GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecD in Hafnia paralvei ATCC 29927

Align iron(III) dicitrate transport system permease protein FecD (characterized)
to candidate WP_061060069.1 M988_RS10210 iron ABC transporter permease

Query= CharProtDB::CH_004160
         (318 letters)



>NCBI__GCF_001655005.1:WP_061060069.1
          Length = 333

 Score =  198 bits (503), Expect = 2e-55
 Identities = 128/326 (39%), Positives = 187/326 (57%), Gaps = 13/326 (3%)

Query: 2   KIALVIFITLALAGCALLSLHMGVIPVPWRALLTDWQAGHEH--YYVLMEYRLPRLLLAL 59
           +IA  + I L LA   L S +MG + + +  L   W+   +   + V +  RLPR+LLA 
Sbjct: 7   RIAFSVLIVLLLA-LGLGSANMGALRLSFHTL---WETPLDDAMWQVWLNIRLPRVLLAT 62

Query: 60  FVGAALAVAGVLIQGIVRNPLASPDILGVNHAASLAS----VGALLLMPSLPVMVLPLLA 115
            VG ALAV+G ++QG+ RNPLA P +LG++  ASL      V  + L P+L +    L A
Sbjct: 63  VVGIALAVSGAIMQGLFRNPLADPTLLGISSGASLCVALVIVMPMTLAPTLALYSHMLAA 122

Query: 116 FAGGMAGLILLKMLAKT-HQPM-KLALTGVALSA-CWASLTDYLMLSRPQDVNNALLWLT 172
           F G +   +L+  L++  H  + +L L G+A++A C+A +     +S  Q +    LW  
Sbjct: 123 FGGSLIISLLIYGLSRGGHGSLSRLLLAGIAINALCFALVGVLSYISNDQQLRQFSLWSM 182

Query: 173 GSLWGRDWSFVKIAIPLMILFLPLSLSFCRDLDLLALGDARATTLGVSVPHTRFWALLLA 232
           GSL    W  +  A  L++     +L   R L+LL LGD  A  LG++V  T+   LLL+
Sbjct: 183 GSLGQAQWGTLLAATSLILPASAAALLMARRLNLLQLGDEEAHYLGINVAKTKRQLLLLS 242

Query: 233 VAMTSTGVAACGPISFIGLVVPHMMRSITGGRHRRLLPVSALTGALLLVVADLLARIIHP 292
             +    VA  G I FIGLV+PH++R   G  HR LLP SAL GA LL+ AD LAR +  
Sbjct: 243 AVLVGAAVAVSGVIGFIGLVIPHLVRMRLGADHRWLLPCSALGGACLLLTADTLARTLVS 302

Query: 293 PLELPVGVLTAIIGAPWFVWLLVRMR 318
           P E+PVG+LT++IG P+F+WL++R +
Sbjct: 303 PAEMPVGMLTSLIGGPYFLWLILRQK 328


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: 268
Number of extensions: 13
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: 333
Length adjustment: 28
Effective length of query: 290
Effective length of database: 305
Effective search space:    88450
Effective search space used:    88450
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: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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