GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Pseudomonas fluorescens FW300-N2C3

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate AO356_28790 AO356_28790 cysteine synthase

Query= metacyc::MONOMER-20568
         (299 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28790
          Length = 347

 Score =  145 bits (366), Expect = 1e-39
 Identities = 102/314 (32%), Positives = 159/314 (50%), Gaps = 20/314 (6%)

Query: 1   MIYDNILETIGNTPLVRINHLNPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGKL 60
           MI + + + IGNTP++ I+   P+   ++  K+E  NP GS+KDR+A  M+  A   G+L
Sbjct: 1   MILNKVSDLIGNTPMLGIDI--PDTHARLLLKIEKNNPGGSIKDRMARNMVLAALKSGRL 58

Query: 61  HPGSTIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILT----- 115
            PG  ++E++SGNTGIGLAM     G + I V+    + ++  ++KA GA++        
Sbjct: 59  KPGGVVVESSSGNTGIGLAMAAVEFGLHFIAVVDHHAAQDKIAVMKALGADVRFVAGHYR 118

Query: 116 DKKLGTDGAIRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVA 175
           + ++      R  AEL ++ PG  F  NQ  N  N    Y     E  AQ +G V  +V 
Sbjct: 119 EDEVAVVERQRMAAELAQQIPGAVF-MNQSDNAAN-AGGYSDFVRETIAQVEGKVGAYVG 176

Query: 176 AVGTSGTLMGVGKNLREKNPEIKIIEAQPTK----GH-----YIQGLKSMEEAIVPAIYQ 226
            VGT G++ G+ + L+  NP+   +  +P      GH     Y  G  +     V  +  
Sbjct: 177 CVGTGGSMTGIARGLKLHNPDTVTVAVEPAGSIVFGHPGYPYYQSGTGTPAGDTVGLVLD 236

Query: 227 ADKIDEHILIESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEK-IDSGVIVVLFAD 285
              ID  + +   +AF  AR I    G+ +G S+G A+  A +   K + +G +VV  AD
Sbjct: 237 YSCIDLGVQVTDSQAFETARYIARNLGLLVGGSTGGAIFKALEFIHKGVLTGNVVVPIAD 296

Query: 286 RGEKYLSTKLFDTE 299
            GEKYL T +FD +
Sbjct: 297 GGEKYLHT-VFDDQ 309


Lambda     K      H
   0.315    0.133    0.367 

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: 279
Number of extensions: 22
Number of successful extensions: 6
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: 299
Length of database: 347
Length adjustment: 28
Effective length of query: 271
Effective length of database: 319
Effective search space:    86449
Effective search space used:    86449
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: 42 (22.0 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