GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Nostoc punctiforme ATCC 29133; PCC 73102

Align Probable aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.78; Transaminase A (uncharacterized)
to candidate WP_336884956.1 NPUN_RS00030 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= curated2:O33822
         (383 letters)



>NCBI__GCF_000020025.1:WP_336884956.1
          Length = 314

 Score =  168 bits (426), Expect = 2e-46
 Identities = 110/312 (35%), Positives = 169/312 (54%), Gaps = 15/312 (4%)

Query: 77  VAEKFRRENGLEVTPEETI-VTVGGKQALFNLFQAILDPGDEVIVLAPYWVSYPEMVRFA 135
           +A K R   GL++ PE  I VT G  +A+ ++  A +DPGDEVIV  PY+ +Y      A
Sbjct: 1   MASKVRWYLGLDIDPETQITVTCGSTEAMASVMLATVDPGDEVIVFEPYYENYGPDAILA 60

Query: 136 GGVPVEVPTLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGVVYPEEVLRALAEMALQ 195
           G  P  V TL    +  D  ++ +A    TKA+++N+P+NPTG V+  E L  +AE+  +
Sbjct: 61  GATPRYV-TLHPPHWTFDEAQLHQAFNANTKAIIINTPHNPTGKVFTREELTLIAELCQK 119

Query: 196 HDFYLVSDEIYEHLIYEGA-HFSPGTL--APEHTITVNGAAKAFAMTGWRIGYACGPKAV 252
            D    +DEIYEH++Y+G  H +  TL    E TIT+NG +K +++TGWR+GY     A+
Sbjct: 120 WDVLAFTDEIYEHILYDGTQHIALATLPGMEERTITINGLSKTYSVTGWRVGYILANPAL 179

Query: 253 IKAMADVSSQSTTSPDTIAQWATLEALTNREASMAFIAMAREAYRKRRDLLLEGLSRIGL 312
             A+  V    T       Q A + A+   +   ++     + Y ++RD +L+ L  +G+
Sbjct: 180 TGAIRKVHDFLTVGAPAPLQRAGVTAM---QLPPSYYEELGKLYHQKRDSILQILDGVGI 236

Query: 313 EAVRPSGAFYVLMDTSPFA-PNEVEAAERLLM-AGVAVVPGTEFAA---FGH--VRLSYA 365
               P GA+YVL D S F    ++E    L+   GVAVVPG+ F +    GH  +R  ++
Sbjct: 237 PYFLPQGAYYVLADISKFGYKTDIEFTYHLIKNIGVAVVPGSSFFSQPEKGHSLIRFCFS 296

Query: 366 TGEENLKKALER 377
              E L+ A +R
Sbjct: 297 KTPETLQAASDR 308


Lambda     K      H
   0.317    0.133    0.382 

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: 315
Number of extensions: 14
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: 383
Length of database: 314
Length adjustment: 29
Effective length of query: 354
Effective length of database: 285
Effective search space:   100890
Effective search space used:   100890
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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