GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Methanobacterium lacus AL-21

Align alanine—glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate WP_013644315.1 METBO_RS03630 pyridoxal phosphate-dependent aminotransferase

Query= metacyc::MONOMER-21143
         (387 letters)



>NCBI__GCF_000191585.1:WP_013644315.1
          Length = 372

 Score =  223 bits (569), Expect = 5e-63
 Identities = 124/366 (33%), Positives = 209/366 (57%), Gaps = 12/366 (3%)

Query: 19  LAEAKKL-EAQGKPMIHLGLGQPDFKTPQHVVDAAKKALDEGHHGYVLSNGILECRQAVT 77
           L+E +++ E  G+  I LGLG+PDFKTPQ+++DAA +A++EG   Y  + GI+E R+A+ 
Sbjct: 16  LSEIRRMFEIAGENAISLGLGEPDFKTPQNIIDAATQAMNEGFTHYTSNMGIIELREAIA 75

Query: 78  RKIKKLYNKDIDPERVLIMPGGKPTMYYAIQCFGEPGAEIIHPTPAFPIYESMINYTGST 137
            K++K        + V++  G    +Y  +Q    PG E++ P P F  Y +        
Sbjct: 76  DKLEKENGISSSADSVIVTVGASEAVYVCMQALINPGDEVLIPDPGFLSYSACAKLADGV 135

Query: 138 PVPYDLTEDKDLKFDPEKILSLITDKTRLLILINPNNPTGSFVEKSAIDVLAEGLKKHPH 197
           PV   + E+ DL+   + +L  IT KT+ +IL +P+NP GS ++K  +  +AE +     
Sbjct: 136 PVGIKIKEENDLRMTCDDVLESITPKTKAIILNSPSNPIGSVMKKKDVKGIAE-IADDND 194

Query: 198 VAILSDEIYSRQIYDGKEMPTFFNYPDLQDRLIVLDGWSKAYAMTGWRMGWSVWPEELIP 257
           + I+SDE+Y + IYD K     ++     +  I ++ +SK YAMTG+R+G+    + +  
Sbjct: 195 IYIISDEVYEKIIYDSKH----YSAGQFSENAITINAFSKTYAMTGFRIGYISANDSIAE 250

Query: 258 HVNKLIINSVSCVNAPSQFAGIAALDGPDDAIHEMMVKFDQRRKLIHEGLNSLPGVECSL 317
            + K+     +C ++ +Q A + AL+GP +++  M+ +F +RR LI + L+ + G++C +
Sbjct: 251 ELLKVHQYIAACASSMAQKAALEALEGPQNSVKSMVSEFKKRRDLIIKRLSGM-GIDCPV 309

Query: 318 PGGAFYAFPKVIGTGMNGSEFAKKCMHEAGVAIVPGTAFGKTCQDYVRFSYAASQDNISN 377
           P GAFY FPKV       S+  KK     GV +V G AFG+   D+VR SYA + D +  
Sbjct: 310 PEGAFYVFPKVDNPEKFVSDGLKK-----GVVMVNGKAFGEQGSDHVRLSYATAYDKLEE 364

Query: 378 ALENIK 383
           A++ ++
Sbjct: 365 AMDRLE 370


Lambda     K      H
   0.319    0.137    0.414 

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: 343
Number of extensions: 22
Number of successful extensions: 5
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: 387
Length of database: 372
Length adjustment: 30
Effective length of query: 357
Effective length of database: 342
Effective search space:   122094
Effective search space used:   122094
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 (21.7 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