GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Phaeobacter inhibens BS107

Align branched-chain-amino-acid transaminase (EC 2.6.1.42) (characterized)
to candidate GFF2835 PGA1_c28810 transcriptional regulator, GntR family

Query= BRENDA::A0A060PQX5
         (417 letters)



>FitnessBrowser__Phaeo:GFF2835
          Length = 491

 Score =  142 bits (358), Expect = 2e-38
 Identities = 94/309 (30%), Positives = 150/309 (48%), Gaps = 14/309 (4%)

Query: 111 DIMITSGSQQALDLIGRVFINPGDIVVVEAPTYLAALQAFKYYEPEFVQIPLDDEGMRVD 170
           +I+IT G+Q AL L+ ++ + PG    +E PTY        Y   E   +P+D +G+  D
Sbjct: 193 EILITLGAQNALWLVTQLLLGPGRKAALEDPTYYTLRDQLVYRGCEIDCLPVDHDGLPPD 252

Query: 171 LLEEKLQELEKEGKKVKLVYTIPTFQNPAGVTMSEKRRKRLLELASEYDFLIVEDNPYGE 230
            + +             +++T P+ Q+P   TM   RRK+LLE A E D +IVED+   E
Sbjct: 253 TIRDDTD----------VIFTTPSHQSPTTATMPMARRKQLLERAREIDAVIVEDDYEFE 302

Query: 231 LRYSGEPVKPIKAWDDEGRVMYLGTFSKILAPGFRIGWIAAEPHLIRKLEIAKQSVDLCT 290
           + + G P   +K+ D +GRV+Y+G+FSK L PG R+G++      IR+    + +V    
Sbjct: 303 MSFLGAPSPALKSLDADGRVVYVGSFSKSLFPGLRLGYLVGSEPFIRQARALRANVLRHP 362

Query: 291 NPFSQVIAWKYVEGGHLDNHIPNIIEFYKPRRDAMLKALEEFMPEGVRWTKPEGGMFVWV 350
               Q     ++  GH D  I  + +    RR  +  A+       V      GG  +W+
Sbjct: 363 PGHVQRTVAYFLSLGHYDAQIRRMAKVLHDRRCVIEDAVTHH-GLSVAGVGVYGGSSLWM 421

Query: 351 TLPEGIDTKLMLEKAVAKGVAYVPGEAFFA--HRDVKNTMRLNFTYVPEEKIREGIKRLA 408
              EG+DT  + +   A  V   PG  FFA  HR  +N  RL ++ +P  +I  G+  +A
Sbjct: 422 RADEGVDTAAVAQSLKATSVLIEPGAPFFAAEHRK-QNYYRLGYSSIPSNRIAPGLALIA 480

Query: 409 ETIKEEMKK 417
           E ++    K
Sbjct: 481 EALRPSRAK 489


Lambda     K      H
   0.318    0.137    0.398 

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: 418
Number of extensions: 24
Number of successful extensions: 3
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: 417
Length of database: 491
Length adjustment: 33
Effective length of query: 384
Effective length of database: 458
Effective search space:   175872
Effective search space used:   175872
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