GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Herbaspirillum seropedicae SmR1

Align D-lactate transporter, permease component 1 (characterized)
to candidate HSERO_RS23260 HSERO_RS23260 ABC transporter permease

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



>FitnessBrowser__HerbieS:HSERO_RS23260
          Length = 334

 Score =  170 bits (430), Expect = 6e-47
 Identities = 121/374 (32%), Positives = 183/374 (48%), Gaps = 67/374 (17%)

Query: 13  LVVAILTLFAPFILNPFPTGSALAQFNAGYPDLMQRFVIFGIFAIGFNILFGLTGYLSFG 72
           L+ A + L  P +L   P+G+           L    ++F + A+G N+L G TG +SFG
Sbjct: 11  LLAAAVALLLPLLL---PSGT-----------LATEVLVFALAALGCNLLLGYTGLMSFG 56

Query: 73  HAAFLGVGSYSAVWMFKLLSMNVVPAIVLSVIVAGLFALVIGYVSLRRSGIYFSILTLAF 132
              F GVGSY+A  +   L + ++PA+ L+ +   L AL++G+ S+R+ G YF +LTLAF
Sbjct: 57  QGIFFGVGSYTAGVVLLQLKLALLPALALAALGGALVALLVGWFSIRQRGTYFVMLTLAF 116

Query: 133 AQMSFNLAYSVLTPITNGETGLQLTLDDPRVLGVSATADGSIPVTSLFGLEMRSTFEMVV 192
           AQM + LAY+ +  +T G+ GL   LD PR            P  +LFGL +  T     
Sbjct: 117 AQMFYFLAYT-MKDVTGGDNGL---LDIPR------------PPLALFGLTLLPT----T 156

Query: 193 GPWAFQFNAGYYLCALILLAAFYLSIRIFRSPFGLMLKAVKSNQQRMNYTGLNTRPYTLA 252
             W +     Y + A++ +  F+L  R+  S  G  L AV+ N+ R +  G + R   LA
Sbjct: 157 SSWQY-----YTVVAILFVLVFWLLQRVVDSVLGKTLLAVRENEARASALGYDVRLLKLA 211

Query: 253 AFVISGMYAGLAGGLMASMDPLAGAERMQWTASGEVVLMTILGGAGTLIGPVLGAGFIKY 312
           AFVISG   GLAGGL A M  +A    +++  S  +++MT++GG G L   VLGA F   
Sbjct: 212 AFVISGAVTGLAGGLHAMMTGVAPLSNIEYHTSEAILVMTVIGGTGNLFASVLGASFYVL 271

Query: 313 FENIFSKINDNVLHSWFSFMPDGIEDAMVFIVHPFIGKGWHLTLGILFMLVVIFLPGGLV 372
             N            W S                 +   W + LG+L + V +++  GL 
Sbjct: 272 VGN------------WLS----------------TLWPRWLMLLGLLLIAVSLYMQKGLF 303

Query: 373 EGGQKLRGWIQGRK 386
               K+   ++G K
Sbjct: 304 GLAMKIIDAVRGNK 317


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: 398
Number of extensions: 30
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 400
Length of database: 334
Length adjustment: 30
Effective length of query: 370
Effective length of database: 304
Effective search space:   112480
Effective search space used:   112480
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 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