GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Coprobacter fastidiosus NSB1

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_022389822.1 NSB1T_RS15660 acyl-CoA dehydrogenase family protein

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



>NCBI__GCF_000473955.1:WP_022389822.1
          Length = 568

 Score =  185 bits (470), Expect = 2e-51
 Identities = 118/358 (32%), Positives = 190/358 (53%), Gaps = 37/358 (10%)

Query: 50  GLLGMVVPEEWGGTYVDYVAYALAVEEISAGDGATGAFMSIHNSVGCGPVL-NYGSEEQK 108
           GL+G+ +P  + G     V Y +A + +S  D     F++I     C   +  + SEEQK
Sbjct: 102 GLMGISIPRRYNGLNFSLVPYIMAADMVSRADAG---FVNIWGLQDCAETIYEFASEEQK 158

Query: 109 QTWLADLASGQVIGCFCLTEPQAGSEAHNLRTRAEL--RDGQWVINGAKQFVSNGKRAKL 166
           Q +L  + +G+ +    LTEP AGS+   +  +A    +DG W +NG K+F++NG    +
Sbjct: 159 QKYLPRVCAGETMA-MDLTEPDAGSDLQAVMLKATYSEKDGCWYLNGVKRFITNGD-GHI 216

Query: 167 AIVFAVTDPDLGK-RGISAFLVPTDTAGFIVDRTEHKMGIRASDTCAVTLNNCTIPEANL 225
           A+V A ++      RG+S F+   +  G  V R E+KMGI+ S TC +   N    +A L
Sbjct: 217 ALVLARSEEGTKDGRGLSMFIYDKNDGGVTVRRIENKMGIKGSPTCELVFKNA---KAEL 273

Query: 226 LGERGKGLA-IALSNLEGGRIGIAAQALGIARAAFEAALAYSRDRVQFGKAINEHQSIAN 284
            G+R  GL    ++ + G R+GIAAQ++G++ AA+  AL Y+++R QFGKAI E  ++  
Sbjct: 274 CGDRKMGLIKYVMALMNGARLGIAAQSVGVSEAAYREALTYAQERRQFGKAIIEFPAVYE 333

Query: 285 LLADMHMQLNAARLMILHAARL--------------------RTAGKPCLSEASQAKLFA 324
           +L+ M  +L+A+R ++    R                     R   K    +A      A
Sbjct: 334 MLSLMKAKLDASRSLLYETTRFVDMYKVYEDISKERKLEKEERDEMKKYQRQADAFTPLA 393

Query: 325 SEMAEKVCS----SAIQIHGGYGYLEDYPVEKYYRDARITQIYEGSSEIQRMVIAREL 378
             M+ + C+      +QIHGG G+++DY  E+ YRDARIT IYEG++++Q +   R +
Sbjct: 394 KGMSSEFCNQNAYDCVQIHGGSGFMKDYACERIYRDARITSIYEGTTQLQVVAAIRHV 451


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: 419
Number of extensions: 15
Number of successful extensions: 5
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: 568
Length adjustment: 33
Effective length of query: 350
Effective length of database: 535
Effective search space:   187250
Effective search space used:   187250
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: 51 (24.3 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