GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Alkalihalobacterium alkalinitrilicum DSM 22532

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_078430315.1 BK574_RS23575 acetylornithine transaminase

Query= reanno::Koxy:BWI76_RS11670
         (406 letters)



>NCBI__GCF_002019605.1:WP_078430315.1
          Length = 376

 Score =  303 bits (775), Expect = 7e-87
 Identities = 159/373 (42%), Positives = 222/373 (59%), Gaps = 11/373 (2%)

Query: 14  MMPVYAPAAFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPRLVKALTEQAGKFWH 73
           + P YA       + +G+ L D   KEY+DF  GI V  LGH HP + + + EQ  + WH
Sbjct: 4   IFPTYARWDVTVQKADGAILVDTNDKEYLDFTSGIGVCNLGHNHPTVKEKVIEQLDQVWH 63

Query: 74  TGNGYTNEPVLRLAKQLIDATFADRVFFCNSGAEANEAALKLARKYAHDRFGSEKSGIVA 133
             N +      + A  L + T  D VFFCNSGAE NE A+KLARKY      + K  I++
Sbjct: 64  VSNLFHIPTQEQAAMMLTEHTCGDYVFFCNSGAEGNEGAIKLARKY------TGKWKIIS 117

Query: 134 FKNAFHGRTLFTVSAGGQPAYSQDFAPLPPQIQHAIYNDLDSAKALIDDNTCAVIVEPMQ 193
           FK +FHGRT  ++SA GQ    + + PL P  ++A +ND+DS K+L+DD   AV++E +Q
Sbjct: 118 FKQSFHGRTFGSMSATGQDKIHEGYGPLLPSFEYATFNDIDSVKSLVDDQVAAVMIEVIQ 177

Query: 194 GEGGVVPADADFLRGLRELCDAHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLSTAKA 253
           GEGGV PAD  F+  L +LC  +  LLI DEVQTG+GRTG+ +AY HY ++PD++ +AK 
Sbjct: 178 GEGGVHPADPVFMEALEQLCQENGILLIVDEVQTGIGRTGKAFAYEHYNISPDIIVSAKG 237

Query: 254 LGGGFPIGALLASERCASVMTVGTHGTTYGGNPLACAVAGEVFATINTREVLNGVKQRHQ 313
           LG GFPIGA++  E+       G+HG+TYGGNPLA A A  V + +   E L  V++   
Sbjct: 238 LGNGFPIGAVIGKEKLKEAFGPGSHGSTYGGNPLATAAASAVMSEVFRPEFLKQVEENGH 297

Query: 314 WFCERLNAINARYGLFKEIRGLGLLIGCVLKDEYAGKAKAISNQAAEEGLMILIAGANVV 373
           +F + L          KEI+G GL+IG     E  G+   +  Q  EEG + L AG NV+
Sbjct: 298 YFMKLLTE-KLTSSFVKEIKGKGLMIGI----ECTGEVGPLLTQMREEGFLALSAGPNVI 352

Query: 374 RFAPALIISEDEV 386
           R  P L +++D++
Sbjct: 353 RLLPPLTVTKDQL 365


Lambda     K      H
   0.321    0.137    0.412 

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: 383
Number of extensions: 22
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: 406
Length of database: 376
Length adjustment: 31
Effective length of query: 375
Effective length of database: 345
Effective search space:   129375
Effective search space used:   129375
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 (21.8 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