GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Sulfurivirga caldicuralii DSM 17737

Align [amino group carrier protein]-C-terminal-L-glutamyl-γ-L-lysine aminotransferase (EC 2.6.1.118; EC 2.6.1.124) (characterized)
to candidate WP_074201116.1 BUQ81_RS04050 glutamate-1-semialdehyde 2,1-aminomutase

Query= metacyc::MONOMER-18314
         (387 letters)



>NCBI__GCF_900141795.1:WP_074201116.1
          Length = 432

 Score =  154 bits (389), Expect = 5e-42
 Identities = 103/305 (33%), Positives = 157/305 (51%), Gaps = 26/305 (8%)

Query: 14  IVKGEAQYVWDIEGRRYLDFHTGIGVAFLGHRNPIILEYLKNQLENISILSTSFSTPIKD 73
           I + +  YVWD++G+RY+D+    G A LGH +P ++E ++ Q E    LS    T ++ 
Sbjct: 36  IDRAKGAYVWDVDGKRYIDYVGSWGPAILGHAHPEVVEAVQKQAEKG--LSYGAPTELEV 93

Query: 74  EMLQALDKVKPDKMDNAMLLNSGTEAVEAALKTARKITGRKKIIAFKNAFHGRT------ 127
           EM   + ++ P  +D   ++NSGTEA   A++ AR  TGR +I+ F+  +HG +      
Sbjct: 94  EMADLICELIPS-VDMVRMVNSGTEATMTAIRLARGATGRDRIVKFEGGYHGHSDSLLVK 152

Query: 128 AGSLSVTWNKKYREPFEP-----LVGPVEFLTFNNIEDL----SKIDNETAAVIVEPIQG 178
           AGS ++T    +  P  P     L      LT+N+ E +     ++ +E A +IVEP+ G
Sbjct: 153 AGSGALT----HGVPSSPGVPKCLAEQTLTLTYNDAEQVRNVFDEVGDEIACIIVEPVAG 208

Query: 179 ESGVIPANIEFMKALKEKTENTGSLLIFDEIQTGFGRTGKLWAYKHYNIVPDILTAGKAI 238
               IP    F++ L++  +  G++LIFDE+ TGF R G   A   Y I PD+ T GK I
Sbjct: 209 NMNCIPPVPGFLETLRQVCDAHGAILIFDEVMTGF-RVGLTGAQGRYGITPDLTTFGKVI 267

Query: 239 GGGFPVSVVFLPDHIANKLEEGD---HGSTYGGNPMAMAAVTAACKVIEKENVVEQANQK 295
           GGG PV  +     I ++L          T  GNP+AMAA     K I +    E    K
Sbjct: 268 GGGMPVGALGGKREIMSQLAPTGPVYQAGTLSGNPLAMAAGLTTLKRISQPGFFEDLEAK 327

Query: 296 GQQFS 300
            Q+ +
Sbjct: 328 TQKLA 332


Lambda     K      H
   0.317    0.136    0.385 

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: 344
Number of extensions: 18
Number of successful extensions: 5
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: 387
Length of database: 432
Length adjustment: 31
Effective length of query: 356
Effective length of database: 401
Effective search space:   142756
Effective search space used:   142756
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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