GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Trichormus variabilis ATCC 29413

Align Alanine--glyoxylate aminotransferase; EC 2.6.1.44 (characterized)
to candidate WP_011321708.1 AVA_RS25680 alanine--glyoxylate aminotransferase family protein

Query= SwissProt::Q3LSM4
         (393 letters)



>NCBI__GCF_000204075.1:WP_011321708.1
          Length = 381

 Score =  339 bits (870), Expect = 7e-98
 Identities = 169/368 (45%), Positives = 241/368 (65%), Gaps = 3/368 (0%)

Query: 13  EPLVTPNKLLMGPGPSNAPQRVLDAMSRPILGHLHPETLKIMDDIKEGVRYLFQTNNIAT 72
           EPL  P++LL+GPGPSNA   VL AM+   +GHL P  L +MD+I+  +RY++QT N  T
Sbjct: 16  EPLEVPSRLLLGPGPSNAHPAVLQAMNVSPVGHLDPAFLALMDEIQSLLRYVWQTENPLT 75

Query: 73  FCLSASGHGGMEATLCNLLEDGDVILIGHTGHWGDRSADMATRYGADVRVVKSKVGQSLS 132
             +S +G   MEAT+ N +E GDV+LIG  G++G+R  DMA RYGADVR +    GQ  S
Sbjct: 76  IAVSGTGTAAMEATIANAVEPGDVVLIGVAGYFGNRLVDMAGRYGADVRTISKPWGQVFS 135

Query: 133 LDEIRDALLIHKPSVLFLTQGDSSTGVLQGLEGVGALCHQHNCLLIVDTVASLGGAPMFM 192
           L+E+R AL  ++P++L L   ++STG  Q LEGVG LC +   LL+VDTV SLGG P+F+
Sbjct: 136 LEELRTALENNRPAILALVHAETSTGARQPLEGVGELCREFGTLLLVDTVTSLGGVPIFL 195

Query: 193 DRWEIDAMYTGSQKVLGAPPGITPVSFSHRAVERYKRRNTKVKVYYWDMSLVGDYWGCFG 252
           D W +D  Y+ SQK LG  PG +P + S RA+E+ +RR TKV  +Y DM+L+G YW   G
Sbjct: 196 DGWGVDLAYSCSQKGLGCSPGASPFTMSSRAIEKLQRRRTKVANWYLDMNLLGKYW---G 252

Query: 253 RPRIYHHTISSTLLYGLREAIAMACEEGLPALIARHEDCAKRLYRGLQDAGFELYADPKD 312
             R+YHHT    L Y LREA+ +  +EGL     RH+   + L+  L+D G  L+ + + 
Sbjct: 253 SERVYHHTAPINLYYALREALRLIAQEGLANCWQRHQKNVEYLWERLEDIGLSLHVEKEY 312

Query: 313 RLSTVTTIKVPQGVDWLKAAQYAMKTYLVEISGGLGPTAGQVFRIGLMGQNATTERVDRV 372
           RL T+TT+++P GVD    A+  +  + +E+ GGLG  AG+V+R+GLMG N+  E VD++
Sbjct: 313 RLPTLTTVRIPDGVDGKAVARQLLNEHNIEVGGGLGELAGKVWRVGLMGFNSRKESVDQL 372

Query: 373 LQVFQEAV 380
           +   ++ +
Sbjct: 373 IPALEQVL 380


Lambda     K      H
   0.321    0.137    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: 385
Number of extensions: 20
Number of successful extensions: 2
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: 393
Length of database: 381
Length adjustment: 30
Effective length of query: 363
Effective length of database: 351
Effective search space:   127413
Effective search space used:   127413
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 Apr 09 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