GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Pseudomonas putida KT2440

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate PP_3491 PP_3491 Enoly-coenzyme A hydratase/isomerase family protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2986
         (356 letters)



>FitnessBrowser__Putida:PP_3491
          Length = 357

 Score =  546 bits (1407), Expect = e-160
 Identities = 266/346 (76%), Positives = 294/346 (84%)

Query: 3   AMQNEVLAEVRNHIGHLTLNRPAGLNALTLDMVRNLHRQLDAWAQDSQVHAVVLRGAGEK 62
           A  + VLAEVRN IGHLTLNRPAGLNALTLDMVR+L + LD WA + QV AVVLRG G K
Sbjct: 9   AATDHVLAEVRNQIGHLTLNRPAGLNALTLDMVRSLRQHLDQWADNPQVRAVVLRGEGPK 68

Query: 63  AFCAGGDIRSLHDSFKSGDTLHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLVQ 122
            FCAGGDIRSL+DSFK+GDTLHE FFVEEYALDL IH YRKP+L +MDGF LGGGMGL Q
Sbjct: 69  GFCAGGDIRSLYDSFKAGDTLHETFFVEEYALDLVIHRYRKPILVVMDGFTLGGGMGLAQ 128

Query: 123 GADLRVVTEKSRLAMPEVGIGYFPDVGGSYFLSRIPGELGIYLGVSGVQIRAADALYCGL 182
           G DLRVVTE+SRL MPEVGIGYFPDVGGSYFLSR+PGELGIYLGVSG QI+AADALYCGL
Sbjct: 129 GCDLRVVTERSRLGMPEVGIGYFPDVGGSYFLSRLPGELGIYLGVSGAQIQAADALYCGL 188

Query: 183 ADWYLESGKLGVLDEKLDQLEWHDTPLKDLQGLLAKFAVQQLPDAPLATLRPAIDHFFAQ 242
           ADWYL S +L  LD+ LDQL++ D PLKDLQ LLA+   Q L DAPL  LRPAIDHFFA 
Sbjct: 189 ADWYLASDQLAALDQGLDQLDFSDHPLKDLQNLLARLGTQVLDDAPLEKLRPAIDHFFAL 248

Query: 243 PDVPSIVEQLRQVTVADSHEWAVTTADLLETRSPLAMAVTLEMLRRGRELPLEQCFALEL 302
           PD+P+IVEQLR V++ DSH WAV TAD LETRSPLAMAVTLEMLRRGREL ++ CFA+EL
Sbjct: 249 PDLPAIVEQLRAVSIGDSHAWAVATADQLETRSPLAMAVTLEMLRRGRELGIDDCFAMEL 308

Query: 303 HLDRQWFERGDLIEGVRALLIDKDKTPRWNPPTLQALDAEHVASFF 348
           HLDRQWF+ GD+IEGVRAL+IDKDK PRWNPPTL AL ++ V  FF
Sbjct: 309 HLDRQWFQHGDIIEGVRALIIDKDKQPRWNPPTLAALQSQRVEQFF 354


Lambda     K      H
   0.322    0.139    0.419 

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: 563
Number of extensions: 17
Number of successful extensions: 1
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: 356
Length of database: 357
Length adjustment: 29
Effective length of query: 327
Effective length of database: 328
Effective search space:   107256
Effective search space used:   107256
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 (21.9 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