GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Magnetospirillum magneticum AMB-1

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_011386326.1 AMB_RS20100 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_000009985.1:WP_011386326.1
          Length = 393

 Score =  384 bits (986), Expect = e-111
 Identities = 190/364 (52%), Positives = 250/364 (68%), Gaps = 5/364 (1%)

Query: 30  PLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWDSA 89
           P+ LDCG  L   ++ Y+TYG+LN + SNA+LICHAL+GDH+ A  H  T  KPGWW   
Sbjct: 26  PIRLDCGVELGPIQVAYQTYGRLNADKSNAILICHALTGDHYVADPHPIT-AKPGWWHEL 84

Query: 90  IGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYRLM 149
           +GPG+  DTDR+F++C N LGGC G+TGP+  +PA+G+ +G DFP++T+ D V  Q RL+
Sbjct: 85  VGPGRVFDTDRYFLICSNVLGGCMGTTGPVDENPATGQAWGLDFPVITIGDMVKVQARLV 144

Query: 150 QYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQAII 209
            +LG+     V+GGS+GGMQVL+W+  YP+ V  A+ IA+A R SAQNIAF+EV RQAI+
Sbjct: 145 DHLGIDQLFCVVGGSMGGMQVLKWAQVYPERVFSAIPIASAARHSAQNIAFHEVGRQAIM 204

Query: 210 TDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELR-AGQVQYGFDVEF 268
            DP++  G Y      P RGL +ARM  HITYLS+ A+  KFGR L+    V YGFD +F
Sbjct: 205 ADPDWCEGNYLQEGKRPHRGLAVARMAAHITYLSEPALHQKFGRNLQNRDTVTYGFDADF 264

Query: 269 QVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVAALAEVKAHFLVVSFTS 328
           QVESYLR+QG +FVDRFDAN+YL +T+A+DYFD A  S   L  A    +  F VVSFTS
Sbjct: 265 QVESYLRHQGNTFVDRFDANSYLYITRAMDYFDLAAESGGVLANAFRGTRTRFCVVSFTS 324

Query: 329 DWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLAGYMANIDFAST 388
           DW F    SR +V AL A    VS+ EI+S+ GHDAFL+  P +H  L G+   ++ A+T
Sbjct: 325 DWLFPTPESRAVVHALNAVAANVSFVEIKSDKGHDAFLLDEPEFHATLTGF---LEGAAT 381

Query: 389 PRGV 392
            RG+
Sbjct: 382 HRGL 385


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: 500
Number of extensions: 16
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: 393
Length adjustment: 31
Effective length of query: 372
Effective length of database: 362
Effective search space:   134664
Effective search space used:   134664
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 09 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