GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Desulfotomaculum ruminis DSM 2154

Align Homoserine O-acetyltransferase; HAT; Homoserine transacetylase; HTA; EC 2.3.1.31 (characterized)
to candidate WP_013841857.1 DESRU_RS09305 homoserine O-succinyltransferase

Query= SwissProt::A5N8M0
         (309 letters)



>NCBI__GCF_000215085.1:WP_013841857.1
          Length = 305

 Score =  458 bits (1179), Expect = e-134
 Identities = 212/304 (69%), Positives = 256/304 (84%)

Query: 1   MPIKIKDDLPAAEILNSENIFIMPENVAFHQDIRPLKIAILNLMPIKITTEVQLLRLIGN 60
           MPIKI D LPA++IL +ENIF+M E  A  QDIRPLK+AILNLMP KITTE QLLRL+GN
Sbjct: 1   MPIKIPDHLPASQILTNENIFVMHETRAVRQDIRPLKMAILNLMPTKITTETQLLRLLGN 60

Query: 61  TALQIEIELLHLKTHVCKNTSEEYLTNFYRTFDEIKNEKFDGLIITGAPIEQLEFSRVNY 120
           T LQ+E+ELLH  +H  KNT E++L  FY+TF+E+KN+KFDGLIITGAP+EQLEF++V+Y
Sbjct: 61  TPLQVEVELLHTGSHWSKNTPEDHLAVFYKTFEEVKNQKFDGLIITGAPVEQLEFNQVDY 120

Query: 121 WEELKDIMEWSKCHVYSTLHICWGAQAGLYYHYGIPKYILKEKLFGVFKHEVTEEKEKLV 180
           WEEL++IMEWSK HV STLHICW AQAGLYYHYGIPKY L  KLFGVFKH +     KL+
Sbjct: 121 WEELQEIMEWSKDHVTSTLHICWAAQAGLYYHYGIPKYDLPAKLFGVFKHWINRSHIKLL 180

Query: 181 RGFDDEFYVPHSRYTEVKREDVEKVKELTILAQSKKAGVYLILDNKGRRIFVTGHSEYDP 240
           RGFDDEFYVPHSRYTEV+R D+E+V+EL IL++S +AGVY++     R  F+TGHSEYDP
Sbjct: 181 RGFDDEFYVPHSRYTEVRRRDIERVEELEILSESDEAGVYIVAAKNRRMFFITGHSEYDP 240

Query: 241 LTLKDEYMRDISKGEDIKMPENYFPDDNPDRKPVVKWRSHADLLFSNWLNYYVYQETPYD 300
           LTLK EY RD+ KG DI +P+NY+P+DNP+ +PVVKWR HA LLFSNWLNYYVYQETP++
Sbjct: 241 LTLKGEYERDVKKGLDILVPQNYYPEDNPENEPVVKWRGHAHLLFSNWLNYYVYQETPFN 300

Query: 301 LSEM 304
           L+E+
Sbjct: 301 LTEI 304


Lambda     K      H
   0.320    0.139    0.420 

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: 413
Number of extensions: 11
Number of successful extensions: 1
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: 309
Length of database: 305
Length adjustment: 27
Effective length of query: 282
Effective length of database: 278
Effective search space:    78396
Effective search space used:    78396
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: 48 (23.1 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