GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Thiomicrospira microaerophila ASL8-2

Align UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_044408414.1 NA59_RS04185 epimerase

Query= curated2:Q56623
         (328 letters)



>NCBI__GCF_000934765.1:WP_044408414.1
          Length = 345

 Score =  246 bits (628), Expect = 6e-70
 Identities = 147/339 (43%), Positives = 204/339 (60%), Gaps = 35/339 (10%)

Query: 12  ILLTGSTGFVGTNLVKSLTLKSDYIVKSAVRHAVNK-DDGLLFEVGDINASTDFELP--- 67
           + LTG+TGFVG+ L+ S  +     V++ VR  ++   D +   VGD+    D E     
Sbjct: 3   VFLTGATGFVGSALL-SRFVADGVSVRALVRRRLDGLPDAVEQVVGDLLGFVDVESSPSP 61

Query: 68  ----------LKNTTVVVHCAARAHVMDDKEAEPLTLYREVNTAGTVNLAKQAIDSGVKR 117
                      K   VVVH AARAH+M D+ A+PL  YR+VN   T+ LA+ A  +GV R
Sbjct: 62  QPSPIEGEGAFKGVDVVVHVAARAHIMRDEVADPLAEYRKVNRGATLALARLAAQAGVGR 121

Query: 118 FIFISSIKVNGEGT----LVGCP------------FKTEDNHAPEDDYGLSKSEAEKQLV 161
           F+F+SS+KVNGE T    L   P            F+ +D   P D YGLSK EAE+ L+
Sbjct: 122 FVFVSSVKVNGEMTFSHSLSPSPQPSPIEGEGVTKFRPDDKFVPTDPYGLSKYEAEQGLL 181

Query: 162 ALAKDSSMEVVIIRPTIVYGPGVKANFASLMRLVSKGIPLPFGSITQNKRSLVSINNLVD 221
           A+A+++ +EVVIIRP +VYGP VK NFAS++  V KG+PLP G++  N RSLV+++NLVD
Sbjct: 182 AIARETGVEVVIIRPPLVYGPNVKGNFASMVNWVKKGVPLPLGAVC-NLRSLVALDNLVD 240

Query: 222 LIVTCIDH---PKAANQVFLVSDGHDVSTAEMVRELAIALDKPTWQLPVPIWCYKLFGKL 278
            I  C D    PKAAN+VFL+SDG DVST++++R++A A    +  LPVP+   +   K 
Sbjct: 241 FIALCADRERSPKAANEVFLISDGVDVSTSDLLRKVAKACGVKSRLLPVPVGLMRFAAKA 300

Query: 279 FGKSDIVDRLTGTLQVDISHTKETLGWKPPQTLQEGFKQ 317
             K  + DRL G LQVD S  ++ LGW+P  T+ E  ++
Sbjct: 301 LSKGAVADRLFGNLQVDSSKAQDLLGWQPVVTMDEALER 339


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: 279
Number of extensions: 15
Number of successful extensions: 5
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: 345
Length adjustment: 28
Effective length of query: 300
Effective length of database: 317
Effective search space:    95100
Effective search space used:    95100
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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