GapMind for Amino acid biosynthesis

 

Alignments for a candidate for OAT in Desulfotalea psychrophila LSv54

Align Ornithine aminotransferase, mitochondrial; Ornithine delta-aminotransferase; Ornithine--oxo-acid aminotransferase; EC 2.6.1.13 (characterized)
to candidate WP_011188057.1 DP_RS04140 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::P04181
         (439 letters)



>NCBI__GCF_000025945.1:WP_011188057.1
          Length = 430

 Score =  132 bits (333), Expect = 2e-35
 Identities = 99/315 (31%), Positives = 158/315 (50%), Gaps = 11/315 (3%)

Query: 59  PVALERGKGIYLWDVEGRKYFDFLSSYSAVNQGHCHPKIVNALKSQVDKLTLTSRAFYNN 118
           P+ +ER +G Y++D +G+KY DF++S+  +  GH HP I+ A++      T +  A  ++
Sbjct: 35  PLFIERAEGSYIYDADGQKYLDFVNSWGPMIMGHAHPDIIKAIQDAAVYGT-SYGAPTSS 93

Query: 119 VLGEYEEYITKLFNYHKVLPMNTGVEAGETACKLARKWGYTVKG-IQKYKAKIVFAAGNF 177
            +      +  + +  KV  +++G EA  +A +LAR  GYT K  I K+       A +F
Sbjct: 94  EVDLASMVVEAVPSIEKVRFVSSGTEATMSAVRLAR--GYTGKNVIVKFDGCYHGHADSF 151

Query: 178 WGRTLSAISSSTDPTSYDGFGPFMPGFDIIPYNDLPALERALQDP--NVAAFMVEPIQGE 235
             +  S + +   P S       +     IPYN + ALE  L+D   N+A  +VEP+ G 
Sbjct: 152 LVKAGSGVLTLGIPGSPGVPEDIVKNTISIPYNSVEALETTLRDADLNIACVIVEPVAGN 211

Query: 236 AGVVVPDPGYLMGVRELCTRHQVLFIADEIQTGLARTGRWLAVDYENVRPDIVLLGKALS 295
            G V P PG+L  +RE+     ++ I DE+ TG  R     A  Y  V PD+  LGK + 
Sbjct: 212 MGCVPPAPGFLQKLREITAEEGIVLIFDEVITGF-RLSYGGAQQYYGVTPDLTCLGKIIG 270

Query: 296 GGLYPVSAVLCDDDIMLTIKPG---EHGSTYGGNPLGCRVAIAALEVLEEENLAENADKL 352
           GGL PV A     DIM ++ P        T  GNPL      AAL++L+++   E+ ++ 
Sbjct: 271 GGL-PVGAYGGKADIMNSVAPDGPVYQAGTLSGNPLAMAAGKAALKLLQQDGFYEDLNQK 329

Query: 353 GIILRNELMKLPSDV 367
                + L+++   V
Sbjct: 330 SAAYADGLLEVAGRV 344


Lambda     K      H
   0.319    0.138    0.415 

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: 455
Number of extensions: 28
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: 439
Length of database: 430
Length adjustment: 32
Effective length of query: 407
Effective length of database: 398
Effective search space:   161986
Effective search space used:   161986
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: 51 (24.3 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