GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Stenotrophomonas chelatiphaga DSM 21508

Align N-acetyl-L-citrulline deacetylase; ACDase; Acetylcitrulline deacetylase; EC 3.5.1.- (characterized)
to candidate WP_057687252.1 ABB28_RS15380 acetylornithine deacetylase

Query= SwissProt::Q8P8J5
         (366 letters)



>NCBI__GCF_001431535.1:WP_057687252.1
          Length = 362

 Score =  631 bits (1628), Expect = 0.0
 Identities = 314/360 (87%), Positives = 335/360 (93%), Gaps = 1/360 (0%)

Query: 4   LLASTLEHLETLVSFDTRNPPRAIAAEGGIFDYLRAQLPGFQVEVIDHGDGAVSLYAVRG 63
           +L  TL HL+ LVSFDTRNPPRAI   GGIFDYLR  LPGF VEV+DHGDGAVSL+AVRG
Sbjct: 1   MLEQTLHHLQALVSFDTRNPPRAITT-GGIFDYLRDNLPGFNVEVVDHGDGAVSLHAVRG 59

Query: 64  TPKYLFNVHLDTVPDSPHWSADPHVMRRTEDRVIGLGVCDIKGAAAALVAAANAGDGDAA 123
            PKYLFNVHLDTVPDSPHWSADPHVMRR +DRV+GLGVCDIKGAAAALVAAANA +GDAA
Sbjct: 60  APKYLFNVHLDTVPDSPHWSADPHVMRRLDDRVVGLGVCDIKGAAAALVAAANASEGDAA 119

Query: 124 FLFSSDEEANDPRCIAAFLARGLPYDAVLVAEPTMSEAVLAHRGISSVLMRFAGRAGHAS 183
           FLFSSDEEANDPRCIAAFLARGLPY+AVLVAEPTMSEAVLAHRGISSVLM+FAGRAGHAS
Sbjct: 120 FLFSSDEEANDPRCIAAFLARGLPYEAVLVAEPTMSEAVLAHRGISSVLMQFAGRAGHAS 179

Query: 184 GKQDPAASALHQAMRWGGKALDHVESLAHARFGGLTGLRFNIGRVDGGIKANMIAPAAEL 243
           GKQD AASALHQAMRWG +ALDHV+SL+ ARFGGLTGLRFNIGRV+GGIKANMIAPAAEL
Sbjct: 180 GKQDAAASALHQAMRWGNRALDHVDSLSTARFGGLTGLRFNIGRVEGGIKANMIAPAAEL 239

Query: 244 RFGFRPLPSMDVDGLLATFAGFADPAAAHFEETFRGPSLPSGDIARAEERRLAARDVADA 303
           RFGFRPLPSMD+D LLATFAGFA+P AA F ETFRGPSLP+GDIA AE RRLAARDVADA
Sbjct: 240 RFGFRPLPSMDIDALLATFAGFAEPEAAVFTETFRGPSLPAGDIADAENRRLAARDVADA 299

Query: 304 LDLPIGNAVDFWTEASLFSAGGYTALVYGPGDIAQAHTADEFVTLAQLQRYVESVNRIIN 363
           LDLPIGNAVDFWTEASLFSAGGYT LV+GPGDIAQAHTADEFVTL QLQRY ++V+RII+
Sbjct: 300 LDLPIGNAVDFWTEASLFSAGGYTTLVFGPGDIAQAHTADEFVTLEQLQRYADAVHRIIS 359


Lambda     K      H
   0.321    0.136    0.406 

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: 488
Number of extensions: 9
Number of successful extensions: 2
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: 366
Length of database: 362
Length adjustment: 29
Effective length of query: 337
Effective length of database: 333
Effective search space:   112221
Effective search space used:   112221
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