GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Salinicoccus carnicancri Crm

Align alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate WP_017548713.1 C792_RS0106810 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= BRENDA::D2Z0I0
         (402 letters)



>NCBI__GCF_000330705.1:WP_017548713.1
          Length = 384

 Score =  181 bits (459), Expect = 3e-50
 Identities = 113/364 (31%), Positives = 182/364 (50%), Gaps = 12/364 (3%)

Query: 35  IVDLGMGNPDIPPSQHIIDKLCEVANRPNVHGYSASKGIPRLRKAICDFYKRRYGVELDP 94
           +++L +G PD      I   + +    P    Y   +G    + AI   YK+ Y V L  
Sbjct: 29  LLNLAVGIPDGETPDVIKKAVADSVYLPENQRYGVFRGKRSFKDAIIRLYKKHYDVTLH- 87

Query: 95  ERNAIMTIGAKEGYSHLMLAMLEPGDTVIVPNPTYPIHYYAPIICGGDAISVPILPEEDF 154
           E N  +  G K G     +  +EPG+ V +PNP YP +     +  G+   +P+L   DF
Sbjct: 88  EENIALLYGTKSGLVQFPMTFIEPGEGVYLPNPGYPDYMAGVKLARGEIYDLPLLAGNDF 147

Query: 155 PEVFLRRLYDLIKTSFRKPKAVVLSFPHNPTTLCVDLEFFQEVVKLAKQEGIWIVHDFAY 214
               L     L K      + + L++P NP       EFF E V+  +     IVHDFAY
Sbjct: 148 ----LPDFDSLDKDELSNARLIYLNYPSNPLGAVATKEFFDETVERFRGTRTRIVHDFAY 203

Query: 215 ADLGFDGYTPPSILQVEGALDVAVELYSMSKGFSMAGWRVAFVVGNEMLIKNLAHLKSYL 274
           A   FD    PSIL  + +L+  +E+YS+SKGF+M+G+RV F VGN+ +++++   + + 
Sbjct: 204 AAFSFDE-KHPSILSSDPSLECCMEIYSLSKGFNMSGFRVGFAVGNKEMVESINLYQDHT 262

Query: 275 DYGVFTPIQVASIIALESPYEVVEKNREIYRRRRDVLVEGLNRVGWEVKKPKGSMFVWAK 334
             G++  +Q AS+ ALE   E++      +++RRD   + +   G  +   KG +F W  
Sbjct: 263 QTGMWGVLQDASVAALEHEEEILSMQHVKFQKRRDFFEKAVIESGIPLNPLKGGIFGWIA 322

Query: 335 VPEEVGMNSLDFSLFLLREAKVAVSPGIGFGEYGEGYVRFALVENEHRIRQAVRGIKKAL 394
           VP+  G +   F+ FL+RE  + V+PG  FG  G+ Y+R +L  ++      +  + + L
Sbjct: 323 VPK--GYDGESFADFLIREKSILVTPGRPFGSRGKNYIRISLAVDD----AVLDAVIERL 376

Query: 395 DKIK 398
           D IK
Sbjct: 377 DTIK 380


Lambda     K      H
   0.322    0.141    0.425 

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: 431
Number of extensions: 20
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: 402
Length of database: 384
Length adjustment: 31
Effective length of query: 371
Effective length of database: 353
Effective search space:   130963
Effective search space used:   130963
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 26 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