GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Burkholderia phytofirmans PsJN

Align UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate BPHYT_RS04375 BPHYT_RS04375 epimerase

Query= curated2:Q56623
         (328 letters)



>FitnessBrowser__BFirm:BPHYT_RS04375
          Length = 318

 Score =  209 bits (532), Expect = 7e-59
 Identities = 126/314 (40%), Positives = 181/314 (57%), Gaps = 12/314 (3%)

Query: 12  ILLTGSTGFVGTNLVKSLTLKSDYIVKSAVRHAVNKDDGLLFEVGDINASTDFE------ 65
           +L+TG+ GFVG  L ++L   +   V   VR  + ++ G+   V   + S DF       
Sbjct: 4   VLVTGANGFVGRALCRALR-DAGNTVTGLVRRQMPREYGVDEWV---DPSVDFAGMDAGW 59

Query: 66  LPLKNTTVVVHCAARAHVMDDKEAEPLTLYREVNTAGTVNLAKQAIDSGVKRFIFISSIK 125
                   VVH AAR HVM +  A+P   ++  N  GT+  A+ A   GV+RF+F+SSIK
Sbjct: 60  PEALQVDCVVHLAARVHVMLEDAADPEAAFQATNVEGTLRCARAAWRHGVRRFVFVSSIK 119

Query: 126 VNGEGTLVGCPFKTEDNHAPEDDYGLSKSEAEKQLVALAKDSSMEVVIIRPTIVYGPGVK 185
              E    G P + +D+ AP+D YG SK  AE+ L+ L   + +E+VI+RP +VYGP V+
Sbjct: 120 AMTEADS-GRPVREDDSPAPQDPYGRSKRAAEEALIRLGAQTGLEIVIVRPPLVYGPDVR 178

Query: 186 ANFASLMRLVSKGIPLPFGSITQNKRSLVSINNLVDLIVTCIDHPKAANQVFLVSDGHDV 245
           ANF SLM  V KG+PLP G++   +RSLV ++NL D +V C    +AA Q F V+D   +
Sbjct: 179 ANFLSLMNAVWKGVPLPLGALGA-RRSLVYVDNLADALVHCATDARAAQQCFHVADSDAL 237

Query: 246 STAEMVRELAIALDKPTWQLPVPIWCYKLFGKLFGKSDIVDRLTGTLQVDISHTKETLGW 305
           + AE+ R L   L +P   LPVP    +L G+L G++  VDRL G+LQ+D S  +  LGW
Sbjct: 238 TIAELARALGRHLGRPARLLPVPESWLRLAGRLTGRTAQVDRLVGSLQLDTSRIRTVLGW 297

Query: 306 KPPQTLQEGFKQTA 319
           + P + +EG   TA
Sbjct: 298 QAPYSTEEGLAATA 311


Lambda     K      H
   0.318    0.134    0.388 

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: 228
Number of extensions: 8
Number of successful extensions: 4
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: 328
Length of database: 318
Length adjustment: 28
Effective length of query: 300
Effective length of database: 290
Effective search space:    87000
Effective search space used:    87000
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