GapMind for Amino acid biosynthesis

 

Alignments for a candidate for OAT in Stenotrophomonas chelatiphaga DSM 21508

Align Ornithine aminotransferase; Orn-AT; Lysine aminotransferase; Lys-AT; EC 2.6.1.13; EC 2.6.1.36 (characterized)
to candidate WP_057509163.1 ABB28_RS13760 glutamate-1-semialdehyde-2,1-aminomutase

Query= SwissProt::Q5JEW1
         (445 letters)



>NCBI__GCF_001431535.1:WP_057509163.1
          Length = 426

 Score =  134 bits (338), Expect = 4e-36
 Identities = 99/315 (31%), Positives = 147/315 (46%), Gaps = 29/315 (9%)

Query: 37  PIVIERGEGIRVYDVDGNVFYDFASGVGVINVGHSHPRVVEAIKKQAEKFTHYSLTDFFY 96
           P  +ER +G  ++DVDGN + D+    G + VGH+HP V +A+KK A+    +       
Sbjct: 35  PFFVERADGAYLHDVDGNRYIDYVGSWGPMIVGHNHPAVRQAVKKAADSGLSFGAP---C 91

Query: 97  ENAIILAEKLIELAPG-DIERKVVYGNSGAEANEAAMKLVKYGTGRKQFLAFYHAFHGRT 155
              + +AE L  L P  ++ R V   NSG EA  +A++L +  TGR + + F   +HG  
Sbjct: 92  AAEVTMAETLTRLVPSCEMVRMV---NSGTEATLSAIRLARGATGRSRIVKFEGCYHGHG 148

Query: 156 QAVLSLTASKWVQQDGFFPTMPGVTHIPYPNPYRNTWGIDGYEEPDELTNRVLDFIEEYV 215
            + L    S  +      PT PGV                G  E   LT    DF     
Sbjct: 149 DSFLVKAGSGMLTLG--VPTSPGVP--------------AGLSEL-TLTLPYNDFDAATA 191

Query: 216 FRHVPPHEIGAIFFEPIQGEGGYVVPPKGFFKALKKFADEYGILLADDEVQMGIGRTGKF 275
                  +I  +  EP+ G    + P +G+ + L+     +G +L  DEV  G  R    
Sbjct: 192 LFEAQGEQIAGLIIEPVVGNANCIPPREGYLQHLRALCTRFGTVLIFDEVMTGF-RVALG 250

Query: 276 WAIEHFGVEPDLIQFGKAIGGGLPLAGVIHRAD----ITFDKPGRHATTFGGNPVAIAAG 331
            A  H+GV PDL  FGK IGGG+P+     + +    I+   P   A T  GNPVA+AAG
Sbjct: 251 GAQAHYGVTPDLTTFGKIIGGGMPVGAYGGKRELMQQISPAGPIYQAGTLSGNPVAMAAG 310

Query: 332 IEVVEIVKELLPHVQ 346
           + ++E+V++   H Q
Sbjct: 311 LAMLELVQQPGFHAQ 325


Lambda     K      H
   0.320    0.141    0.418 

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: 455
Number of extensions: 31
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: 445
Length of database: 426
Length adjustment: 32
Effective length of query: 413
Effective length of database: 394
Effective search space:   162722
Effective search space used:   162722
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: 51 (24.3 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