GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Nocardioides dokdonensis FR1436

Align [amino group carrier protein]-gamma-(L-lysyl)-L-glutamate aminotransferase (EC 2.6.1.118) (characterized)
to candidate WP_068111454.1 I601_RS15155 acetylornithine transaminase

Query= BRENDA::Q93R93
         (395 letters)



>NCBI__GCF_001653335.1:WP_068111454.1
          Length = 396

 Score =  298 bits (762), Expect = 2e-85
 Identities = 172/367 (46%), Positives = 219/367 (59%), Gaps = 6/367 (1%)

Query: 29  LLIVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMAMPQTLPTPM 88
           L +VRG+GA VWDA+G EY+D +GG  V  LGH +P +V AV  Q  TL  +     +  
Sbjct: 30  LTLVRGEGAHVWDADGKEYVDLLGGIAVNALGHAHPALVAAVTDQLSTLGHISNFFTSVP 89

Query: 89  RGEFYRTLTAILPPELNRVFPVNSGTEANEAALKFARAHTGRKKFVAAMRGFSGRTMGSL 148
           + E    L A++     +VF  NSG EANEAA K  R  TGR   V A  GF GRTMG+L
Sbjct: 90  QVELAEKLVALVGAGPGKVFLANSGAEANEAAFKMTR-RTGRTHVVVAEGGFHGRTMGAL 148

Query: 149 SVTWEPKYREPFLPLVEPVEFIPYNDVEALKRAVDEETAAVILEPVQGEGGVRPATPEFL 208
           ++T +  YREPF PL   V F+PY DV+AL+ AV E TAA++LEP+QGE GV  A   +L
Sbjct: 149 ALTSKAAYREPFEPLPGDVTFVPYGDVDALREAVTETTAAILLEPIQGEAGVVMAPAGYL 208

Query: 209 RAAREITQEKGALLILDEIQTGMGRTGKRFAFEHFG-IVPDILTLAKALGGGVPLGVAVM 267
           RAAR +  E GALL LDE+QTGMGRTG  FA  H G +VPDILTLAK LGGG P+G  V 
Sbjct: 209 RAARALADESGALLWLDEVQTGMGRTGDWFA--HAGHVVPDILTLAKGLGGGYPIGAVVG 266

Query: 268 REEVARSMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAELGPWFMEKLRAIPSP 327
               A  +  G HGTTFGG+P+A AA +A IR +E   L E     G    E L A    
Sbjct: 267 LGRAADLLEPGNHGTTFGGSPVACAAALAVIRTIEEDGLLEHVRRAGERLREGLAA--DA 324

Query: 328 KIREVRGMGLMVGLELKEKAAPYIARLEKEHRVLALQAGPTVIRFLPPLVIEKEDLERVV 387
           ++ EVRG GL++GL+L  + A  +    +    +     P+ IR  PPLV+   D+E  +
Sbjct: 325 RVTEVRGEGLLIGLDLVSETAAAVVEAAQRAGFIVNMPTPSRIRLAPPLVLTDADIESFL 384

Query: 388 EAVRAVL 394
            A   +L
Sbjct: 385 TAWPTIL 391


Lambda     K      H
   0.319    0.137    0.403 

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: 447
Number of extensions: 17
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: 395
Length of database: 396
Length adjustment: 31
Effective length of query: 364
Effective length of database: 365
Effective search space:   132860
Effective search space used:   132860
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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