GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdB in Sinorhizobium meliloti 1021

Align 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (EC 1.2.4.4) (characterized)
to candidate SM_b20020 SM_b20020 pyruvate dehydrogenase E1 component, subunits alpha and beta

Query= reanno::Smeli:SMc03202
         (337 letters)



>FitnessBrowser__Smeli:SM_b20020
          Length = 692

 Score =  246 bits (627), Expect = 2e-69
 Identities = 140/337 (41%), Positives = 195/337 (57%), Gaps = 21/337 (6%)

Query: 3   RMTMIEAVRSAMDVSMARDDNVVVFGEDVGYFGGVFRCTQGLQAKYGKTRCFDTPISESG 62
           R+ M+ A+R  +D  M  +  VV+FGED+G  GGV   T GLQ K+G  R FDT +SE G
Sbjct: 373 RINMVTAIRRTLDHEMTVNQRVVLFGEDIGPKGGVHAVTLGLQEKFGTARVFDTSLSEEG 432

Query: 63  IVGTAIGMAAYGLKPCVEIQFADYMYPAYDQLTQEAARIRYRSNGDFTCPIVVRMPTGGG 122
           I+G A+GMA  GL P  EIQF  Y  PA +QL  +   IR+R++  F  PIVVRM  G  
Sbjct: 433 IIGRAVGMALAGLVPVPEIQFRKYAEPAIEQL-NDCGTIRWRTSNRFAAPIVVRMAGGFL 491

Query: 123 IFGGQTHSQSPEALFTHVCGLKVVVPSNPYDAKGLLISAIEDPDPVMFLEPKRLYNGPFD 182
             G   HSQ+ E  F H  G K+ VPSN  DA GLL +A+   DPV+F E + + + P  
Sbjct: 492 KCGDPWHSQTNEVAFVHQPGWKIAVPSNAEDAVGLLRTALRGNDPVIFFEHRAMLDHP-- 549

Query: 183 GHHERPVTAWSKHELGDVPDGHYTIPIGKAEIRRKGSGVTVIAYGTMVHVALAAAEETGI 242
                    W++      P   + +P GKA+  R+G  +T++ +G MV     AAE  GI
Sbjct: 550 ---------WARR---PYPGDAFALPFGKAKFTREGRDITIVTWGAMVPRCEEAAE--GI 595

Query: 243 DAEVIDLRSLLPLDLETIVQSAKKTGRCVVVHEATLTSGFGAELAALVQEHCFYHLESPV 302
            A+VIDLR+L+P D + ++ S ++T RC++VHE   T+GFGAE+AA V +  F  L++P+
Sbjct: 596 SADVIDLRTLMPWDRKAVIASVRRTRRCLIVHEDLATAGFGAEIAAAVADEAFIDLDAPI 655

Query: 303 VRLTGWDTPYPH---AQEWDYFPGPARVGRALAEAME 336
            RLT  D P PH     +W   P   R+ R + + +E
Sbjct: 656 SRLTMPDIPSPHNPALLDW-AVPSTERIRRKIIDLLE 691


Lambda     K      H
   0.321    0.138    0.424 

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: 611
Number of extensions: 32
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: 337
Length of database: 692
Length adjustment: 34
Effective length of query: 303
Effective length of database: 658
Effective search space:   199374
Effective search space used:   199374
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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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