GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecD in Pseudomonas fluorescens GW456-L13

Align iron(III) dicitrate transport system permease protein FecD (characterized)
to candidate PfGW456L13_3769 Hemin ABC transporter, permease protein

Query= CharProtDB::CH_004160
         (318 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3769
          Length = 345

 Score =  172 bits (436), Expect = 1e-47
 Identities = 123/337 (36%), Positives = 184/337 (54%), Gaps = 27/337 (8%)

Query: 6   VIFITLALAGCALLSLHMGVIPVPWRALLT----------DWQAGHEHYYVLMEYRLPRL 55
           +IF+ L L     LSL +G + +P    L           D     +   +L + RLPR 
Sbjct: 11  LIFLLLLLVLVFWLSLALGPVSLPLGDTLLGGMRLLGLPLDGGDTQQAELILGQIRLPRS 70

Query: 56  LLALFVGAALAVAGVLIQGIVRNPLASPDILGVNHAASLASVGALL---LMPSLPVMVLP 112
           LL + VG+ LA++GV +QG+ RNPLA P ++GV+  A+L +  A++   L+  LP ++ P
Sbjct: 71  LLGIAVGSVLALSGVAMQGLFRNPLADPGLVGVSGGAALGAALAIVGGSLLGGLPPVIEP 130

Query: 113 LL----AFAGGMAGLILLKMLAKTHQPMKLA---LTGVALSA-CWASLTDYLMLSRPQDV 164
            L    AFAGG+    ++    + +    +A   L GVA++A   A +  +  L+    +
Sbjct: 131 YLLSVCAFAGGLIVTAVVYRFGRRNGQTDVATMLLAGVAMTAMAGAGVGLFTYLADDATL 190

Query: 165 NNALLWLTGSLWGRDWSFVKIAIPLMILFLPLSLSFCRD---LDLLALGDARATTLGVSV 221
                W  GSL G  +  +    PL+I+ L ++L   R    L+ L LG++ A  LG  +
Sbjct: 191 RTLTFWNLGSLNGASYPRLW---PLLIVTLGVALWLPRRAAALNALLLGESEARHLGFDI 247

Query: 222 PHTRFWALLLAVAMTSTGVAACGPISFIGLVVPHMMRSITGGRHRRLLPVSALTGALLLV 281
              +   +L         VAA G I FIGLVVPH+MR + G  HR LLP S L GA LL+
Sbjct: 248 ERIKLELVLCTALGVGAAVAAAGLIGFIGLVVPHLMRLLVGPDHRVLLPASLLAGASLLL 307

Query: 282 VADLLARIIHPPLELPVGVLTAIIGAPWFVWLLVRMR 318
           +ADL AR++  P ELP+G++TA+IGAP+F++LLVR R
Sbjct: 308 LADLAARLLLAPAELPIGIVTALIGAPFFLYLLVRGR 344


Lambda     K      H
   0.330    0.142    0.447 

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: 304
Number of extensions: 15
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: 318
Length of database: 345
Length adjustment: 28
Effective length of query: 290
Effective length of database: 317
Effective search space:    91930
Effective search space used:    91930
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: 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