GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Thermodesulforhabdus norvegica DSM 9990

Align Putative [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate WP_093392448.1 BM091_RS00090 N-acetyl-gamma-glutamyl-phosphate reductase

Query= curated2:A0RWW0
         (348 letters)



>NCBI__GCF_900114975.1:WP_093392448.1
          Length = 346

 Score =  278 bits (712), Expect = 1e-79
 Identities = 156/350 (44%), Positives = 214/350 (61%), Gaps = 8/350 (2%)

Query: 1   MKVGVVGASGYVGGETLRLLVNHPDVEIAAVTSRQHVGEYLHRVQPSLRGFTDLTFSELD 60
           +KVGV+G SGY G E +RLL  HP+V+I AV+SR      +    P+ R F DL +   D
Sbjct: 2   LKVGVLGGSGYTGFELIRLLATHPEVKIVAVSSRAQEESAVSEHYPAFRKFVDLRYVLPD 61

Query: 61  YDRLSDSCDLVFTAVPHGTATDIVRALYDRDIKVIDLSADYRLHDPADYTKWYGWEHPHP 120
                   D+VF+A+PHG +   V  L ++ ++VIDLSAD+R+ D A Y +WY   H  P
Sbjct: 62  DPVFEKGVDVVFSALPHGASMKAVSGLVEKGVRVIDLSADFRIRDAAVYEQWYE-PHTSP 120

Query: 121 DYLSKSVFGIPELHREEIRSAKLVSCPGCMAVTSILALAPPVREGLVDTEHIVVDSKIGS 180
           D L  +V+G+PEL+R EI SA+LV+ PGC   + ILALAP ++  L++ + I++DSK G 
Sbjct: 121 DLLKDAVYGLPELYRREIASARLVANPGCYPTSIILALAPLLKNRLIEEDSIIIDSKSGV 180

Query: 181 SGAGAGAG-TAHAMRAGV-IRPYK-PAKHRHTGEIEQELSGIAGKKIRVSMSPHAVDVVR 237
           +GAG G   T H        + YK    HRH  EIEQELS I+GK+IRV+ +PH V + R
Sbjct: 181 TGAGRGLSLTTHFCEVNEGFKAYKVGGVHRHIPEIEQELSLISGKEIRVTFTPHLVPMSR 240

Query: 238 GILCTNHVFLTREASEKDLWKMYRQAYGEERFVRLIRDKKGLYKFPDPKFLVGSNFCDIG 297
           GIL T +V         ++ + YR  Y +E FVRL+    G  + P    + GSNFCDIG
Sbjct: 241 GILSTLYVVPREGVKAGEIDEAYRTMYADEPFVRLV----GSGEMPSTLQVRGSNFCDIG 296

Query: 298 FDLDEDNNRLVAISASDNLMKGAAGSAIQNMNIMAGLDEMSGLRYTPLTP 347
           + LD  + RL+ +SA DNL +GA+G A+ NMNIM G+ E +GL Y P  P
Sbjct: 297 WKLDGRSGRLIVVSAIDNLTRGASGQAVCNMNIMFGIPETTGLFYVPWQP 346


Lambda     K      H
   0.320    0.137    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: 329
Number of extensions: 17
Number of successful extensions: 4
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: 348
Length of database: 346
Length adjustment: 29
Effective length of query: 319
Effective length of database: 317
Effective search space:   101123
Effective search space used:   101123
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: 49 (23.5 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