GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5403 in Cupriavidus basilensis 4G11

Align ABC transporter for D-Alanine, permease component 2 (characterized)
to candidate RR42_RS02580 RR42_RS02580 amino acid ABC transporter permease

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



>FitnessBrowser__Cup4G11:RR42_RS02580
          Length = 242

 Score = 94.4 bits (233), Expect = 3e-24
 Identities = 81/247 (32%), Positives = 123/247 (49%), Gaps = 21/247 (8%)

Query: 125 WYFAVFLSMPGPRAAHNFGDTFFVSSRGLNMPAALVAEGFWPFVISVVLAIVAIVLMTRW 184
           W++ VFL     +AA N     ++ S GL +  AL   G   ++I++V+  V  VL T  
Sbjct: 5   WHWGVFLE----QAAQNETYLDWMIS-GLKVTIAL---GLSSWIIALVIGSVLGVLRTV- 55

Query: 185 ANKRFEATGEPFHKFWVGLALFLVIPALSALLFGAPVHWEMPELK--GFNFVGGWVLIPE 242
            NK        +      + +F  IP L  L      ++ MPEL   G +F        +
Sbjct: 56  PNKWLSGLAATY------VEIFRNIPLLVQLFIW---YFVMPELLPGGESFKQMNPFAQQ 106

Query: 243 LLALTLALTVYTAAFIAEIVRSGIKSVSHGQTEAARSLGLRNGPTLRKVIIPQALRVIIP 302
            LA  L L  +TAA + E VRSGI S+  GQ  A  ++G     T R V++P + RVI+P
Sbjct: 107 FLAAMLCLGTFTAARVCEQVRSGINSLPPGQRNAGLAMGFTLAQTYRYVLLPMSFRVIVP 166

Query: 303 PLTSQYLNLAKNSSLAAGIGYPEMVSLFAGTVLNQTGQAIEVIAITMSVYLAISISISLL 362
           PLTS++LN+ KNS++A+ IG  E+ +     +++ T +  E       +Y  I+I + LL
Sbjct: 167 PLTSEFLNIFKNSAVASTIGLLELAAQ-GRQLVDYTARPYESFIAVTIMYALINIVVMLL 225

Query: 363 MNWYNKR 369
           M W   R
Sbjct: 226 MRWVEGR 232



 Score = 58.9 bits (141), Expect = 1e-13
 Identities = 29/76 (38%), Positives = 45/76 (59%)

Query: 60  DSYARVFLIGLLNTLLVTFIGVILATILGFIIGVARLSQNWIISKLATVYVEVFRNIPPL 119
           ++Y    + GL  T+ +     I+A ++G ++GV R   N  +S LA  YVE+FRNIP L
Sbjct: 18  ETYLDWMISGLKVTIALGLSSWIIALVIGSVLGVLRTVPNKWLSGLAATYVEIFRNIPLL 77

Query: 120 LQILFWYFAVFLSMPG 135
           +Q+  WYF +   +PG
Sbjct: 78  VQLFIWYFVMPELLPG 93


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: 239
Number of extensions: 15
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 2
Length of query: 375
Length of database: 242
Length adjustment: 27
Effective length of query: 348
Effective length of database: 215
Effective search space:    74820
Effective search space used:    74820
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