GapMind for catabolism of small carbon sources

 

Aligments for a candidate for aatJ in Dechlorosoma suillum PS

Align ABC transporter for L-asparagine and L-glutamate, periplasmic substrate-binding component (characterized)
to candidate Dsui_0635 Dsui_0635 periplasmic component of amino acid ABC-type transporter/signal transduction system

Query= reanno::pseudo1_N1B4:Pf1N1B4_771
         (304 letters)



>FitnessBrowser__PS:Dsui_0635
          Length = 299

 Score =  370 bits (949), Expect = e-107
 Identities = 188/289 (65%), Positives = 224/289 (77%), Gaps = 2/289 (0%)

Query: 10  AAIAAALISTPVFAAELTGTLKKIKESGTITLGHRDASIPFSYIADASGKPVGYSHDIQL 69
           A I +AL + PV A E + TLKKIK++G+ITLGHR++SIPFSY  D   + +GYSH++ L
Sbjct: 11  AVIGSALCAAPVLAQE-SPTLKKIKDTGSITLGHRESSIPFSYYDDKQ-QVIGYSHEMML 68

Query: 70  KIVEAIKKDLDMPNLQVKYNLVTSQTRIPLVQNGTVDVECGSTTNNVERQQQVDFSVGIF 129
           K V+AIK +L +  L VK   VTS  RI L+QNGTVD+ECGSTTNN+ERQ+QV FS  IF
Sbjct: 69  KAVDAIKAELKLAKLDVKLMPVTSANRITLLQNGTVDMECGSTTNNLERQKQVGFSTSIF 128

Query: 130 EIGTKLLSKKDSAYKDFADLKGKNVVTTAGTTSERILKSMNADKQMGMNVISAKDHGESF 189
            IGT+L++KKD+  KDF DL GKNVVTTAGTTSER+++ MN +KQM MN+ISAKDHGESF
Sbjct: 129 VIGTRLMAKKDAGVKDFPDLAGKNVVTTAGTTSERLIRKMNEEKQMKMNIISAKDHGESF 188

Query: 190 QMLETGRAVAFMMDDALLAGEMAKAKKPTDWAVTGTAQSNEIYGCMVRKGDAPFKKAVDD 249
             LE+GRAVAFMMDDALL GEMAKAK+P DW V GTAQS E YGCM+RK DA FKK VD 
Sbjct: 189 LTLESGRAVAFMMDDALLYGEMAKAKRPGDWVVVGTAQSKEAYGCMLRKDDAGFKKVVDA 248

Query: 250 AIIATYKSGEINKIYEKWFMQPIPPKGLNLMFPMSEELKALIANPTDKA 298
           A+     SGE  KIY KWFM PIPPKGLNL  P+S+++KAL   P DKA
Sbjct: 249 ALTKAMTSGEAEKIYNKWFMNPIPPKGLNLNMPLSDDMKALYKAPNDKA 297


Lambda     K      H
   0.315    0.131    0.365 

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: 317
Number of extensions: 6
Number of successful extensions: 2
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: 304
Length of database: 299
Length adjustment: 27
Effective length of query: 277
Effective length of database: 272
Effective search space:    75344
Effective search space used:    75344
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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 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