GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Epibacterium ulvae U95

Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate WP_090215547.1 CV091_RS07085 aspartate aminotransferase family protein

Query= curated2:Q9X2A5
         (385 letters)



>NCBI__GCF_002796795.1:WP_090215547.1
          Length = 444

 Score =  207 bits (526), Expect = 6e-58
 Identities = 130/369 (35%), Positives = 201/369 (54%), Gaps = 33/369 (8%)

Query: 8   SRFPATFVYGKGSWIYDEKGNAYLDFTSGIAVNVLGHSHPRLVEAIKDQAEKLIHCSNLF 67
           +  P   + G G ++YD  G AY D + G AV+ LGH    ++ AIK Q + +      F
Sbjct: 10  NNLPPIGMKGDGVYLYDTDGKAYFDGSGGAAVSCLGHGDQDIINAIKRQLDSMAFAHTGF 69

Query: 68  W-NRPQMELAELLSKNTFGG--KVFFANTGTEANEAAIKIARKYGKKKSE-KKYRILSAH 123
             ++P  +LA+LL K+       V+F + G+EA EAA+K+AR+Y  +  + ++ +I++  
Sbjct: 70  LGSQPAEDLADLLVKHAPESLEHVYFVSGGSEAVEAALKLARQYFVEIGQSQRSKIIARR 129

Query: 124 NSFHGRTLGSLTATGQPKYQKPFEPLV-------PGFEY---------FEFNN------V 161
            S+HG TLG+L   G    +  F PL+       P +EY         FE+         
Sbjct: 130 QSYHGNTLGALAVGGNEWRRAQFAPLLIDVSHIGPCYEYRNRRAEETSFEYGQRVANELE 189

Query: 162 EDLRRKMSEDVCAVFLEPIQGES-GIVPATKEFLEEARKLCDEYDALLVFDEVQCGMGRT 220
           E++ R   + V A   EP+ G + G VP+ + + +  R++CD Y  LL+ DEV CGMGRT
Sbjct: 190 EEILRLGPDQVMAFIAEPVVGATMGAVPSVEGYFKRIREICDTYGVLLILDEVMCGMGRT 249

Query: 221 GKLFAYQKYGVVPDVLTTAKGLGGGV-PIGAVIVN-ERANVLEPG----DHGTTFGGNPL 274
           G LFA ++  + PD+ T AKGLG G  PIGA + + E  N ++ G     HG T+ G+P 
Sbjct: 250 GTLFAAEQEEISPDICTIAKGLGAGYQPIGATLCSGEIFNTIKNGSGFFQHGHTYIGHPT 309

Query: 275 ACRAGVTVIKELTKEGFLEEVEEKGNYLMKKLQEMKEEYDVVADVRGMGLMIGIQFREEV 334
           AC AG+ V+++LT+ G +E V  KG  L+  LQ+    +  V D+RG GL +G++F  + 
Sbjct: 310 ACSAGLAVVQKLTQGGVVEHVTAKGQQLLDLLQQEFGRHPNVGDIRGRGLFVGMEFVADR 369

Query: 335 SNREVATKC 343
             + V   C
Sbjct: 370 GRKAVIDPC 378


Lambda     K      H
   0.318    0.138    0.402 

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: 450
Number of extensions: 24
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: 385
Length of database: 444
Length adjustment: 31
Effective length of query: 354
Effective length of database: 413
Effective search space:   146202
Effective search space used:   146202
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 Jul 26 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