GapMind for catabolism of small carbon sources

 

Aligments for a candidate for acdH in Herbaspirillum seropedicae SmR1

Align 2-methyl-branched-chain-enoyl-CoA reductase (EC 1.3.8.5) (characterized)
to candidate HSERO_RS04640 HSERO_RS04640 butyryl-CoA dehydrogenase

Query= reanno::acidovorax_3H11:Ac3H11_2996
         (376 letters)



>FitnessBrowser__HerbieS:HSERO_RS04640
          Length = 382

 Score =  496 bits (1277), Expect = e-145
 Identities = 239/376 (63%), Positives = 297/376 (78%)

Query: 1   MLLTQDQEMIRDAVRDFAQTELWPHAARWDKEHHFPKDAHQGLAALGAYGICVPEEFGGA 60
           MLL+ + EMIRDA+R FAQ  L P AA WD+ H FP +A + LA LGA G+CVPE++GGA
Sbjct: 1   MLLSPEHEMIRDAMRHFAQERLLPFAADWDRNHTFPAEALKELAELGAMGMCVPEQWGGA 60

Query: 61  NLDYLTLALVLEEIAAGDGGTSTAISVTNCPVNAILMRYGNAQQKRDWLTPLARGEMLGA 120
            +DY++L L LEEIAAGDG TST +SV N     I  +YG+  QK  WL PLARGEMLG 
Sbjct: 61  GMDYMSLVLALEEIAAGDGATSTIVSVQNSLACGITEKYGSPTQKEQWLKPLARGEMLGC 120

Query: 121 FCLTEPHVGSDASALRTTAVKQGDEYVINGVKQFITSGKNGQVAIVIAVTDKGAGKKGMS 180
           FCLTEPH GSDA+A+RT A + GD++++NG KQFITSGK+  VAIV AVTD+ AGKKG+S
Sbjct: 121 FCLTEPHTGSDAAAIRTRAERDGDDFILNGTKQFITSGKHAGVAIVFAVTDRSAGKKGIS 180

Query: 181 AFLVPTNNPGYVVARLEDKLGQHSSDTAQINFDNCRIPAENLIGAEGEGYKIALGALEGG 240
            FLVP + PG+VV R E+K+GQH+SDT QI  DNCR+PA  L+G EGEGY+IAL  LE G
Sbjct: 181 CFLVPCDTPGFVVGRSEEKMGQHASDTVQIMLDNCRVPATALLGKEGEGYRIALSNLEAG 240

Query: 241 RIGIAAQSVGMARSAFDAALAYSKERESFGTAIFNHQAVGFRLADCATQIEAARQLIWHA 300
           RIGIAAQSVGMAR+AF+AA++Y+++RESFG  I  HQAV FRLAD  T ++AAR ++W A
Sbjct: 241 RIGIAAQSVGMARAAFEAAVSYARQRESFGVPIIEHQAVNFRLADMNTLLDAARLMVWRA 300

Query: 301 AALRDAGKPCLKEAAMAKLFASEMAERVCSAAIQTLGGYGVVNDFPVERIYRDVRVCQIY 360
           A L+D G+PCLKEA+MAK+FASE AE++ S AIQ  GG G  +DFPVERIYRDVR+CQIY
Sbjct: 301 AQLKDQGRPCLKEASMAKMFASEAAEKIASDAIQIHGGVGYTSDFPVERIYRDVRICQIY 360

Query: 361 EGTSDVQKIIIQRALA 376
           EG +D+Q+++I RA+A
Sbjct: 361 EGANDIQRLVIGRAIA 376


Lambda     K      H
   0.319    0.134    0.396 

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: 457
Number of extensions: 11
Number of successful extensions: 1
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: 376
Length of database: 382
Length adjustment: 30
Effective length of query: 346
Effective length of database: 352
Effective search space:   121792
Effective search space used:   121792
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 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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