GapMind for Amino acid biosynthesis

 

Alignments for a candidate for moeZ in Dyella japonica UNC79MFTsu3.2

Align Probable adenylyltransferase/sulfurtransferase MoeZ; EC 2.7.7.-; EC 2.8.1.- (characterized)
to candidate N515DRAFT_2678 N515DRAFT_2678 Molybdopterin or thiamine biosynthesis adenylyltransferase

Query= SwissProt::P9WMN7
         (392 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2678
          Length = 388

 Score =  227 bits (579), Expect = 4e-64
 Identities = 123/251 (49%), Positives = 161/251 (64%), Gaps = 8/251 (3%)

Query: 14  ALSREEVARYSRHLIIPDLGVDGQKRLKNARVLVIGAGGLGAPTLLYLAAAGVGTIGIVD 73
           AL  +   RYSR L +P +G  GQ +L  AR++++GAGGLGAP  LYLAAAGVG I ++D
Sbjct: 122 ALDADAAERYSRQLRLPQVGEAGQAKLGAARIVLLGAGGLGAPAALYLAAAGVGQITLID 181

Query: 74  FDVVDESNLQRQVIHGVADVGRSKAQSARDSIVAINPLIRVRLHELRLAPSNAVDLFKQY 133
            D V+ SNL RQVIH  A VG +K +SAR ++ A+NP +R+   E RL   N   L   +
Sbjct: 182 DDRVERSNLHRQVIHADARVGMAKTESARLALNALNPRVRIETREERLRADNVERLLADH 241

Query: 134 DLILDGTDNFATRYLVNDAAVLAGKPYVWGSIYRFEGQASVF---WEDAPDGLGVNYRDL 190
           DL++DG DNF  RYLV  A+   G P V+G++ RF GQ SVF    +DAP      YR L
Sbjct: 242 DLVIDGADNFPARYLVAAASRRLGLPMVYGAVERFTGQVSVFDPRRDDAP-----CYRCL 296

Query: 191 YPEPPPPGMVPSCAEGGVLGIICASVASVMGTEAIKLITGIGETLLGRLLVYDALEMSYR 250
           +PEPP     P+C+E GVLG++   +  +  TEA+KLI  +GETL GRLL  DAL M +R
Sbjct: 297 FPEPPSAAEAPNCSEAGVLGVLPGLIGLLQATEALKLILELGETLSGRLLHVDALTMRFR 356

Query: 251 TITIRKDPSTP 261
              +R+DPS P
Sbjct: 357 ETRLRRDPSCP 367



 Score = 29.6 bits (65), Expect = 2e-04
 Identities = 21/82 (25%), Positives = 35/82 (42%)

Query: 306 LIDVRDPVEWDIVHIDGAQLIPKSLINSGEGLAKLPQDRTAVLYCKTGVRSAEALAAVKK 365
           LIDVR+  E       GA  + +  +       +  +DR  +  C +G RS  A  A+++
Sbjct: 36  LIDVREDHERADGTPAGALGLSRGFLELRIEQTEANRDRPILALCGSGQRSLLAAEALQR 95

Query: 366 AGFSDAVHLQGGIVAWAKQMQP 387
            G+     + GG   W  +  P
Sbjct: 96  MGYRQVSSVAGGFNRWKAEGLP 117


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: 441
Number of extensions: 25
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 392
Length of database: 388
Length adjustment: 31
Effective length of query: 361
Effective length of database: 357
Effective search space:   128877
Effective search space used:   128877
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: 50 (23.9 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