GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Sulfuritalea hydrogenivorans DSM 22779

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_041096163.1 SUTH_RS00215 acyl-CoA dehydrogenase family protein

Query= reanno::acidovorax_3H11:Ac3H11_2991
         (396 letters)



>NCBI__GCF_000828635.1:WP_041096163.1
          Length = 388

 Score =  322 bits (826), Expect = 9e-93
 Identities = 167/365 (45%), Positives = 237/365 (64%), Gaps = 3/365 (0%)

Query: 28  FAQAEIAPRAADIDKSDQFPMDLWRKMGDLGVLGITVPEQYGGAAMGYLAHMVAMEEISR 87
           +AQ    P    +D  D FP D +R+MG++G+LG TVPE  GG  +  ++     E +S 
Sbjct: 23  YAQERHHPLLRRMDDDDWFPADEYRRMGEVGLLGTTVPESLGGPGLDLVSQFFIGEALSY 82

Query: 88  ASASVGLSYGAHSNLCVNQINRNGNEAQKAKYLSKLISGEHVGALAMSEPGAGSDVI-SM 146
            +  +G S+GA  NLCVN + RN +  Q+A++L +++SG  +GAL ++EPGAGSD + SM
Sbjct: 83  WNNMLGASWGASENLCVNNLVRNASAEQQARFLPRMLSG--IGALGLTEPGAGSDALGSM 140

Query: 147 KLKAEDKGGYYLLNGSKMWITNGPDADTLVVYAKTEPELGARGVTAFLIEKGMKGFSIAQ 206
           K  A   G +Y+LNG KM+ITNGP AD L+VYAKT PE G  G++AF++EKGM GFS+AQ
Sbjct: 141 KTSARRDGDHYVLNGRKMFITNGPVADLLLVYAKTTPERGQHGISAFVVEKGMPGFSVAQ 200

Query: 207 KLDKLGMRGSHTGELVFQDVEVPAENVLGGLNQGAKVLMSGLDYERAVLTGGPLGIMQSV 266
            L K+G RGS TGEL+F D  VPA N++GG ++G KV+MSGLD ER   +G  +GI Q  
Sbjct: 201 SLKKMGWRGSPTGELLFDDCRVPAANLIGGEDKGVKVVMSGLDIERVFFSGHVIGIAQRA 260

Query: 267 MDNVIPYIHDRKQFGQSIGEFQLIQGKVADMYTVLQAGRSFAYTVAKNLDMLGTDHVRQV 326
           +D  + Y   R QFGQ I  FQL+QG +ADMY  L++ R+F+Y + K +   G     ++
Sbjct: 261 LDLSLDYAKTRVQFGQPIAGFQLVQGMLADMYAALESVRAFSYQLLKEITAAGEAGRGEI 320

Query: 327 RKDCASVILWCAEKATWMAGEGVQIYGGNGYINEYPLGRLWRDAKLYEIGAGTSEIRRML 386
            K  A+ +L        +    VQI+GGNG++ E  +  L+R  KL EIGAGT+++R+++
Sbjct: 321 HKRSAAAVLHAGYMLKTVLDHAVQIHGGNGFMWETEVNCLYRAGKLIEIGAGTTQVRQLI 380

Query: 387 IGREL 391
           I  EL
Sbjct: 381 IAGEL 385


Lambda     K      H
   0.318    0.136    0.400 

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: 458
Number of extensions: 19
Number of successful extensions: 3
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: 396
Length of database: 388
Length adjustment: 31
Effective length of query: 365
Effective length of database: 357
Effective search space:   130305
Effective search space used:   130305
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 Apr 09 2024. 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