GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Halopiger salifodinae KCY07-B2

Align D-lactate transporter, permease component 1 (characterized)
to candidate WP_049988462.1 LT39_RS00200 branched-chain amino acid ABC transporter permease

Query= reanno::Phaeo:GFF1249
         (400 letters)



>NCBI__GCF_000784335.1:WP_049988462.1
          Length = 396

 Score =  148 bits (373), Expect = 3e-40
 Identities = 100/360 (27%), Positives = 161/360 (44%), Gaps = 65/360 (18%)

Query: 45  LMQRFVIFGIFAIGFNILFGLTGYLSFGHAAFLGVGSYSAVWMFKLLSMNVVPAI----- 99
           L   F+I  +FA+ FN+L+G TG LSFGHA F G G+Y    + +     +  A+     
Sbjct: 49  LFTEFLIIALFAVAFNLLYGYTGLLSFGHAMFFGAGAYGLAIVMRDYQAAIGDAVGSGLA 108

Query: 100 -VLSVIVAGLFALV--------IGYVSLRRSGIYFSILTLAFAQMSFNLAYSVLTPITNG 150
            + + +V GL  L+        +GY+S+R   IYF+++TLAF  + ++L       +T+G
Sbjct: 109 PLATFVVGGLAGLLLALVLAVPVGYLSVRLEEIYFALITLAFGMLFYSLLIQDPYGLTDG 168

Query: 151 ETGLQLTLDDPRVLGVSATADGSIPVTSLFGLEMRSTFEMVVGPWAFQFNAGYYLCALIL 210
             G+ + L    + G              F L  R T+              YYL A ++
Sbjct: 169 TDGIFILLGTVELGGAE------------FRLGERRTY--------------YYLTAAVV 202

Query: 211 LAAFYLSIRIFRSPFGLMLKAVKSNQQRMNYTGLNTRPYTLAAFVISGMYAGLAGGLMAS 270
           +A+ Y   RI  SPFG + KA++ +  R    G+N   +    FV+S ++ G+AG L+A 
Sbjct: 203 VASIYAIWRIVNSPFGTVCKAIRESPDRATALGVNVTVHRWMTFVVSALFVGVAGVLIAG 262

Query: 271 MDPLAGAERMQWTASGEVVLMTILGGAGTLIGPVLGAGFIKYFENIFSKINDNVLHSWFS 330
              +A      WT S   V+ T++GGA    GP++GA    Y   + S+           
Sbjct: 263 FASVATPNEAHWTMSATPVVATVIGGATYFGGPIVGAFVYHYVRWLISRF---------- 312

Query: 331 FMPDGIEDAMVFIVHPFIGKGWHLTLGILFMLVVIFLPGGLVEGGQKLRGWIQGRKAKKD 390
                          P +   W L  GI+ ++VV++   G   G   L  W++  +A  D
Sbjct: 313 ---------------PALEAYWELFFGIMLIVVVLYFKRGAAGGLVMLGAWLRDVRAAYD 357


Lambda     K      H
   0.327    0.143    0.435 

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: 504
Number of extensions: 35
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: 400
Length of database: 396
Length adjustment: 31
Effective length of query: 369
Effective length of database: 365
Effective search space:   134685
Effective search space used:   134685
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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