+G++S A+L   +      T    ++L   A  
Sbjct: 65  VITGATLGLSGAVLQGLLRNPLAEPGLIGVSSSASLGAVIAIYTGITLTMPFALPIFALA 124

Query: 128 GGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDH--AYGIFYWL 185
             G++  L+    GG   T     LILAG+A+S+    LT + L L+ +   A  I +W+
Sbjct: 125 SAGIAAALLPLLAGGRGQTLT---LILAGVAISSIATALTSLALNLSPNPFAAMEIVFWM 181

Query: 186 AGGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINML 245
            G ++    Q ++ + P ++    ++ +    LN L+L + TAHT+GV+L  LR      
Sbjct: 182 LGSLNDRSMQHLYIIAPFIMVGWGLLFVTGKGLNALSLGEETAHTMGVSLPTLRFCAIAG 241

Query: 246 VLLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALA 305
               VGA  +V G + FIGL+VPHL R     +   +L  S L GA L+ LAD+  +   
Sbjct: 242 TAASVGAVTAVTGTIGFIGLIVPHLLRKMVDDEPARLLLPSALAGACLLTLADIAVKLFG 301

Query: 306 FPGDLPAGAVLALIGSPCFVWLVRRR 331
              +L  G + AL+G+P F+WL+ ++
Sbjct: 302 PQSNLKLGVLTALVGAPFFLWLILKQ 327


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: 329
Number of extensions: 14
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: 332
Length adjustment: 28
Effective length of query: 304
Effective length of database: 304
Effective search space:    92416
Effective search space used:    92416
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 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