GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Desulfotalea psychrophila LSv54

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_011188057.1 DP_RS04140 glutamate-1-semialdehyde 2,1-aminomutase

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



>NCBI__GCF_000025945.1:WP_011188057.1
          Length = 430

 Score =  144 bits (364), Expect = 4e-39
 Identities = 96/310 (30%), Positives = 156/310 (50%), Gaps = 22/310 (7%)

Query: 12  LTIVKGEAQYVWDIEGRRYLDFHTGIGVAFLGHRNPIILEYLKNQLENISILSTSFSTPI 71
           L I + E  Y++D +G++YLDF    G   +GH +P I++     +++ ++  TS+  P 
Sbjct: 36  LFIERAEGSYIYDADGQKYLDFVNSWGPMIMGHAHPDIIK----AIQDAAVYGTSYGAPT 91

Query: 72  KDEM-LQALDKVKPDKMDNAMLLNSGTEAVEAALKTARKITGRKKIIAFKNAFHGRT--- 127
             E+ L ++       ++    ++SGTEA  +A++ AR  TG+  I+ F   +HG     
Sbjct: 92  SSEVDLASMVVEAVPSIEKVRFVSSGTEATMSAVRLARGYTGKNVIVKFDGCYHGHADSF 151

Query: 128 -----AGSLSVTWNKKYREPFEPLVGPVEFLTFNNIEDLSKI----DNETAAVIVEPIQG 178
                +G L++        P E +V     + +N++E L       D   A VIVEP+ G
Sbjct: 152 LVKAGSGVLTLGIPGSPGVP-EDIVKNTISIPYNSVEALETTLRDADLNIACVIVEPVAG 210

Query: 179 ESGVIPANIEFMKALKEKTENTGSLLIFDEIQTGFGRTGKLWAYKHYNIVPDILTAGKAI 238
             G +P    F++ L+E T   G +LIFDE+ TGF R     A ++Y + PD+   GK I
Sbjct: 211 NMGCVPPAPGFLQKLREITAEEGIVLIFDEVITGF-RLSYGGAQQYYGVTPDLTCLGKII 269

Query: 239 GGGFPVSVVFLPDHIANKLEEGD---HGSTYGGNPMAMAAVTAACKVIEKENVVEQANQK 295
           GGG PV        I N +          T  GNP+AMAA  AA K+++++   E  NQK
Sbjct: 270 GGGLPVGAYGGKADIMNSVAPDGPVYQAGTLSGNPLAMAAGKAALKLLQQDGFYEDLNQK 329

Query: 296 GQQFSNILVK 305
              +++ L++
Sbjct: 330 SAAYADGLLE 339


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: 399
Number of extensions: 21
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: 430
Length adjustment: 31
Effective length of query: 356
Effective length of database: 399
Effective search space:   142044
Effective search space used:   142044
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