GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astC in Pandoraea thiooxydans ATSB16

Align Succinylornithine transaminase; SOAT; EC 2.6.1.81; Succinylornithine aminotransferase (uncharacterized)
to candidate WP_047216038.1 PATSB16_RS01020 acetylornithine transaminase

Query= curated2:Q3Z295
         (406 letters)



>NCBI__GCF_001931675.1:WP_047216038.1
          Length = 399

 Score =  297 bits (761), Expect = 3e-85
 Identities = 168/362 (46%), Positives = 221/362 (61%), Gaps = 5/362 (1%)

Query: 28  GEGSRLWDQQGKEYIDFAGGIAVNALGHAHPELREALNEQASKFWHTGNGYTNEPVLRLA 87
           G+GS ++D  GK Y+DF  G AVN LGH +  +  AL EQA K  +    Y NEP+ RLA
Sbjct: 25  GKGSWIFDHTGKRYLDFIQGWAVNCLGHCNEGMIRALTEQAGKLINPSPAYYNEPMARLA 84

Query: 88  KKLIDATFADRVFFCNSGAEANEAALKLARKFAH---DRYGSHKSGIVAFKNAFHGRTLF 144
             L   +  D+VFF NSGAEANE A+KLARK+     +  G  +  I+ F ++FHGRTL 
Sbjct: 85  GLLTKNSCFDKVFFTNSGAEANEGAIKLARKWGQKHPNAAGGARFEIITFDHSFHGRTLA 144

Query: 145 TVSAGGQPAYSQDFAPLPPDIRHAAYNDINSASALIDDATCAVIVEPIQGEGGVVPASNA 204
           T+SA G+P + + FAP  P    A  NDI S   LI   T AV++EP+QGEGGV+PA+  
Sbjct: 145 TMSASGKPGWDKIFAPQVPGFPKAELNDIASVEKLIGPDTVAVMLEPVQGEGGVIPATRE 204

Query: 205 FLQGLRELCDRHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLTTAKALGGGFPVGALL 264
           F+  LREL  RHN LLI DEVQTG GRTG+L+AY   G+TPD++T  K +GGG P+ ALL
Sbjct: 205 FMLQLRELTHRHNLLLIVDEVQTGCGRTGKLFAYELSGITPDIMTLGKGIGGGVPLAALL 264

Query: 265 TTEECASVMTVGTHGTTYGGNPLASAVAGKVLELINTPEMLNGVKQRHDWFVERLNTINH 324
           +T   A V   G  G TY GNPL +AV   V+E +  P  L  V Q  ++  E+L  +  
Sbjct: 265 STAAVA-VFEAGDQGGTYNGNPLMTAVGISVIEQLTAPGFLENVTQLGNYLREQLLALCD 323

Query: 325 RYGLFSEVRGLGLLIGCVLNADYAGQAKQISQEAAKAGVMVLIAGGNVVRFAPALNVSEE 384
            YG F   RG GLL   +L  D   Q  + ++  +  G++V  A  N++RF PALNV+ E
Sbjct: 324 TYG-FEGERGEGLLRALLLGKDIGPQIVEKARNLSPDGLLVNAARPNLLRFMPALNVTRE 382

Query: 385 EV 386
           E+
Sbjct: 383 EI 384


Lambda     K      H
   0.319    0.136    0.408 

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: 453
Number of extensions: 19
Number of successful extensions: 4
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: 399
Length adjustment: 31
Effective length of query: 375
Effective length of database: 368
Effective search space:   138000
Effective search space used:   138000
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 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