GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astC in Hippea alviniae EP5-r

Align Succinylornithine transaminase; SOAT; Succinylornithine aminotransferase; EC 2.6.1.81 (characterized)
to candidate WP_022669880.1 G415_RS0101830 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::Q8ZPV2
         (408 letters)



>NCBI__GCF_000420385.1:WP_022669880.1
          Length = 433

 Score =  130 bits (327), Expect = 7e-35
 Identities = 99/321 (30%), Positives = 154/321 (47%), Gaps = 23/321 (7%)

Query: 22  PFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPALREALNEQANRFWHIGNGYTNE 81
           P    + +GS+++D+ G E+ID+        LGHA   + + + E   + +  G     E
Sbjct: 34  PLFIAKAKGSKIYDEDGNEFIDYVNSWGPAILGHADDEVIDKIEEVLEKGFSFGAPTILE 93

Query: 82  PALRLAKKLIDATFA-ERVFFCNSGAEANEAALKLARKYAHDRVGNHKSGIVAFKNAFHG 140
               +AK++++A  + E V F +SG EA  +A++LAR          +  I+ F   +HG
Sbjct: 94  T--EIAKRIVNAFDSIELVRFVSSGTEAAMSAIRLARGVTG------RDNILKFTGCYHG 145

Query: 141 RT--LFTVSAGGQPTYSQDFAP-LPPDI-RH---AAYNDLNSASALID---DNTCAVIVE 190
            +  L   +  G  T+    +  +P D  +H   A +NDL++   +     ++  AVIVE
Sbjct: 146 HSDSLLVGAGSGSSTFGVPSSKGVPIDFAKHTLLAEFNDLDAVEDIFKKYGNSIAAVIVE 205

Query: 191 PVQGEGGVIPATKAFLQGLRELCDRHQALLIFDEVQTGVGRTGELYAYMHYGVTPDILTT 250
           PV G  GVI   + FL+GLR +CD + A+LIFDEV TG   T     ++ Y V PDI   
Sbjct: 206 PVAGNMGVIRPVEGFLEGLRRVCDDYGAILIFDEVMTGFRLTYGGAQHI-YNVKPDITIL 264

Query: 251 AKALGGGFP---IGAMLTTQDYASVMTPGTHGTTYGGNPLATAVAGKVLDIINTPEMQNG 307
            K +GGGFP    GA     +Y +         T  GNP+A A     LDI+        
Sbjct: 265 GKVVGGGFPAACFGARKEIMEYLAPEGEVYQAGTLSGNPIAMAAGIATLDILKRKNPYEE 324

Query: 308 VRQRHDAFIERLNTLNVRFGM 328
           + +     I R+  L V +G+
Sbjct: 325 LNKNTQKIISRIIGLGVEYGI 345


Lambda     K      H
   0.320    0.137    0.413 

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: 431
Number of extensions: 23
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: 408
Length of database: 433
Length adjustment: 32
Effective length of query: 376
Effective length of database: 401
Effective search space:   150776
Effective search space used:   150776
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