GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Methylocella silvestris BL2

Align Homoserine O-acetyltransferase; HAT; EC 2.3.1.31; Homoserine transacetylase; HTA (uncharacterized)
to candidate WP_012591475.1 MSIL_RS12645 hypothetical protein

Query= curated2:Q6ADB9
         (402 letters)



>NCBI__GCF_000021745.1:WP_012591475.1
          Length = 345

 Score =  130 bits (328), Expect = 4e-35
 Identities = 97/310 (31%), Positives = 147/310 (47%), Gaps = 33/310 (10%)

Query: 48  IGAFGFESGESLPFVRIAYETWGELSPARDNAVLVLHALTGDSHAVGAAGPGHRTSGWWQ 107
           +G F  ESG+ +  +++AY T+GEL+P + NA+L     +G ++ + +A           
Sbjct: 18  LGDFDLESGDKIRGLKLAYATFGELAPDKSNAILFPTWYSGTTNILESA----------- 66

Query: 108 GIIGPGKAIDTDRWFVAVPNMLGGCQGTTGPTSIAPDGAEWGARFPFTTIRDQVKAQAAF 167
             +G G+A+D  ++F+ + N +G    T+   + AP  A   ARFP  +I D V+AQ   
Sbjct: 67  -YLGEGRALDASKYFIILVNQIGNGLSTSPSNTPAPFNA---ARFPKISIADDVRAQRRL 122

Query: 168 -ADALGIGRWAAVVGGSMGGMQALEWAVGFPERVERLAVIAAPPHSTADQIAFNSVQLGA 226
            A+  G+ + A V+GGSMG     EWAV FPE VER A IA     TA      S  + A
Sbjct: 123 IAEKFGLEKLALVLGGSMGAQMTFEWAVRFPEAVERAAPIAGTARGTAHNRLLVSTFIEA 182

Query: 227 IRTDPLFHGGSYYDEKDGEGPHQGLALARRMALITYRSLSELNDRFER-TWQSGISPLGD 285
           I +DP F GG Y D       H+GL    R+    + +     D + R  W+S       
Sbjct: 183 IESDPAFDGGWYAD----GAAHRGLRRHARL----FAAAGFTPDLYNRAAWRS------- 227

Query: 286 GGRFAVESYLDFHGNKFTRRFDANSYLTLVQAMNSHDVGHD-GSGLAAALSRVTATTLVV 344
            G  + E +L           D N+ + L      +D     G  + AAL+ + A T V+
Sbjct: 228 LGFTSSEDFLTGFVEAHFLPQDPNNLILLATKWRENDAARRFGGDIVAALASIKAKTFVI 287

Query: 345 GIDSDRLFPV 354
            I+ D  FP+
Sbjct: 288 AIEEDGFFPL 297


Lambda     K      H
   0.319    0.137    0.427 

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: 399
Number of extensions: 21
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: 402
Length of database: 345
Length adjustment: 30
Effective length of query: 372
Effective length of database: 315
Effective search space:   117180
Effective search space used:   117180
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: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 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