GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Luteimonas huabeiensis HB2

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_024890485.1 Z164_RS0109600 acyl-CoA dehydrogenase

Query= reanno::Phaeo:GFF1011
         (386 letters)



>NCBI__GCF_000559025.1:WP_024890485.1
          Length = 382

 Score =  286 bits (731), Expect = 9e-82
 Identities = 160/376 (42%), Positives = 226/376 (60%), Gaps = 1/376 (0%)

Query: 6   MTFDLGEDVNALRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITVPEEFG 65
           M F   E+   ++D+  R AQER+ P A+  D+  EFP E  + +GE GL+GI VP E+G
Sbjct: 1   MEFGFSEEQLMIQDVARRIAQERIAPSAEAFDRSGEFPLENIRLLGENGLMGIEVPTEYG 60

Query: 66  GAGMSYLAHTVAVEEIARASASVSLSYGAHSNLCVNQIKLNGNAEQKAKYLPRLVSGEHV 125
           GAGM  +A+ +A+ EIA A A+ S     +++L  N I  +G   QK  Y+  +  G  +
Sbjct: 61  GAGMDPVAYVLAMVEIAAADAAHSTIMSVNNSLFCNGILTHGTEAQKQTYVRAIAEGREI 120

Query: 126 GALAMSEAGAGSDVVSMSLRAEKRND-HYRLNGNKYWITNGPDADTLVVYAKTDPDAGSK 184
           GA A++E  +GSD  SM  RA  + D  + +NG K WIT+GP A  +V++A TDP  G++
Sbjct: 121 GAFALTEPQSGSDATSMRCRAVAQADGSFVVNGKKSWITSGPVARYIVLFATTDPAQGAR 180

Query: 185 GMTAFLIEKEFKGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVLGEEGKGVRVLMSGL 244
           G+TAFL++ + +GF   +   KLG+R S T E+ F+D  V  + VLG+ G+G ++ MS L
Sbjct: 181 GITAFLVDTQREGFHRGKTEPKLGIRASATCEIEFQDYVVRADEVLGQPGQGFKIAMSVL 240

Query: 245 DYERVVLAGIGTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTARAYV 304
           D  R+ +A    GI  A  +  + Y+KERK FGQPIG FQ+ Q KIADM   ++ +    
Sbjct: 241 DAGRIGIASQAIGIARAAYEATIAYVKERKAFGQPIGAFQMTQAKIADMKCKLDASLLLT 300

Query: 305 YEVAKACDKGTVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRDAKLM 364
              A    +G     +A+   L ASE AM  AHQAVQ  GG GY  + PV R FRDAK+ 
Sbjct: 301 LRAAWLKRQGQRFTTEASVAKLTASEAAMWIAHQAVQIHGGMGYSKEMPVERYFRDAKIT 360

Query: 365 EIGAGTSEIRRMLIGR 380
           EI  GTSEI+R++I R
Sbjct: 361 EIYEGTSEIQRLVIAR 376


Lambda     K      H
   0.318    0.132    0.382 

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: 358
Number of extensions: 17
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: 386
Length of database: 382
Length adjustment: 30
Effective length of query: 356
Effective length of database: 352
Effective search space:   125312
Effective search space used:   125312
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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