GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Pseudomonas simiae WCS417

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate GFF2674 PS417_13640 ribose ABC transporter permease

Query= uniprot:D8IZC8
         (344 letters)



>FitnessBrowser__WCS417:GFF2674
          Length = 325

 Score =  324 bits (830), Expect = 2e-93
 Identities = 177/326 (54%), Positives = 232/326 (71%), Gaps = 11/326 (3%)

Query: 17  ARRSSSTTAQWLLHRLGMLPVLVVLYLLFYGLTLYLSGDGTSNFASAENTMNILRQVAIN 76
           A  + +  A+ L+  +GMLPVL+   LL  G  L      + NF + +N   I +Q ++N
Sbjct: 7   ATTNKAERARELMRTVGMLPVLI---LLLVGFAL-----ASENFLTMQNLSIISQQASVN 58

Query: 77  LVLAAGMTFVILTAGIDLSVGSVLAVSAVLGMQVSLGAAPG-WAIPMFIFSGLVMGMVNG 135
           +VLAAGMTFVILTAGIDLSVG++LA SAV+ +Q S+    G + I   I  GL++G+VNG
Sbjct: 59  VVLAAGMTFVILTAGIDLSVGAILAASAVVALQASMSPQFGMFGIAAGIGFGLLLGLVNG 118

Query: 136 AMVALLNINAFVVTLGTMTAFRGAAYLLADGTTVLNNDIPSFEWIGNGDFLHVPWLIWVA 195
            ++A + +  F+VTLG +TA RG A LLAD  TV N D+P F +IGN   L VPWL+ +A
Sbjct: 119 GLIAFMRLPPFIVTLGALTAMRGLARLLADDKTVFNPDLP-FAFIGNDSLLGVPWLVIIA 177

Query: 196 VAVVLLSWVILRKTVLGMHIYAIGGNLQAARLTGIRVGLVLLFVYSISGLFSGLAGAMSA 255
           VAVV LSW ILR+TV+G+ IY++GGN +AARL+GI+V  VLLFVY++SG  +GL   MSA
Sbjct: 178 VAVVALSWFILRRTVMGVQIYSVGGNPEAARLSGIKVWKVLLFVYAMSGALAGLGAVMSA 237

Query: 256 SRLYGANG-NWGSGYELDAIAAVVLGGTSLMGGVGSIWGTVVGALIIGVMNNGLTILGLS 314
           SRL+ ANG   G  YELDAIAAV+LGGTS  GGVG+I GT++GALII V+ NGL +LG+S
Sbjct: 238 SRLFAANGLQLGQSYELDAIAAVILGGTSFTGGVGTIGGTLIGALIIAVLTNGLVLLGVS 297

Query: 315 SFWQYVAKGAVIVLAVILDKWRQKDA 340
             WQY+ KG VI+ AV LD++RQ  A
Sbjct: 298 DIWQYIIKGIVIIGAVALDRYRQSGA 323


Lambda     K      H
   0.324    0.138    0.417 

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: 385
Number of extensions: 27
Number of successful extensions: 4
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: 344
Length of database: 325
Length adjustment: 28
Effective length of query: 316
Effective length of database: 297
Effective search space:    93852
Effective search space used:    93852
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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