GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Geobacter lovleyi SZ

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_012471501.1 GLOV_RS17225 homoserine O-acetyltransferase

Query= SwissProt::S2L5R8
         (390 letters)



>NCBI__GCF_000020385.1:WP_012471501.1
          Length = 367

 Score =  321 bits (823), Expect = 2e-92
 Identities = 164/369 (44%), Positives = 229/369 (62%), Gaps = 4/369 (1%)

Query: 14  SVGLVAPQTAHFDVPLALACGKTLQSYDLVYETYGKLNASRSNAVLICHALSGHHHAAGY 73
           S+G+V  QT  F+  + L  G+ L    LVYE YG +NA  SN +++ HA +G  H AG 
Sbjct: 2   SIGVVHEQTITFEAGIRLESGRILAPITLVYELYGTMNADCSNVIMVEHAWTGDAHLAGK 61

Query: 74  HSREDRKPGWWDAHIGPGKSIDTDRFFVISLNNLGGCHGSTGPCAINPDTGRQWGPDFPM 133
              +D KPGWWDA +GPG+ +DTDR+ V+  N +G C+GSTGP +INP TG+++   FP+
Sbjct: 62  RREDDPKPGWWDAIVGPGRLLDTDRYCVLCSNVIGSCYGSTGPASINPRTGKRYNLSFPV 121

Query: 134 MTVGDWVHSQARLADRLGIERFAAVIGGSLGGMQVLQWSLAYPERIANAVVIAATPKLSA 193
           +TV D V +Q  L D LGI R   V+GGS+GGMQ L+W+  YPER+A+ V +A TP+ S 
Sbjct: 122 ITVRDMVRAQELLLDHLGIRRLLCVMGGSMGGMQALEWATQYPERVASVVALATTPRPSP 181

Query: 194 QNIAFNEVARQAIRSDPDFYDGWYAEHDTLPRRGLKLARMVGHITYLSEDAMGSKFGRDL 253
           Q I+ N VAR AI +DP +  G Y  +   P+ GL LAR +GHIT+LS+++M  KF R  
Sbjct: 182 QAISLNAVARWAIYNDPTWKKGEYKHN---PKDGLALARGIGHITFLSDESMWQKFERRF 238

Query: 254 RSDDLNFGYDVEFQVESYLRYQGDTFSTSFDANTYLLMTKALDYFDPAAAHDGDLAAAVA 313
            + D  F +  +F+VE YL Y G  F   FDAN +L + KALD +D A  ++  +  A +
Sbjct: 239 SAKDGLFDFFGQFEVERYLNYNGYNFVDRFDANCFLYLAKALDLYDVAWGYE-SMTDAFS 297

Query: 314 PASCPFLVVSFSTDWRFPPSRSRELVDALIRAGKPVSYVCIDSPHGHDAFLLPETRYQAI 373
             + P    +FS+DW +PP ++ E+V  L   GK V Y  I S +GHDAFLL    +  +
Sbjct: 298 RITAPIQFFAFSSDWLYPPYQTEEMVTCLQGLGKEVEYHLIQSAYGHDAFLLEHETFTPM 357

Query: 374 FASFMGRVA 382
             S + RVA
Sbjct: 358 VRSLLERVA 366


Lambda     K      H
   0.321    0.136    0.428 

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: 393
Number of extensions: 15
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: 390
Length of database: 367
Length adjustment: 30
Effective length of query: 360
Effective length of database: 337
Effective search space:   121320
Effective search space used:   121320
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