GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Acidovorax sp. GW101-3H11

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate Ac3H11_1610 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1610
          Length = 362

 Score =  253 bits (646), Expect = 6e-72
 Identities = 148/357 (41%), Positives = 211/357 (59%), Gaps = 14/357 (3%)

Query: 20  LEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQIMLD 79
           L++ ++TK Y    AV  ++L++ KGE  +LLG SGCGK+T L+M+AGFE  ++G+I L 
Sbjct: 4   LQLTDVTKFYGSTCAVQSMNLSVEKGEFVSLLGPSGCGKTTTLQMVAGFEAVTSGRIELA 63

Query: 80  GVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLGLVHM 139
           G D++      R + ++FQSYALFPHMTV  N++FGL+  K+PKAE   RV + LGLVH+
Sbjct: 64  GRDITHAKANTRGLGIVFQSYALFPHMTVADNVSFGLEMRKVPKAERKDRVAQALGLVHL 123

Query: 140 QEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDILERV 199
           ++ A R P +LSGGQRQRVALAR+L   P +LLLDEP+  LD KLR+ MQ E+  I  +V
Sbjct: 124 EKHAGRYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDAKLREEMQFELRQIQRKV 183

Query: 200 GVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVNVFEGV 259
           G T VMVTHDQ EAM+++ R+ +M  G+  QI  P  +YEHP TR+ + F+G  N+  G 
Sbjct: 184 GTTTVMVTHDQSEAMSISDRVVVMEAGRATQIDHPHRVYEHPRTRFISTFVGKANLVPGQ 243

Query: 260 LKERQEDGLVLDSPGLVHPLKVDAD-ASVVDNVPVHVALRPEKIMLCEEPPANGCNFAVG 318
           +         + +     P++V  + A       V +++RPEK+ L   P   G     G
Sbjct: 244 VTTASATHTHVGA----GPIEVRVEGAQFRPGAAVLLSVRPEKLQLV--PTVQG--RIDG 295

Query: 319 EVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRLCWEVDSCVVL 375
           EV    +LG   +Y V    G ++      A    +G    G+   L W  D C+ L
Sbjct: 296 EVCERFFLGSQWLYRVGTGMGDLMVL----APNDGRGALEEGERTGLDWP-DHCMRL 347


Lambda     K      H
   0.321    0.137    0.400 

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: 334
Number of extensions: 15
Number of successful extensions: 1
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: 377
Length of database: 362
Length adjustment: 30
Effective length of query: 347
Effective length of database: 332
Effective search space:   115204
Effective search space used:   115204
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: 49 (23.5 bits)

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

Links

Downloads

Related tools

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