GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12660 in Pseudomonas simiae WCS417

Align D-lactate transporter, permease component 2 (characterized)
to candidate GFF522 PS417_02660 branched-chain amino acid transporter permease subunit LivH

Query= reanno::Phaeo:GFF1250
         (340 letters)



>FitnessBrowser__WCS417:GFF522
          Length = 304

 Score =  140 bits (352), Expect = 5e-38
 Identities = 103/338 (30%), Positives = 166/338 (49%), Gaps = 44/338 (13%)

Query: 1   MDAILLQ-ILNGLDKGSAYALIALGLTLIFGTLGVVNFAHGALFMIGAFCAVTVQRVLSL 59
           MD I LQ ++NGL  GS Y LIA+G T+++G +G++NFAHG ++MI A+ A     +L+ 
Sbjct: 1   MDGIFLQQLVNGLTLGSVYGLIAIGYTMVYGIIGMINFAHGEVYMISAYLAAISLALLA- 59

Query: 60  SFETVDETQKDFLGNPLKVKTPYVESWFGPEVGGAIIDWAVPLAILFAIPIMIGV-GYVM 118
                                     +FG E    +I     L  L    ++ GV G+V+
Sbjct: 60  --------------------------YFGIESFPLLI-----LGTLIFTVVVTGVYGWVI 88

Query: 119 ERGLIKHFYKRPHADQILVTFGLAIVLQEVVKYFYGANPIQTPAPDALNGVVNLGSIIGM 178
           ER   K          ++   G++++LQ   +   GA   Q   P  L G   +   IG 
Sbjct: 89  ERVAYKPLRNSTRLAPLISAIGISLILQNYAQIAQGAK--QQGIPTLLAGAWRVD--IGS 144

Query: 179 DIVYPVWRVVYFFFAVVIIGGIFSF-LQFTTFGMVVRAGMADRETVGLLGINIDRRFTIM 237
             V   +  V+   A      + ++ +++T  G + RA   DR+   +LGIN DR  + +
Sbjct: 145 GFVQLTYTKVFILVAAFAGMALLTYVIKYTKLGRMCRATQQDRKMASILGINTDRVISYV 204

Query: 238 FGIAAAVAGLAGVMYT-PINSPNYHMGMDFLVLSFVVVVVGGMGSLPGAVLAGFLLGVLE 296
           F I AA+A LAGV+ T    + +++ G    + +F   V+GG+GSLPGA+L G +LG+ E
Sbjct: 205 FVIGAAMAALAGVLITLNYGTFDFYAGFIIGIKAFTAAVLGGIGSLPGAMLGGIILGISE 264

Query: 297 SFASMNEIKSLIPGIDQIIIYVVAIIILLTRPRGLMGR 334
           S  S      +      +  + + ++IL+ RP+GL+GR
Sbjct: 265 SLFS----GLINSDYKDVFSFSLLVVILIFRPQGLLGR 298


Lambda     K      H
   0.329    0.147    0.439 

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: 253
Number of extensions: 15
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 340
Length of database: 304
Length adjustment: 28
Effective length of query: 312
Effective length of database: 276
Effective search space:    86112
Effective search space used:    86112
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 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