GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Methanobacterium lacus AL-21

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_013645701.1 METBO_RS10535 glutamate-1-semialdehyde-2,1-aminomutase

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



>NCBI__GCF_000191585.1:WP_013645701.1
          Length = 420

 Score =  134 bits (338), Expect = 4e-36
 Identities = 97/326 (29%), Positives = 160/326 (49%), Gaps = 25/326 (7%)

Query: 16  KGEAQYVWDIEGRRYLDFHTGIGVAFLGHRNPIILEYLKNQLENISILSTSFSTPIKDEM 75
           K E   + D++G  Y+D+    G   LGH NP ++  ++ QL    +  +++  P + E+
Sbjct: 34  KAEGSKLTDVDGNSYIDYCLAYGPMVLGHSNPEVVSEVEKQL----VKGSAYGVPTEKEI 89

Query: 76  LQALDKVKPDKM---DNAMLLNSGTEAVEAALKTARKITGRKKIIAFKNAFHGRTAGSLS 132
              L K+  +++   D    +NSGTEA  +A++ AR    + KII F+ A+HG     L 
Sbjct: 90  --ELAKMVVNRVPCADMVRFVNSGTEATMSAIRLARAAKSKNKIIKFEGAYHGAHDNVLV 147

Query: 133 VTWNKKYREPFEPLVGPVE------FLTFNNIEDLSKIDNET----AAVIVEPIQGESGV 182
            + +     P  P V P E       + FNN E + +I N+     AA+I+EPI G  G+
Sbjct: 148 KSGSGAAGLPDSPGV-PEETTRNTLLIPFNNEESVIEIINKNKDSIAAIIIEPIMGNVGL 206

Query: 183 IPANIEFMKALKEKTENTGSLLIFDEIQTGFGRTGKLWAYKHYNIVPDILTAGKAIGGGF 242
           IP    F++ L++ T      LIFDE+ TGF R  +  A +++ + PD++T GK +GGGF
Sbjct: 207 IPPKNGFLEFLRKITLENDITLIFDEVITGF-RIAQGGAQEYFKVTPDLVTFGKILGGGF 265

Query: 243 PVSVVFLPDHIANKLEEGD---HGSTYGGNPMAMAAVTAACKVIEKENVVEQANQKGQQF 299
           P+  +         +          T+ GNP+++ A  A  K ++++      N KG+ F
Sbjct: 266 PMGAITGKKEYMEMIAPSGSVYQAGTFNGNPISITAGLATLKQLDQQ-FYSDMNSKGKNF 324

Query: 300 SNILVKNLADLKVVREVRGKGLMIGI 325
              +   L D  +  +V G   M  I
Sbjct: 325 REGIRNILEDKNLNYQVAGVSSMFQI 350


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: 387
Number of extensions: 13
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: 387
Length of database: 420
Length adjustment: 31
Effective length of query: 356
Effective length of database: 389
Effective search space:   138484
Effective search space used:   138484
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 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