GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Thermus aquaticus YT-1

Align succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_053767489.1 BVI061214_RS04805 aspartate aminotransferase family protein

Query= BRENDA::O30508
         (406 letters)



>NCBI__GCF_001280255.1:WP_053767489.1
          Length = 396

 Score =  283 bits (725), Expect = 5e-81
 Identities = 159/377 (42%), Positives = 226/377 (59%), Gaps = 15/377 (3%)

Query: 21  YAPAAFIPVRGEGSRVWDQSGRELIDFAGGIAVTSLGHAHPALVKALTEQAQRIWHVSNV 80
           Y     + VRG+G+RVWD  G E ID  GG  V +LGH +P +V+A+  QA+ +  +   
Sbjct: 24  YTKHDLLIVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMVMPQT 83

Query: 81  FTNEPALRLARKLVDATFAE--RVFLANSGAEANEAAFKLARRYANDVYGPQKYEIIAAS 138
                     R LV     E  RVF  NSG EANEAA K AR +     G +K+  +AA 
Sbjct: 84  LPTPARGEFYRTLVSLLPPELNRVFPVNSGTEANEAALKFARAHT----GRKKF--VAAM 137

Query: 139 NSFHGRTLFTVNVGGQPKYSDGFGPKFEGITHVPYNDLEALKAAISDKTCAVVLEPIQGE 198
             F GRT+ +++V  +PKY + F P    +  +PYND+EAL+ A+ ++T AV+LEP+QGE
Sbjct: 138 RGFSGRTMGSLSVTWEPKYREPFLPLVGPVEFIPYNDVEALRRAVDEETAAVILEPVQGE 197

Query: 199 GGVLPAQQAYLEGARKLCDEHNALLVFDEVQSGMGRVGELFAYMHYGVVPDILSSAKSLG 258
           GGV PA+  +L+ AR++  E  ALL+ DE+Q+GMGR G  FA+ HYGVVPDIL+ AK+LG
Sbjct: 198 GGVRPAKPEFLQAAREITREKGALLILDEIQTGMGRTGRRFAFEHYGVVPDILTLAKALG 257

Query: 259 GGFPIGAMLTTGEIAKHLSVGTHGTTYGGNPLASAVAEAALDVINTPEVLDGVKAKHERF 318
           GG PIGA++   E+A+ +  G HGTT+GGNPLA A   AA+  +    + +        F
Sbjct: 258 GGVPIGAVVMRKEVAESMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAELGPWF 317

Query: 319 KSRLQKIGQEYGIFDEIRGMGLLIGAALTDEWKGKARDVLNAAEKE-AVMVLQASPDVVR 377
             +L++I        E+RG+GL++G     E K K+   +   EKE  ++ LQA P V+R
Sbjct: 318 MEKLREIPSPK--IREVRGLGLMVGL----ELKEKSAPYIQKLEKEHRILTLQAGPTVIR 371

Query: 378 FAPSLVIDDAEIDEGLE 394
           F P LVID  +++  +E
Sbjct: 372 FLPPLVIDREDLERVVE 388


Lambda     K      H
   0.318    0.135    0.394 

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: 441
Number of extensions: 21
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: 406
Length of database: 396
Length adjustment: 31
Effective length of query: 375
Effective length of database: 365
Effective search space:   136875
Effective search space used:   136875
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 (21.7 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