GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Psest_0085 in Pseudomonas fluorescens FW300-N2E2

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate Pf6N2E2_321 TRAP transporter solute receptor, unknown substrate 1

Query= reanno::psRCH2:GFF85
         (317 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_321
          Length = 316

 Score =  454 bits (1167), Expect = e-132
 Identities = 242/317 (76%), Positives = 267/317 (84%), Gaps = 2/317 (0%)

Query: 1   MRLTKRLGLLAAAAAFTASTAAVAAPTFINILTGGTSGVYYPIGVALSQQYNK-IDGAKT 59
           MR+ K   LLAAAAA   ST A AAP +INILTGGTSGVYYPIGV LSQ Y+  I  AKT
Sbjct: 1   MRVNKHFTLLAAAAALVVSTTAQAAPVYINILTGGTSGVYYPIGVGLSQIYSSGIQDAKT 60

Query: 60  SVQATKASVENLNLLQAGRGELAFSLGDSVEDAWNGVEDAGFKAPLKRLRAIAGTYNNYI 119
           SVQATKASVENLNLLQAGRGELA +LGDSV DA NGVEDAGFKAPL +LRAIAG Y NYI
Sbjct: 61  SVQATKASVENLNLLQAGRGELALALGDSVADAKNGVEDAGFKAPLTKLRAIAGAYPNYI 120

Query: 120 QIVASAESGIKTLDDLKGKRISVGAPKSGTELNARAIFKAAGLDYKDMGRVEFLPYAESV 179
           QIVAS ESGIKTL DLKGK +SVGA KSGTELNARAIFKAAGL Y+DM +V++LP+AESV
Sbjct: 121 QIVASQESGIKTLADLKGKTVSVGAAKSGTELNARAIFKAAGLTYQDM-KVQYLPFAESV 179

Query: 180 ELIKNRQLDATLQSSGLGMAAIRDLASTMPVTFVEIPAEVVEKIESDAYLAGVIPAGTYD 239
           +LIKNRQLDATLQSSGLGMAAIRDLASTM +++V +P +VVEKI + AY + +IPA TYD
Sbjct: 180 DLIKNRQLDATLQSSGLGMAAIRDLASTMALSYVAVPTDVVEKIGNPAYQSAMIPANTYD 239

Query: 240 GQDADVPTVAITNILVTHEKVSDEVAYQMTKLMFDNLAALGNAHSAAKDIKLENATKNLP 299
           GQ   VPTVAITNILVT E V DEVAYQMTKL+F+NL  LG +HSAAKDI L+NA KNLP
Sbjct: 240 GQAEAVPTVAITNILVTREDVPDEVAYQMTKLLFENLTRLGTSHSAAKDITLKNAAKNLP 299

Query: 300 IPLHPGAERFYKEAGVL 316
           I LHPGAER+YKE G L
Sbjct: 300 IALHPGAERYYKEVGAL 316


Lambda     K      H
   0.314    0.131    0.359 

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: 347
Number of extensions: 6
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: 317
Length of database: 316
Length adjustment: 27
Effective length of query: 290
Effective length of database: 289
Effective search space:    83810
Effective search space used:    83810
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: 42 (22.0 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