GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Dinoroseobacter shibae DFL-12

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate 3607593 Dshi_1002 Cystathionine gamma-synthase (RefSeq)

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__Dino:3607593
          Length = 380

 Score =  208 bits (530), Expect = 2e-58
 Identities = 131/342 (38%), Positives = 188/342 (54%), Gaps = 14/342 (4%)

Query: 63  PGNVYSRYTNPTVRTFEERIAALEGAEQAVATASGMSAILALVMSLCSSGDHVLVSRSVF 122
           P N+YSR  +  +R  E  +AALEG   A+A  SGM+A  A+  +L  +G  V++   ++
Sbjct: 48  PDNIYSRDDSEALRAVETLLAALEGGAGALAFPSGMAATAAVFRTL-PAGARVVLQSGIY 106

Query: 123 GSTISLFDKYFKRFGIQVDYPPLSDLAAWEAACKPNTKLFFVESPSNPLAELVDIAALAE 182
             T      +  R G+ +     +D  A  +AC   T L FVE+PSNP  + VDI A A 
Sbjct: 107 WGTTKWVRDFCARRGVTLVEVDAADAHALGSACAAPTALVFVETPSNPWLKTVDIRAAAA 166

Query: 183 IAHAKGALLAVDNCFCTPALQQPLKLGADVVIHSATKYIDGQGRGMGG--VVAGRG-EQM 239
            AH  GALL VD+   TP L +PL LGAD+V+HSATK ++G    + G  V A  G E  
Sbjct: 167 AAHGAGALLVVDSTAATPVLTRPLGLGADLVMHSATKGLNGHSDVLAGALVTADAGHETW 226

Query: 240 KEVVGFLRTAGPTLSPFNAWLFLKGLETLRIRMQAHSASALALAEWLERQPGIERVYYAG 299
             +      AG  L PF AWL L+G+ TL +R+   SA+AL LA+ L     +  V+Y G
Sbjct: 227 ARIATDRHDAGAVLGPFEAWLLLRGMRTLPLRVARMSATALELAQRLSTDTRVADVFYPG 286

Query: 300 LPSHPQHELARRQQS-GFGAVVSFDVKGGRDAAWRFIDATRMVSITTNLGDTKTTIAHPA 358
           LP H  H++A  Q + GFG ++SF V G R  A   +    +    T+LG  ++ + H A
Sbjct: 287 LPGHAGHDIAVAQMTGGFGGLMSFLVHGDRQTALEVVGRLELFQRATSLGGVESLVEHRA 346

Query: 359 TTSHGRLSPEDRARAGIGDSLIRVAVGLEDLDDLKADMARGL 400
           T     + P+    +GI ++L+R++VG+ED  DL AD+ R L
Sbjct: 347 T-----IEPD----SGIPETLVRLSVGIEDAGDLWADLDRAL 379


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: 368
Number of extensions: 19
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: 403
Length of database: 380
Length adjustment: 31
Effective length of query: 372
Effective length of database: 349
Effective search space:   129828
Effective search space used:   129828
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