GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Caulobacter crescentus NA1000

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate CCNA_02254 CCNA_02254 isovaleryl-CoA dehydrogenase

Query= reanno::Smeli:SM_b21121
         (387 letters)



>FitnessBrowser__Caulo:CCNA_02254
          Length = 386

 Score =  543 bits (1398), Expect = e-159
 Identities = 271/381 (71%), Positives = 314/381 (82%), Gaps = 2/381 (0%)

Query: 2   FEAGLNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITAD 61
           F   ++FALGE  DA+R +  RFA+++IAP+A   D +N+FP  LW  MG+LGL GIT +
Sbjct: 5   FAPSMDFALGETADAIRETTARFAADKIAPIAAKIDETNSFPRELWVPMGDLGLHGITVE 64

Query: 62  EAHGGAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLIS 121
           E  GG GLGYL H VAMEE+SRASASVGLSYGAHSNLCVNQI R   P QK+RYLPKLIS
Sbjct: 65  EEFGGLGLGYLEHVVAMEEVSRASASVGLSYGAHSNLCVNQIRRWATPEQKARYLPKLIS 124

Query: 122 GEHVGALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAA 181
           GEHVG+LAMSE GAGSDVVSMKL+A++ GDRY+LNG+K WITN P AD LVVYAKT    
Sbjct: 125 GEHVGSLAMSEAGAGSDVVSMKLRAEQVGDRYILNGTKFWITNAPHADTLVVYAKT--GE 182

Query: 182 GPRGITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLM 241
           G RGITAF+VEK   GFS  +KLDK+GMRGS+T+EL+F DCE+PEENV+G VG GV VLM
Sbjct: 183 GSRGITAFIVEKGMKGFSVSKKLDKMGMRGSDTAELVFEDCEIPEENVMGPVGGGVGVLM 242

Query: 242 SGLDYERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAAR 301
           SGLDYER VL+AGPLGIM ACLDVV+PY+ +RKQFGQPIG FQLMQGK+ADMYV +N+AR
Sbjct: 243 SGLDYERAVLAAGPLGIMQACLDVVLPYVRDRKQFGQPIGSFQLMQGKIADMYVALNSAR 302

Query: 302 AYVYAVAAACDRGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDA 361
           AYVYAVA ACD G+T R DAAG IL A+E A  ++LEAIQALGG GYT ++P  RLLRDA
Sbjct: 303 AYVYAVAKACDAGKTTRFDAAGAILMASENAVKVSLEAIQALGGAGYTKEWPVERLLRDA 362

Query: 362 KLYEIGAGTSEIRRMLIGREL 382
           KLY+IGAGT+EIRR LIGREL
Sbjct: 363 KLYDIGAGTNEIRRFLIGREL 383


Lambda     K      H
   0.318    0.135    0.391 

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: 433
Number of extensions: 15
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: 387
Length of database: 386
Length adjustment: 30
Effective length of query: 357
Effective length of database: 356
Effective search space:   127092
Effective search space used:   127092
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 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