GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CBS in Sinorhizobium meliloti 1021

Align cystathionine β-synthase (O-acetyl-L-serine) monomer (EC 4.2.1.22; EC 2.5.1.134; EC 2.5.1.47) (characterized)
to candidate SMc00421 SMc00421 O-acetylserine sulfhydrylase A

Query= metacyc::HP_RS00545-MONOMER
         (306 letters)



>FitnessBrowser__Smeli:SMc00421
          Length = 322

 Score =  223 bits (569), Expect = 4e-63
 Identities = 125/306 (40%), Positives = 185/306 (60%), Gaps = 3/306 (0%)

Query: 3   IITTMQDAIGRTPVFKFTNKDYPIPLNSAIYAKLEHLNPGGSVKDRLGQYLIGEGFKTGK 62
           + +++ + IG TP+ +         + + + AKLE  NP GSVKDR+G  +I      GK
Sbjct: 12  VFSSITETIGDTPIVRLDKLAKEKGVKANLLAKLEFFNPIGSVKDRIGVAMIESLEAQGK 71

Query: 63  IT-SKTTIIEPTAGNTGIALALVAIKHHLKTIFVVPEKFSTEKQQIMRALGALVINTPTS 121
           IT  +TT++EPT+GNTGIALA VA     + I  +PE  S E+++++  LGA ++ T  +
Sbjct: 72  ITPGRTTLVEPTSGNTGIALAFVAAAKGYRLILTMPETMSVERRKMLTLLGAELVLTEGA 131

Query: 122 EGISGAIKKSKELAESIPDSYLPLQFENPDNPAAYYHTLAPEIVQELGTNLTSFVAGIGS 181
           +G+ GAI K++EL E++PD+ +P QFENP NP  +  T A EI  +    +   V+GIG+
Sbjct: 132 KGMKGAIAKAQELTETLPDAIIPQQFENPANPEIHRTTTAEEIWNDTEGAVDILVSGIGT 191

Query: 182 GGTFAGTARYLKERIPAIRLIGVEPEGS-ILNGGEPGPHEIEGIGVEFIPPFFENLDIDG 240
           GGT  G  + LK R P++R+I VEPE S IL+GG PGPH+I+GIG  F P   +    D 
Sbjct: 192 GGTITGAGQVLKARKPSVRVIAVEPEESPILSGGAPGPHKIQGIGAGFAPAILDTSVYDE 251

Query: 241 FETISDEEGFSYTRKLAKKNGLLVGSSSGAAFVAALKEAQRLPE-GSQVLTIFPDVADRY 299
             T++  E     R +A+  G+ VG S+GAA  AA++  QR    G  ++ I P  A+RY
Sbjct: 252 VVTVNAGEAIEAARLVARLEGVPVGISAGAALQAAIEVGQREENAGRNIVVIIPSFAERY 311

Query: 300 LSKGIY 305
           LS  ++
Sbjct: 312 LSTVLF 317


Lambda     K      H
   0.316    0.137    0.389 

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: 267
Number of extensions: 13
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: 306
Length of database: 322
Length adjustment: 27
Effective length of query: 279
Effective length of database: 295
Effective search space:    82305
Effective search space used:    82305
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 (21.6 bits)
S2: 48 (23.1 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