GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Acidovorax sp. GW101-3H11

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate Ac3H11_227 Hemin ABC transporter, permease protein

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_227
          Length = 360

 Score =  173 bits (438), Expect = 7e-48
 Identities = 119/329 (36%), Positives = 177/329 (53%), Gaps = 15/329 (4%)

Query: 16  AALIIIFWLSLFCYSAIPVSGADATRALLP--GHTPTL---PEALVQ-NLRLPRSLVAVL 69
           AAL+ + ++      A  ++ A   + LL   G  P+    PE LV  N+RLPR L+ V 
Sbjct: 28  AALVGLSFVWASTRGAYAIAPAQLWQVLLQAVGAAPSAEQAPEYLVFINIRLPRLLMGVA 87

Query: 70  IGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALS-------PTPIAGYSLS 122
            GA L LAG L+Q L  NP+A P L+G++SGAALA A+T  L        P  +  ++L 
Sbjct: 88  AGAGLGLAGALMQGLFRNPLADPGLVGVSSGAALAAAVTIVLGMHWLPDMPRTLGSWALV 147

Query: 123 FIAACGGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCM-GLTRITLLLAEDHAYGI 181
            +A  GG +   L+     G   T     ++LAG+A++A  + GL  +  +  ++    +
Sbjct: 148 SMAFGGGLLVTALIYALAQGDGGTR-MGLMLLAGVAVNALALAGLGYLNFISTDEQLRNL 206

Query: 182 FYWLAGGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLV 241
             WL G +  ARW  V  +  +V  A  + L+LA  LN + L ++ A  LGV + R + +
Sbjct: 207 QMWLLGSLGGARWSAVALVGAIVAVACGLGLVLARPLNAIALGEAQAALLGVPVERTKRL 266

Query: 242 INMLVLLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLA 301
             ++  L VGA  +  G + FIGL+ PH  R  AG D R VLP S LLGA L+L AD +A
Sbjct: 267 AVLVTALAVGAVTAATGIIGFIGLVAPHWVRLVAGPDHRVVLPGSALLGAALVLAADGVA 326

Query: 302 RALAFPGDLPAGAVLALIGSPCFVWLVRR 330
           R +  P +LP G + A IG P F+ ++R+
Sbjct: 327 RTIVQPAELPLGVLTAFIGVPLFLAMLRQ 355


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: 369
Number of extensions: 11
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: 360
Length adjustment: 29
Effective length of query: 303
Effective length of database: 331
Effective search space:   100293
Effective search space used:   100293
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