GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Phaeobacter inhibens BS107

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate GFF1710 PGA1_c17340 acyl-CoA dehydrogenase AcdA

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2985
         (383 letters)



>FitnessBrowser__Phaeo:GFF1710
          Length = 381

 Score =  259 bits (663), Expect = 7e-74
 Identities = 152/378 (40%), Positives = 214/378 (56%), Gaps = 5/378 (1%)

Query: 3   DIELSEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDGLVAKMGELGLLGMVVPEEWGG 62
           D  L+EEQ  I DMA  F +  IAP A+ WE  G I   L  ++GELG   + V EE GG
Sbjct: 2   DFALTEEQTAIFDMAFAFGQEHIAPFARQWEAEGTIPKSLWPQIGELGFGALYVSEETGG 61

Query: 63  TYVDYVAYALAVEEISAGDGATGAFMSIHNSVGCGPVLN-YGSEEQKQTWLADLASGQVI 121
             +  +   L  E +S    +  AF+SIHN   C  +L+ + S+E K   + D+ S + +
Sbjct: 62  AGLSRLDATLVFEALSMACPSVAAFLSIHNM--CAKMLDSFASDEMKARIMPDILSMKTV 119

Query: 122 GCFCLTEPQAGSEAHNLRTRAELRDGQWVINGAKQFVSNGKRAKLAIVFAVTDPDLGKRG 181
             +CLTEP +GS+A  L+TRA   +  + +NG K F+S G  +  A V  V   + G +G
Sbjct: 120 LSYCLTEPGSGSDAAALKTRAAKTNEGYTLNGTKAFISGGGYSD-AYVCMVRSGEDGPKG 178

Query: 182 ISAFLVPTDTAGFIVDRTEHKMGIRASDTCAVTLNNCTIPEANLLGERGKGLAIALSNLE 241
           +S   V   TAG      E KMG ++  T  V  ++C IP ANL+GE GKG   A+  L+
Sbjct: 179 VSTVYVEDGTAGLSFGGLEEKMGWKSQPTAQVQFDDCKIPAANLVGEEGKGFTYAMKGLD 238

Query: 242 GGRIGIAAQALGIARAAFEAALAYSRDRVQFGKAINEHQSIANLLADMHMQLNAARLMIL 301
           GGR+ IA+ +LG A+ A    L Y  +R  FGK+I++ Q +   LADM ++L AAR+ + 
Sbjct: 239 GGRLNIASCSLGAAQQALTMTLQYMSERKAFGKSIDQFQGLQFRLADMEIELQAARVFLR 298

Query: 302 HAARLRTAGKPCLSE-ASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVEKYYRDARIT 360
            AA     G P  S+  + AK F +E   KV    +Q+HGGYGYL DY +EK  RD R+ 
Sbjct: 299 QAAWKLDQGAPDASKHCAMAKKFVTEAGSKVVDQCLQLHGGYGYLADYGIEKLVRDLRVH 358

Query: 361 QIYEGSSEIQRMVIAREL 378
           QI EG++EI R++ AR L
Sbjct: 359 QILEGTNEIMRVITARHL 376


Lambda     K      H
   0.319    0.134    0.393 

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: 348
Number of extensions: 19
Number of successful extensions: 4
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: 383
Length of database: 381
Length adjustment: 30
Effective length of query: 353
Effective length of database: 351
Effective search space:   123903
Effective search space used:   123903
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 (21.8 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