GapMind for catabolism of small carbon sources

 

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

Align ABC transporter for L-Histidine, periplasmic substrate-binding component (characterized)
to candidate PfGW456L13_3631 Histidine ABC transporter, histidine-binding protein (TC 3.A.1)

Query= reanno::pseudo5_N2C3_1:AO356_09620
         (322 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3631
          Length = 316

 Score =  502 bits (1293), Expect = e-147
 Identities = 232/316 (73%), Positives = 273/316 (86%)

Query: 7   LLTTLLSMGLLASAGATQAAGWCESGKPVKFAGLNWESGMLLTDVLQVVLEKGYDCKTDS 66
           LLT+LL++GLL  + ++QA+GWCESGK VKFAGLNWESGMLLTD++ +VL+ GY C TD 
Sbjct: 1   LLTSLLTLGLLVGSASSQASGWCESGKSVKFAGLNWESGMLLTDIMMIVLKDGYGCTTDQ 60

Query: 67  LPGNSITMENALSSNDIQVFAEEWVGRSEVWNKAEKAGKVVGVGAPVVGAIEGWYVPRYV 126
           L GN+I +E AL+ NDIQVF EEW+ RSEVW KA  AGKVVGVGAP++GA +GWYVPRYV
Sbjct: 61  LVGNTIILETALAGNDIQVFGEEWMERSEVWKKAVAAGKVVGVGAPIIGATQGWYVPRYV 120

Query: 127 VEGDAKRKLEAKAPGLKNIADLGQYAAVFKDPEEPSKGRFYNCPAGWTCELDNSEMLKSY 186
           VEGDAKR   A+AP L+ +ADL +YA+VF+D EEPSKGRFYNCPAGW CE DN+EMLK Y
Sbjct: 121 VEGDAKRNRPAQAPDLRTVADLSKYASVFRDSEEPSKGRFYNCPAGWICEQDNTEMLKEY 180

Query: 187 GLEKTYTNFRPGTGPALDAAVLSSYKRGEPILFYYWSPTPLMGQVDLVKLEEKPGVDKSV 246
           GLE T+TNFRPGTG ALDAAVLSSYKRGEP+LFYYWSPTPLMGQ+D ++LEEK G +K V
Sbjct: 181 GLENTFTNFRPGTGAALDAAVLSSYKRGEPVLFYYWSPTPLMGQIDAIRLEEKTGANKDV 240

Query: 247 SIKVGLSKTFHDEAPELVAVLEKVNLPIDILNQNLGRMAKERIESPKLAKIFLKEHPEVW 306
              VGLSK FH++APELVAVLEKVN+PID+LNQNL RM +ERIESPKLA++FLKEHPE+W
Sbjct: 241 ITMVGLSKAFHEQAPELVAVLEKVNIPIDLLNQNLARMTRERIESPKLARMFLKEHPEIW 300

Query: 307 HAWVSEDAAKKIDAAL 322
           HAWV E AAKKI+A+L
Sbjct: 301 HAWVDEAAAKKIEASL 316


Lambda     K      H
   0.314    0.133    0.398 

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: 373
Number of extensions: 10
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: 322
Length of database: 316
Length adjustment: 28
Effective length of query: 294
Effective length of database: 288
Effective search space:    84672
Effective search space used:    84672
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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