GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Pseudomonas putida KT2440

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate PP_2426 PP_2426 coniferyl alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__Putida:PP_2426
          Length = 350

 Score =  333 bits (854), Expect = 4e-96
 Identities = 167/346 (48%), Positives = 237/346 (68%), Gaps = 7/346 (2%)

Query: 13  AFGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGH 72
           A G+AA+  T  L+P  F RR+    DV + +L+CGVCHSD H   N WG   YP++PGH
Sbjct: 4   AIGYAAQTPTSPLAPMTFQRRSPRPDDVAIDILYCGVCHSDIHQARNEWGIAVYPLMPGH 63

Query: 73  EIVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHC-ENTIDTYGS-IYFD 130
           EI+G VT VG KV   KVGD VG+GC+V SCR+CE+C  + E +C E    TY +    D
Sbjct: 64  EIIGRVTAVGDKVTAHKVGDLVGVGCMVDSCRTCEACAKDLEQYCLEGPTMTYATPDRVD 123

Query: 131 GTMTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVV 190
           G+ T GGYS ++V  EHF++R P  + L S AP+LCAGITTYSPLK++G+  PG KIG++
Sbjct: 124 GSNTMGGYSSSIVVSEHFVVRIPAGMDLPSAAPILCAGITTYSPLKHHGVG-PGHKIGIL 182

Query: 191 GLGGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDG 250
           G+GGLGH+ +K+AKA GA+VT+   S++K +EA  + GAD  ++++D EQM+ A    D 
Sbjct: 183 GMGGLGHMGIKLAKALGAEVTLFTRSQAKAEEA-RRQGADHVIVSTDAEQMRAAAGRFDF 241

Query: 251 IIDTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFE--LPVFSLLKGRKLLGGTINGGIKE 308
           ++DT+PV H L P  + LK +G  ++VG  E P +  L   +L+  R++L G++ GGI E
Sbjct: 242 LLDTIPVQHDLNPYLETLKFDGVHILVGLIE-PIDPALHAANLVMKRRVLAGSLIGGIAE 300

Query: 309 TQEMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDIA 354
           TQE+LDF A+H+I  D+E++ +  +N A ER++  DV+YRFVID+A
Sbjct: 301 TQEVLDFCAEHDIRCDIEMLDIRNINQAYERMIAGDVKYRFVIDMA 346


Lambda     K      H
   0.319    0.137    0.415 

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: 349
Number of extensions: 17
Number of successful extensions: 5
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: 365
Length of database: 350
Length adjustment: 29
Effective length of query: 336
Effective length of database: 321
Effective search space:   107856
Effective search space used:   107856
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 (21.7 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