GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Sphingomonas koreensis DSMZ 15582

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 Ga0059261_3452 Ga0059261_3452 Cysteine synthase

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__Korea:Ga0059261_3452
          Length = 330

 Score =  147 bits (371), Expect = 3e-40
 Identities = 101/309 (32%), Positives = 153/309 (49%), Gaps = 26/309 (8%)

Query: 11  LGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADGLLRP 70
           +GNTPLV L+   P    G D     ++ K E  NP  S+KDR A+ +++ AEA GLL P
Sbjct: 11  IGNTPLVRLK--GPSTAAGCD-----IYGKCEFANPGASVKDRAALFIVQDAEARGLLAP 63

Query: 71  GATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAAEGGSN 130
           G TI+E T+GNTGI LA+    KGY+ I VMPE  S E+   L   GA+++   A   SN
Sbjct: 64  GGTIVEGTAGNTGIGLALVGNAKGYKTIIVMPETQSREKMDTLRALGAELVLVPAAPYSN 123

Query: 131 TA--VATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGLGTTG 187
               V T++ +A   P+ +   Q+ N AN  +H  GT  E+   +   I  F    GT G
Sbjct: 124 PGHFVHTSRRIAEETPNAIWANQFDNIANRKAHIVGTAEEIWTQMEGRIDGFTCAAGTGG 183

Query: 188 TLMGTGRFLREHVANVKIVAAEPR-------------YGEGVYALRNMDEGFVPELYDPE 234
           T+ G G  L+E    V I  ++P                EG      + +G +    +  
Sbjct: 184 TIAGVGLGLKEKDERVTIALSDPHGAALYEYYAHGELKAEGSSVAEGIGQGRITANLEGA 243

Query: 235 ILTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVA 294
            +  ++ +   + +     L+  EG+  G+S+G  +  A+ +G   L  G+R  IA ++ 
Sbjct: 244 PIDTQFRISDEEGLEWVERLLAEEGLCLGLSSGINVAGAVRLGR-ELGPGKR--IATILC 300

Query: 295 DAGWKYLST 303
           D G++YLST
Sbjct: 301 DTGFRYLST 309


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: 304
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: 323
Length of database: 330
Length adjustment: 28
Effective length of query: 295
Effective length of database: 302
Effective search space:    89090
Effective search space used:    89090
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