GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Psest_0085 in Pseudomonas putida KT2440

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate PP_3954 PP_3954 periplasmic binding subunit of unknown solute

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



>FitnessBrowser__Putida:PP_3954
          Length = 316

 Score =  448 bits (1152), Expect = e-131
 Identities = 232/311 (74%), Positives = 261/311 (83%), Gaps = 1/311 (0%)

Query: 7   LGLLAAAAAFTASTAAVAAPTFINILTGGTSGVYYPIGVALSQQYNK-IDGAKTSVQATK 65
           L L  A+  F  S AA AAPTFINILTGGTSGVYYP+GV +SQ Y+  I+G+KT+VQATK
Sbjct: 5   LRLALASTLFAVSAAAQAAPTFINILTGGTSGVYYPVGVGISQIYSHGIEGSKTTVQATK 64

Query: 66  ASVENLNLLQAGRGELAFSLGDSVEDAWNGVEDAGFKAPLKRLRAIAGTYNNYIQIVASA 125
           ASVENLNLLQAGRGELAF+LGDSV DAW G  +AGFK PLK+LRAIAGTY NYIQIVAS 
Sbjct: 65  ASVENLNLLQAGRGELAFALGDSVADAWKGDAEAGFKTPLKKLRAIAGTYPNYIQIVASK 124

Query: 126 ESGIKTLDDLKGKRISVGAPKSGTELNARAIFKAAGLDYKDMGRVEFLPYAESVELIKNR 185
           ESGI +L DLKGKRISVGAPKSGTELNARAIFKAAGL Y+DMG+VE+LPYAESVELIKNR
Sbjct: 125 ESGITSLSDLKGKRISVGAPKSGTELNARAIFKAAGLTYQDMGKVEYLPYAESVELIKNR 184

Query: 186 QLDATLQSSGLGMAAIRDLASTMPVTFVEIPAEVVEKIESDAYLAGVIPAGTYDGQDADV 245
           QLDATLQSSGLG AAIRDLA+T+PV FV IPAEVV +I ++AY    IPA TYDGQ ADV
Sbjct: 185 QLDATLQSSGLGQAAIRDLAATLPVVFVPIPAEVVTRIGNNAYQPATIPANTYDGQSADV 244

Query: 246 PTVAITNILVTHEKVSDEVAYQMTKLMFDNLAALGNAHSAAKDIKLENATKNLPIPLHPG 305
            T AI NILVT   + D++AYQMTKL+F+NL  L  AH+AAKDI+ ENA KNLPIPLHPG
Sbjct: 245 STAAINNILVTRADIGDDLAYQMTKLIFENLPRLVTAHAAAKDIQAENAAKNLPIPLHPG 304

Query: 306 AERFYKEAGVL 316
           A R++KE  +L
Sbjct: 305 AARYFKEKNLL 315


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: 360
Number of extensions: 6
Number of successful extensions: 2
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