GapMind for Amino acid biosynthesis

 

Alignments for a candidate for moeZ in Pedobacter sp. GW460-11-11-14-LB5

Align Probable adenylyltransferase/sulfurtransferase MoeZ; EC 2.7.7.-; EC 2.8.1.- (characterized)
to candidate CA265_RS12640 CA265_RS12640 molybdopterin biosynthesis protein

Query= SwissProt::P9WMN7
         (392 letters)



>FitnessBrowser__Pedo557:CA265_RS12640
          Length = 368

 Score =  225 bits (574), Expect = 1e-63
 Identities = 139/364 (38%), Positives = 204/364 (56%), Gaps = 15/364 (4%)

Query: 22  RYSRHLIIPDLGVDGQKRLKNARVLVIGAGGLGAPTLLYLAAAGVGTIGIVDFDVVDESN 81
           RY+R +I+   G + Q++L  A+VLVIGAGGLG P L YLAAAG+G IGIVD D +  SN
Sbjct: 5   RYNRQIILKGFGEEAQQKLLRAKVLVIGAGGLGCPALQYLAAAGIGHIGIVDDDTISLSN 64

Query: 82  LQRQVIHGVADVGRSKAQSARDSIVAINPLIRVRLHELRLAPSNAVDLFKQYDLILDGTD 141
           L RQ++   AD+G+ K + A   +  +N  I +  H +RL  +N +D+  +YD ILDGTD
Sbjct: 65  LHRQILFTTADIGKLKVEVAAKRLQEMNTQIGIIRHPIRLQKNNILDIVSRYDYILDGTD 124

Query: 142 NFATRYLVNDAAVLAGKPYVWGSIYRFEGQASVFWEDAPDGL--GVNYRDLYPEPPPPGM 199
           NF +RYL+NDA  L  KP ++ ++  FEGQ ++F  +APD L    NYRDL+P PP  G 
Sbjct: 125 NFESRYLINDACALLNKPLIFAAVSGFEGQLAIF--NAPDHLTPSTNYRDLFPIPPDKGE 182

Query: 200 VPSCAEGGVLGIICASVASVMGTEAIKLITGIGETLLGRLLVYDALEMSYRTITIRKDP- 258
           V +CAE G++G++   + ++   E IKLI  IG+ L  ++L Y+ L     TI I     
Sbjct: 183 VANCAENGIIGVLPGILGTMAAAETIKLIAKIGQALTNKILSYNLLTQEQYTINISHGGG 242

Query: 259 -STPKITELVDYEQFCGVVADDAAQAAKGSTITPRELRDWLDSGRKLALIDVRDPVEWDI 317
            + PK       ++F  +   D ++  +G           L       LIDVR+  E  I
Sbjct: 243 YTLPKTV-----DEFLNMDYQDTSEGPQGYIEIDAGELVKLQQLESTILIDVRERHEVPI 297

Query: 318 VHIDGAQLIPKSLINSGEGLAKLPQDRTAVLYCKTGVRSAEALAAV-KKAGFSDAVH-LQ 375
           +       +P S    G  ++K    +  VL C+ G+RS  A  A+ +K G +  ++ L+
Sbjct: 298 LDKQIFTQVPMS--EFGAFMSKEFYQKHVVLICQHGIRSVAAAEAMQEKYGDAKKIYSLK 355

Query: 376 GGIV 379
           GGIV
Sbjct: 356 GGIV 359


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: 358
Number of extensions: 16
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: 392
Length of database: 368
Length adjustment: 30
Effective length of query: 362
Effective length of database: 338
Effective search space:   122356
Effective search space used:   122356
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