GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Thioalkalivibrio thiocyanodenitrificans ARhD 1

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_018232220.1 THITHI_RS0106275 glutamate-1-semialdehyde 2,1-aminomutase

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



>NCBI__GCF_000378965.1:WP_018232220.1
          Length = 428

 Score =  138 bits (347), Expect = 3e-37
 Identities = 103/339 (30%), Positives = 158/339 (46%), Gaps = 20/339 (5%)

Query: 8   GDRGLTIVKGEAQYVWDIEGRRYLDFHTGIGVAFLGHRNPIILEYLKNQLENISILSTSF 67
           G   L I + E  Y++D +G+RY+D+    G    GH +P +LE ++  + +   LS   
Sbjct: 30  GGDPLFIERAEGAYLYDADGKRYIDYVGSWGPMIAGHAHPEVLEAVRETIAHG--LSFGA 87

Query: 68  STPIKDEMLQALDKVKPDKMDNAMLLNSGTEAVEAALKTARKITGRKKIIAFKNAFHGR- 126
            T I+  M   + ++ P  MD   ++NSGTEA  +A++ AR  TGR KII F+  +HG  
Sbjct: 88  PTEIEIRMADRVCELVPS-MDMVRMVNSGTEATMSAIRLARGFTGRDKIIKFEGCYHGHG 146

Query: 127 -----TAGSLSVTWNKKYREPFEPLVGPVEFLT--FNNIEDL----SKIDNETAAVIVEP 175
                 AGS ++T       P  P       LT  +N+++ +    S +  + A VIVEP
Sbjct: 147 DSLLVKAGSGALTLGVP-SSPGVPAALAEHTLTLAYNDLDQVRDTFSHVGGQVACVIVEP 205

Query: 176 IQGESGVIPANIEFMKALKEKTENTGSLLIFDEIQTGFGRTGKLWAYKHYNIVPDILTAG 235
           + G    IP    F++ L+   +  G+LLIFDE+ TGF R         YN+ PD+ T G
Sbjct: 206 VAGNMNCIPPEPGFLEGLRALCDEYGALLIFDEVMTGF-RVALGGVQALYNVKPDLTTLG 264

Query: 236 KAIGGGFPVSVVFLPDHIANKLEEGD---HGSTYGGNPMAMAAVTAACKVIEKENVVEQA 292
           K IGGG PV        +  +L          T  GNP+AMAA     +++      +  
Sbjct: 265 KVIGGGMPVGAFGGRREVMEQLAPLGPVYQAGTLSGNPVAMAAGLKTLELVSSPGFYDLL 324

Query: 293 NQKGQQFSNILVKNLADLKVVREVRGKGLMIGIDIRFQP 331
            +K     + ++    D  +       G M G+    QP
Sbjct: 325 GEKVNTLVDGILAAARDTGIPMTANRVGGMFGLFFTDQP 363


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: 16
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: 428
Length adjustment: 31
Effective length of query: 356
Effective length of database: 397
Effective search space:   141332
Effective search space used:   141332
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