GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Rhizobium leguminosarum 3841

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_011654402.1 RL_RS29285 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2392
         (383 letters)



>NCBI__GCF_000009265.1:WP_011654402.1
          Length = 386

 Score =  234 bits (598), Expect = 2e-66
 Identities = 144/381 (37%), Positives = 211/381 (55%), Gaps = 13/381 (3%)

Query: 6   LSEDQRMIRDMARDFARREIAPHAQAWEKAGWID----DTLVAQMGELGLLGMVVPEEWG 61
           LSE+Q MI +  R F   EI PH    E++G +     D +  +  +LG      PEE G
Sbjct: 5   LSEEQEMIVETVRAFVETEIYPHENEVERSGIVPPELGDEIRRKCIDLGFYACNFPEEVG 64

Query: 62  GSYIDYVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGSQAQKDEWLTELASGRAI 121
           G+ +D+V + L   E+  G G+ G  +      G   +L      Q++ +L     G  I
Sbjct: 65  GAGLDHVTFTLVEREL--GRGSLGLTVFFGRPSG---ILMACEGEQRERYLLPAVRGEKI 119

Query: 122 GCFALTEPQAGSEAHNLRTRAELVDGHWVLNGSKQFCSNAKRSKLAIVFAVTDPELGKKG 181
              A+TEP AGS+   ++  A      +VLNG+K F S+A  +   IVFA T  E   KG
Sbjct: 120 DALAITEPDAGSDMRGMKCAARRDGSDFVLNGTKHFISHADVADFVIVFAATGEEETPKG 179

Query: 182 L----SAFLVPTDTPGFAVERSEHKMGIRASDTCGVSLSDCRIPEANLLGERGKGLAIAL 237
           +    +AFLV   TPGF + +    +  R      +S +DCRIP + +LGE  +G  IA 
Sbjct: 180 IKKKITAFLVDRGTPGFEILKGYDSVSHRGYHNSTLSFTDCRIPGSQVLGEVHRGFEIAN 239

Query: 238 SNLEGGRIGIGAQALGIARAAFEAALLYARERVQFGKPIAEHQSIANMLADMQTQLNAAR 297
             L G R+ + A  +G AR  F+  L YA ER QFGKPI  +Q ++  LADM T+++AA 
Sbjct: 240 QWLYGTRLTVAATCVGRARRVFDMTLPYAAERKQFGKPIGANQGVSFKLADMITEIDAAD 299

Query: 298 LLILHAARLKSAGLPCLSEASQAKLFASEMAEKVCSQAVQIHGGYGYLEDYPVERYYRDA 357
            L L AA    AGL    + + AKL++SEM  +V  +A+QI GG G ++D P+ R++RDA
Sbjct: 300 WLTLAAAWRLDAGLSADRQIASAKLYSSEMLARVTDEAIQIFGGMGLMDDLPLARFWRDA 359

Query: 358 RITQIYEGSSEIQRLLIAREL 378
           R+ +I++G+SEIQR +I+R+L
Sbjct: 360 RVERIWDGTSEIQRHIISRDL 380


Lambda     K      H
   0.318    0.133    0.390 

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: 331
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: 386
Length adjustment: 30
Effective length of query: 353
Effective length of database: 356
Effective search space:   125668
Effective search space used:   125668
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