GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Jeotgalibacillus soli P9

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate WP_041086373.1 KP78_RS03515 iron ABC transporter permease

Query= SwissProt::P15030
         (332 letters)



>NCBI__GCF_000829435.1:WP_041086373.1
          Length = 334

 Score =  182 bits (461), Expect = 1e-50
 Identities = 111/323 (34%), Positives = 180/323 (55%), Gaps = 7/323 (2%)

Query: 10  LWGLPVAALIIIFWLSLFCYSAIPVSGA-DATRALLPGHTPTLPEALVQNLRLPRSLVAV 68
           L GL    +++ F    F  + IP S   +A     P  T  L   ++   RL R+++A+
Sbjct: 12  LVGLLGLVIVLFFGSLAFGQTTIPFSTTWEAITRYDPADTNHL---IIGTSRLTRAVIAL 68

Query: 69  LIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSA-LSPTPIAGYSLSFIAAC 127
           +IG +LA+AG  +Q LT NP+A+P LLGINSGA   + L    L  + +  Y   + A  
Sbjct: 69  VIGMNLAIAGVFVQALTRNPLAAPDLLGINSGAIFFIVLAITWLEVSSLTQYM--WFAFL 126

Query: 128 GGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDHAYGIFYWLAG 187
           G G++  +V   G   R      K+IL+G+ALSA     T+  L++ E     + +W+AG
Sbjct: 127 GAGIAGAVVFFLGSIGRDGLTPIKVILSGVALSALFTSFTQGLLVVDEQSIQTVLFWIAG 186

Query: 188 GVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINMLVL 247
            V+    + +  +LP ++ A+ V L +   + + +  D  A  LG     +++++ +L++
Sbjct: 187 SVAGRDMEMLVSVLPFLLGALIVSLFMGRAIGIFSSGDDVAKGLGQRTGIIKVLMGVLII 246

Query: 248 LLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALAFP 307
           +L G  V+V G V FIGL+VPH+A+   G D R ++P S LLGA L+L AD++AR + FP
Sbjct: 247 ILAGGSVAVVGSVGFIGLIVPHMAKGLVGNDYRWMIPYSALLGAALLLAADIVARFIIFP 306

Query: 308 GDLPAGAVLALIGSPCFVWLVRR 330
            ++P G + A IG P F++L R+
Sbjct: 307 QEVPIGVMTAFIGGPFFIYLARK 329


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: 308
Number of extensions: 12
Number of successful extensions: 2
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: 334
Length adjustment: 28
Effective length of query: 304
Effective length of database: 306
Effective search space:    93024
Effective search space used:    93024
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