GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dddA in Sphingomonas histidinilytica UM2

Align 3-hydroxypropanonate dehydrogenase (EC 1.1.1.59) (characterized)
to candidate WP_139385133.1 B5X82_RS18185 3-hydroxyisobutyrate dehydrogenase

Query= metacyc::MONOMER-18957
         (354 letters)



>NCBI__GCF_900167915.1:WP_139385133.1
          Length = 296

 Score =  127 bits (319), Expect = 4e-34
 Identities = 95/320 (29%), Positives = 155/320 (48%), Gaps = 36/320 (11%)

Query: 20  GFIGLGLMGQHMARHVYNQLEPSDKLYVYDVDPKHTTQFLTEVTSQTPQNAPLLTPLNSL 79
           GFIGLG MG  MA    N  +    +  +D+  +   + +                    
Sbjct: 5   GFIGLGNMGGGMAA---NLAKKGHDVRAFDLSKEAVDRAVAAGCVAAGS----------- 50

Query: 80  KDFTTEVDSQLDFIVTMVPEGKHVKSVVSELVGHYKSTGNYDPSIKTTFLDSSTIDIPTS 139
               +E     +++VTM+P G+HV++V       Y++            +D STID+ ++
Sbjct: 51  ---ASEAVKDAEYVVTMLPAGQHVRAV-------YENDVFGSAPASALLMDCSTIDVASA 100

Query: 140 RDVHQLVKSSIPEFDFIDTPVSGGVAGARKGTLSFML--SRETHDDIDPSLTALLSKMGI 197
           R V+    ++      +D PVSGG+A A  GTL+FM+  S E     +P    +L+ MG 
Sbjct: 101 RAVN--AAAAAQGLAMVDAPVSGGIAAANGGTLTFMVGGSAEHFARAEP----VLALMGK 154

Query: 198 NIFPCGATHGTGLAAKLANNYLLAITNIAAADSFQLAESFGLNLQNYAKLVAVSTGKSWA 257
            +   G   G+G AAK+ NN +L  T +A  ++F LA   GL+LQ +  + + ++G+SW+
Sbjct: 155 AVIHAGGA-GSGQAAKIVNNMILGATMVATCEAFALASKLGLDLQTFYDISSKASGQSWS 213

Query: 258 SVDNCPIPGVYPDNNLPSDVNYEGGFITKLTRKDVVLATESAKFNNRFLMLGDIGRHWYD 317
               CP+PGV P +  P+D +Y+GGF   L  KD+ LA E+A+     + +G      Y 
Sbjct: 214 MTSYCPVPGVGPQS--PADNDYQGGFAAGLMLKDLKLAVEAAQGVGASVPMGGHAESLY- 270

Query: 318 KACEREDIANRDLSVLFEWL 337
           +A      A +D S + + L
Sbjct: 271 QAFANLGGAGKDFSAIIKLL 290


Lambda     K      H
   0.317    0.134    0.392 

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: 218
Number of extensions: 8
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 354
Length of database: 296
Length adjustment: 28
Effective length of query: 326
Effective length of database: 268
Effective search space:    87368
Effective search space used:    87368
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 (21.6 bits)
S2: 48 (23.1 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