GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Thiothrix lacustris DSM 21227

Align Homoserine O-acetyltransferase; HAT; Homoserine transacetylase; HTA; EC 2.3.1.31 (characterized)
to candidate WP_028489154.1 Q394_RS0109900 homoserine O-succinyltransferase

Query= SwissProt::A0A1D3PDD4
         (309 letters)



>NCBI__GCF_000621325.1:WP_028489154.1
          Length = 361

 Score =  148 bits (374), Expect = 2e-40
 Identities = 111/337 (32%), Positives = 164/337 (48%), Gaps = 43/337 (12%)

Query: 7   MPIKIPDHLPAKEILLKENIFIMDESRAYTQDIRPLKICILNLMPTKQ--ETETQLLRLL 64
           MP+     LP  E L +E   ++ E  A+ QDIR L I  LN+MP      TE Q  RL+
Sbjct: 1   MPLVAHTALPTFERLRQEGQTVLSEDYAFNQDIRELHIGFLNMMPDAALAATERQFFRLV 60

Query: 65  GNTPLQVDVSLLHPSTHS--PRNTSKE-HLNLFYKTIDEVKQQKFDGMIITGAPVETLPF 121
           G + L     + HP T    PR+   + +++  Y+  +++++Q  D +IITGA       
Sbjct: 61  GESNLIAQFHI-HPFTLDSLPRSDKAQAYIDQHYEKFEDLRKQGLDALIITGANPSAAHL 119

Query: 122 HDVNYWNEMTSILDWTTTNVTSTLHICWGAQAGLYHHYGIKKKPLTTKLFGVYSHKLEVK 181
            D  +W  +  +  W   NVTSTL  C  + A + H +GI+++PL  K +GVYSH + + 
Sbjct: 120 EDEPFWEGLCEVAAWAMENVTSTLCSCLASHALVQHLWGIRRRPLGFKRWGVYSHAVTMP 179

Query: 182 NVNLLRGFDDVFYAPHSRHTTVSREDIERVDELIVLSSSEEAGVYIASSKDGKR-VFVMG 240
              L+   +  F  PHSR   + R  +E V  + VL  S+EAGV++A S D  R +F+ G
Sbjct: 180 EHPLVNDLNTRFDVPHSRFNQIDRVQLEAVG-VQVLVESDEAGVHMAVSPDLFRMIFLQG 238

Query: 241 HSEYDAHTLKQEYERDVKR---GIACD-PPF--NY------------------------- 269
           H EYD  +L +EY R+  R   G   D PPF  NY                         
Sbjct: 239 HPEYDQVSLLKEYRRETMRWFEGAREDYPPFPENYLRPKAKAILNEYRLTQRLAKRQGKP 298

Query: 270 ---FPEGNVDALPPLQWRAHSNLLFSNWLNYYVYQET 303
              FPE  + ++    WR  + + +SNW+   VYQ T
Sbjct: 299 LPDFPEALLLSMLHNTWRDTAKVFYSNWIG-KVYQIT 334


Lambda     K      H
   0.319    0.136    0.416 

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: 325
Number of extensions: 21
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 309
Length of database: 361
Length adjustment: 28
Effective length of query: 281
Effective length of database: 333
Effective search space:    93573
Effective search space used:    93573
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