GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Desulfotalea psychrophila LSv54

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_011187683.1 DP_RS02180 acetylornithine transaminase

Query= reanno::WCS417:GFF4238
         (406 letters)



>NCBI__GCF_000025945.1:WP_011187683.1
          Length = 397

 Score =  322 bits (825), Expect = 1e-92
 Identities = 176/374 (47%), Positives = 239/374 (63%), Gaps = 9/374 (2%)

Query: 14  DQVMVPNYA--PAAFIPVRGEGSRVWDQAGRELIDFAGGIAVNVLGHAHPALVGALTEQA 71
           D+V+V NY   P AF    G G  + D  G++ +DF  GIAV  LGH HP +V A+ EQ+
Sbjct: 11  DKVLVGNYGRYPVAF--TEGTGCVLTDANGKKYVDFLAGIAVCSLGHCHPRIVNAIREQS 68

Query: 72  HKLWHVSNVFTNEPALRLAHKLIDATFAERVFFCNSGAEANEAAFKLARRVAFDRFGSEK 131
            +L HVSN++  E   RLA  L++ +F ++VFFCNSGAEANEAA KLAR  A     + K
Sbjct: 69  ERLIHVSNLYYTEAQTRLAELLVENSFGDKVFFCNSGAEANEAAIKLARIHA----PAGK 124

Query: 132 YEIIAALNSFHGRTLFTVNVGGQSKYSDGFGPKITGITHVPYNDLDALKAAVSDKTCAVV 191
            +II+   +FHGRT+ T+   GQ+++  GF P  TG    P+ DLDAL+A + D  CAV+
Sbjct: 125 NKIISLTGAFHGRTMVTLAATGQARFCAGFEPIPTGFAAAPFADLDALEAMIDDTVCAVL 184

Query: 192 LEPIQGEGGVLPAELAYLQGARDLCDANNALLVFDEVQTGMGRSGHLFAYQHYGVTPDIL 251
            EP+QGEGGV P    YLQG RD+CD +  LL+FDEVQTG+GRSG LFA+Q +GV PDI+
Sbjct: 185 CEPLQGEGGVRPLGREYLQGIRDICDRHGVLLIFDEVQTGVGRSGSLFAHQVFGVEPDIM 244

Query: 252 TSAKSLGGGFPIAAMLTTEALAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLAGV 311
           T AK L  G PI A++T +A+A  LV G+HG+T+GGNP+ CA A   ++VI     LA V
Sbjct: 245 TLAKGLASGMPIGAIITRDAVAASLVPGSHGSTFGGNPVVCAAASTNLEVILEDGFLAEV 304

Query: 312 NAKHDLFKARLEQIGKQY-GIFTEVRGMGLLLGCVLSDAFKGKAKDVFNAAEKENLMILQ 370
            +  +     L ++ K++  IFTE RG+GLL G V+++  K     +     ++  +I  
Sbjct: 305 KSVAEHLAQSLGKLVKEFPAIFTEERGLGLLRGLVMTEEGKKSGSKIVMEMLEKGFLINF 364

Query: 371 AGPDVVRFAPSLVV 384
           AG   +RFAP LVV
Sbjct: 365 AGGVALRFAPPLVV 378


Lambda     K      H
   0.320    0.137    0.400 

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: 433
Number of extensions: 20
Number of successful extensions: 3
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: 397
Length adjustment: 31
Effective length of query: 375
Effective length of database: 366
Effective search space:   137250
Effective search space used:   137250
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