GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Azospirillum thiophilum BV-S

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 WP_052709915.1 AL072_RS06975 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_001305595.1:WP_052709915.1
          Length = 437

 Score =  227 bits (578), Expect = 4e-64
 Identities = 121/293 (41%), Positives = 178/293 (60%)

Query: 9   QQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGLDSV 68
           QQ++N  TV   Y L+A+GYT+VY I+G IN A GE+ M+G+ +  IA AGL M G  + 
Sbjct: 139 QQVINAATVACVYGLLALGYTLVYAILGQINLAMGELTMLGAMLTAIAAAGLGMAGWATW 198

Query: 69  PLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNTVLLSQDSK 128
           P  +  A +  +  T+  G++++R+ +R LRG     PLI A+G+SI  Q  V L   ++
Sbjct: 199 PPALLGALVLVMGFTAVQGWTMDRLVFRRLRGVRSHTPLIVAVGLSIAYQEGVRLLHGAR 258

Query: 129 DKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACRACAE 188
           D     ++ G   +   GA  V     Q+ +  +T      L   + R+  GRA RAC +
Sbjct: 259 DWWPAPVLTGRHDLLSDGAFTVTALTAQLAILGLTGGLYALLWGIMQRTAFGRAHRACTD 318

Query: 189 DIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTAAVLG 248
           D+  A L+G++ N  +A+TF IG  LAA A  ++++ YG +N   G+L+G KA  AAV+G
Sbjct: 319 DVAAAELVGVDVNRTVAVTFAIGGGLAAAAGSVIALYYGGVNFFTGYLIGFKALAAAVVG 378

Query: 249 GIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGILGR 301
           GIGS+PGAMLGG +LG+ E F +  F   YKD+VAFGLL L L++RP G+LG+
Sbjct: 379 GIGSVPGAMLGGALLGLVETFWSAYFAIAYKDIVAFGLLTLFLIYRPQGLLGQ 431


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: 359
Number of extensions: 17
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: 307
Length of database: 437
Length adjustment: 30
Effective length of query: 277
Effective length of database: 407
Effective search space:   112739
Effective search space used:   112739
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 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