GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Klebsiella variicola At-22

Align Acetylornithine deacetylase; AO; Acetylornithinase; EC 3.5.1.16; N-acetylornithinase; NAO (uncharacterized)
to candidate WP_012968503.1 KVAR_RS15665 M20 family metallopeptidase

Query= curated2:O68873
         (380 letters)



>NCBI__GCF_000025465.1:WP_012968503.1
          Length = 391

 Score =  145 bits (367), Expect = 1e-39
 Identities = 110/323 (34%), Positives = 154/323 (47%), Gaps = 24/323 (7%)

Query: 57  KVNLVAVKGGSGSGRAALALVGHSDCVPYDAAW-TDALRLTEKDGRLYARGACDTKGFIA 115
           + N++AV   +G G    A   H D VP  + W +D   LTE+DGRLY RGACD KG + 
Sbjct: 57  RTNVIAVLN-NGPG-PCFAFNTHLDTVPAGSGWASDPFTLTERDGRLYGRGACDAKGPLV 114

Query: 116 CALHA----ALNAEQLKAPLMVVLTADEEVGLTGAKKLVEAGLGRARHAIVGEPTRLIPV 171
             + A    A N +Q    LM V TADEEV   GAK  V         A++GEPT     
Sbjct: 115 AMVEALRLLAANRQQWSGTLMGVFTADEEVASEGAKFYVRDNPPAIDFAVIGEPTSNATF 174

Query: 172 RANKGYCLAEVEVRGKEGHSAYPDSGASAIFRAGRFLQRLE---HLALTVLREDLDEGFQ 228
            A+KG     V V+G   HS  P+ G +AI+++ R L  +E   H  +     DL     
Sbjct: 175 SAHKGSLRPRVRVKGVTAHSGTPELGVNAIYQSARLLGLIEEAHHQQVRCRCHDLVGN-- 232

Query: 229 PPFTTVNVGVIQGGKAKNVIPGACRFVVEWRPIPGQPPERVSQLLETIRQELVRDEPAFE 288
               ++ V  I GG A NV+P +C  +++ R +PG+  E V   L+ +           E
Sbjct: 233 ---ASLTVTRIHGGHADNVVPESCELLLDRRMVPGEDEEVVKAELQQLLDHAYA-HAGVE 288

Query: 289 AQIRVVRTDRGVNTRAD---AEVVRFLAEA-----SGNAPETVSFGTEAPQMTELGAEAV 340
           A+I   +   G  T+ D   A V + LA       S   P     G +      LGA+ V
Sbjct: 289 AEIIAWQPTTGGATQTDSREAIVEQSLAACRRHGQSEPGPFGFQGGCDLVHFRSLGAKGV 348

Query: 341 VFGPGDIRVAHQTGEYVPVEDLV 363
           V GPG + VAH+  E+VPV++ +
Sbjct: 349 VIGPGSLAVAHKPDEFVPVDEFI 371


Lambda     K      H
   0.319    0.136    0.396 

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: 407
Number of extensions: 22
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: 380
Length of database: 391
Length adjustment: 30
Effective length of query: 350
Effective length of database: 361
Effective search space:   126350
Effective search space used:   126350
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