GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Chlorobium phaeobacteroides BS1

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_012473666.1 CPHAMN1_RS01040 glutamate-1-semialdehyde 2,1-aminomutase

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



>NCBI__GCF_000020545.1:WP_012473666.1
          Length = 431

 Score =  147 bits (370), Expect = 7e-40
 Identities = 102/316 (32%), Positives = 154/316 (48%), Gaps = 45/316 (14%)

Query: 8   GDRGLTIVKGEAQYVWDIEGRRYLDFHTGIGVAFLGHRNPIILEYLKNQLENISILSTSF 67
           G   + + KG+  Y+ D++G  YLD+    G   LG  +P I   ++N L  I    TSF
Sbjct: 33  GGTPIFMAKGQGAYMTDVDGNTYLDYVGSWGPFILGSMHPRITAAIENTLTKIG---TSF 89

Query: 68  STPIKDEM--LQALDKVKPDKMDNAMLLNSGTEAVEAALKTARKITGRKKIIAFKNAFHG 125
            TPI+ E+   + L ++ P  ++   ++NSGTEA  +A++ AR  TGR KII F+  +HG
Sbjct: 90  GTPIEMEIEIAELLTQIVPS-IEMVRMVNSGTEATMSAVRLARGYTGRDKIIKFEGCYHG 148

Query: 126 R-----------------------TAGSLSVTWNKKYREPFEPLVGPVEFLTFNNIEDLS 162
                                   T G+ + T N KY +     +  V  L   N + + 
Sbjct: 149 HGDSFLIKAGSGALTLGAPDSPGVTKGTANDTLNAKYND-----IESVRVLVKENKDSI- 202

Query: 163 KIDNETAAVIVEPIQGESGVIPANIEFMKALKEKTENTGSLLIFDEIQTGFGRTGKLWAY 222
                 AA+I+EP+ G +GVIPA  +F++AL++     G +LIFDE+  GF R     A 
Sbjct: 203 ------AAIIIEPVAGNTGVIPAKTDFLQALRDLCTEEGIVLIFDEVMCGF-RVALGGAQ 255

Query: 223 KHYNIVPDILTAGKAIGGGFPVSVVFLPDHIANKLEE-GD--HGSTYGGNPMAMAAVTAA 279
           + Y I PD+ T GK IGGG PV        I  ++   GD     T  GNP+A+ A    
Sbjct: 256 ERYGITPDLTTMGKIIGGGLPVGAFGGKREIMQRVAPIGDVYQAGTLSGNPLALTAGLET 315

Query: 280 CKVIEKENVVEQANQK 295
            K++  +N   +  +K
Sbjct: 316 LKILRDDNPYPELERK 331


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: 400
Number of extensions: 11
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: 431
Length adjustment: 31
Effective length of query: 356
Effective length of database: 400
Effective search space:   142400
Effective search space used:   142400
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