GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Pseudomonas putida KT2440

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate PP_0501 PP_0501 NAD-dependent epimerase/dehydratase family protein

Query= BRENDA::F2NQX6
         (314 letters)



>FitnessBrowser__Putida:PP_0501
          Length = 310

 Score =  200 bits (508), Expect = 4e-56
 Identities = 119/308 (38%), Positives = 174/308 (56%), Gaps = 15/308 (4%)

Query: 3   VLVTGGAGFIGSHLVHALHQKGIPVAVLDDLSTGKRAHIPPDVP---LYQTDIRDLNAVL 59
           +L+TGGAGFIGSHL  AL  KG  V +LDD STG+R+++  D P   L + D+ D   V 
Sbjct: 6   ILITGGAGFIGSHLCDALLDKGYAVRILDDFSTGRRSNLQVDHPRLELIEGDVADAGLVT 65

Query: 60  HAFQDFQPTHVAHQAAQASVKHSVQNPCKDAEINLLGGLNILEAMRATGTQKIVFASTGG 119
            A    +   V H AA ASV+ SV++P +  + N +G LN+ EAMR  G ++++FAS+  
Sbjct: 66  QAAAGCRA--VVHLAAVASVQASVEDPVRTHQSNFIGTLNVCEAMRVHGVRRVLFASSA- 122

Query: 120 AIYGEVPEGRRAPETWPPKPKSPYAASKAAFEHYLEVYRQTHGLTYTTLRYANVYGPRQD 179
           A+YG   EG    E  P  P +PYA  K A E YL+ YR+ HGL     R+ N++GPRQD
Sbjct: 123 AVYGNNGEGESISEDTPKAPLTPYAVDKLASEQYLDFYRRQHGLEPVVFRFFNIFGPRQD 182

Query: 180 PHGE-AGVVAIFTNRLLHAQPVTLYARKEPGDPGCIRDYIHVEDVTRANLLALETNL--E 236
           P    +GV++IF  R +   P+T++     GD    RD+++V D+ +  + ALE     E
Sbjct: 183 PSSPYSGVISIFCERAVQGLPITVF-----GDGEQTRDFLYVGDLVQVMVQALEQPQVEE 237

Query: 237 GTYNVSTGQGRTTEDVLYTIARALGTTPRVTYAPPRDGDLEVSVLDPTQLQAHGWRPQV- 295
           G  N+   Q  +   +L  + + +G+ P ++YA  R GD+  S  D  +L A     QV 
Sbjct: 238 GAVNIGLNQATSLNQLLAALEKVVGSLPAISYAAARSGDIRHSRADNQRLLARFEFAQVT 297

Query: 296 PFEEGIRR 303
           P  EG+ +
Sbjct: 298 PMVEGLTK 305


Lambda     K      H
   0.318    0.135    0.411 

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: 241
Number of extensions: 15
Number of successful extensions: 6
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: 314
Length of database: 310
Length adjustment: 27
Effective length of query: 287
Effective length of database: 283
Effective search space:    81221
Effective search space used:    81221
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 (21.7 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