GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Bacillus alkalinitrilicus DSM 22532

Align Probable aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.78; Transaminase A (uncharacterized)
to candidate WP_078430887.1 BK574_RS15655 aminotransferase class V-fold PLP-dependent enzyme

Query= curated2:O67781
         (394 letters)



>NCBI__GCF_002019605.1:WP_078430887.1
          Length = 380

 Score =  275 bits (704), Expect = 1e-78
 Identities = 153/358 (42%), Positives = 216/358 (60%), Gaps = 9/358 (2%)

Query: 33  DVIGFGAGEPDFDTPDFIKEACIRALREGKTKYAPSAGIPELREAIAEKLLKENKVEYKP 92
           DVI    G PDF TP+ I  A ++A  EG   Y+ +AGI  LR+AIA K  ++N + Y P
Sbjct: 18  DVIDLTIGAPDFTTPENIVNANVKASLEGHHYYSSNAGIMSLRKAIAAKFERDNGISYDP 77

Query: 93  -SEIVVSAGAKMVLFLIFMAILDEGDEVLLPSPYWVTYPEQIRFFGGVPVEVPLKKEKGF 151
            +EI V+ GA   L L+ M +L+ GDEV+L  P W  Y  QI   GGVPV VP  +E GF
Sbjct: 78  ETEIDVTIGATEALGLLMMTLLNPGDEVILADPTWPNYITQILMAGGVPVRVPTYEEDGF 137

Query: 152 QLSLEDVKEKVTERTKAIVINSPNNPTGAVYEEEELKKIAEFCVERGIFIISDECYEYFV 211
            L +E V+  +TE+T+AI+IN+PNNPTGA+ E++ +++  E   +  +++ISDE YE  +
Sbjct: 138 SLQVEAVEAAITEKTRAILINTPNNPTGALLEKKSVQEFVELAKKHEVYLISDEVYEKII 197

Query: 212 YGDAKFVSPASFSDEVKNITFTVNAFSKSYSMTGWRIGYVACPEEYAKVIASLNSQSVSN 271
           Y + +  SPAS     K +  TVN+FSKSY+M GWR+GYVA  E     +  L     S 
Sbjct: 198 YDENEHFSPASLPG-AKEVVITVNSFSKSYAMCGWRVGYVAASENVIAPLLKLQEGMASC 256

Query: 272 VTTFAQYGALEALKNPKSKDFVNEMRNAFERRRDTAVEELSKIPGMDVVKPEGAFYIFPD 331
             T AQ  A+ AL+ P  +D V+EM   ++ RRD  VE L+KIPG+ V+KP GAFY+F +
Sbjct: 257 ANTMAQMAAVAALEGP--QDAVDEMVKRYKERRDLMVEGLNKIPGISVIKPGGAFYLFVN 314

Query: 332 FSAYAEKLGGDVKLSEFLLEKAKVAVVPGSAFG--APGFLRLSYALSEERLVEGIRRI 387
                +      + +  LL++  V  VPGS FG    G++R+ YA S+E L + + RI
Sbjct: 315 IKELGK---SSQEFATELLKQTGVMTVPGSGFGEAGEGYIRICYAKSDELLQQALERI 369


Lambda     K      H
   0.317    0.135    0.383 

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: 372
Number of extensions: 21
Number of successful extensions: 6
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: 394
Length of database: 380
Length adjustment: 30
Effective length of query: 364
Effective length of database: 350
Effective search space:   127400
Effective search space used:   127400
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