GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Pseudomonas putida KT2440

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate PP_1018 PP_1018 mannose/glucose ABC transporter - ATP binding subunit

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__Putida:PP_1018
          Length = 384

 Score =  296 bits (758), Expect = 6e-85
 Identities = 163/361 (45%), Positives = 228/361 (63%), Gaps = 28/361 (7%)

Query: 1   MAGIKIDKINKFYGT--TQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSG 58
           MA +++  +NK YG+     L DI L I+DGEF++ VGPSGCGKSTL+  +AGLE ++ G
Sbjct: 1   MATLELRNVNKTYGSGLPDTLKDIQLSIKDGEFLILVGPSGCGKSTLMNCIAGLEQITGG 60

Query: 59  RIEIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAA 118
            I I  +DV+ + P DRD+AMVFQSYALYP M+VREN+EFG+K+         E +A  A
Sbjct: 61  AILIDEQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKLPQAAIDEEVARVA 120

Query: 119 RVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEG 178
           ++LQ+E  L RKP QLSGGQ+QRVA+GRA+ + P ++LFDEPLSNLDAKLRV+MR E++ 
Sbjct: 121 KLLQIEHLLARKPAQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180

Query: 179 LHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPA 238
           +H++L  T +YVTHDQ+EAMT+ DK+ V+  G I+Q G+P  +Y+ P ++FVA FIGSP 
Sbjct: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPQQIYNDPANQFVASFIGSPP 240

Query: 239 MNVFSSDVGLQD----------------------ISLDASAAFVGCRPEHIEI-VPDGDG 275
           MN     +  QD                       +L+     +G RPE I +   DG+G
Sbjct: 241 MNFIPVRLARQDGRLLALLDSGQARCELPLGEAADALEGREIILGIRPEQIALGAADGNG 300

Query: 276 --HIAATVHVKERLGGESLLYLGLKGGGQIVARVGGDDETKVGAAVSLRFSRHRLHQFDE 333
              I A V V E  G + L+++ L    ++  R+  D   +VG  ++L+F   R+  FD 
Sbjct: 301 LPAIRAEVQVTEPTGPDLLVFVTL-NQTKVCCRLAPDVACRVGDTLNLQFDPARVLLFDA 359

Query: 334 A 334
           A
Sbjct: 360 A 360


Lambda     K      H
   0.320    0.139    0.396 

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: 9
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: 338
Length of database: 384
Length adjustment: 29
Effective length of query: 309
Effective length of database: 355
Effective search space:   109695
Effective search space used:   109695
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.

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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