GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolM in Sinorhizobium meliloti 1021

Align scyllo-inosose 3-dehydrogenase; 2-keto-myo-inositol dehydrogenase; EC 1.1.1.- (characterized)
to candidate SMc01214 SMc01214 zinc-containing alcohol dehydrogenase

Query= SwissProt::Q9WYP3
         (395 letters)



>FitnessBrowser__Smeli:SMc01214
          Length = 347

 Score =  150 bits (379), Expect = 5e-41
 Identities = 112/344 (32%), Positives = 175/344 (50%), Gaps = 38/344 (11%)

Query: 40  VRVEEVPEPRIEKPTEIIIKVKACGICGSDVHMAQTDEEGYILYPGLTGFPVTLGHEFSG 99
           VR   +PEP    P ++++KV+ACGICG+D H+   +      +P     PVTLGHEF G
Sbjct: 14  VRNVGIPEPG---PDDLLVKVEACGICGTDRHLLHGE------FPSTP--PVTLGHEFCG 62

Query: 100 VVVEAGPEAINRRTNKRFEIGEPVCAEEMLWCGHCRPCAEGFPNHCENLNELGFNVDGAF 159
           +VVEAG         +    G  +  +  + CG C  C  G  N C NL  +G + DG F
Sbjct: 63  IVVEAGSAV------RDIAPGARITGDPNISCGRCPQCQAGRVNLCRNLRAIGIHRDGGF 116

Query: 160 AEYVKVDAKYAWSLR-ELEGVYEGDRLFLAGSLVEPTSVAYNAVIVRGGGIRPGDNVVIL 218
           AEYV V  K A+ +   L+ V+        G+  EP +   + V +   GI+ G  V IL
Sbjct: 117 AEYVLVPRKQAFEIPLTLDPVH--------GAFCEPLACCLHGVDL--SGIKAGSTVAIL 166

Query: 219 GGGPIGLAAVAILKHAGASKVILSEPSEVRRNLAKELGADHVIDPTKENFVEAVLDYTNG 278
           GGG IGL  V + + AGA+ VILS     +R LA+E+GA   +DP+  + VEA+     G
Sbjct: 167 GGGVIGLLTVQLARLAGATTVILSTRQATKRRLAEEVGATATVDPSAGDVVEAIAGPV-G 225

Query: 279 L---GAKLFLEATGVPQLVWPQIEEVIWRARGINATVAIVARADAKIPLTGEVFQVRRAQ 335
           L   G  + +E  GV + V       + +A G    + ++ + + K+ +       R  +
Sbjct: 226 LVPGGVDVVIECAGVAETVKQSTR--LAKAGGTVVILGVLPQGE-KVEIEPFDILFRELR 282

Query: 336 IVGSQGHSGHGTFPRVISLMASG-MDMTKIISKTVSMEEIPEYI 378
           ++GS          R   L+A+G +++ ++IS+ +S++E P+ I
Sbjct: 283 VLGS--FINPFVHRRAADLVATGAIEIDRMISRRISLDEAPDVI 324


Lambda     K      H
   0.319    0.138    0.418 

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: 345
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: 395
Length of database: 347
Length adjustment: 30
Effective length of query: 365
Effective length of database: 317
Effective search space:   115705
Effective search space used:   115705
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 (21.7 bits)
S2: 49 (23.5 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:

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