Aligments for a candidate for actP in Pseudomonas putida KT2440

GapMind for catabolism of small carbon sources

Aligments for a candidate for actP in Pseudomonas putida KT2440

Align Cation/acetate symporter ActP; Acetate permease; Acetate transporter ActP (characterized)
to candidate PP_1743 PP_1743 acetate permease

Query= SwissProt::P32705
         (549 letters)



>FitnessBrowser__Putida:PP_1743
          Length = 554

 Score =  851 bits (2199), Expect = 0.0
 Identities = 430/533 (80%), Positives = 473/533 (88%), Gaps = 1/533 (0%)

Query: 18  AADAISGAVERQPTNWQAIIMFLIFVVFTLGITYWASKRVRSRSDYYTAGGNITGFQNGL 77
           AADA++G V++QP N  AI MF+ FV FTLGITYWASKR +S SDYY AGG ITGFQNGL
Sbjct: 22  AADALTGEVQKQPLNVSAIAMFVAFVAFTLGITYWASKRNKSASDYYAAGGKITGFQNGL 81

Query: 78  AIAGDYMSAASFLGISALVFTSGYDGLIYSLGFLVGWPIILFLIAERLRNLGRYTFADVA 137
           AIAGDYMSAASFLGISALVFTSGYDGLIYS+GFLVGWPIILFLIAERLRNLG+YTFADVA
Sbjct: 82  AIAGDYMSAASFLGISALVFTSGYDGLIYSIGFLVGWPIILFLIAERLRNLGKYTFADVA 141

Query: 138 SYRLKQGPIRILSACGSLVVVALYLIAQMVGAGKLIELLFGLNYHIAVVLVGVLMMMYVL 197
           SYRL Q  IR LSA GSLVVVA YLIAQMVGAGKLIELLFGL+YH+AV+LVG+LM +YVL
Sbjct: 142 SYRLGQKEIRTLSASGSLVVVAFYLIAQMVGAGKLIELLFGLDYHVAVILVGILMCLYVL 201

Query: 198 FGGMLATTWVQIIKAVLLLFGASFMAFMVMKHVGFSFNNLFSEAMAVHPKGVDIMKPGGL 257
           FGGMLATTWVQIIKAVLLL GASFMA MVMKHVGF FN LFSEA+ VH KG  IM PGGL
Sbjct: 202 FGGMLATTWVQIIKAVLLLSGASFMALMVMKHVGFDFNTLFSEAIKVHAKGEAIMSPGGL 261

Query: 258 VKDPISALSLGLGLMFGTAGLPHILMRFFTVSDAREARKSVFYATGFMGYFYILTFIIGF 317
           VKDPISA SLGL LMFGTAGLPHILMRFFTVSDA+EARKSV YATGF+GYFYILTFIIGF
Sbjct: 262 VKDPISAFSLGLALMFGTAGLPHILMRFFTVSDAKEARKSVLYATGFIGYFYILTFIIGF 321

Query: 318 GAIMLVGANPEYKDAAGHLIGGNNMAAVHLANAVGGNLFLGFISAVAFATILAVVAGLTL 377
           GAI+LV  NPE+KDAAG L+GGNNMAAVHLANAVGG++FLGFISAVAFATILAVVAGLTL
Sbjct: 322 GAILLVSTNPEFKDAAGALLGGNNMAAVHLANAVGGSVFLGFISAVAFATILAVVAGLTL 381

Query: 378 AGASAVSHDLYANVFKKG-ATEREELRVSKITVLILGVIAIILGVLFENQNIAFMVGLAF 436
           AGASAVSHDLYA+V++KG A +++E+RVSKIT + LGV+AI LG+LFE QNIAFMVGLAF
Sbjct: 382 AGASAVSHDLYASVWRKGKANDKDEIRVSKITTVALGVLAIGLGILFEKQNIAFMVGLAF 441

Query: 437 AIAASCNFPIILLSMYWSKLTTRGAMMGGWLGLITAVVLMILGPTIWVQILGHEKAIFPY 496
           +IAASCNFP++LLSMYW KLTTRGAM+GGWLGL++AV LMILGPTIWVQILGHEK I+PY
Sbjct: 442 SIAASCNFPVLLLSMYWKKLTTRGAMIGGWLGLVSAVTLMILGPTIWVQILGHEKPIYPY 501

Query: 497 EYPALFSITVAFLGIWFFSATDNSAEGARERELFRAQFIRSQTGFGVEQGRAH 549
           EYPALFS+ +AF+ IWFFS TD S     ER LF  QF+RSQTG G     +H
Sbjct: 502 EYPALFSMAIAFVSIWFFSVTDKSKAAEDERALFFPQFVRSQTGLGASGAVSH 554


Lambda     K      H
   0.329    0.142    0.424 

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: 1033
Number of extensions: 44
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: 549
Length of database: 554
Length adjustment: 36
Effective length of query: 513
Effective length of database: 518
Effective search space:   265734
Effective search space used:   265734
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 53 (25.0 bits)

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

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources