GapMind for Amino acid biosynthesis

 

Aligments for a candidate for PSSH in Desulfovibrio vulgaris Miyazaki F

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 8501944 DvMF_2658 cysteine synthase (RefSeq)

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__Miya:8501944
          Length = 310

 Score =  191 bits (485), Expect = 2e-53
 Identities = 119/305 (39%), Positives = 168/305 (55%), Gaps = 17/305 (5%)

Query: 7   LLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADG 66
           + + +G TPLV L R+S       +G    + AKLE  NP  S+KDR A+ MI+ A   G
Sbjct: 7   MTELVGRTPLVRLNRVS-------EGCAAEVVAKLEFNNPCASVKDRIALAMIDGAMERG 59

Query: 67  LLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAAE 126
            L PG  ++EPTSGNTG+ LA  A ++G  L+  MPE+ S ER+ LL  +GA+++ + A 
Sbjct: 60  ELAPGGLLVEPTSGNTGVGLAFVAAVRGLTLVLTMPESMSNERKALLRGFGARLVLTPAS 119

Query: 127 GGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGLGT 185
            G   A+  A+ + A  P  VML Q+ NP N   H   T  E+ AD   ++  FVAG+GT
Sbjct: 120 KGMRGAIEEAERIVAETPGAVMLGQFVNPDNPLVHRKTTAEEIWADTDGKVDAFVAGVGT 179

Query: 186 TGTLMGTGRFLREHVANVKIVAAEPRY-------GEGVYALRNMDEGFVPELYDPEILTA 238
            GT+ GTGR LRE   ++K+ A EP           G + ++ +  GFVP + D ++   
Sbjct: 180 GGTVTGTGRRLRELNPDIKVFAVEPDESPVLSGGAPGPHPIQGIGAGFVPPVLDTKVYDE 239

Query: 239 RYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVADAGW 298
              V   DA+   R L+  EGI  G+S+GA   AA+ V      AG+R  +  VV D G 
Sbjct: 240 IIRVPGKDALVTARRLLREEGILCGVSSGANAFAAMAVARRPEMAGKR--VVFVVCDTGE 297

Query: 299 KYLST 303
           +YLST
Sbjct: 298 RYLST 302


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: 285
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: 323
Length of database: 310
Length adjustment: 27
Effective length of query: 296
Effective length of database: 283
Effective search space:    83768
Effective search space used:    83768
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 Aug 03 2021. The underlying query database was built on Aug 03 2021.

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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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.

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