GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Malonomonas rubra DSM 5091

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_072906806.1 BUB13_RS06080 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_900142125.1:WP_072906806.1
          Length = 373

 Score =  327 bits (837), Expect = 5e-94
 Identities = 167/371 (45%), Positives = 234/371 (63%), Gaps = 2/371 (0%)

Query: 13  LSRSVGIVEPKTARFSEPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHA 72
           ++ SVG+V+ + A F   L L+ GR L    + +E YGQLN    N +L+ HA +GD HA
Sbjct: 1   MNDSVGLVKTEYADFDVELRLESGRLLGPLTIAFERYGQLNAAKDNVILVTHAWTGDAHA 60

Query: 73  AGFHAETDRKPGWWDSAIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPD 132
           AG H E DRKPGWWD+ IGPGK  DTD++FV+C N +G CKGSTGP S+DP +G+PY   
Sbjct: 61  AGVHDEEDRKPGWWDNMIGPGKVFDTDKYFVLCSNVIGSCKGSTGPTSIDPKTGRPYRLK 120

Query: 133 FPIVTVKDWVHAQYRLMQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPR 192
           FP + V+D V AQ  L+ +LG++   AV+GGS+G MQ ++W+I YP+ +   V IA   R
Sbjct: 121 FPSLMVRDMVRAQKLLIDHLGITSIHAVVGGSMGAMQAIEWAIHYPEMIRAIVPIAGTGR 180

Query: 193 LSAQNIAFNEVARQAIITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFG 252
            S   IA N +ARQAI  DP +  G Y   +  P  GL LAR +GHI++LSD +M  KFG
Sbjct: 181 TSPMAIALNALARQAIFNDPLWKKGNYRPEHP-PADGLALARAVGHISFLSDASMWLKFG 239

Query: 253 RELRAGQVQYGFDVEFQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVA 312
           R        + F  +F++E YL Y G +FVDRFD N++L + KALD +D A  + D L  
Sbjct: 240 RRFSVRDGMFDFFGKFEIERYLDYNGGNFVDRFDTNSFLYLAKALDLYDVAW-NFDSLSE 298

Query: 313 ALAEVKAHFLVVSFTSDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYY 372
           AL  +    L  +FTSDW ++P++++E+V  L    K V Y  IES++GHD+FL+    +
Sbjct: 299 ALDRLNCPSLWFAFTSDWLYTPQQTQEVVDELRRLNKPVDYHLIESDYGHDSFLVEPEKF 358

Query: 373 HRVLAGYMANI 383
             +L  ++A +
Sbjct: 359 IPILQTFLAEV 369


Lambda     K      H
   0.320    0.135    0.412 

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: 448
Number of extensions: 25
Number of successful extensions: 3
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: 403
Length of database: 373
Length adjustment: 30
Effective length of query: 373
Effective length of database: 343
Effective search space:   127939
Effective search space used:   127939
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: 50 (23.9 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