GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Thermus aquaticus YT-1

Align Alanine--glyoxylate aminotransferase; EC 2.6.1.44 (characterized)
to candidate WP_053767477.1 BVI061214_RS04695 aminotransferase class V-fold PLP-dependent enzyme

Query= SwissProt::Q3LSM4
         (393 letters)



>NCBI__GCF_001280255.1:WP_053767477.1
          Length = 353

 Score =  196 bits (497), Expect = 1e-54
 Identities = 133/365 (36%), Positives = 192/365 (52%), Gaps = 19/365 (5%)

Query: 21  LLMGPGPSNAPQRVLDAMSRPILGHLHPETLKIMDDIKEGVRYLFQTNNIATFC-LSASG 79
           LL+ PGP+  P+RV  A+ RP+ GHL PE L +   I+E +R LF     A    L+ SG
Sbjct: 2   LLLTPGPTPIPERVQRALLRPMRGHLDPEVLAVNRAIQERLRVLFDPGEGALVAALAGSG 61

Query: 80  HGGMEATLCNLLEDGDVILIGHTGHWGDRSADMATRYGADVRVVKSKVGQSLSLDEIRDA 139
             GMEA L NL  D   +L+   G +  R A+MA  +G +  V++   G+++  + ++ A
Sbjct: 62  SLGMEAGLANL--DRGPVLVLVNGAFSQRVAEMAHLHGLEPTVLEFPPGEAVDPEAVKKA 119

Query: 140 LLIHKPSVLFLTQGDSSTGVLQGLEGVGALCHQHNCLLIVDTVASLGGAPMFMDRWEIDA 199
           L   +  ++ L  G++STGVL     +GAL  +   L  +D V +LG  P  M    +D 
Sbjct: 120 LARRRYRMVALVHGETSTGVLNPAPAIGALAKEAGALFFLDAVTTLGMLPFSMRAMGVDY 179

Query: 200 MYTGSQKVLGAPPGITPVSFSHRAVERYKRRNTKVKVYYWDMSLVGDYWGCFGRPRIYHH 259
            +TGSQK L APPG+ P++ S   +  +  R    + +Y D++ V ++W   G    YHH
Sbjct: 180 AFTGSQKCLSAPPGLAPIAVSQEGLRAFTGR----RGWYLDLARVAEHWERGG----YHH 231

Query: 260 TISSTLLYGLREAIAMACEEGLPALIARHEDCAKRLYRGLQDAGFELYADPKDR-LSTVT 318
           T    L Y L EA+ +A EEG+ A   R E     L   L   GF  Y  PK+  L TV 
Sbjct: 232 TTPVLLHYALLEALDLALEEGIEARKKRAEALYAWLLEELGLRGFRPY--PKESPLPTVL 289

Query: 319 TIKVPQGV--DWLKAAQYAMKTYLVEISGGLGPTAGQVFRIGLMGQNATTERVDRVLQVF 376
            ++ P+GV  D L  A YA     V ++GG+GPT GQV R+GLMG+ A  E     L+  
Sbjct: 290 VVRPPEGVEADRLVRALYAEG---VAVAGGIGPTRGQVLRLGLMGEGARREAYGVFLEAL 346

Query: 377 QEAVA 381
              +A
Sbjct: 347 DRVLA 351


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: 371
Number of extensions: 25
Number of successful extensions: 4
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: 353
Length adjustment: 30
Effective length of query: 363
Effective length of database: 323
Effective search space:   117249
Effective search space used:   117249
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