GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Sulfurimonas denitrificans DSM 1251

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_011372739.1 SUDEN_RS05820 glutamate-1-semialdehyde 2,1-aminomutase

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



>NCBI__GCF_000012965.1:WP_011372739.1
          Length = 430

 Score =  142 bits (359), Expect = 1e-38
 Identities = 113/348 (32%), Positives = 165/348 (47%), Gaps = 38/348 (10%)

Query: 8   GDRGLTIVKGEAQYVWDIEGRRYLDFHTGIGVAFLGHRNPII----LEYLKNQLENISIL 63
           G   L I  G   Y+ DI+G RY+DF    G    GHR+  I    +E +K+ L      
Sbjct: 32  GGTPLFIANGSGAYLTDIDGNRYVDFVQSWGPLLFGHRDESIESAVIEAVKHGL------ 85

Query: 64  STSFSTPIKDEM-LQALDKVKPDKMDNAMLLNSGTEAVEAALKTARKITGRKKIIAFKNA 122
             SF  P + E  L AL     D ++    ++SGTEAV +A++ AR  T    I+ F   
Sbjct: 86  --SFGAPTQAESDLAALVISMFDSIEKIRFVSSGTEAVMSAIRLARGYTNCDDIVKFTGC 143

Query: 123 FHGRT------AGSLSVTWNKKYREPFEPLVGPVEFLT------FNNIEDLSKI---DNE 167
           +HG +      AGS + T+      P  P V P +F        +NNIE + K      +
Sbjct: 144 YHGHSDSLLVQAGSGAATFGN----PSSPGV-PADFTKHTLLAEYNNIESVKKCFSDSKD 198

Query: 168 TAAVIVEPIQGESGVIPANIEFMKALKEKTENTGSLLIFDEIQTGFGRTGKLWAYKHYNI 227
            A VI+EPI G  G++PA+ EF++ L+E  +  G+LLIFDE+ +GF R     A     +
Sbjct: 199 VACVIIEPIAGNMGLVPADKEFLRELRELCDANGALLIFDEVMSGF-RASVHGAESITGV 257

Query: 228 VPDILTAGKAIGGGFPVSVVFLPDHIANKLE-EGD--HGSTYGGNPMAMAA-VTAACKVI 283
            PDI+T GK IGGG PV        I  KL  EG      T  GNP+AMAA + A  K+ 
Sbjct: 258 KPDIVTLGKVIGGGMPVGAFGARAEIMAKLSPEGPVYQAGTLSGNPVAMAAGLAAITKLK 317

Query: 284 EKENVVEQANQKGQQFSNILVKNLADLKVVREVRGKGLMIGIDIRFQP 331
           +   ++   N +  +    + +      +  ++  +G M G     +P
Sbjct: 318 QNGQIISVLNSRATRLVEGMQEAAKTYGIAMQIDTRGSMFGFFFNEKP 365


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: 359
Number of extensions: 12
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 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