GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Nostoc punctiforme PCC 73102 ATCC 29133; PCC 73102

Align Succinylornithine transaminase; SOAT; EC 2.6.1.81; Succinylornithine aminotransferase (uncharacterized)
to candidate WP_012410441.1 NPUN_RS20670 glutamate-1-semialdehyde 2,1-aminomutase

Query= curated2:Q3Z295
         (406 letters)



>NCBI__GCF_000020025.1:WP_012410441.1
          Length = 432

 Score =  150 bits (379), Expect = 7e-41
 Identities = 111/297 (37%), Positives = 145/297 (48%), Gaps = 27/297 (9%)

Query: 22  PFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPELREALNEQASKFWHTGNGYTNE 81
           P +  R +G+ +WD  G +YID+ G       GHAHPE+  AL+E   K    G   T E
Sbjct: 40  PIVFDRVKGAYIWDVDGNQYIDYVGTWGPAICGHAHPEVIAALHEALEKGTSFGAPSTLE 99

Query: 82  PVLRLAKKLIDATFA-DRVFFCNSGAEANEAALKLARKFAHDRYGSHKSGIVAFKNAFHG 140
            VL  A+ +IDA  + + V F NSG EA    L+L R F      +++  I+ F+  +HG
Sbjct: 100 NVL--AEMVIDAVPSIEMVRFVNSGTEACMGVLRLMRAF------TNRDKIIKFEGCYHG 151

Query: 141 RT-LFTVSAGGQPAYSQDFAPLPPDIRHAA--------YNDINSASALID---DATCAVI 188
               F V AG   A      P  P +  AA        YND+ S  AL +   D    VI
Sbjct: 152 HADTFLVKAGSGVATLG--LPDSPGVPKAATSTTLTAPYNDLESVKALFEENRDEIAGVI 209

Query: 189 VEPIQGEGGVVPASNAFLQGLRELCDRHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLL 248
           +EP+ G  G +     FL+GLREL   + ALL+FDEV TG  R     A   +GVTPDL 
Sbjct: 210 LEPVVGNAGFIAPDAGFLEGLRELTHEYGALLVFDEVMTGF-RIAYGGAQEKFGVTPDLT 268

Query: 249 TTAKALGGGFPVGALLTTEECASVMTVG---THGTTYGGNPLASAVAGKVLELINTP 302
           T  K +GGG PVGA     +  S++          T  GNPLA     K LEL+  P
Sbjct: 269 TLGKVIGGGLPVGAYGGRRDIMSMVAPAGPVYQAGTLSGNPLAMTAGIKTLELLQKP 325


Lambda     K      H
   0.319    0.136    0.408 

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: 467
Number of extensions: 25
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: 432
Length adjustment: 32
Effective length of query: 374
Effective length of database: 400
Effective search space:   149600
Effective search space used:   149600
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