GapMind for catabolism of small carbon sources

 

Aligments for a candidate for ans in Pseudomonas simiae WCS417

Align L-asparaginase (EC 3.5.1.1) (characterized)
to candidate GFF5498 PS417_28140 asparaginase

Query= reanno::pseudo3_N2E3:AO353_09960
         (334 letters)



>FitnessBrowser__WCS417:GFF5498
          Length = 325

 Score =  524 bits (1350), Expect = e-153
 Identities = 265/326 (81%), Positives = 288/326 (88%), Gaps = 4/326 (1%)

Query: 8   AAQHVMVLYTGGTIGMQASANGLAPASGFEARMRDYLHSQPDLVVPNWRFREMTPLIDSA 67
           ++ +VMVLYTGGTIGMQAS +GLAPASGFEARMR+ L   P    P WRF+EM PLIDSA
Sbjct: 3   SSSNVMVLYTGGTIGMQASTHGLAPASGFEARMREQLAHLP---APAWRFQEMAPLIDSA 59

Query: 68  NMTPAYWQRLRDAVIEAVDVDGCDSVLILHGTDTLAYSAAAMSFQLLGLHARVLFTGSML 127
           NMTPAYWQRLR AV+EAVD DGCD+VLILHGTDTLAYSAAAMSFQLLGL A V+FTGSML
Sbjct: 60  NMTPAYWQRLRTAVVEAVD-DGCDAVLILHGTDTLAYSAAAMSFQLLGLPAPVVFTGSML 118

Query: 128 PAGVPDSDAWENLGGALVALGQGLAPGVQLYFHGELLDPTRCAKIRSFGRHPFARLQRQG 187
           PAGVPDSDAWEN+ GAL ALG+G+APGV LYFHG L+ PTRCAKIRSFGR+PFA L RQG
Sbjct: 119 PAGVPDSDAWENVSGALAALGKGIAPGVHLYFHGALMAPTRCAKIRSFGRNPFAALNRQG 178

Query: 188 GGVKAPALPTALEYRQSKQLAKVGVLPLFPGIGAEQLDGVLNSGIQGLVLECFGSGTGPS 247
           G  +A ++P AL+YRQ K LA VGVLPL PGIGA QLD V+ SGIQ L+LECFGSGTGPS
Sbjct: 179 GAARAESIPQALDYRQPKALASVGVLPLVPGIGAAQLDAVIGSGIQALILECFGSGTGPS 238

Query: 248 DNPEFLASLARARDQGVVVVAITQCHEGGVELDVYEAGSRLRGVGVLSGGGMTREAAFGK 307
           DNPEFLASL RA+DQGVVVVAITQCHEGGVELDVYEAGSRLRGVGVLSGGGMTREAAFGK
Sbjct: 239 DNPEFLASLQRAQDQGVVVVAITQCHEGGVELDVYEAGSRLRGVGVLSGGGMTREAAFGK 298

Query: 308 LHALLGADLDTAEVRRLVELDLCGEL 333
           L+AL+GA LDT EVRRLVELDLCGEL
Sbjct: 299 LNALIGAGLDTQEVRRLVELDLCGEL 324


Lambda     K      H
   0.320    0.138    0.415 

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: 453
Number of extensions: 14
Number of successful extensions: 3
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: 334
Length of database: 325
Length adjustment: 28
Effective length of query: 306
Effective length of database: 297
Effective search space:    90882
Effective search space used:    90882
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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