GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astC in Acidovorax sp. GW101-3H11

Align succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate Ac3H11_3991 Glutamate-1-semialdehyde aminotransferase (EC 5.4.3.8)

Query= BRENDA::O30508
         (406 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3991
          Length = 434

 Score =  106 bits (264), Expect = 2e-27
 Identities = 87/301 (28%), Positives = 140/301 (46%), Gaps = 22/301 (7%)

Query: 30  RGEGSRVWDQSGRELIDFAGGIAVTSLGHAHPALVKALTEQAQRIWHVSNVFTNEPALRL 89
           R +G+  WD + +  ID+ G      LGH HPA+++A+  Q+  +   S     E  + L
Sbjct: 42  RAQGAYFWDANDQRFIDYIGSWGPMILGHGHPAVLEAV--QSAALEGFSFGAPTEREVEL 99

Query: 90  ARKLVDATFA-ERVFLANSGAEANEAAFKLARRYANDVYGPQKYEIIAASNSFHGRTLFT 148
           A +++    + E + L +SG EA  +A +LAR       G  K+         H  +L  
Sbjct: 100 AEEILGLVPSMEMIRLVSSGTEAGMSAIRLAR----GATGRSKFIKFEGCYHGHADSLLV 155

Query: 149 VNVGGQPKYSDGF--GPKFEGITH---VPYNDLEALKAAIS---DKTCAVVLEPIQGEGG 200
               G   + +    G   E + H   + YN++  L+ A +    +   V++EPI G   
Sbjct: 156 KAGSGLATFGNATSAGVPPEVVQHTIVLEYNNVAQLEEAFALHGKELACVMIEPIAGNMN 215

Query: 201 VLPAQQAYLEGARKLCDEHNALLVFDEVQSG----MGRVGELFAYMHYGVVPDILSSAKS 256
           ++ A   +++  R+LC EH ALLV DEV +G    +G    ++A    G  PD+    K 
Sbjct: 216 LVRASVPFMKRCRELCTEHGALLVLDEVMTGFRVALGSAQSVYAKSIPGFKPDLTVLGKV 275

Query: 257 LGGGFPIGAMLTTGEIAKHLSV--GTH-GTTYGGNPLASAVAEAALDVINTPEVLDGVKA 313
           +GGG P+ A      I +HL+   G +   T  GNP+A+A   A L  I  P   D + A
Sbjct: 276 IGGGMPLAAFGGPRAIMEHLAPLGGVYQAGTLSGNPVATACGLATLREIKKPGFFDALSA 335

Query: 314 K 314
           +
Sbjct: 336 R 336


Lambda     K      H
   0.318    0.135    0.394 

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: 436
Number of extensions: 19
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: 406
Length of database: 434
Length adjustment: 32
Effective length of query: 374
Effective length of database: 402
Effective search space:   150348
Effective search space used:   150348
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 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