GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatA in Nocardiopsis lucentensis DSM 44048

Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_017600915.1 D471_RS0123665 amidase

Query= curated2:B8HY89
         (482 letters)



>NCBI__GCF_000341125.1:WP_017600915.1
          Length = 307

 Score = 89.4 bits (220), Expect = 2e-22
 Identities = 102/330 (30%), Positives = 135/330 (40%), Gaps = 43/330 (13%)

Query: 166 ALGSDTGGSIRQPASFCGVVGLKPTYGLVSRYGLVAYASSLDQIGPFATNVEDAALLLGA 225
           A GSD GGS+R PAS CG+ GLKPT G +S   L      L   GP    V DAALLL A
Sbjct: 2   AHGSDGGGSLRIPASACGLFGLKPTRGRISGGPLKPDLVGLSTAGPLTHTVLDAALLLDA 61

Query: 226 IAGHDPQDSTSLNVPIPDYTQFLIPDLKGK---KIGIIQE--TYGEGLDPQVEQVTHKAI 280
           +AG    D      P+P    F     +     ++G   +  +    + P V      A 
Sbjct: 62  MAGARSGDLYGA-PPLPPGETFADHARRAPGRLRVGRYADAGSVDAPVHPHVRAAYDAAS 120

Query: 281 QQLEELGAEVREISCP---RFRYGLP-TYYIIAPSEASANLARYDGVKYGFRSPDPENLL 336
             L ELG EV EI  P    F    P  + ++  + ASA+             PD E+ L
Sbjct: 121 DLLVELGHEVEEIPTPGDAHFGGTFPEDFGVLWAAMASASPV----------DPDREHDL 170

Query: 337 SMYTRTRAEGFGPEVKRRIMIGTYALSAGYYDAYYLKAQK-VRTLIKQDFEAAFEQVDVL 395
              TR   E               A     Y A   + Q+ VR+LI      A E  DVL
Sbjct: 171 RPITRWLRE------------RARATPVPDYIAACARLQRGVRSLI-----TATEPYDVL 213

Query: 396 VCPT-----APTTAFAAGAKTADPLSMYLSDLMTIPVNLAGLPGLSLPCGFDQQGLPIGL 450
           + PT      P   F  G    +   M      T   N++G P +S+P  +   GLPIG+
Sbjct: 214 LSPTLALPPVPIGHFDQGGPEEEFRRMTEFTPFTSVYNVSGQPSVSVPLHWSPDGLPIGV 273

Query: 451 QLIGNVLREDLVFQVAYAYEQATPWHDRHP 480
            L G +  E  +  ++   E+A PW  R P
Sbjct: 274 MLTGRMGGEGTLLSLSAQMEEARPWAHRVP 303


Lambda     K      H
   0.317    0.134    0.388 

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: 365
Number of extensions: 21
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 482
Length of database: 307
Length adjustment: 30
Effective length of query: 452
Effective length of database: 277
Effective search space:   125204
Effective search space used:   125204
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 (21.6 bits)
S2: 50 (23.9 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