GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Klebsiella variicola At-22

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate WP_012542131.1 KVAR_RS15830 fructose-asparagine asparaginase

Query= curated2:Q8TR66
         (424 letters)



>NCBI__GCF_000025465.1:WP_012542131.1
          Length = 347

 Score =  105 bits (263), Expect = 2e-27
 Identities = 96/334 (28%), Positives = 155/334 (46%), Gaps = 33/334 (9%)

Query: 82  KLPKIAILSTGGTIASKI-------DYRTGAVTSQFTADDILAAIPELKEIADFKGRVIS 134
           +LP I IL+TGGTIA           Y+ GA+  Q     ++ A+PE+ +IA  +G  ++
Sbjct: 23  RLPHIVILATGGTIAGSAASNTQTTGYKAGAIGVQ----TLINAVPEMSKIAHVEGEQVA 78

Query: 135 SILSENMDSDSWQNLSKAVVEEIEAG-ADGVIVTHGTDTMMYSAAALSFMIKTPVPIVFV 193
           +I SENM SD    LSK V   +     DGV++THGTDT+  +   L+  +K+  P+VF 
Sbjct: 79  NIGSENMTSDIILELSKRVNALLARDDVDGVVITHGTDTLDETPYFLNLTVKSNKPVVFT 138

Query: 194 GSQRSADRPSSDNAMNAICAARVAISDIAE---VVVVMHGTTSDDFCEIHRGTKVRKLHT 250
            + R A   S+D  MN + A  VA    A    V+VV++         I     V K + 
Sbjct: 139 AAMRPATAISADGPMNLLEAVTVAADPDARGRGVMVVLND-------RIGAARFVTKTNA 191

Query: 251 SRRDAFKSVNSLPVGTVDYGTGEIKTFID--YTRRGEKALKFKPGMEPKCALVKFTPGAD 308
           +  D F++     +G V  G  + +T +D  +T R    ++    + PK  ++       
Sbjct: 192 TSLDTFRAPEEGYLGVVVGGKPQFETRVDKIHTLRSVFDVRQLKTL-PKVVIIYGYQDDP 250

Query: 309 PTVLDYYISNGYKGLVVEGTGLGHISTKWIPLLRKATDAKMPVIVTSQCLNGRICDRVYD 368
             + D  I++   G++  GTG G +S +    ++KA  A + V+  S+  +G +      
Sbjct: 251 EYMYDAAIAHHADGIIYAGTGAGSVSVRSAAGIKKAQQAGIVVVRASRTGSGVVPPDDSQ 310

Query: 369 TGRDMLKAGAIEGEDTLPETALVKLMWVLGQTDD 402
            G        +  +   P  A + LM  L QT D
Sbjct: 311 PG--------LVSDSLNPAKARILLMTALTQTKD 336


Lambda     K      H
   0.316    0.134    0.386 

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: 313
Number of extensions: 24
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: 424
Length of database: 347
Length adjustment: 30
Effective length of query: 394
Effective length of database: 317
Effective search space:   124898
Effective search space used:   124898
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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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