GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Phaeobacter inhibens BS107

Align cystathionine gamma-lyase (EC 4.4.1.1); cysteine-S-conjugate beta-lyase (EC 4.4.1.13) (characterized)
to candidate GFF1649 PGA1_c16720 putative pyridoxal phosphate-dependent transferase

Query= BRENDA::A2RM21
         (380 letters)



>FitnessBrowser__Phaeo:GFF1649
          Length = 383

 Score =  204 bits (520), Expect = 3e-57
 Identities = 129/369 (34%), Positives = 199/369 (53%), Gaps = 19/369 (5%)

Query: 19  TGAVSVPIYQTS--------TYKQNGLGQPKEYEYSRSGNPTRHALEELIADLEGGVQGF 70
           +GA++ PI QTS         ++    G+     Y+R  NPT  A E L+A  E G    
Sbjct: 19  SGAITPPIVQTSLFSFDSYEAFEDRMAGRSNAAIYTRVQNPTVAAFESLMAKAEQGEAAV 78

Query: 71  AFSSGLAGIHAVLSLF-SAGDHIILADDVYGGTFRLMDKVLTKTGIIYDLVDLSNLDDLK 129
           AF+SG+A I + L  F   GD I   + VY  ++R M+++L   G+  D      L++ +
Sbjct: 79  AFASGMAAISSTLLAFVKPGDRIACVEHVYPDSYRFMERMLRPFGVEIDYYAPHQLEE-E 137

Query: 130 AAFKEETKAIYFETPSNPLLKVLDIKEISAIAKAHDALTLVDNTFATPYLQQPIALGADI 189
                  +  Y E+PS+ + + L++K+++A AK H  LT++DN++A+P  Q+P+  G DI
Sbjct: 138 PELLNGVRLAYLESPSSVVFQPLNLKKVTAHAKRHGVLTMIDNSWASPVFQKPLTQGVDI 197

Query: 190 VLHSATKYLGGHSDVVAGLVTTNSKELASEIGFLQNSIGAVLGPQDSWLVQRGIKTLALR 249
           VLHSA+KY+ GHSD VAG+V    + +          +GA L P +++L+ RG++TL+ R
Sbjct: 198 VLHSASKYISGHSDTVAGVVVAAQQHIDRIRDLTLPLLGAKLAPFEAFLLTRGLRTLSAR 257

Query: 250 MEAHSANAQKIAEFLETSKAVSKVYYPGLNSHPGHEIAKKQMSAFGGMISFELTDENAVK 309
           M  H A A    + L     V +V+ PG N  PG       ++   G+++ E  D   + 
Sbjct: 258 MRQHQATATLFIDRLSALPQVRRVHSPGPNEVPG-------LTGRSGLMAVEFDDSVDIP 310

Query: 310 DFVENLSYFTLAESLGGVESLIEVPAVMTHASIPKE-LREEIGIKDGLIRLSVGVEAIED 368
            F   LS+F L  S GG ESLI +PA +  A I +E   +  G+   L+RL++G+E  ED
Sbjct: 311 AFSNALSHFRLGVSWGGFESLI-LPARVGLAQIGEENSMQRFGVSPNLVRLNLGLEEAED 369

Query: 369 LLTDIKEAL 377
           L  DI  AL
Sbjct: 370 LWADITSAL 378


Lambda     K      H
   0.315    0.133    0.366 

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: 290
Number of extensions: 17
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: 380
Length of database: 383
Length adjustment: 30
Effective length of query: 350
Effective length of database: 353
Effective search space:   123550
Effective search space used:   123550
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: 42 (22.0 bits)
S2: 50 (23.9 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