GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Sinorhizobium meliloti 1021

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate SMc01976 SMc01976 hypothetical protein

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__Smeli:SMc01976
          Length = 390

 Score =  221 bits (562), Expect = 4e-62
 Identities = 135/365 (36%), Positives = 199/365 (54%), Gaps = 16/365 (4%)

Query: 43  TSSYVFRTAADAAARFAGEVPGNVYSRYTNPTVRTFEERIAALEGAEQAVATASGMSAIL 102
           TS + F+   +  A + GE    +Y+R  NPTVR FEE +A LEGAE A+  ASGMSAI 
Sbjct: 33  TSLFTFKDYDEMVASYRGERVRPIYTRGLNPTVRHFEEMLAKLEGAEDAIGFASGMSAIS 92

Query: 103 ALVMSLCSSGDHVLVSRSVFGSTISLFDKYFKRFGIQVDYPPLSDLAAWEAACKPNTKLF 162
           + V+S    GD ++  + V+     LF  + KR  ++V Y    D  A  A   P  KLF
Sbjct: 93  STVLSFVEPGDRIVAVKHVYPDAFRLFGTHLKRMRVEVTYVDGRDEEA-VAKALPGAKLF 151

Query: 163 FVESPSNPLAELVDIAALAEIAHAKGALLAVDNCFCTPALQQPLKLGADVVIHSATKYID 222
           ++ESP++ + +  D+AALA +A  +G +  +DN + +P  QQP+ LG D+VIHSA+KY+ 
Sbjct: 152 YMESPTSWVMDTHDVAALAALARRQGIVTVIDNSWASPVFQQPVSLGVDLVIHSASKYLG 211

Query: 223 GQGRGMGGVVAGRGEQMKEVVGFLRT-----AGPTLSPFNAWLFLKGLETLRIRMQAHSA 277
           G    + GVVAG G    E++G +R+      G  LSPF+AWL ++G+ TL +RM+AH  
Sbjct: 212 GHSDVVAGVVAGSG----ELIGRIRSEAYPYLGGKLSPFDAWLLIRGMRTLPVRMKAHER 267

Query: 278 SALALAEWLERQPGIERVYYAGLPSHPQHELARRQQSGFGAVVSFDVKGGRDAAWRFIDA 337
           SALA+A  L   P +E V + GL +H    L     SG   + SF  + G D   RF D 
Sbjct: 268 SALAVARRLAEHPLVETVCHPGLGNHLPPGL-----SGTSGLFSFIFREGVDVR-RFADH 321

Query: 338 TRMVSITTNLGDTKTTIAHPATTSHGRLSPEDRARAGIGDSLIRVAVGLEDLDDLKADMA 397
            ++  +  + G  ++ I         +  P   A  GI    +R+ VGLE  + L +D+ 
Sbjct: 322 LKLFKLGVSWGGHESLIVPGEVVLAQKAEPNSAAAFGISPRSVRLHVGLEGTEALWSDLE 381

Query: 398 RGLAA 402
             + A
Sbjct: 382 AAMTA 386


Lambda     K      H
   0.319    0.133    0.392 

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: 377
Number of extensions: 17
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: 403
Length of database: 390
Length adjustment: 31
Effective length of query: 372
Effective length of database: 359
Effective search space:   133548
Effective search space used:   133548
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: 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