GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Sulfurivirga caldicuralii DSM 17737

Align Putative [LysW]-aminoadipate semialdehyde/glutamate semialdehyde transaminase; EC 2.6.1.118; EC 2.6.1.124 (uncharacterized)
to candidate WP_074200562.1 BUQ81_RS01125 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= curated2:Q9YBY6
         (388 letters)



>NCBI__GCF_900141795.1:WP_074200562.1
          Length = 428

 Score =  128 bits (321), Expect = 3e-34
 Identities = 101/309 (32%), Positives = 156/309 (50%), Gaps = 34/309 (11%)

Query: 29  DSGRKYLDCHAGHGAAFLGHSNPAIVEAVVRQAREL--VAASSSFSTPSLEEALTEFSRI 86
           + GR+ +D  +   AA  G+++P +V AV RQ + +  +        P+++ A  +   +
Sbjct: 38  EDGRRLVDGMSSWWAAIHGYNHPELVLAVARQLKTMPHIMFGGLTHEPAVDLA-EKLVTL 96

Query: 87  APPWAEEIVFLNTGTEAVEAALKAA---WLATGKRG---IVALKNSFHGRTLASLSVTW- 139
           +P   +++ F ++G+ AVE ALK A   W+A  K      + ++N +HG T  ++SVT  
Sbjct: 97  SPVPLKKVFFADSGSVAVEVALKIALQYWMARRKPQKHIFLTVRNGYHGDTFGAMSVTDP 156

Query: 140 -NPRYRRGVPVLDTRFLSPSTDPGEVEKLVP----------------EDTAAIIVEPI-Q 181
            N  +     VL   + +P+   G   KL                  ++ AAII+EPI Q
Sbjct: 157 DNGMHSLFAGVLPKHYFAPAPHMGFDLKLDEPADDIAALAAFLDHHHDEIAAIILEPIVQ 216

Query: 182 GEGGLTKIYAELAKALREAADRVGALLIFDEIQTGFGRTGRVWAHESLGVEPDIMTAGKS 241
           G GG+        + LR  AD    LLIFDEI TGFGRTG+++A E  G+ PDIMT GK+
Sbjct: 217 GAGGMRFYRPAYVRQLRAIADDYNVLLIFDEIATGFGRTGKLFACEWAGISPDIMTVGKA 276

Query: 242 IAGG-LPASAVLSREGVLATLASG-----RHGSTHAANPLSMAAVAAASRFLREEGVPDK 295
           + GG +  +A L+ E V  TL +       HG T  ANP + AA  A+   L +    D+
Sbjct: 277 LTGGMMTLAATLTTEEVAYTLCNNPPRALMHGPTFMANPTACAAANASIELLLKSAWQDR 336

Query: 296 ARAAGALLE 304
            +   A L+
Sbjct: 337 IQHIEAHLQ 345


Lambda     K      H
   0.319    0.136    0.398 

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: 327
Number of extensions: 14
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: 388
Length of database: 428
Length adjustment: 31
Effective length of query: 357
Effective length of database: 397
Effective search space:   141729
Effective search space used:   141729
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 Jul 25 2024. The underlying query database was built on Jul 25 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