GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Trichodesmium erythraeum IMS101

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate WP_011612342.1 TERY_RS13460 spermidine/putrescine ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>NCBI__GCF_000014265.1:WP_011612342.1
          Length = 381

 Score =  298 bits (764), Expect = 1e-85
 Identities = 162/362 (44%), Positives = 234/362 (64%), Gaps = 8/362 (2%)

Query: 20  LEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQIMLD 79
           +E+R + K ++G  AV  V   I +GE F++LG SGCGK+T LR++AGFE PSAG+I++ 
Sbjct: 19  VELRKVFKVFEGHTAVKGVDFNIRQGEFFSILGPSGCGKTTTLRLIAGFETPSAGEIIIR 78

Query: 80  GVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLGLVHM 139
           G  +SQ P Y RP+N +FQSYALF H++V+ NIAFGL+  +L K E   +V + L LV M
Sbjct: 79  GQSMSQTPAYRRPVNTVFQSYALFNHLSVKDNIAFGLRIKRLGKTETEEKVAQALQLVKM 138

Query: 140 QEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDILERV 199
           ++FA R P+Q+SGGQ+QRVALAR+L  RP +LLLDEP+GALD KLR +MQ+E+ +I + +
Sbjct: 139 EKFADRYPNQISGGQQQRVALARALVNRPAVLLLDEPLGALDLKLRKQMQMELSNIHKDL 198

Query: 200 GVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVNVFEGV 259
           GVT VMVTHDQ+EAM+M+ RIA+M+ G+  QIG P+EIYE P + + A+FIG  N+F+G 
Sbjct: 199 GVTFVMVTHDQQEAMSMSDRIAVMHEGRIEQIGSPQEIYECPESPFVADFIGDTNLFQGC 258

Query: 260 LKERQEDGLVLDS-PGL---VHPLKVDA-DASVVDNVPVHVALRPEKIMLCEEPPANGCN 314
           ++      LV+ +  GL       KV+  +  +     V +++RPEK+ L   PP    N
Sbjct: 259 VEYNNNSSLVVKTDSGLNISAEYKKVNGKNGEIYGGTSVVLSVRPEKVNLSLYPPDVSEN 318

Query: 315 FAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRLCWEVDSCVV 374
              G + ++ Y+G    Y V L SG  +  +  N  R    LP     + + W   +C+ 
Sbjct: 319 CFEGRLRNVMYMGTHVHYQVNLLSGDQMMVRQPNTER---TLPNLDTPMYVYWSKQNCLA 375

Query: 375 LT 376
           L+
Sbjct: 376 LS 377


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: 333
Number of extensions: 13
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: 381
Length adjustment: 30
Effective length of query: 347
Effective length of database: 351
Effective search space:   121797
Effective search space used:   121797
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 Sep 24 2021. 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