GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5403 in Halomonas desiderata SP1

Align ABC transporter for D-Alanine, permease component 2 (characterized)
to candidate WP_086509148.1 BZY95_RS06445 amino acid ABC transporter permease

Query= reanno::pseudo6_N2E2:Pf6N2E2_5403
         (375 letters)



>NCBI__GCF_002151265.1:WP_086509148.1
          Length = 396

 Score =  443 bits (1140), Expect = e-129
 Identities = 218/374 (58%), Positives = 286/374 (76%)

Query: 2   RAWVFQVVTVVAVIALGWFLFDNTQTNLQHRGITSGFGFLERSAGFGIAQHLIDYTEADS 61
           RA +FQV+ + AV A   ++  NTQ NL  RGIT+GFGFL+R+AGFGI Q LI+Y+   +
Sbjct: 23  RALLFQVLLIAAVAAFLLYIIGNTQDNLAARGITTGFGFLDRTAGFGIGQSLIEYSSQST 82

Query: 62  YARVFLIGLLNTLLVTFIGVILATILGFIIGVARLSQNWIISKLATVYVEVFRNIPPLLQ 121
           Y R F++GLLNTLLV+ +GVI ATI+GFI+G+ARLS NW+I++LA+ Y+E+FRNIP LLQ
Sbjct: 83  YGRTFVVGLLNTLLVSALGVIAATIIGFIVGIARLSPNWLIARLASGYIEIFRNIPLLLQ 142

Query: 122 ILFWYFAVFLSMPGPRAAHNFGDTFFVSSRGLNMPAALVAEGFWPFVISVVLAIVAIVLM 181
           I FWYFAV  +MP  R +++ G+  F++ RGL +P  L   GF    ++ V+AIVA + +
Sbjct: 143 IFFWYFAVLRAMPAARDSYSLGEVIFLNVRGLYLPEPLFESGFGLIPLTFVVAIVASIAL 202

Query: 182 TRWANKRFEATGEPFHKFWVGLALFLVIPALSALLFGAPVHWEMPELKGFNFVGGWVLIP 241
             W  +R EATG+     W+ LAL L +P L  +  G PV W++PEL+GFNF GG  +IP
Sbjct: 203 VIWNKRRHEATGKRLPAGWISLALILGLPMLVLVATGVPVTWDVPELRGFNFRGGITIIP 262

Query: 242 ELLALTLALTVYTAAFIAEIVRSGIKSVSHGQTEAARSLGLRNGPTLRKVIIPQALRVII 301
           E LAL LAL++YTA+FIAEIVRSGI+++ HGQTEAA++L L     LR V++PQALRVII
Sbjct: 263 EFLALWLALSIYTASFIAEIVRSGIQAIPHGQTEAAQALSLPQKLVLRLVVVPQALRVII 322

Query: 302 PPLTSQYLNLAKNSSLAAGIGYPEMVSLFAGTVLNQTGQAIEVIAITMSVYLAISISISL 361
           PPLTSQYLNL KNSSLA  IGYP++VS+FAGT LNQTGQAIEVI++TM+VYL IS+ +S+
Sbjct: 323 PPLTSQYLNLIKNSSLATAIGYPDLVSVFAGTTLNQTGQAIEVISMTMAVYLIISLLVSM 382

Query: 362 LMNWYNKRIALIER 375
            MNW+N R+AL+ER
Sbjct: 383 FMNWFNARVALVER 396


Lambda     K      H
   0.328    0.141    0.430 

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: 513
Number of extensions: 18
Number of successful extensions: 1
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: 375
Length of database: 396
Length adjustment: 30
Effective length of query: 345
Effective length of database: 366
Effective search space:   126270
Effective search space used:   126270
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: 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