GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Sulfurihydrogenibium azorense Az-Fu1

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_012674541.1 SULAZ_RS03715 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_000021545.1:WP_012674541.1
          Length = 302

 Score =  224 bits (571), Expect = 2e-63
 Identities = 114/302 (37%), Positives = 183/302 (60%), Gaps = 7/302 (2%)

Query: 9   IWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGPVVFR--HREHMQRLHDSAK 66
           ++F  + V  E+AK+ + +++ HYGT+VFEGIR Y + +   ++    +EH +RL  + +
Sbjct: 4   VYFENKFVEEEEAKISIKTNSFHYGTAVFEGIRAYYNKENDTMYGLFFKEHYERLFKNMR 63

Query: 67  IYRFPVSQSIDELMEACRDVIRKNN-LTSAYIRPLIFVGDVGMGVNPPAGYSTDVIIAAF 125
           I    + +SID+L+E  ++++++NN     YIRP+++  D+ +G     GY+  + I   
Sbjct: 64  ILNMEIEESIDQLVEITKELVKRNNHKEDVYIRPIVYFSDLAIGPKL-IGYTAKIAIYTL 122

Query: 126 PWGAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQEGIA 185
           P G Y+      +GI A VSSW R   N IP   K  G Y++S L  +EA   G +E I 
Sbjct: 123 PLGDYIDTN---KGIKAKVSSWVRLNDNMIPPRLKVTGAYVNSALAKTEALLSGAEEAIV 179

Query: 186 LDVNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVREQVLSRE 245
           L+ +G++SEG+ EN+F  +DG L TPP +   L GITR A++ +A +LGI V E+ +SR 
Sbjct: 180 LNKDGFVSEGSAENIFIARDGKLITPPVSDDILEGITRKAVMDIATDLGIPVIERSISRT 239

Query: 246 SLYLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLFTGETEDKWGWLD 305
            LY+ADEVF  GT A+I+PV  +DG ++G G  G +TK+I+  +F    G+ E    W+ 
Sbjct: 240 ELYVADEVFFCGTGAQISPVIEIDGRKIGNGTVGDITKKIKDIYFDAVRGKVEKYKNWVV 299

Query: 306 QV 307
           ++
Sbjct: 300 EI 301


Lambda     K      H
   0.319    0.136    0.413 

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: 245
Number of extensions: 13
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: 309
Length of database: 302
Length adjustment: 27
Effective length of query: 282
Effective length of database: 275
Effective search space:    77550
Effective search space used:    77550
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: 48 (23.1 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