GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astC in Marinomonas arctica 328

Align Succinylornithine transaminase; SOAT; EC 2.6.1.81; Succinylornithine aminotransferase (uncharacterized)
to candidate WP_111605742.1 DK187_RS02410 4-aminobutyrate--2-oxoglutarate transaminase

Query= curated2:Q3Z295
         (406 letters)



>NCBI__GCF_003259225.1:WP_111605742.1
          Length = 425

 Score =  220 bits (560), Expect = 7e-62
 Identities = 146/402 (36%), Positives = 207/402 (51%), Gaps = 35/402 (8%)

Query: 21  APFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPELREALNEQASKFWHTGNGYTN 80
           AP    R   + +WD +GK YIDF  GIAV   GH HP+++ A   Q  +F HT    + 
Sbjct: 22  APVYVDRALNAEIWDVEGKRYIDFGAGIAVVNTGHNHPKVKAATIAQIERFTHTCVMVSP 81

Query: 81  -EPVLRLAKKLIDATFAD---RVFFCNSGAEANEAALKLARKFAHDRYGSHKSGIVAFKN 136
            E  + LA+KL  A   +   +  F  +GAEA E  +K+AR  AH    + + GI+AF  
Sbjct: 82  YESAVALAEKLNAAAPGNTPKKSIFVTTGAEAVENCVKIAR--AH----TGRPGIIAFNG 135

Query: 137 AFHGRTLFTVSAGGQP-AYSQDFAPLPPDIRHAAY-ND---INSASALID---------- 181
            +HGRT  T+   G+   Y   F P P DI H  Y ND   I    AL D          
Sbjct: 136 GYHGRTNMTMGLTGKVNPYKIGFGPFPSDIFHVPYPNDYLGITEEQALADLQLRFTCDIE 195

Query: 182 -DATCAVIVEPIQGEGGVVPASNAFLQGLRELCDRHNALLIFDEVQTGVGRTGELYAYMH 240
                A+I+EP+QGEGG   AS +FLQ LR+LCD H  LLI DE+Q+G  RTG ++ +  
Sbjct: 196 PSRVAAIIIEPVQGEGGFYKASTSFLQKLRKLCDDHGMLLILDEIQSGFARTGTMFCHEQ 255

Query: 241 YGVTPDLLTTAKALGGGFPVGALLTTEECASVMTVGTHGTTYGGNPLASAVAGKVLELIN 300
            G+  DL+TTAK + GG P+ A++           G  G TYGG+P+  A    V E+I 
Sbjct: 256 AGIEADLMTTAKGIAGGVPLAAVVGKANIMDAPIPGGLGGTYGGSPVGCAAGLAVFEVIE 315

Query: 301 TPEMLNGVKQRHDWFVERLNTINHRY-GLFSEVRGLGLLIGCV------LNADYAGQAKQ 353
             ++     Q    FVE L  +   +  +  +VR  G +I         +N  Y   AK+
Sbjct: 316 EEKLCERATQIGTRFVEHLTALQAEFPNIIGDVRNSGAMIAVEFVHDGDVNKPYPELAKK 375

Query: 354 ISQEAAKAGVMVLIAG--GNVVRFAPALNVSEEEVTTGLDRF 393
           +S +A++ G+++L  G  GNV+RF PAL +  E +  G++ F
Sbjct: 376 LSGKASENGLVLLSCGIRGNVIRFLPALTIEMELIDEGMEIF 417


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: 493
Number of extensions: 19
Number of successful extensions: 6
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: 425
Length adjustment: 31
Effective length of query: 375
Effective length of database: 394
Effective search space:   147750
Effective search space used:   147750
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