GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Thioalkalivibrio halophilus HL17

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_018947109.1 B1A74_RS01550 homoserine O-succinyltransferase

Query= SwissProt::L0E1U3
         (356 letters)



>NCBI__GCF_001995255.1:WP_018947109.1
          Length = 356

 Score =  565 bits (1456), Expect = e-166
 Identities = 267/352 (75%), Positives = 301/352 (85%)

Query: 1   MPLVAHSNLPTFERLRKEGGTVLPNDYALHQDIRALHIGLLNMMPDAALAATERQFFRLV 60
           MPLVAHS LPTFERLR EG +VLPND+A  Q+IRALHIGLLNMMPDAALAATERQFFRL+
Sbjct: 1   MPLVAHSGLPTFERLRSEGESVLPNDFARQQEIRALHIGLLNMMPDAALAATERQFFRLI 60

Query: 61  GESNQIAQFYMHPFTLAELPRGPGGQAHVERYYETFDTIQREGLDALIITGANVSQPDLA 120
           GESNQIAQFY+HPFTL +L RG  G+ HVE YYE F+ ++ EGLDALIITGANV+QPDLA
Sbjct: 61  GESNQIAQFYIHPFTLPQLKRGRKGREHVENYYEDFEQLKEEGLDALIITGANVTQPDLA 120

Query: 121 LEPFWEPLAEVVEWAWKNVTSTLCSCLTTHAVMQSRYGERRRHRGAKLWGVFDHRVVDRT 180
           LEPFWEPLAEVV+WAW NVTSTLCSCL THAV+QS YGE R+H G KLWGVF HRVVDR 
Sbjct: 121 LEPFWEPLAEVVDWAWDNVTSTLCSCLATHAVLQSHYGEHRQHMGEKLWGVFPHRVVDRR 180

Query: 181 HPLVAGVNTRFDVPHSRFNDVSREQFDRHRLKVLVESERAGVHLAVSEDGFRLVFFQGHP 240
           HPLV GVNTRFDVPHSR+N V+R+QF+ H L+VLVESE AG+HL  S DGFR+VFFQGHP
Sbjct: 181 HPLVTGVNTRFDVPHSRYNKVTRDQFEHHGLRVLVESEEAGIHLGASPDGFRMVFFQGHP 240

Query: 241 EYDSISLLKEYKREVLRFVNGEREEFPPLPERYLSPQAAAILEEHRERVEQARQRRVPAP 300
           EYDSISLLKEYKREV+R++ G+R+ +PPLPE YL PQAAAIL+EHRE VE A +     P
Sbjct: 241 EYDSISLLKEYKREVVRYIEGDRKAYPPLPENYLMPQAAAILDEHREHVEAALEHCTEIP 300

Query: 301 ELPEPLLVGRLDNTWHDSALAVVNNWIGNVYQFTNHDRRIPFRPGVDPNAPL 352
            LPE LL+ RLDNTWHD+ALAV+NNW+GNVYQ TN DRR PFR  VDP+ PL
Sbjct: 301 ALPEALLLDRLDNTWHDTALAVINNWLGNVYQLTNLDRRKPFRDSVDPDDPL 352


Lambda     K      H
   0.322    0.138    0.429 

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: 509
Number of extensions: 10
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: 356
Length of database: 356
Length adjustment: 29
Effective length of query: 327
Effective length of database: 327
Effective search space:   106929
Effective search space used:   106929
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 (21.9 bits)
S2: 49 (23.5 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