GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galactonolactonase in Mucilaginibacter mallensis MP1X4

Align D-galactono-lactonase (EC 3.1.1.-) (characterized)
to candidate WP_091380910.1 BLU33_RS22265 lactonase family protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3314
         (389 letters)



>NCBI__GCF_900105165.1:WP_091380910.1
          Length = 382

 Score =  235 bits (599), Expect = 2e-66
 Identities = 132/365 (36%), Positives = 206/365 (56%), Gaps = 17/365 (4%)

Query: 26  YQLLVGSYTAGQSQGIYRLAFDSRTGQI----DASPLQVIKSANPSWLTLSKDQRHLFVV 81
           Y +L+G+YT G S+GIY       TG++    + + +      NPS+L +S + + ++ V
Sbjct: 28  YDVLIGTYTNGTSKGIYVYRLYEETGKLSYLNEFTNVDDTAFTNPSYLCVSDNNKFVYAV 87

Query: 82  NENGPGQTDPVGRVSSFAIDPKTHALSLISQVQSLGNEPTHSSLSIDGSHLFVSNYSVAE 141
           NEN  G       V++   +  T  +  I+   S G +P   ++  D  ++F++NYS   
Sbjct: 88  NENKKGG------VTALTFNANTGKMKFINSQLSQGADPCFVAVDKDQKNIFIANYS--- 138

Query: 142 DPGGTLAVLPVAADGKLKAVVQMSSHPASRVNPERQASAHVHSTIPSPDGRYVFANDLGA 201
              G+LAVLPV  DG ++   Q+     +    +RQ   HVH    SP+ +Y+   DLG 
Sbjct: 139 --SGSLAVLPVNKDGSIRPASQVIQDAGTGPVKDRQEGPHVHMAALSPNEKYLLYTDLGT 196

Query: 202 DKVFAYRFDPKANPELPLTPATPAFVQLPPGSGPRHLLFSADGKHAWLTMEMSAQVAVFD 261
           DK+   R+  KA+   PL+PA PAFV + PG+GPRH++FSADGK+ +L  E+   V  + 
Sbjct: 197 DKINVQRY--KASKPQPLSPAEPAFVSVAPGNGPRHMVFSADGKYVYLLQEIGGFVNAYT 254

Query: 262 YHDGQLEQTQMVDLAAGQPVSDKAAAALHASADGKFLYVSNRGTANQLLVFAIDPATGHL 321
           Y +G+L Q Q VD+   +   +  +AA+  S DG+FLY SNRG AN+++ +AI+   G L
Sbjct: 255 YDNGKLTQIQSVDMKRPEFGGNIGSAAIKISPDGRFLYASNRGNANEIVQYAINAENGQL 314

Query: 322 SELQRRAVEGDHPREFSLDPSGKFLLIANQKSNQIVVVERDARTGLLGKTVQKLPMDAPS 381
           S + R    G  PR+FS+DP GKFL+++NQ S+ I V   D ++G +G  V  L +  P 
Sbjct: 315 SFVARVPSLGKGPRDFSIDPQGKFLIVSNQNSDTIYVYRIDQKSGWIGSVVSTLKIGNPV 374

Query: 382 DLRFL 386
            L+ +
Sbjct: 375 CLKIV 379


Lambda     K      H
   0.316    0.132    0.382 

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: 472
Number of extensions: 32
Number of successful extensions: 11
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 389
Length of database: 382
Length adjustment: 30
Effective length of query: 359
Effective length of database: 352
Effective search space:   126368
Effective search space used:   126368
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 (21.6 bits)
S2: 50 (23.9 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