GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Desulfacinum infernum DSM 9756

Align UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_073040696.1 BUB04_RS20145 hybrid nucleoside-diphosphate sugar epimerase/sugar transferase

Query= curated2:Q56623
         (328 letters)



>NCBI__GCF_900129305.1:WP_073040696.1
          Length = 525

 Score =  244 bits (623), Expect = 3e-69
 Identities = 134/312 (42%), Positives = 194/312 (62%), Gaps = 3/312 (0%)

Query: 12  ILLTGSTGFVGTNLVKSLTLKSDYIVKSAVRHAVN--KDDGLLFEVGDINASTDFELPLK 69
           IL+TG++GF+G+ LV+ L  +    V +  R   +   +D +  + GD        LP  
Sbjct: 3   ILVTGASGFIGSALVRRLAGREGLQVIAMGRSTPHGLPEDVVPLQTGDFLHLRSNPLPPW 62

Query: 70  NTTVVVHCAARAHVMDDKEAEPLTLYREVNTAGTVNLAKQAIDSGVKRFIFISSIKVNGE 129
              V +H AAR              +   NT  TV LA+ A ++GV+RFIFISS KV+GE
Sbjct: 63  KPDVCIHLAARVDAPPRGRENNEGSFHLTNTVATVRLARWAAEAGVRRFIFISSAKVHGE 122

Query: 130 GTLVGCPFKTEDNHAPEDDYGLSKSEAEKQLVALAKDSSMEVVIIRPTIVYGPGVKANFA 189
            +  G PF+ +D  APED Y  SK +AE+ L  +++++ ME+V+IRP +VYGPGVK NFA
Sbjct: 123 TSRPGRPFREDDPAAPEDAYARSKWDAERALEEISRETGMELVVIRPPLVYGPGVKGNFA 182

Query: 190 SLMRLVSKGIPLPFGSITQNKRSLVSINNLVDLIVTCIDHPKAANQVFLVSDGHDVSTAE 249
            LM  + +GIPLP G++  N+RSL +++NLVDLI TC++HP AA   FLVSDG D+STAE
Sbjct: 183 RLMGWMRRGIPLPLGAVRDNRRSLAALDNLVDLIETCVEHPAAAGHAFLVSDGEDLSTAE 242

Query: 250 MVRELAIALDKPTWQ-LPVPIWCYKLFGKLFGKSDIVDRLTGTLQVDISHTKETLGWKPP 308
           ++R LA+A+ + + + LPVP    +   +L G+ D+V RL G+ Q+DI   +  LGW PP
Sbjct: 243 LLRRLALAMGRRSPRLLPVPAPLLETTAQLLGRQDMVRRLLGSFQLDIFKARRLLGWVPP 302

Query: 309 QTLQEGFKQTAQ 320
             + E  ++TAQ
Sbjct: 303 VGVDEALRRTAQ 314


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: 336
Number of extensions: 10
Number of successful extensions: 3
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: 525
Length adjustment: 31
Effective length of query: 297
Effective length of database: 494
Effective search space:   146718
Effective search space used:   146718
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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