GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Shewanella loihica PV-4

Align Branched-chain amino acid ABC transporter permease LivH; SubName: Full=Branched-chain amino acid transporter permease subunit LivH; SubName: Full=L-leucine ABC transporter membrane protein /L-isoleucine ABC transporter membrane protein /L-valine ABC transporter membrane protein (characterized, see rationale)
to candidate 5210165 Shew_2609 inner-membrane translocator (RefSeq)

Query= uniprot:A0A0D9B2B6
         (307 letters)



>FitnessBrowser__PV4:5210165
          Length = 297

 Score =  135 bits (339), Expect = 2e-36
 Identities = 89/305 (29%), Positives = 162/305 (53%), Gaps = 21/305 (6%)

Query: 9   QQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGLDSV 68
           Q ++NGL VG  Y ++ + + +VY    ++NFA GE  ++G++V +      A +    +
Sbjct: 8   QLIINGLIVGLLYGVVGMCFVLVYKSTQIVNFAQGEFLLVGAWVCW------AFLTYFQL 61

Query: 69  PLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNTVLLSQDSK 128
           P  +   F+ ++   + +G  ++ I  RP+ G   +  ++  IG+SIF Q+         
Sbjct: 62  PFFV--GFLFTLCFMAVFGVLLQMIVLRPMIGEPIISVIMVTIGLSIFFQSLTKWIFGVS 119

Query: 129 DKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACRACAE 188
            +S P +     +I   G +  L   M  V+ ++ + A     LF   S+ G A RA A 
Sbjct: 120 PQSYPQVFDTQ-SIAIFGLNIELAYLMSTVIAILIMAAFF---LFFKYSKHGLAMRATAF 175

Query: 189 DIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTAAVLG 248
           D ++A  LGI+   + A+++ I A ++A A V++ M  GV +  +   +G+K F A +LG
Sbjct: 176 DQQVAQSLGISVKQVFAMSWGIAATVSATAGVVIGMVNGVSDSLS--TIGIKVFPAVILG 233

Query: 249 GIGSIPGAMLGGLVLGVAEAFGADIFGDQY------KDVVAFGLLVLVLLFRPTGILGRP 302
           G+ SI GA++GG+V+GV E   A+ F  Q+       D+  F +L+++L F+P G+ G  
Sbjct: 234 GLDSIVGAIVGGVVIGVLENI-AEFFDSQWLHIGNMYDIAPFYVLLVILWFKPYGLFGTR 292

Query: 303 EVEKV 307
           ++E++
Sbjct: 293 DIERI 297


Lambda     K      H
   0.327    0.144    0.411 

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: 248
Number of extensions: 18
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: 307
Length of database: 297
Length adjustment: 27
Effective length of query: 280
Effective length of database: 270
Effective search space:    75600
Effective search space used:    75600
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: 48 (23.1 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