GapMind for Amino acid biosynthesis

 

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

Align Fructose-1,6-bisphosphate aldolase/phosphatase; FBP A/P; FBP aldolase/phosphatase; EC 3.1.3.11; EC 4.1.2.13 (uncharacterized)
to candidate WP_053768266.1 BVI061214_RS10025 fructose-1,6-bisphosphate aldolase/phosphatase

Query= curated2:Q72K02
         (363 letters)



>NCBI__GCF_001280255.1:WP_053768266.1
          Length = 363

 Score =  653 bits (1685), Expect = 0.0
 Identities = 325/363 (89%), Positives = 341/363 (93%)

Query: 1   MKVTLSVLKADIGSVGGHTLPSRKVLAKVEEVVREEVGRLLLDAYVFHIGDDIVLLLSHT 60
           M++TLSVLKADIGSVGGHTLPS  VLA V+EVV E  G LLLDAYVFHIGDDIVLLLSHT
Sbjct: 1   MRITLSVLKADIGSVGGHTLPSPAVLAAVKEVVEEAKGSLLLDAYVFHIGDDIVLLLSHT 60

Query: 61  RGVRNQEVHALAWKAFREGTEVARAEGLYGAGQDLLKDAFTGNLHGLGPQVAEMEFTERP 120
           +GV +  +H LAWKAFREGTEVA+ EGLYGAGQDLLKDAFTGNLHGLGPQVAEMEF ERP
Sbjct: 61  QGVAHPAIHELAWKAFREGTEVAKREGLYGAGQDLLKDAFTGNLHGLGPQVAEMEFAERP 120

Query: 121 AEPFMVLAADKTEPGAFNLPLYLAFADPMYSSGLLLSPELRPGFRFRIMDLAQTERDSYI 180
           +EPFMVLAADKTEPGAFNLPLYLAFADPMYSSGLLLSPELRPGFRFRIMDLAQTERDSYI
Sbjct: 121 SEPFMVLAADKTEPGAFNLPLYLAFADPMYSSGLLLSPELRPGFRFRIMDLAQTERDSYI 180

Query: 181 ELDAPERLYDIATLLRDSHRFAIESIWSRKHGEQAAVVSTTRLRNIAGRYVGKDDPVAIV 240
           ELDAPERLYDIA LLRDSHRFAI SIW RK+GE AAVVSTTRLRNIAGRYVGKDDPVA+V
Sbjct: 181 ELDAPERLYDIAALLRDSHRFAIASIWLRKYGEVAAVVSTTRLRNIAGRYVGKDDPVALV 240

Query: 241 RTQKIFPATEEFGPVFALAPYVAGDTRGSHHMPLMPVRANTPASTFFCVPMVCGLAFSLR 300
           RTQKIFPATEEFGP FALAP+VAGDTRGSHH+PLMPV+ANTPASTFFCVPMVC L FSL+
Sbjct: 241 RTQKIFPATEEFGPPFALAPFVAGDTRGSHHLPLMPVKANTPASTFFCVPMVCALGFSLK 300

Query: 301 EGRLSEPVDLFADPVWEAVRAKVVEKAQEMRRQGFYGPAMLPMEELEYTGIAERLKALER 360
           EGRL+ PVDLFADPVW+AVRAKVVEKAQEMRRQGFYGPAMLPMEELEYTGIAERLK LER
Sbjct: 301 EGRLTGPVDLFADPVWDAVRAKVVEKAQEMRRQGFYGPAMLPMEELEYTGIAERLKELER 360

Query: 361 EFS 363
           EFS
Sbjct: 361 EFS 363


Lambda     K      H
   0.321    0.138    0.405 

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: 575
Number of extensions: 15
Number of successful extensions: 1
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: 363
Length of database: 363
Length adjustment: 29
Effective length of query: 334
Effective length of database: 334
Effective search space:   111556
Effective search space used:   111556
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: 49 (23.5 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