GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Desulfovibrio vulgaris Hildenborough

Align [CysO sulfur-carrier protein]-thiocarboxylate-dependent cysteine synthase (EC 2.5.1.113); O-phosphoserine sulfhydrylase (EC 2.5.1.65) (characterized)
to candidate 206086 DVU0663 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>MicrobesOnline__882:206086
          Length = 308

 Score =  208 bits (529), Expect = 2e-58
 Identities = 119/310 (38%), Positives = 175/310 (56%), Gaps = 17/310 (5%)

Query: 6   SLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEAD 65
           S+   +G TP+V L +++        G    + AKLE+ NP  S+KDR A+ M+E A A 
Sbjct: 6   SMTDLVGKTPMVRLNKVTL-------GCVAEVVAKLENFNPCSSVKDRIALNMVEAAIAR 58

Query: 66  GLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAA 125
           G + PGA ++EPTSGNTG+ LA    ++G +L+  MPE+ S ERR LL+ +G  ++ + A
Sbjct: 59  GEIAPGAVLVEPTSGNTGVGLAFVCAVRGLKLVLTMPESMSAERRALLKAFGTTLVLTPA 118

Query: 126 EGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGLG 184
             G   AV  A+ + A  P  VML Q+ NP N  +H   TGPE+ AD    I  FVAG+G
Sbjct: 119 AKGMRGAVEEAERIVADTPGAVMLQQFANPDNPAAHEATTGPEIWADTDGMIDCFVAGVG 178

Query: 185 TTGTLMGTGRFLREHVANVKIVAAEPRY-------GEGVYALRNMDEGFVPELYDPEILT 237
           T GT+ GTGR+L+    +++++A EP           G +A++ +  GFVP + D  +  
Sbjct: 179 TGGTITGTGRYLKGRNPDIRVIAVEPAESAVLSGGAPGPHAIQGIGAGFVPPVLDTSVYD 238

Query: 238 ARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVADAG 297
               V   DA+   R L+  EGI  GIS+GA +HAA+        AG+R  +  ++ D G
Sbjct: 239 EVMPVPGADALTMARRLLQEEGILCGISSGANVHAAIAYARRPENAGKR--VVCIICDTG 296

Query: 298 WKYLSTGAYA 307
            +YLST  +A
Sbjct: 297 ERYLSTPLFA 306


Lambda     K      H
   0.317    0.134    0.398 

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: 287
Number of extensions: 16
Number of successful extensions: 4
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: 323
Length of database: 308
Length adjustment: 27
Effective length of query: 296
Effective length of database: 281
Effective search space:    83176
Effective search space used:    83176
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