GapMind for catabolism of small carbon sources

 

Alignments for a candidate for puuA in Hippea alviniae EP5-r

Align Gamma-glutamyl-putrescine synthetase (EC 6.3.1.11) (characterized)
to candidate WP_022670511.1 G415_RS0104980 type I glutamate--ammonia ligase

Query= reanno::BFirm:BPHYT_RS23160
         (444 letters)



>NCBI__GCF_000420385.1:WP_022670511.1
          Length = 470

 Score =  154 bits (389), Expect = 6e-42
 Identities = 122/364 (33%), Positives = 173/364 (47%), Gaps = 39/364 (10%)

Query: 67  VTDPDMVCVPDASTIRMIPWAVDPTAQVIHDCVH-FDGTPVAISPRRVLRRVLELYKAKG 125
           + + DM+ +PD +T  M P+A   T  +I D V      P    PR + ++  E  K+ G
Sbjct: 61  INESDMLVMPDPATAFMDPFAEVATLNIICDIVDPITREPYERHPRAIAKKAEEFLKSSG 120

Query: 126 WKPV--IAPELEFYLVDMNKDPDLPLQPP-----------IGRTGRPETGRQAYSIEAVN 172
              V    PELEF+++D   D    ++P            I  +G+ E     Y I+   
Sbjct: 121 IADVAFFGPELEFFILD---DVRYDVKPNTSYYAVDSVEGIWNSGKDEDPNLGYKIKHKE 177

Query: 173 EFDP---------LFEDIYEYCEVQELEVDTLIHEVGAA-QMEINFMHGDPLKLADSVFL 222
            + P         L  +I    E   +EV+   HEV  A Q EI+  +   L+ AD+V  
Sbjct: 178 GYFPVAPLDSLQDLRSEIVLELEKAGIEVEAHHHEVATAGQAEIDIKYASLLQQADNVMK 237

Query: 223 FKRTVREAALRHKMYATFMAKPMEGEPGSAMHMHQSLVDEETGHNLFTGPDGKPTS-LFT 281
           +K   +  A  +    TFM KP+ G+ G+ MH HQSL  +  G  LF G      S +  
Sbjct: 238 YKYIAKNVAFMYGKTITFMPKPIAGDNGTGMHTHQSLWKD--GKPLFAGNGYAGLSEIGL 295

Query: 282 SYIAGLQKYTPALMPIFAPYINSYRRLSRFMAAPINVAWGYDNRTVGFRIPHSGPA--AR 339
            YI G+ K+  AL     P +NSY+RL     APIN+A+   NR+   RIP   P+  A+
Sbjct: 296 YYIGGILKHGKALAAFTNPTMNSYKRLVPGFEAPINLAYSSRNRSAAVRIPMYSPSPKAK 355

Query: 340 RIENRIPGVDCNPYLAIAATLAAGYLGMTQKLEATEPLLSDGYELP-------YQLPRNL 392
           RIE R P    NPYLA  A L AG  G+  K++  EPL  + Y+LP        ++PRNL
Sbjct: 356 RIEVRFPDPSANPYLAFTAMLMAGIDGIINKIDPGEPLDKNIYDLPPEELAKVEKMPRNL 415

Query: 393 EEGL 396
           EE L
Sbjct: 416 EEAL 419


Lambda     K      H
   0.321    0.138    0.418 

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: 563
Number of extensions: 38
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: 444
Length of database: 470
Length adjustment: 33
Effective length of query: 411
Effective length of database: 437
Effective search space:   179607
Effective search space used:   179607
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 (21.8 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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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