GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Shewanella loihica PV-4

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate 5208004 Shew_0520 O-succinylhomoserine (thiol)-lyase (RefSeq)

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__PV4:5208004
          Length = 388

 Score =  257 bits (656), Expect = 5e-73
 Identities = 141/337 (41%), Positives = 207/337 (61%), Gaps = 2/337 (0%)

Query: 67  YSRYTNPTVRTFEERIAALEGAEQAVATASGMSAILALVMSLCSSGDHVLVSRSVFGSTI 126
           YSR  NPT     + IA LE     V T +GM+AI  LV SL    D ++V    +G + 
Sbjct: 47  YSRSGNPTRSILGDAIAELEQGATGVVTCTGMAAI-TLVTSLLGPEDLLVVPHDCYGGSY 105

Query: 127 SLFDKYFKRFGIQVDYPPLSDLAAWEAACKPNTKLFFVESPSNPLAELVDIAALAEIAHA 186
            LF    K+   ++     +D  A E A   + K+ ++E+PSNPL  +VDI A+A+ +H 
Sbjct: 106 RLFTNLAKKGAFKLLVVDQTDERALEQALTQSPKMVWLETPSNPLLRVVDIEAIAQASHK 165

Query: 187 KGALLAVDNCFCTPALQQPLKLGADVVIHSATKYIDGQGRGMGGVVAGRGEQMKEVVGFL 246
            GA + VDN F +P LQQPL+LGAD+V+HS TKYI+G    +GG V  +  ++ E++ + 
Sbjct: 166 VGAQVVVDNTFLSPVLQQPLQLGADIVVHSTTKYINGHSDVVGGAVVAKDPEVGELLHWW 225

Query: 247 -RTAGPTLSPFNAWLFLKGLETLRIRMQAHSASALALAEWLERQPGIERVYYAGLPSHPQ 305
             T G T S F+++L L+GL TL +R++ H A+A  +   L     +E+VYY GL  HP 
Sbjct: 226 SNTLGLTGSAFDSYLTLRGLRTLAVRIREHQANAQKVLALLCDHKAVEKVYYPGLAEHPG 285

Query: 306 HELARRQQSGFGAVVSFDVKGGRDAAWRFIDATRMVSITTNLGDTKTTIAHPATTSHGRL 365
           HE+A RQQ GFGA++SF++KGG  A   F+DA +  S+  +LG  ++ +A PAT +H  +
Sbjct: 286 HEIAARQQKGFGAMLSFELKGGESALVAFLDALQYFSVAESLGGVESLVAVPATMTHRAM 345

Query: 366 SPEDRARAGIGDSLIRVAVGLEDLDDLKADMARGLAA 402
            P+ R  AG+ D+LIR++VG+ED +DL AD+  GL A
Sbjct: 346 DPDARREAGVKDTLIRLSVGIEDGEDLVADILAGLEA 382


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: 361
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: 388
Length adjustment: 31
Effective length of query: 372
Effective length of database: 357
Effective search space:   132804
Effective search space used:   132804
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