GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Phaeacidiphilus oryzae TH49

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate WP_084703891.1 BS73_RS07930 ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>NCBI__GCF_000744815.1:WP_084703891.1
          Length = 389

 Score =  231 bits (589), Expect = 3e-65
 Identities = 143/377 (37%), Positives = 211/377 (55%), Gaps = 17/377 (4%)

Query: 3   DAIPRPQAKTRKALTPLLEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLL 62
           DA P P A+      P +   ++T +Y  Q  ++  +L +  GE+ ALLG SG GK+T L
Sbjct: 20  DAGPAPAARR-----PGISFEDVTVAYRDQVVLNGFTLDVAAGEVVALLGPSGSGKTTAL 74

Query: 63  RMLAGFEQPSAGQIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLP 122
           R +AGF  P  G++ + G D++ +PP+ R I M+ Q YALFPH+ VEQN+AFGLK  + P
Sbjct: 75  RTVAGFTAPVRGRVGIGGRDVTGLPPHRRGIGMVVQQYALFPHLRVEQNVAFGLKAHRTP 134

Query: 123 KAEIASRVNEMLGLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDK 182
           +A++  RV E L +  M  +A+R P +LSGGQ+QRVALAR+LA RP++LLLDEP+ ALD 
Sbjct: 135 RAQVPGRVAEALEMTGMAGYARRYPRELSGGQQQRVALARALAIRPEVLLLDEPLSALDA 194

Query: 183 KLRDRMQLEVVDI-LERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHP 241
            LR  M  E+  +  E   V+ + VTHDQ EA+T+A RIA++   + V  G PE +Y  P
Sbjct: 195 GLRAGMLAELARLHRELPEVSILYVTHDQIEALTLADRIAVLRDARLVDCGTPERLYRRP 254

Query: 242 TTRYSAEFIGSVN---VFEGVLKERQEDGLVLDSPGLVHPLKVDADASVVDNVPVHVALR 298
              ++A F+G  N   V  G   +R   G      G V  L++ A        P  + +R
Sbjct: 255 ADAFTASFVGRANLLPVTAGQEPDRVVLGAATHRTGAVE-LRITAQDGFPAGSPALLCVR 313

Query: 299 PEKIMLCEEPPANGCNFAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPT 358
           P ++    E    G N   G V  + +LG      V L +G  ++A+L       +  P 
Sbjct: 314 PHQLRPATE---GGPNLLRGRVSDVQWLGSTHRVQVDLDAGPRVAAELSGL----RVPPA 366

Query: 359 WGDEVRLCWEVDSCVVL 375
            G+E+ L ++ +  V+L
Sbjct: 367 AGEELALGFDPEDGVLL 383


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: 390
Number of extensions: 16
Number of successful extensions: 2
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: 389
Length adjustment: 30
Effective length of query: 347
Effective length of database: 359
Effective search space:   124573
Effective search space used:   124573
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: 50 (23.9 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