GapMind for Amino acid biosynthesis

 

Alignments for a candidate for moeZ in Pseudomonas simiae WCS417

Align Probable adenylyltransferase/sulfurtransferase MoeZ; EC 2.7.7.-; EC 2.8.1.- (characterized)
to candidate GFF4107 PS417_21040 sulfurylase

Query= SwissProt::P9WMN7
         (392 letters)



>FitnessBrowser__WCS417:GFF4107
          Length = 620

 Score =  305 bits (780), Expect = 3e-87
 Identities = 167/384 (43%), Positives = 233/384 (60%), Gaps = 11/384 (2%)

Query: 14  ALSREEVARYSRHLIIPDLGVDGQKRLKNARVLVIGAGGLGAPTLLYLAAAGVGTIGIVD 73
           ALS EEV RY RH+ +P +G +GQ  LK A+VL+IG GGLG+P  LYLAAAGVGT+G+VD
Sbjct: 243 ALSNEEVQRYVRHITLPGVGREGQLNLKKAKVLIIGTGGLGSPISLYLAAAGVGTLGLVD 302

Query: 74  FDVVDESNLQRQVIHGVADVGRSKAQSARDSIVAINPLIRVRLHELRLAPSNAVDLFKQY 133
           FDVV+ SNLQRQ++HG + +G  K +SAR  +  +N  I++  H+  L   NA++L   Y
Sbjct: 303 FDVVESSNLQRQIVHGNSTLGMPKVESARQRLQDLNRHIQINAHDTALNADNALELVGAY 362

Query: 134 DLILDGTDNFATRYLVNDAAVLAGKPYVWGSIYRFEGQASVFWEDAPDGLGVNYRDLYPE 193
           DL++DGTDNF TRYLVNDA V  GKP V+G+IYRF+GQ SV         G  YR L+P 
Sbjct: 363 DLVIDGTDNFDTRYLVNDACVQLGKPLVYGAIYRFDGQISVLNYKG----GPCYRCLFPS 418

Query: 194 PPPPGMVPSCAEGGVLGIICASVASVMGTEAIKLITGIGETLLGRLLVYDALEMSYRTIT 253
            PP  + P+C+ GGV+G++   V  +  TEAIKL+ GIGE L GRL+ +DAL M +  I 
Sbjct: 419 APPAELAPNCSAGGVIGVLPGVVGMIQATEAIKLLIGIGEPLSGRLMRFDALAMKFSEIR 478

Query: 254 IRKDPSTPKITELVDYE----QFCGVVADDAAQAAKGSTITPRELRDWLDSGRKL-ALID 308
            ++    P  +EL   E      C          A+   I P+ L+  L+       L+D
Sbjct: 479 FKRRADCPCCSELRHSETRAPAACADTMPSPPSLAEERYIKPQVLKQVLEHHSSADVLLD 538

Query: 309 VRDPVEWDIVHIDGAQLIPKSLINSGEGLAKLPQDRTAVLYCKTGVRSAEALAAVKKAGF 368
           VRD  E ++  + G   IP + ++    L +L +D T  L C  G R+ +A + +  AGF
Sbjct: 539 VRDASELEVCKLPGVVHIPLAELDG--HLDRLSRDNTHYLICYAGTRAEQAASTLLAAGF 596

Query: 369 SDAVHLQGGIVAWAKQMQPDMVMY 392
           ++   LQGG+  W + ++PDM +Y
Sbjct: 597 ANTKVLQGGMKHWVRDVEPDMPLY 620


Lambda     K      H
   0.319    0.137    0.404 

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: 656
Number of extensions: 30
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: 392
Length of database: 620
Length adjustment: 34
Effective length of query: 358
Effective length of database: 586
Effective search space:   209788
Effective search space used:   209788
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 (21.7 bits)
S2: 52 (24.6 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