GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Pseudomonas fluorescens FW300-N1B4

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate Pf1N1B4_2638 UDP-glucose 4-epimerase (EC 5.1.3.2)

Query= BRENDA::F2NQX6
         (314 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2638
          Length = 309

 Score =  209 bits (531), Expect = 9e-59
 Identities = 126/306 (41%), Positives = 178/306 (58%), Gaps = 11/306 (3%)

Query: 3   VLVTGGAGFIGSHLVHALHQKGIPVAVLDDLSTGKRAHIPPDVPLYQTDIRDL-NAVLHA 61
           VL+TGGAGFIGSHL  AL  KG  V +LDDLSTGKR+++P D PL +  + D+ +A L A
Sbjct: 6   VLITGGAGFIGSHLTDALLAKGHSVRILDDLSTGKRSNLPLDNPLVELIVGDVADAALVA 65

Query: 62  FQDFQPTHVAHQAAQASVKHSVQNPCKDAEINLLGGLNILEAMRATGTQKIVFASTGGAI 121
                 + VAH AA ASV+ SV +P K  + N +G LN+ EAMR TG ++++FAS+  A+
Sbjct: 66  QAMVGCSAVAHLAAVASVQASVDDPVKTHQSNFIGSLNVCEAMRQTGVKRVLFASSA-AV 124

Query: 122 YGEVPEGRRAPETWPPKPKSPYAASKAAFEHYLEVYRQTHGLTYTTLRYANVYGPRQDPH 181
           YG   EG    E  P  P +PYAA K A EHY + YR+ H L     R+ N++GPRQDP 
Sbjct: 125 YGNNGEGESIDEDTPKAPLTPYAADKLASEHYFDFYRRQHSLEPVIFRFFNIFGPRQDPS 184

Query: 182 GE-AGVVAIFTNRLLHAQPVTLYARKEPGDPGCIRDYIHVEDVTRANLLALE-TNLE-GT 238
              +GV++IF+ R     P+T++     GD    RD+++VED+    + A+E   +E G 
Sbjct: 185 SPYSGVISIFSERAQKGLPITVF-----GDGEQTRDFVYVEDLVGVLVQAIEKPQVEVGA 239

Query: 239 YNVSTGQGRTTEDVLYTIARALGTTPRVTYAPPRDGDLEVSVLDPTQ-LQAHGWRPQVPF 297
            NV   Q  T + +L  +   +G  P V+Y P R GD+  S  +  + L+   +  Q P 
Sbjct: 240 VNVGWNQATTLKQMLEALEAVVGELPPVSYGPARSGDIRHSRANNRRLLERFTYPQQTPM 299

Query: 298 EEGIRR 303
             G+ R
Sbjct: 300 SVGLAR 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: 250
Number of extensions: 16
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: 309
Length adjustment: 27
Effective length of query: 287
Effective length of database: 282
Effective search space:    80934
Effective search space used:    80934
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.

Links

Downloads

Related tools

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