GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysT in Shewanella amazonensis SB2B

Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate 6936140 Sama_0337 isopropylmalate isomerase large subunit (RefSeq)

Query= curated2:Q8PZT3
         (391 letters)



>FitnessBrowser__SB2B:6936140
          Length = 470

 Score =  238 bits (606), Expect = 3e-67
 Identities = 142/359 (39%), Positives = 195/359 (54%), Gaps = 44/359 (12%)

Query: 75  EGICHQVLPENGFALPGKLLVGADSHSCTYGAFGAFATGVGATDMAEIFATGKLWFKVPE 134
           +GI H + PE G  LPG ++V  DSH+ T+GAFGA A G+G +++  + AT  L     +
Sbjct: 105 QGIVHVMGPELGITLPGTVIVCGDSHTATHGAFGALAFGIGTSEVEHVLATQTLRQLKAK 164

Query: 135 SFRMTVEGSLDKHVYAKDLTLYLIGKTGIAGATYKAVEFYGQAISELSVAGRMTLCNMAI 194
           + ++ V G +   + AKD+ L +IGK G+ G T   VEF G+AI +LS+ GRMTLCNMAI
Sbjct: 165 TMKIEVRGKVADGITAKDIVLAIIGKIGMDGGTGYVVEFCGEAIRDLSMEGRMTLCNMAI 224

Query: 195 EMGAKTGIVPPDEKTFDFLKNRAVAP-----------YEPVYSDPDASYLKEFVYDAGDI 243
           EMGAK G+V PDE TF +L+ R  AP           +  +++D DA +  E V +A  I
Sbjct: 225 EMGAKAGMVAPDETTFAYLEGREFAPKGDAWQQALADWRELHTDADAVFDAEVVLEAAAI 284

Query: 244 EPQV--------------ACPHQVDNVKPVGEVE------------GT-----HVDQVFI 272
            PQ+                P+  D   PV                GT      +++VFI
Sbjct: 285 APQLTWGTNPGQVVAIDGVVPNPADETNPVVRTSMEKALAYVDLTPGTPMTDIAINKVFI 344

Query: 273 GTCTNGRLEDLEVAASVLKGKKVT--VRTIIIPASRSTLLAAIKNGTMEILLKAGVTLAT 330
           G+CTN R+EDL  AA+  KG+KV   V  I++P S    L A   G  +I L+AG     
Sbjct: 345 GSCTNSRIEDLRAAAAQAKGRKVASGVTAIVVPGSGQVKLQAEAEGLDKIFLEAGFEWRL 404

Query: 331 PGCGPCLGAHQGVLGEGEVCVSTANRNFKGRMGKDGFIYLASPATAAASALTGEITDPR 389
           PGC  CL  +   L  G+ C ST+NRNF+GR G+    +L SPA AAA+A+ G   D R
Sbjct: 405 PGCSMCLAMNDDRLEAGDRCASTSNRNFEGRQGRGSRTHLVSPAMAAAAAVAGHFVDIR 463


Lambda     K      H
   0.318    0.135    0.401 

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: 425
Number of extensions: 19
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: 391
Length of database: 470
Length adjustment: 32
Effective length of query: 359
Effective length of database: 438
Effective search space:   157242
Effective search space used:   157242
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: 51 (24.3 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