GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12660 in Pseudomonas fluorescens GW456-L13

Align D-lactate transporter, permease component 2 (characterized)
to candidate PfGW456L13_4608 High-affinity branched-chain amino acid transport system permease protein LivH (TC 3.A.1.4.1)

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



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4608
          Length = 307

 Score =  123 bits (308), Expect = 7e-33
 Identities = 97/338 (28%), Positives = 158/338 (46%), Gaps = 50/338 (14%)

Query: 7   QILNGLDKGSAYALIALGLTLIFGTLGVVNFAHGALFMIGAFCA-VTVQRVLSLSFETVD 65
           Q++NGL  GS YALIA+G T+++G +G++NFAHG ++MIG++ A + +  +  L  ++V 
Sbjct: 10  QLVNGLTIGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMLGLDSV- 68

Query: 66  ETQKDFLGNPLKVKTPYVESWFGPEVGGAIIDWAVPLAILFAIPIMIGVGYVMERGLIKH 125
                    PL +                        A L  I +    GY +ER   + 
Sbjct: 69  ---------PLLMTA----------------------AFLATIVVTSAYGYSIERIAYRP 97

Query: 126 FYKRPHADQILVTFGLAIVLQEVVKYFYGANPIQTPAPDALNGVVNLGSIIGMDIVYPVW 185
                    ++   G++I LQ  V      +      P+ + G    G     +++    
Sbjct: 98  LRGSNRLIPLISAIGMSIFLQNTV--LLAQDSKDKSIPNLIPGNFAFGPGGAHEVLISYM 155

Query: 186 RVVYFFFAVVIIGGIFSFLQFTTFGMVVRAGMADRETVGLLGINIDRRFTIMFGIAAAVA 245
           ++V F   +V + G+  F+  +  G   RA   D +   LLGIN +    + F I AA+A
Sbjct: 156 QIVVFVVTLVAMLGLTLFISRSRLGRACRACAEDIKMANLLGINTNNIIALTFVIGAALA 215

Query: 246 GLAGVM----YTPINSPNYHMGMDFLV--LSFVVVVVGGMGSLPGAVLAGFLLGVLESFA 299
            +A V+    Y  IN PN      FLV   +F   V+GG+GS+PGA+L G +LGV E+F 
Sbjct: 216 AIAAVLLSMQYGVIN-PN----AGFLVGLKAFTAAVLGGIGSIPGAMLGGLVLGVAEAFG 270

Query: 300 SMNEIKSLIPGIDQIIIYVVAIIILLTRPRGLMGRKGV 337
           +             ++ + + +++LL RP GL+GR  V
Sbjct: 271 A----DIFGDQYKDVVAFGLLVLVLLFRPTGLLGRPEV 304


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: 290
Number of extensions: 18
Number of successful extensions: 2
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: 307
Length adjustment: 28
Effective length of query: 312
Effective length of database: 279
Effective search space:    87048
Effective search space used:    87048
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