GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garD in Halomonas desiderata SP1

Align L-talarate dehydratase (EC 4.2.1.156); galactarate dehydratase (EC 4.2.1.42) (characterized)
to candidate WP_086510675.1 BZY95_RS14785 mandelate racemase/muconate lactonizing enzyme family protein

Query= BRENDA::Q8ZL58
         (398 letters)



>NCBI__GCF_002151265.1:WP_086510675.1
          Length = 378

 Score =  153 bits (386), Expect = 9e-42
 Identities = 103/306 (33%), Positives = 155/306 (50%), Gaps = 23/306 (7%)

Query: 100 LLGEDPNDIDKIYTKLLWAGASVGRSGMAVQAISPIDIALWDMKAKRAGLPLAKLLGAH- 158
           L+G+DP   ++++ +L       G+ G+ V A+S IDIALWD+K KR G+P++ LLG   
Sbjct: 66  LIGQDPLQTERLWLELYNRLRDQGQRGLTVTALSGIDIALWDIKGKRFGVPISTLLGGRF 125

Query: 159 RDSVQCYNTSGGFLHTPLDQVLKN---VVISRENGIGGIKLKVGQPNCAEDIRRLTAVRE 215
           RDSV+ Y T G F    +D+V  N   V   R  G   +K+K+G     ED+R + AVRE
Sbjct: 126 RDSVRAYAT-GSFRRAGVDRVEDNAREVAGYRREGFHAVKIKIGF-GVDEDLRVIEAVRE 183

Query: 216 ALGDEFPLMVDANQQWDRETAIRMGRKMEQFNLIWIEEPLDAYDIEGHAQLAAALDTPIA 275
           ++G +  LM+DAN  +D   A+ +GR+  +F + W EEP+    +  +  + A    P+A
Sbjct: 184 SIGPDMRLMIDANHGYDYLEAVEVGRRAAKFGIDWFEEPVLPEHVSAYRAVRADQPIPVA 243

Query: 276 TGEMLTSFREHEQLILGNASDFVQPDAPRVGGISPFLKIMDLAAKHGRKLAPH-----FA 330
            GE         + +   A D +QPD   VGG +   ++ D+AA HG +L PH       
Sbjct: 244 GGETWHGRYAMHEPLATRAVDIIQPDICGVGGFTEIRRVADMAALHGVRLVPHVWGTAVC 303

Query: 331 MEVHLHLSAAY--------PLEPWLEHFEWLNP----LFNEQLELRDGRMWISDRHGLGF 378
           +   L   AA         P+EP LE     NP    +    +E   G + I D  GLG 
Sbjct: 304 LAASLQFMAALLPNPPRRDPIEPILEFDRTENPFRQAVVTTPIEHDRGVVAIPDGPGLGI 363

Query: 379 TLSEQA 384
            +  +A
Sbjct: 364 EIDREA 369


Lambda     K      H
   0.319    0.136    0.410 

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: 393
Number of extensions: 24
Number of successful extensions: 2
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: 398
Length of database: 378
Length adjustment: 30
Effective length of query: 368
Effective length of database: 348
Effective search space:   128064
Effective search space used:   128064
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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